Sistema OPTIMA XR200/220amx
Manual de Pre – Instalación
Manual de Instalación
Optima XR200amx Manual del Operador (Ingles)
Optima XR220amx Manual del Operador (Ingles)
Manual de Esquemáticos
Optima XR200amx Actualización Digital OM (Ingles)
Optima XR200amx Conformidad DICOM
Manual con partes ilustradas
Optima XR220amx Conformidad DICOM
EMC Estatuto de Conformidad
Estatuto IHE
Especificaciones del Tubo de Rayos X
Check List PM (EN) Check List PM (ES-LA) Check List PM (PT-BR)
CAPITULO 1 – Introducción
Sección 1 – Visión en Conjunto
Esta declaración de integración de IHE describe la conformidad prevista de
este producto de GE con el IHE Marco técnico. El Marco Técnico de IHE define
un subconjunto de funcional componentes de la empresa de salud, llamados
IHE Actors, y especifica sus interacciones en términos de un conjunto de
transacciones coordinadas basadas en estándares. Estas transacciones están
organizadas en unidades funcionales llamadas perfiles de integración que
destacan su capacidad para abordar necesariamente.
Los usuarios familiarizados con estos conceptos pueden usar Declaraciones de
integración como una ayuda para determinar qué nivel de integración que este
producto admite con otros sistemas y qué beneficios clínicos y operativos tal
integración podría proporcionar.
Otras declaraciones de integración de GE, así como más información sobre IHE
se pueden encontrar en Internet en:
ge.com/ihe
Sección 2 – Observaciones Importantes
El uso de estas Declaraciones de integración IHE, por sí solo, no es suficiente
para garantizar que la interoperación sea exitosa.
El usuario debe proceder con precaución y asegurarse de que la integración
de un sistema calificado (como la proporcionada por los Servicios
profesionales de TI de GE) aborde al menos cuatro problemas:
- Integración: la integración de cualquier sistema en un departamento o
empresa integrada requiere un análisis de los requisitos de las
aplicaciones. El diseño de una solución que integra Los sistemas GE con
sistemas no GE son responsabilidad del usuario y no deben ser
subestimado Se debe tener especial cuidado al definir el flujo de trabajo
esperado, el condiciones especiales, y la práctica clínica a ser apoyada
para asegurar un seguro y efectivo operación.
- Validación: prueba del rango completo de posibles interacciones entre
cualquier sistema de GE y el sistema no GE, antes de que la integración
se declare operativa, no debe pasarse por alto. Por lo tanto, el usuario
debe asegurarse de que cualquier proveedor que no sea GE acepte la
plena responsabilidad de todos validación requerida para su conexión
con los sistemas de GE. Esto incluye la precisión del datos una vez que
ha cruzado la interfaz y la estabilidad de los datos para las aplicaciones
previstas. Tal validación es necesaria antes de realizar cualquier uso
clínico (diagnóstico y / o tratamiento).
- Evolución futura: GE entiende que el Marco Técnico de IHE y el los
estándares de comunicación evolucionarán para cumplir con los
crecientes requisitos del usuario. GE está activamente involucrado en el
desarrollo del Marco Técnico de IHE y los estándares subyacentes. Tales
evoluciones pueden requerir cambios en los sistemas ya instalados.
Además, GE se reserva el derecho de descontinuar o hacer cambios a las
características del producto, incluidas las reflejadas por esta Declaración
de integración de IHE. El usuario debe asegurarse de que cualquier
sistema no GE que se conecta con los sistemas de GE también planifica
la evolución futura de IHE. No hacerlo es probable como resultado la
pérdida de función y / o conectividad a medida que evolucionan los
perfiles de IHE Integration y GE Los productos se han mejorado para
admitir estos cambios.
Optima XR200amx / XR220amx
Manual de Pre-Instalación
Warning
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR
SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X
représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement
X entraîne des dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les
personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour ellesmêmes. Avant chaque manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se
renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique,
Annales 26: Recommandations de la Commission Internationale sure la Protection Radiologique et les normes
nationales en vigueur.
WARNING
X-RAY EQUIPMENT IS DANGEROUS TO BOTH PATIENT AND OPERATOR UNLESS MEASURES OF
PROTECTION ARE STRICTLY OBSERVED.
Though this equipment is built to the highest standards of electrical and mechanical safety, the useful x-ray beam
becomes a source of danger in the hands of the unauthorized or unqualified operator. Excessive exposure to x-radiation
causes damage to human tissue.
Therefore, adequate precautions must be taken to prevent unauthorized or unqualified persons from operating this
equipment or exposing themselves or others to its radiation.
Before operation, persons qualified and authorized to operate this equipment should be familiar with the
Recommendations of the International Commission on Radiological Protection (ICRP), contained in Annals Number 26
of the ICRP, and with applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS
NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro
al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede
causar daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o
no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán
informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales
No 26: Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE
GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den
Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte
Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden
Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen
Kommission für Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für
Strahlenschutz und anderer nationaler Normenbehörden.
Page 2
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Important information
WARNING
(EN)
ПРЕДУПРЕЖДЕНИЕ
(BG)
警告
(ZH-CN)
警告
(ZH-HK)
警告
(ZH-TW)
This service manual is available in English only.
•
If a customer's service provider requires a language other than English, it is the customer's
responsibility to provide translation services.
•
Do not attempt to service the equipment unless this service manual has been consulted and is
understood.
•
Failure to heed this warning may result in injury to the service provider, operator or patient from
electric shock, mechanical or other hazards.
Tова упътване за работа е налично само на английски език.
•
Ако доставчикът на услугата на клиента изиска друг език, задължение на клиента е да
осигури превод.
•
Не използвайте оборудването, преди да сте се консултирали и разбрали упътването за
работа.
•
неспазването на това предупреждение може да доведе до нараняване на доставчика на
услугата, оператора или пациентa в резултат на токов удар, механична или друга опасност.
本维修手册仅提供英文版本。
•
•
•
如果客户的维修服务人员需要非英文版本，则客户需自行提供翻译服务。
未详细阅读和完全理解本维修手册之前，不得进行维修。
忽略本警告可能对维修服务人员、操作人员或患者造成电击、机械伤害或其他形式的伤
害。
本服務手冊僅提供英文版本。
• 倘若客戶的服務供應商需要英文以外之服務手冊，客戶有責任提供翻譯服務。
• 除非已參閱本服務手冊及明白其內容，否則切勿嘗試維修設備。
• 不遵從本警告或會令服務供應商、網絡供應商或病人受到觸電、機械性或其他的危險。
本維修手冊僅有英文版。
• 若客戶的維修廠商需要英文版以外的語言，應由客戶自行提供翻譯服務。
• 請勿試圖維修本設備，除非 您已查閱並瞭解本維修手冊。
• 若未留意本警告，可能導致維修廠商、操作員或病患因觸電、機械或其他危險而受傷。
UPOZORENJE
(HR)
Ovaj servisni priručnik dostupan je na engleskom jeziku.
•
Ako davatelj usluge klijenta treba neki drugi jezik, klijent je dužan osigurati prijevod.
•
Ne pokušavajte servisirati opremu ako niste u potpunosti pročitali i razumjeli ovaj servisni
priručnik.
•
zanemarite li ovo upozorenje, može doći do ozljede davatelja usluge, operatera ili pacijenta uslijed
strujnog udara, mehaničkih ili drugih rizika.
VÝSTRAHA
(CS)
Tento provozní návod existuje pouze v anglickém jazyce.
• V případě, že externí služba zákazníkům potřebuje návod v jiném jazyce, je zajištění překladu do
odpovídajícího jazyka úkolem zákazníka.
• Nesnažte se o údržbu tohoto zařízení, aniž byste si přečetli tento provozní návod a pochopili jeho
obsah.
• V případě nedodržování této výstrahy může dojít k poranění pracovníka prodejního servisu,
obslužného personálu nebo pacientů vlivem elektrického proudu, respektive vlivem mechanických
či jiných rizik.
Denne servicemanual findes kun på engelsk.
• Hvis en kundes tekniker har brug for et andet sprog end engelsk, er det kundens ansvar at sørge
for oversættelse.
• Forsøg ikke at servicere udstyret uden at læse og forstå denne servicemanual.
• Manglende overholdelse af denne advarsel kan medføre skade på grund af elektrisk stød,
mekanisk eller anden fare for teknikeren, operatøren eller patienten.
ADVARSEL
(DA)
Important Information
Page 3
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
WAARSCHUWING
(NL)
HOIATUS
(ET)
VAROITUS
(FI)
ATTENTION
(FR)
WARNUNG
(DE)
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ
(EL)
FIGYELMEZTETÉS
(HU)
AÐVÖRUN
(IS)
Page 4
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.
• Als het onderhoudspersoneel een andere taal vereist, dan is de klant verantwoordelijk voor de
vertaling ervan.
• Probeer de apparatuur niet te onderhouden alvorens deze onderhoudshandleiding werd
geraadpleegd en begrepen is.
• Indien deze waarschuwing niet wordt opgevolgd, zou het onderhoudspersoneel, de operator of
een patiënt gewond kunnen raken als gevolg van een elektrische schok, mechanische of andere
gevaren.
See teenindusjuhend on saadaval ainult inglise keeles
• Kui klienditeeninduse osutaja nõuab juhendit inglise keelest erinevas keeles, vastutab klient
tõlketeenuse osutamise eest.
• Ärge üritage seadmeid teenindada enne eelnevalt käesoleva teenindusjuhendiga tutvumist ja
sellest aru saamist.
• Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja, operaatori või patsiendi vigastamist
elektrilöögi, mehaanilise või muu ohu tagajärjel.
Tämä huolto-ohje on saatavilla vain englanniksi.
• Jos asiakkaan huoltohenkilöstö vaatii muuta kuin englanninkielistä materiaalia, tarvittavan
käännöksen hankkiminen on asiakkaan vastuulla.
• Älä yritä korjata laitteistoa ennen kuin olet varmasti lukenut ja ymmärtänyt tämän huolto-ohjeen.
• Mikäli tätä varoitusta ei noudateta, seurauksena voi olla huoltohenkilöstön, laitteiston käyttäjän tai
potilaan vahingoittuminen sähköiskun, mekaanisen vian tai muun vaaratilanteen vuoksi.
Ce manuel d’installation et de maintenance est disponible uniquement en anglais.
• Si le technicien d'un client a besoin de ce manuel dans une langue autre que l'anglais, il incombe
au client de le faire traduire.
• Ne pas tenter d'intervenir sur les équipements tant que ce manuel d’installation et de maintenance
n'a pas été consulté et compris.
• Le non-respect de cet avertissement peut entraîner chez le technicien, l'opérateur ou le patient
des blessures dues à des dangers électriques, mécaniques ou autres.
Diese Serviceanleitung existiert nur in englischer Sprache.
• Falls ein fremder Kundendienst eine andere Sprache benötigt, ist es Aufgabe des Kunden für eine
entsprechende Übersetzung zu sorgen.
• Versuchen Sie nicht diese Anlage zu warten, ohne diese Serviceanleitung gelesen und
verstanden zu haben.
• Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des Kundendiensttechnikers, des
Bedieners oder des Patienten durch Stromschläge, mechanische oder sonstige Gefahren
kommen.
Το παρόν εγχειρίδιο σέρβις διατίθεται μόνο στα αγγλικά.
• Εάν ο τεχνικός σέρβις ενός πελάτη απαιτεί το παρόν εγχειρίδιο σε γλώσσα εκτός των αγγλικών,
αποτελεί ευθύνη του πελάτη να παρέχει τις υπηρεσίες μετάφρασης.
• Μην επιχειρήσετε την εκτέλεση εργασιών σέρβις στον εξοπλισμό αν δεν έχετε συμβουλευτεί και
κατανοήσει το παρόν εγχειρίδιο σέρβις.
• Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί τραυματισμός στον τεχνικό
σέρβις, στο χειριστή ή στον ασθενή από ηλεκτροπληξία, μηχανικούς ή άλλους κινδύνους.
Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.
• Ha a vevő szolgáltatója angoltól eltérő nyelvre tart igényt, akkor a vevő felelőssége a fordítás
elkészíttetése.
• Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási kézikönyvben leírtakat nem
értelmezték.
• Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető vagy a beteg áramütés,
mechanikai vagy egyéb veszélyhelyzet miatti sérülését eredményezheti.
Þessi þjónustuhandbók er aðeins fáanleg á ensku.
• Ef að þjónustuveitandi viðskiptamanns þarfnast annas tungumáls en ensku, er það skylda
viðskiptamanns að skaffa tungumálaþjónustu.
• Reynið ekki að afgreiða tækið nema að þessi þjónustuhandbók hefur verið skoðuð og skilin.
• Brot á sinna þessari aðvörun getur leitt til meiðsla á þjónustuveitanda, stjórnanda eða sjúklings frá
raflosti, vélrænu eða öðrum áhættum.
Important Information
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
AVVERTENZA
(IT)
(JA)
경고
(KO)
BRÎDINÂJUMS
(LV)
ĮSPĖJIMAS
(LT)
ADVARSEL
(NO)
OSTRZEŻENIE
(PL)
AVISO
(PT-BR)
ATENÇÃO
(PT-PT)
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Il presente manuale di manutenzione è disponibile soltanto in lingua inglese.
• Se un addetto alla manutenzione richiede il manuale in una lingua diversa, il cliente è tenuto a
provvedere direttamente alla traduzione.
• Procedere alla manutenzione dell'apparecchiatura solo dopo aver consultato il presente manuale
ed averne compreso il contenuto.
• Il mancato rispetto della presente avvertenza potrebbe causare lesioni all'addetto alla
manutenzione, all'operatore o ai pazienti provocate da scosse elettriche, urti meccanici o altri
rischi.
このサービスマニュアルには英語版しかありません。
 サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業者の責任で行
うものとさせていただきます。
 このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでください。
この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、感電や機械
的又はその他の危険により負傷する可能性があります。
본 서비스 매뉴얼은 영어로만 이용하실 수 있습니다 .
• 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우 , 번역 서비스를 제공하는 것은 고객의
책임입니다 .
• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하려고 시도하지 마십시오 .
• 본 경고 사항에 유의하지 않으면 전기 쇼크 , 기계적 위험 , 또는 기타 위험으로 인해 서비스 제공자
, 사용자 또는 환자에게 부상을 입힐 수 있습니다 .
Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.
• Ja klienta apkopes sniedzējam nepieciešama informācija citā valodā, klienta pienākums ir
nodrošināt tulkojumu.
• Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas un saprašanas.
• Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas trieciena, mehānisku vai
citu faktoru izraisītu traumu risks apkopes sniedzējam, operatoram vai pacientam.
Šis eksploatavimo vadovas yra tik anglų kalba.
• Jei kliento paslaugų tiekėjas reikalauja vadovo kita kalba – ne anglų, suteikti vertimo paslaugas
privalo klientas.
• Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar nesupratote šio
eksploatavimo vadovo.
• Jei nepaisysite šio įspėjimo, galimi paslaugų tiekėjo, operatoriaus ar paciento sužalojimai dėl
elektros šoko, mechaninių ar kitų pavojų.
Denne servicehåndboken finnes bare på engelsk.
• Hvis kundens serviceleverandør har bruk for et annet språk, er det kundens ansvar å sørge for
oversettelse.
• Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest og forstått.
• Manglende hensyn til denne advarselen kan føre til at serviceleverandøren, operatøren eller
pasienten skades på grunn av elektrisk støt, mekaniske eller andre farer.
Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.
• Jeśli serwisant klienta wymaga języka innego niż angielski, zapewnienie usługi tłumaczenia jest
obowiązkiem klienta.
• Nie próbować serwisować urządzenia bez zapoznania się z niniejszym podręcznikiem
serwisowym i zrozumienia go.
• Niezastosowanie się do tego ostrzeżenia może doprowadzić do obrażeń serwisanta, operatora
lub pacjenta w wyniku porażenia prądem elektrycznym, zagrożenia mechanicznego bądź innego.
Este manual de assistência técnica encontra-se disponível unicamente em inglês.
•
Se outro serviço de assistência técnica solicitar a tradução deste manual, caberá ao cliente
fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
A não observância deste aviso pode ocasionar ferimentos no técnico, operador ou paciente
decorrentes de choques elétricos, mecânicos ou outros.
Este manual de assistência técnica só se encontra disponível em inglês.
•
Se qualquer outro serviço de assistência técnica solicitar este manual noutro idioma, é da
responsabilidade do cliente fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
O não cumprimento deste aviso pode colocar em perigo a segurança do técnico, do operador ou
do paciente devido a choques eléctricos, mecânicos ou outros.
Important Information
Page 5
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
ATENŢIE
(RO)
ОСТОРОЖНО!
(RU)
UPOZORENJE
(SR)
UPOZORNENIE
(SK)
ATENCION
(ES)
VARNING
(SV)
OPOZORILO
(SL)
DİKKAT
(TR)
Page 6
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Acest manual de service este disponibil doar în limba engleză.
•
Dacă un furnizor de servicii pentru clienţi necesită o altă limbă decât cea engleză, este de datoria
clientului să furnizeze o traducere.
•
Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi înţelegerii acestui manual de
service.
•
Ignorarea acestui avertisment ar putea duce la rănirea depanatorului, operatorului sau pacientului
în urma pericolelor de electrocutare, mecanice sau de altă natură.
Данное руководство по техническому обслуживанию представлено только на английском языке.
•
Если сервисному персоналу клиента необходимо руководство не на английском, а на
каком-то другом языке, клиенту следует самостоятельно обеспечить перевод.
•
Перед техническим обслуживанием оборудования обязательно обратитесь к данному
руководству и поймите изложенные в нем сведения.
•
Несоблюдение требований данного предупреждения может привести к тому, что
специалист по техобслуживанию, оператор или пациент получит удар электрическим током,
механическую травму или другое повреждение
Ovo servisno uputstvo je dostupno samo na engleskom jeziku.
•
Ako klijentov serviser zahteva neki drugi jezik, klijent je dužan da obezbedi prevodilačke usluge.
•
Ne pokušavajte da opravite uređaj ako niste pročitali i razumeli ovo servisno uputstvo.
•
Zanemarivanje ovog upozorenja može dovesti do povređivanja servisera, rukovaoca ili pacijenta
usled strujnog udara ili mehaničkih i drugih opasnosti.
Tento návod na obsluhu je k dispozícii len v angličtine.
•
Ak zákazníkov poskytovateľ služieb vyžaduje iný jazyk ako angličtinu, poskytnutie
prekladateľských služieb je zodpovednosťou zákazníka.
•
Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na obluhu a neporozumiete mu.
•
Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa služieb, obsluhujúcej
osoby alebo pacienta elektrickým prúdom, mechanické alebo iné ohrozenie.
Este manual de servicio sólo existe en inglés.
•
Si el encargado de mantenimiento de un cliente necesita un idioma que no sea el inglés, el cliente
deberá encargarse de la traducción del manual.
•
No se deberá dar servicio técnico al equipo, sin haber consultado y comprendido este manual de
servicio.
•
La no observancia del presente aviso puede dar lugar a que el proveedor de servicios, el
operador o el paciente sufran lesiones provocadas por causas eléctricas, mecánicas o de otra
naturaleza.
Den här servicehandboken finns bara tillgänglig på engelska. .
•
Om en kunds servicetekniker har behov av ett annat språk än engelska, ansvarar kunden för att
tillhandahålla översättningstjänster.
•
Försök inte utföra service på utrustningen om du inte har läst och förstår den här
servicehandboken.
•
Om du inte tar hänsyn till den här varningen kan det resultera i skador på serviceteknikern,
operatören eller patienten till följd av elektriska stötar, mekaniska faror eller andra faror.
Ta servisni priročnik je na voljo samo v angleškem jeziku.
•
Če ponudnik storitve stranke potrebuje priročnik v drugem jeziku, mora stranka zagotoviti prevod.
•
Ne poskušajte servisirati opreme, če tega priročnika niste v celoti prebrali in razumeli.
•
Če tega opozorila ne upoštevate, se lahko zaradi električnega udara, mehanskih ali drugih
nevarnosti poškoduje ponudnik storitev, operater ali bolnik.
Bu servis kılavuzunun sadece ingilizcesi mevcuttur.
•
Eğer müşteri teknisyeni bu kılavuzu ingilizce dışında bir başka lisandan talep ederse, bunu
tercüme ettirmek müşteriye düşer.
•
Servis kılavuzunu okuyup anlamadan ekipmanlara müdahale etmeyiniz.
•
Bu uyarıya uyulmaması, elektrik, mekanik veya diğer tehlikelerden dolayı teknisyen, operatör
veya hastanın yaralanmasına yol açabilir.
Important Information
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Legal notes
TRADEMARKS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2
are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of
their respective holders.
COPYRIGHTS
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material
presented and contained herein may not be reproduced in any form or manner, without the written
permission of General Electric Company, Inc.
Important Information
Page 7
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation
“damage in shipment” written on all copies of the freight or express bill before delivery is accepted
or “signed for” by a General Electric representative or a hospital receiving agent. Whether noted or
concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event,
within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this
14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and
MIS.” Contact your local service coordinator for more information on this process.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT
All electrical installations that are preliminary to positioning of the equipment at the site prepared for
the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds into
the Power Distribution Unit shall be performed by licensed electrical contractors. Other connections
between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE
Healthcare personnel. The products involved (and the accompanying electrical installations) are
highly sophisticated, and special engineering competence is required. In performing all electrical
work on these products, GE will use its own specially trained field engineers. All of GE’s electrical
work on these products will comply with the requirements of the applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to
perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein
contained should be thoroughly read and understood by everyone who will use the equipment
before you attempt to place this equipment in operation. GE Healthcare will be glad to assist and
cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the
useful beam, no practical design of equipment can provide complete protection. Nor can any
practical design compel the operator to take adequate precautions to prevent the possibility of any
persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully
acquainted with the recommendations of the National Council on Radiation Protection and
Measurements (NCRP) as published in NCRP Reports available from NCRP Publications, 7910
Woodmont Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission
on Radiation Protection, and take adequate steps to protect against injury.
The equipment is sold with the understanding that GE Healthcare, its agents, and representatives
have no responsibility for injury or damage which may result from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be
used.
Page 8
Important Information
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
LITHIUM BATTERY CAUTIONARY STATEMENT
DANGER - Risk of Explosion
Danger of explosion if battery is incorrectly replaced.
Replace only with the same or equivalent type recommended by the
manufacturer. Discard used batteries according to the manufacturer’s
instructions.
ATTENTION - Danger d’Explosion
Il y a danger d’explosion s’il y a replacement incorrect de la batterie.
Remplacer uniquement avec une batterie du même type ou d’un type
recommandé par le constructeur. Mettre au rébut les batteries
usagées conformément aux instructions du fabricant.
TECHNICAL MANUAL UPDATES
When operating or servicing GE Healthcare products, please contact your GE representative for
the latest revision of product documentation. Product documentation may also be available on-line
at the GE Healthcare support documentation library.
OMISSIONS AND ERRORS
Customers, please contact your GE Healthcare sales or service representatives.
GE personnel, please use the GE Healthcare complaint handling process to report all omissions,
errors, and defects in this publication.
Important Information
Page 9
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Revision history
Revision
Date
Reason for change
1
03AUG2011
Initial release of document
2
13SEP2012
Added text to front material on how to obtain most recent revisions of
technical manuals. Satisfies FDA recommendation.
3
03DEC2014
Chapter 1, Section 1.4.1, added additional height in the table of 178.8 cm
(70.4 in) for short column 220/200 systems. Updated Fig 1-2 with
additional height. Refer to ECO 2158872.
Chapter 1, Section 1.2, added Wireless Hand Switch (optional, Optima
XR220amx and Optima XR200amx) under "Shipped Separately". Refer
to ECO 2162103.
Chapter 1, Section 1.3.2, added customer’s responsibility for tablet
holder option.
Chapter 1, Section 1.6, added a item of tablet holder in the check off list.
Chapter 5, Section 5.2, added one column “FIPS ON Specification” in the
table 5-1: Access point and network specifications.
Chapter 5, Section 5.2, in the table 5-1: Access point and network
specifications, removed the specification of “FIPS 140-2, AES-256” in the
item of “Security protocol (Compliant with 802.11)”.
Chapter 6, Section 6.1.2, added “If FIPS is enabled” item in the list of
“Network infrastructure”. Removed “FIPS 140-2, AES-256” in the
checklist of “Wireless security”, Added “What is CA certificate?”/ “What is
Client certificate?”/“What is Private key file?”/ “What is Private key
password?” in the checklist of “Wireless security”.
Page 10
Important Information
Preface - PubliGE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Preface Publication Conventions
Standardized conventions for representing information is a uniform way of communicating
information to a reader in a consistent manner. Conventions are used so that the reader can easily
recognize the actions or decisions that must be made. There are a number of character and
paragraph styles used in this publication to accomplish this task. Please become familiar with them
before proceeding forward.
It is important that you read and understand hazard statements, and not just ignore them.
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and
style for safety communications reflected in this publication represents the harmonization of IEC/
ISO 3864 and ANSI Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential
hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify
important safety information. Text (Hazard) styles are applied to the paragraph contents that are
applicable to each specific safety statement.
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert
symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation
mark within it. It Is always used next to the signal word to indicate the severity of the hazard.
Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert
symbol and signal word are placed immediately before any paragraph they affect. Safety
information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Text Format of Signal Words
DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH, IF
NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS SIGNAL
WORD IS LIMITED TO THE MOST EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT
AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Caution - Indicates a potentially hazardous situation which, if not avoided, may result in
minor or moderate injury. It may also be used to alert against unsafe practices.
NOTICE - Indicates information or a company policy that relates directly or indirectly to the
safety of personnel or protection of property. This signal word is associated directly with a
hazard or hazardous situation and is used in place of 'DANGER,' 'WARNING,' or 'CAUTION.'
It can include:
•
Destruction of a disk drive
•
Potential for internal mechanical damage, such as to a X-ray tube
Publication Conventions
Page 11
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Symbols and Pictorials Used
The following Symbols and Pictorials are be used in this publication. These graphical icons
(symbols) may be used to make you aware of specific types of hazards that could possibly cause
harm.
Page 12
keep_up
magnetic
biohazard
compressgas
ppe-hearing
fragile
impact
corrosive
heavyobject
ppe-2people
static_elec
heat
general
laser
ppe-respitory
keep_dry
pinch
radiation
poisongas
ppe-loto
general
explosive
electrical
flammable
ppe-eye
torque
crush/mechanical
tipping
Read Manual
ppe-gloves
ce
instuction
poisonmatl
entanglement
instuction
Publication Conventions
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such
as Purpose, Example, Comment or Note) are used to identify important but non-safety related
information. Text styles are also applied to text within each paragraph modified by the specific
prefix.
EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:
Purpose: Introduces and provides meaning as to the information contained within the chapter,
section or subsection (such as used at the beginning this chapter, for example).
Note:
Example:
Comment:
Conveys information that should be considered important to the reader.
Used to make the reader aware that the paragraph(s) that follow are examples of information
possibly stated previously.
Represents “additional” information that may or may not be relevant to your situation.
Page Layout
Publication Part Number & Revision Number
The current section and its title
are always shown in the footer of
the left (even) page.
An exclamation point in a triangle is used
to indicate important information to the user.
Paragraphs preceeded by Alphanumeric
characters (e.g. numbers) contain information that must be followed in a specific order.
Publication Title
The current chapter and its title
are always shown in the footer of
the right (odd) page.
Paragraphs preceeded by a symbol
(e.g. bullets) contain information that
has no specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location.
The document part number and revision number appears in every header on every page. Odd
numbered page footers indicate the current chapter, its title and current page number. Even page
footers show the current section and its title, as well as the current page number.
Publication Conventions
Page 13
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text
that’s either screen input and output. Mono-spaced fonts, such courier, are used to indicated text
direction. When you type at your keyboard, you are generating computer input. Occasionally you
will see the math operator “greater-than” and “less-than” symbols used to indicate the start and
finish of variable output. When reading text generated by the computer, you are reading it as
computer generated output. In addition to direction, characters are italicized (e.g. italics) to indicate
information specific to your system or site.
Example: Fixed
Output
This paragraph’s font represents computer generated screen “fixed” output.
Its output is fixed from the sense that it does not vary from application
to application. It is the most commonly used style used to indicate
filenames, paths and text that do not change from system to system. The
character style used is a fixed width such as courier.
Example:
Variable Output
This paragraph’s font represents computer screen output that is
“variable”. It is used to represent output that varies from application
to application or system to system. Variable output is sometimes found
placed between greater-than and less-than operators for clarification. For
example: <variable_ouput> or <3.45.120.3>. In both cases, the < and >
operators are not part of the actual input.
Example: Fixed
Input
This paragraph’s font represents fixed input. It is computer input that
is typed-in via the keyboard. Typed input that does not vary from
application to application or system to system. Fixed text the user is
required to supply as input. For example: cd /usr/3p
Example:
Variable Input
This paragraph’s font represents computer input that can vary from
application to application or system to system. With variable text, the
user is required to supply system dependent input or information. Variable
input sometimes is placed between greater-than and less-than operators.
For example: <variable_input>. In these cases, the (<>) operators would
be dropped prior to input. For example: ypcat hosts | grep <3.45.120.3>
would be typed into the computer as:
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or
soft button, switch or key. Physical hardware, such as buttons and switches, are called hard keys
because they are hard wired or mechanical in nature. A keyboard or on/off switch would be a hard
key. Software or computer generated buttons are called soft keys because they are software
generated. Software driven menu buttons are an example of such keys. Soft and hard keys are
represented differently in this publication.
Example: Hard
Keys
A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style
that uses both over and under-lined bold text that is bold. This is a hard key.
Example: Soft
Keys
Whereas the computer MENU button that you would click with your mouse or touch with your hand
uses over and under-lined regular text. This is a soft key.
Page 14
Publication Conventions
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Table of contents
Chapter 1
General requirements .................................................................... 17
Section 1.1 Objectives and overview............................................................ 17
1.1.1
Pre-installation tasks ................................................................................................. 17
Section 1.2 System components and options ............................................. 18
Section 1.3 Customer responsibilities.......................................................... 19
1.3.1
1.3.2
Contract changes ...................................................................................................... 19
Responsibilities of the customer................................................................................ 19
Section 1.4 Delivery requirements ................................................................ 20
1.4.1 Product dimensions and weights...............................................................................
1.4.2 Shipping dimensions and weights .............................................................................
1.4.2.1 United States shipments ..................................................................................
1.4.2.2 International shipments ....................................................................................
1.4.3 Door size requirements .............................................................................................
1.4.3.1 System in crate ................................................................................................
1.4.3.2 System in normal use (not in crate) .................................................................
1.4.4 Minimum elevator depth requirements ......................................................................
20
22
22
23
23
23
23
24
Section 1.5 Product storage and handling requirements ........................... 24
Section 1.6 Pre-installation results ............................................................... 24
Chapter 2
Special construction requirements .............................................. 25
Section 2.1 Radiation protection................................................................... 25
Chapter 3
Environmental (HVAC) requirements .......................................... 27
Section 3.1 Relative humidity and temperature........................................... 27
Section 3.2 Altitude ........................................................................................ 27
3.2.1
Atmospheric pressure ............................................................................................... 28
Section 3.3 Heat output.................................................................................. 28
Section 3.4 Audible noise .............................................................................. 28
Chapter 4
Electrical requirements.................................................................. 29
Section 4.1 Power requirements ................................................................... 29
4.1.1
4.1.2
Chapter 5
Electrical requirements.............................................................................................. 29
Power consumption................................................................................................... 30
Communication requirements....................................................... 31
Section 5.1 Wired networks ........................................................................... 31
5.1.1
Network requirements ............................................................................................... 31
Table of Contents
Page 15
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Section 5.2 Wireless networks....................................................................... 31
5.2.1
Chapter 6
Access points and network capabilities .................................................................... 31
Network / workflow information.................................................... 33
Section 6.1 Network/workflow information................................................... 33
6.1.1
6.1.2
6.1.3
6.1.4
Page 16
Facility information....................................................................................................
Physical network.......................................................................................................
Workflow analysis .....................................................................................................
Remote host data .....................................................................................................
Table of Contents
33
33
36
37
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Chapter 1 General requirements
Section 1.1 Objectives and overview
This document is intended as a guide and informational resource for planning and properly
preparing a location for the installation of the Optima XR200amx/XR220amx system.
To avoid unnecessary expenses and delays, be sure to review all the information in this manual to
determine whether the site is ready for the installation to begin. This is an important process that
helps verify site readiness.
1.1.1 Pre-installation tasks
Pre-installation is a cooperative effort between the customer/purchaser and GE Healthcare. The
diagram below shows the pre-installation process.
Chapter 2 Special
construction requirements
Site data
collected from
field
Radiation
consultant
Chapter 3 Environmental
(HVAC) requirements
Site planning
Chapter 4 Electrical
requirements
Chapter 5 Communication
requirements
Chapter 6 Network /
workflow information
Pre-installation
site work
Planning and
site work
complete?
No
Yes
Delivery and
installation
Chapter 1 General requirements
Page 17
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Section 1.2 System components and options
Available components of the Optima XR200amx/Optima XR220amx system are listed below.
Shipped with the Optima XR200amx/Optima XR220amx system:
•
Optima XR200amx/Optima XR220amx
•
Backup tether for digital detector (Optima XR220amx only)
•
Service keyboard
•
Software CD
•
External CD/DVD-ROM drive
•
Operating System firmware USB drive
•
Tablet holder assembly (optional, Optima XR220amx and Optima XR200amx)
Shipped separately:
•
DAP meter (standard with Optima XR220amx, optional for Optima XR200amx)
•
Digital detector (Optima XR220amx only)
•
Detector batteries (Optima XR220amx only)
•
Detector battery charger (Optima XR220amx only)
•
6:1 grid (Optima XR220amx only)
•
Barcode reader (optional, Optima XR220amx only)
•
Wireless Hand Switch (optional, Optima XR220amx and Optima XR200amx)
Optima XR200amx
Figure 1-1 Optima systems
Page 18
Section 1.2 System components and options
Optima XR220amx
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Section 1.3 Customer responsibilities
1.3.1 Contract changes
The cost of any alterations or modifications not specified in the sales contract are the responsibility
of the customer.
1.3.2 Responsibilities of the customer
The customer is responsible for completing pre-installation activities. This includes procuring and
installing all required materials and services to prepare the site for installation. This responsibility
includes providing:
1.
A clean and safe work environment for installation of the product (finished floor, ceiling, walls,
and proper lighting).
2.
A secure location for storing loose items such as the service keyboard.
3.
A location suitable for charging the system and downloading images (Optima XR220amx
only). See Chapter 3 Environmental (HVAC) requirements.
4.
Electrical power of the required voltage. See Chapter 4 Electrical requirements.
5.
An Ethernet jack as described in Chapter 5 Communication requirements.
6.
If the Wireless Option is purchased, the wireless access point and wireless network
requirements described in Chapter 5 Communication requirements.
7.
If the tablet holder option is purchased, please check with customers the tablet is ready to
install.
Chapter 1 General requirements
Page 19
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Section 1.4 Delivery requirements
1.4.1 Product dimensions and weights
Components not listed are of negligible size and weight.
Product or
component
Optima XR200amx /
Optima XR220amx
Length
Width
Height
Weight
Ref.
404 kg (891 lb)
Figure 1-2
194.0 cm (76.4 in)
standard column
119.3 cm (47 in)
55.2 cm (21.7 in)
or
178.8 cm (70.4 in)
short column
FlashPadTM detector
(Optima XR220amx
or Optima
XR200amx with
digital upgrade)
58 cm (22.8 in)
45.2 cm (17.8 in)
2.7 cm (1.1 in)
4.5 kg (10 lb)
Figure 1-3
DAP (Optima
XR220amx or
Optima XR200amx
with digital upgrade)
146 mm (5.75 in)
198 mm (7.8 in)
45 mm (1.8 in)
0.5 kg (1.1 lb)
Figure 1-4
Barcode Reader
(option, for Optima
XR220amx or
Optima XR200amx
with digital upgrade)
42 mm (1.66 in)
19 mm (0.75 in)
125 mm (4.9 in)
85 g (3 oz)
Figure 1-5
Page 20
Section 1.4 Delivery requirements
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
552
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
Figure 1-2 System dimensions
Figure 1-3 FlashPadTM detector
Chapter 1 General requirements
Page 21
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Figure 1-4 DAP Meter
Figure 1-5 Barcode Reader
1.4.2 Shipping dimensions and weights
Prepare a clear path from the loading dock to the installation location. Consider the shipping
dimensions when reviewing door size, hallway width, corner angles, and elevator size.
Components not listed are of negligible size and weight.
1.4.2.1 United States shipments
Component
Length
Width
Height
Weight
119.4 cm (47 in)
63.5 cm (25 in)
198.2 cm (78 in)
404 kg (891 lb)
FlashPadTM detector
119.4 cm (47 in)
78.8 cm (31 in)
91.5 cm (36 in)
22.7 kg (50 lb)
DAP
250 mm (9.8 in)
450 mm (17.7 in)
120 mm (4.7 in)
<3 kg (<6.6 lbs)
Barcode Reader
250 mm (9.8 in)
450 mm (17.7 in)
120 mm (4.7 in)
<3 kg (<6.6 lbs
Optima XR200amx /
Optima XR220amx
Page 22
Section 1.4 Delivery requirements
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
1.4.2.2 International shipments
Component
Length
Width
Height
Weight
124.5 cm (49 in)
76.2 cm (30 in)
210.9 cm (83 in)
492 kg (1084 lb)
FlashPadTM detector
119.4 cm (47 in)
78.8 cm (31 in)
91.5 cm (36 in)
22.7 kg (50 lb)
DAP
250 mm (9.8 in)
450 mm (17.7 in)
120 mm (4.7 in)
<3 kg (<6.6 lbs)
Barcode Reader
250 mm (9.8 in)
450 mm (17.7 in)
120 mm (4.7 in)
<3 kg (<6.6 lbs)
Optima XR200amx /
Optima XR220amx
1.4.3 Door size requirements
Minimum door sizes also apply to hallways and elevators.
1.4.3.1 System in crate
To accommodate the system in a shipping crate, the minimum door width is 76 cm (30 in), and
the minimum door height is 211 cm (83 in).
1.4.3.2 System in normal use (not in crate)
To accommodate the system during normal use, the minimum door width is 61 cm (24 in), and the
minimum door height is 193 cm (76 in). See the room diagram in Figure 1-6.
1
114.8 cm
(45.2 in)
105 cm
(42 in)
2
55.9 cm
(22 in)
91.5 cm
(36 in)
ITEM
DESCRIPTION
1
Power cord, maximum extended length is 2.75 m (9 ft)
2
Ethernet cable
Figure 1-6 System room diagram
Chapter 1 General requirements
Page 23
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
1.4.4 Minimum elevator depth requirements
See 1.4.1 Product dimensions and weights and 1.4.2 Shipping dimensions and weights.
Section 1.5 Product storage and handling requirements
Refer to Chapter 3 Environmental (HVAC) requirements for temperature, humidity, and
atmospheric pressure requirements.
The maximum incline that the system can navigate is 7 degrees, and the maximum threshold height
over which the system can drive is 2.5 cm (1 in).
The system is not designed to travel over rough or bumpy ground. Take care when moving
the system to avoid sharp bumps, or steps larger than the 2.5 cm (1 in) threshold limit.
Section 1.6 Pre-installation results
After the pre-installation work is completed, you should be able to check off each of these items:
1.
Radiation physicist consulted about radiation protection
2.
Electrical service in place at the ratings specified
3.
Charging/downloading area size adequate for equipment
4.
Secure location to store loose items identified
5.
Network requirements met or exceeded
6.
If wireless option is purchased, wireless network capabilities met
7.
Network/workflow information collected
8.
IP addresses for DICOM and broadband identified
9.
Broadband access provided for InSite ExC connection
10. If tablet holder option is purchased, the tablet is ready to install.
Page 24
Section 1.5 Product storage and handling requirements










GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Chapter 2 Special construction requirements
Section 2.1 Radiation protection
Because X-ray equipment produces radiation, special precautions may need to be taken or special
site modifications may be required. GE Healthcare does not make recommendations regarding
radiation protection. It is the customer’s responsibility to ensure compliance with applicable laws
and regulations.
Chapter 2 Special construction requirements
Page 25
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
Page 26
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Section 2.1 Radiation protection
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Chapter 3 Environmental (HVAC)
requirements
Section 3.1 Relative humidity and temperature
Storage values refer only to equipment that is still in shipping containers. If the equipment is
partially or completely installed, refer to in-use values.
Ensure that the in-use and storage locations meet the temperature and humidity minimums and
maximums listed in Table 3-1.
Table 3-1 Environmental requirements - relative humidity and temperature
Relative humidity (non-condensing)
In-use
Temperature
Storage
In-use
Storage
Min.
Max.
Min.
Max.
Min.
Max.
Min.
Max.
30%
75%
25%
85%
10° C
(50° F)
35° C
(95° F)
-10° C
(14° F)
45° C
(113° F)
Ensure that the in-use and storage location conditions do not fluctuate more than the maximum
rates of change given in Table 3-2.
Table 3-2 Maximum rates of change for relative humidity and temperature
In-use
Storage
Temperature change
< 10° C (50° F)/hour
< 20° C (68° F)/hour
Humidity change
< 30%/hour
< 30%/hour
Section 3.2 Altitude
Storage values refer only to equipment that is still in shipping containers. If the equipment is
partially or completely installed, refer to in-use values.
Ensure that the in-use and storage locations meet the altitude minimums and maximums listed in
Table 3-3.
Table 3-3 Altitude requirements, relative to sea level
In-use
Storage
Min.
Max.
Min.
Max.
-30 m
3,000 m
-30 m
3,000 m
(-98.4 ft)
(9843 ft)
(-98.4 ft)
(9843 ft)
Chapter 3 Environmental (HVAC) requirements
Page 27
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
3.2.1 Atmospheric pressure
Ensure that the in-use and storage locations meet the atmospheric pressure minimums and
maximums listed in Table 3-4.
Table 3-4 Atmospheric pressure requirements
In-use
Storage
Min.
Max.
Min.
Max.
70.1 kPa
106 kPa
70.1 kPa
106 kPa
Ensure that the in-use and storage location conditions do not fluctuate more than the maximum
rates of change given in Table 3-5.
Table 3-5 Atmospheric pressure change rate limits
In-use
Storage
< 1.8 kPa/hour
< 76 kPa/hour
Section 3.3 Heat output
Below are the maximum power and thermal values in summary form:
Table 3-6 Optima XR200amx/XR220amx heat output
State
Watts
BTU/hour
Idle
143
488
Drive
275
938
Charge
261
890
Expose
474
1616
Charge + Expose
611
2084
For reference, a tightly closed room of 3 m x 3 m (10 ft x 10 ft) with a 2.4 m (8 ft) ceiling would require
2100 BTU/hour to raise the temperature by 12.2°C (10°F).
Section 3.4 Audible noise
Noise limits assume that all system covers are installed, and assume background noise of 40 dBA.
Measurements are taken 1 m (3.3 ft) from the equipment. The in-use measurement is taken when
the unit is being driven. Tube rotor and exposure tone noise are not included in these
measurements.
Maximum operating noise generated by the equipment is listed in Table 3-7.
Table 3-7 Audible noise produced by the system
Page 28
In-use
Idle
Upper limit: 55 dBA
Upper limit: 50 dBA
Section 3.3 Heat output
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Chapter 4 Electrical requirements
The purpose of this chapter is to ensure that the product is properly powered and grounded, thus
ensuring the proper operation of the product installed. The information in this chapter should be
adhered to, unless there are written deviations approved by GE Healthcare.
This chapter gives the requirements for powering and grounding the system. If these power and
grounding instructions are not adhered to, proper operation cannot be guaranteed. Any cost
associated and found to be a result of non-conformity may be the responsibility of the institution
and/or their contractor.
Section 4.1 Power requirements
4.1.1 Electrical requirements
•
Customer-supplied electrical outlet (United States style; see Figure 4-1)
In regions that use an electrical plug other than the style used in the United States, the
installation process includes removing the electrical plug and replacing it with the appropriate
hospital-grade plug as dictated by local regulations. Detailed instructions are included in the
Optima XR200amx/Optima XR220amx Installation Manual.
•
System input voltage: 100 VAC or 120 VAC or 220/240 VAC
•
System input current (maximum input current during charging):
-
12 A at 110 V
-
7 A at 220 V
•
System input frequency: 50/60 Hz
•
Maximum 1 cycle in-rush current: 75 A peak
•
The system requires an AC outlet with a ground terminal.
Figure 4-1 Electrical outlet
Chapter 4 Electrical requirements
Page 29
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
4.1.2 Power consumption
Continuous and peak power consumption during use are not applicable for this system, because
power for use is drawn from the batteries (even if the system is connected to wall power).
Power consumption during battery charging (assuming the system is not being used during
charging) is as follows:
•
Draw is less than 1200 W from 100 VAC (50/60 Hz) power outlet.
•
Draw is less than 1300 W from 120 or 220/240 VAC (50/60 Hz) power outlet.
Typical charge time from empty to full is four hours. Charge time varies with the age of the batteries,
and whether the system is in use during charging.
Page 30
Section 4.1 Power requirements
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Chapter 5 Communication requirements
Section 5.1 Wired networks
Verify that the site’s network meets the specifications listed below, and gather the additional
information requested in 6.1.4 Remote host data on page 37.
Be sure to have this information on hand at installation.
5.1.1 Network requirements
Note:
For hardwire network connections DHCP and Static IP address assignment is supported.
The system is equipped with Ethernet hardware for facilities connectivity of HIS/RIS, service
diagnostics, and (for Optima XR220amx only) to transfer digital images.
It is the customer’s responsibility to provide the Ethernet connection in a location convenient for
image transfer (Optima XR220amx only) and remote InSite connectivity. A minimum data rate of
54Mb/s is required to prevent delays when transferring images. A data rate of 100Mb/sec provides
optimal performance.
The network connection must be 802.3-compliant 10/100/1000 Base-T Ethernet, and there must be
at least one RJ45 jack dedicated (for Static IP) to connect the new equipment on the LAN.
Section 5.2 Wireless networks
If the wireless option is purchased, verify that the site’s wireless network meets the specifications
listed below.
In a wireless network environment that has multiple types of wireless devices, it is highly
recommended that the site design the network to minimize disruption to Optima XR200amx/Optima
XR220amx systems. Consult with a professional wireless network company to ensure that these
requirements are met.
5.2.1 Access points and network capabilities
The wireless network and the access points communicating with the Optima XR200amx/Optima
XR220amx must comply with the Optima XR200amx/Optima XR220amx capabilities outlined in
Table 5-1.
Table 5-1 Access point and network specifications
Item
Certification
NO FIPS Specification
Wireless fidelity (Wi-fi)
FIPS ON Specification
Wireless fidelity (Wi-fi)
Wireless network
standard
•
IEEE 802.11a/b/g/n
•
IEEE 802.11a/b/g/n
Data rates
•
802.11b: 1, 2, 5.5, 11 Mbps
•
802.11b: 1, 2, 5.5, 11 Mbps
•
802.11a/g: 6, 9, 12, 18, 24, 36, 48, 54
Mbps
•
802.11a/g: 6, 9, 12, 18, 24, 36, 48, 54
Mbps
•
802.11n
•
802.11n
Chapter 5 Communication requirements
Page 31
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Table 5-1 Access point and network specifications
Item
Uplink
Wireless standards
NO FIPS Specification
Auto-sensing 802.3 10/100/1000 base-T
Ethernet
FIPS ON Specification
Auto-sensing 802.3 10/100/1000 base-T
Ethernet
•
802.11a/b/g/n
•
802.11a/b/g/n
•
802.11d (world-mode)
•
802.11d (world-mode)
Signal and noise
Minimum of -80 dBm signal in an
environment with -95 dBm noise
Minimum of -80 dBm signal in an
environment with -95 dBm noise
Security protocol
Encryption:
Encryption:
(Compliant with
802.11)
•
WEP 64 bit or 128 bit
•
WPATM-PSK (TKIP)
•
WPA2 -PSK (AES)
•
Management Frame Protection (MFP)
TM
•
WPA2TM-PSK (AES)
Authentication:
•
EAP-TLS
Authentication:
Frequency band and
operating channels
(If the installation
country is not listed,
check with the local
regulatory agency.)
•
LEAP
•
LEAP + WEP
•
LEAP + WPATM
•
EAP-PEAP/MSCHAPv2
•
EAP-TLS
•
EAP-TTLS/MSCHAPv2
•
EAP-FAST
•
EAP-SIM
•
PEAP-GTC
Americas (FCC):
Americas (FCC):
•
2.412 to 2.462 GHz; 11 channels
•
2.412 to 2.462 GHz; 11 channels
•
5.15 to 5.35, 5.725 to 5.825 GHz; 12
channels
•
5.15 to 5.35, 5.725 to 5.825 GHz; 12
channels
Europe (ETSI):
•
2.412 to 2.472 GHz; 13 channels
•
5.15 to 5.725 GHz; 19 channels
Japan (TELEC):
Compliance
Page 32
•
2.412 to 2.472 GHz; 13 channels
Orthogonal Frequency Division
Multiplexing (OFDM)
•
2.412 to 2.484 GHz; 14 channels
Complementary Code Keying (CCK)
•
5.15 to 5.25 GHz; 4 channels
Safety:
Safety:
•
UL 60950-1
•
UL 60950-1
•
CAN/CSA C22.2 No. 60950-1
•
CAN/CSA C22.2 No. 60950-1
•
IEC 60950-1
•
IEC 60950-1
•
EN 60950-1
•
EN 60950-1
Section 5.2 Wireless networks
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Chapter 6 Network / workflow information
Section 6.1 Network/workflow information
This section contains questions designed to elicit necessary information about DICOM equipment,
workflow, and dataflow. The information collected here is required for GE Healthcare employees to
install the equipment and to connect it to the site's wired and wireless networks.
6.1.1 Facility information
Name of facility: _______________________________________________________________
Workflow contact: ____________________________________ Phone: __________________
Wired network contact:________________________________
Phone: __________________
Wireless network contact:______________________________
Phone: __________________
DICOM device contact: ________________________________ Phone: __________________
Other contact: _______________________________________ Phone: __________________
6.1.2 Physical network
Network infrastructure
What wired networks and/or wireless uplinks does this facility use?
 Has 100/1000 Base-T installed
 Will have 100/1000 Base-T installed by this date:___________
 Has 10 Base-T installed
 Will have 10 Base-T installed by this date: ___________
 Has a different network installed: _____________________
 If FIPS is enabled: _____________________
 Does not have a network installed
Wireless network standards
What wireless network standard is the site using?
 IEEE 802.11a
 IEEE 802.11b/g
 IEEE 802.11n
Chapter 6 Network / workflow information
Page 33
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
What is the SSID for the wireless network?_____________________
Is the SSID broadcast?  Yes  No
Wireless security
What security protocol does the wireless network use?
 WEP 64 bit or 128 bit
 WPATM-PSK (TKIP)
 Management Frame Protection (MFP)
 LEAP
 LEAP + WEP
 EAP-PEAP/MSCHAPv2)
 EAP-TLS
 EAP-FAST
 EAP-SIM
 Other: _____________________
 WPA2TM-PSK (AES)
 LEAP + WPATM
 EAP-TTLS/MSCHAPv2
 PEAP-GTC
What is the wireless network key type?
 Hexadecimal
 ASCII
 N/A
For WEP security wireless networks, what is the key or key number? _____________________
For PSK security wireless networks, what is the pass phrase? _____________________
For EAP/PEAP security wireless networks:
What is the domain/user name? _____________________
What is the password? _____________________
What is CA certificate? (if required) _____________________
What is Client certificate? (if required) _____________________
What is Private key file? (if required) _____________________
What is Private key password? (if required) _____________________
IMPORTANT: If keys/passwords are not provided here, the holder of those keys/passwords must
be available at installation to provide the information.
What type of access control (filtering) does the facility use? _____________________________
Are there any additional requirements (MAC or IP filtering)? _____________________________
Does the facility use an authentication/RADIUS server?  Yes  No
If yes, provide the manufacturer and model: __________________________________________
Subnets
Is the network segmented using subnets?
 Yes  No
If the facility will place the Optima XR200amx/Optima XR220amx system on a subnet, list the
subnet mask and router IP:
Subnet mask: _ _ _ . _ _ _ . _ _ _ . _ _ _
Router IP: _ _ _ . _ _ _ . _ _ _ . _ _ _
Page 34
Section 6.1 Network/workflow information
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
If the Optima XR220amx system will be on a subnet, is the wireless network routed to a different
network for image viewing?
 Yes  No
IP addresses/names
At the facility, equipment IP addresses are:
 Static
 Acquired via DHCP
 Combination of both methods
Indicate the IP address that will be assigned to the Optima XR200amx/XR220amx system, if static
addresses are used at the site. (Some DICOM-compliant devices require a fixed IP for
authentication. If dynamic addresses are assigned, authentication may not be possible.)
Optima XR200amx/XR220amx IP address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The Optima XR200amx/XR220amx system uses the following IP addresses internally:
•
192.168.1.50
•
192.168.2.45
•
192.168.3.50
If the facility network uses 192.168.x.x, there will be a conflict. If this conflict occurs, contact a GE
Healthcare Service Representative to change the internal IP addresses used by the system.
The host name is the network's name for the Optima XR200amx/XR220amx system.
Optima XR200amx/XR220amx host name: _________________________
The Scheduled Station AE Title (Application Entity Title) is the name the HIS/RIS will use to send
worklist information to the Optima XR200amx/XR220amx system.
Scheduled Station AE Title: _________________________
Bandwidth/capacity
On average, images from the Optima XR220amx require 8.5 Mb per image. Be sure the network
bandwidth is sufficient.
Number of Optima XR220amx units in the facility: _____________________
Wireless network capacity
Number of access points in the area where Optima XR200amx/XR220amx will be used:
_____________
On average, access point utilization should not exceed 50% of its full capacity to support all wireless
devices. Is there sufficient RF coverage in all of the areas where Optima XR200amx/XR220amx will
be used?
 Yes  No
Does the network comply with QoS (Quality of Service) 802.1q?
 Yes  No
Chapter 6 Network / workflow information
Page 35
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
6.1.3 Workflow analysis
Patient data
When the patient arrives in the system room for the exam, how is the patient data entered into the
system?
 Manually typed
 Entered via barcode reader
Barcode format:______________
 Downloaded from HIS/RIS
How is the query structured? Check all that apply:
 By date
 By modality
 By patient information
 Other method - Please explain:
Patient schedule
In retrieving patient schedule information, how often is the query sent?:
 Once at the start of a shift
 Several times during a shift
 Before each patient
Image handling (Optima XR220amx only)
What percent of images acquired are reviewed via soft copy? ______%
What percent of images acquired are printed? ______%
After the diagnostic images are acquired, what is the facility’s default workflow? Pick one:
 Manually send
 Automatically push
Send/push to (pick all that apply):
 Review station(s)
 Archive system(s)
 Printer(s)
When images are configured for automatic push, what images should be sent to PACS/archive/
review stations?
 Raw
 Processed
 Raw and Processed
When images are printed, on what device is the print command originated? Pick all that apply:
 The system
 A review workstation
 A PACS system
How soon after the images are acquired is the first image quality check done?
Page 36
Section 6.1 Network/workflow information
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
 Before next image is shot
 Before patient leaves
 After patient leaves
When it comes to image quality, would the site prefer to:
 Consider all images good unless marked bad
 Consider all images bad unless marked good
6.1.4 Remote host data
The Optima XR200amx/XR220amx system allows configuration of one HIS/RIS server, one MPPS
server (Optima XR220amx only), multiple PACS/archive/review workstations (Optima XR220amx
only), and multiple printers (Optima XR220amx only). The host name of all the nodes configured on
the system should be unique within the system. Complete a Remote Host section below and include
a DICOM Compliance Statement for each device.
Remote host #___
Remote hosts are DICOM devices to which theOptima XR220amx or Optima XR200amx with digital
upgrade system can push an image. Remote hosts can be review workstations, archival devices,
or PACS.
This remote host is a:
 Review workstation
 Archival device
 PACS
 MPPS server
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The host name is the name that appears on the screen, that users will use to identify this device.
Host name: _________________________
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
DICOM supports a number of image types. Indicate if this device supports the DX and/or the CR
image types.
Image types supported:
Supports multi-framing:
 DX
 Yes
 CR
 No
The next four sections address the four services that remote host devices may offer. Each of the
services will have its own AE (application entity) title and port number. The AE title is the name given
to a service or application provided by a DICOM device. The port number is a logical designation
within the device. These pieces of information are available in the device's DICOM Conformance
Statement.
Being a remote host server allows the Optima XR220amx or Optima XR200amx with digital
upgrade system to push images to other devices.
Does the site plan to use this device as a remote host server?
 Yes
 No
If yes, provide: AE title: __________________________ Port number: ___________
Chapter 6 Network / workflow information
Page 37
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Being a query/retrieve service class provider allows the Optima XR220amx or Optima XR200amx
with digital upgrade system to query this device and retrieve images stored there.
 Yes
Query/retrieve?
 No
If yes, provide: Query/retrieve AE title:________________________ Port number:__________
The query/retrieve by study or patient controls how much the user is able to retrieve at one time.
For study, the user may retrieve studies, series, images. For patient, the user may retrieve all of the
study attributes plus a patient's entire image collection.
Query/retrieve by:
 Study
 Patient
A storage commitment provider confirms that images sent by the Optima XR220amx or Optima
XR200amx with digital upgrade system to an archival system were received and stored. This option
is available only when the Optima XR220amx or Optima XR200amx with digital upgrade system is
sending DX type images.
Storage commitment?
 Yes
 No
If yes, provide: Storage commitment AE title: ______________________ Port number:________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The MPPS server receives the messages sent by the Optima XR200amx or Optima XR200amx
with digital upgrade system. These messages consist of information such as when the exam started
and closed, how many images were acquired, dose information, etc. This information is then
updated on the facility’s scheduling system.
 Yes
MPPS server
 No
If yes, provide: AE title: _________________________ Port number:___________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Remote host #___
Remote hosts are DICOM devices to which theOptima XR220amx or Optima XR200amx with digital
upgrade system can push an image. Remote hosts can be review workstations, archival devices,
or PACS.
This remote host is a:
 Review workstation
 Archival device
 PACS
 MPPS server
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The host name is the name that appears on the screen, that users will use to identify this device.
Host name: _________________________
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
DICOM supports a number of image types. Indicate if this device supports the DX and/or the CR
image types.
Image types supported:
Page 38
 DX
 CR
Section 6.1 Network/workflow information
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
 Yes
Supports multi-framing:
 No
The next four sections address the four services that remote host devices may offer. Each of the
services will have its own AE (application entity) title and port number. The AE title is the name given
to a service or application provided by a DICOM device. The port number is a logical designation
within the device. These pieces of information are available in the device's DICOM Conformance
Statement.
Being a remote host server allows the Optima XR220amx or Optima XR200amx with digital
upgrade system to push images to other devices.
Does the site plan to use this device as a remote host server?
 Yes
 No
If yes, provide: AE title: __________________________ Port number: ___________
Being a query/retrieve service class provider allows the Optima XR220amx or Optima XR200amx
with digital upgrade system to query this device and retrieve images stored there.
 Yes
Query/retrieve?
 No
If yes, provide: Query/retrieve AE title:________________________ Port number:__________
The query/retrieve by study or patient controls how much the user is able to retrieve at one time.
For study, the user may retrieve studies, series, images. For patient, the user may retrieve all of the
study attributes plus a patient's entire image collection.
Query/retrieve by:
 Study
 Patient
A storage commitment provider confirms that images sent by the Optima XR220amx or Optima
XR200amx with digital upgrade system to an archival system were received and stored. This option
is available only when the Optima XR220amx or Optima XR200amx with digital upgrade system is
sending DX type images.
Storage commitment?
 Yes
 No
If yes, provide: Storage commitment AE title: ______________________ Port number:________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The MPPS server receives the messages sent by the Optima XR200amx or Optima XR200amx
with digital upgrade system. These messages consist of information such as when the exam started
and closed, how many images were acquired, dose information, etc. This information is then
updated on the facility’s scheduling system.
 Yes
MPPS server
 No
If yes, provide: AE title: _________________________ Port number:___________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Remote host #___
Remote hosts are DICOM devices to which theOptima XR220amx or Optima XR200amx with digital
upgrade system can push an image. Remote hosts can be review workstations, archival devices,
or PACS.
This remote host is a:
 Review workstation
 Archival device
 PACS
 MPPS server
Manufacturer/model: _________________________
Software/firmware version: _________________________
Chapter 6 Network / workflow information
Page 39
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The host name is the name that appears on the screen, that users will use to identify this device.
Host name: _________________________
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
DICOM supports a number of image types. Indicate if this device supports the DX and/or the CR
image types.
 DX
 Yes
Image types supported:
Supports multi-framing:
 CR
 No
The next four sections address the four services that remote host devices may offer. Each of the
services will have its own AE (application entity) title and port number. The AE title is the name given
to a service or application provided by a DICOM device. The port number is a logical designation
within the device. These pieces of information are available in the device's DICOM Conformance
Statement.
Being a remote host server allows the Optima XR220amx or Optima XR200amx with digital
upgrade system to push images to other devices.
Does the site plan to use this device as a remote host server?
 Yes
 No
If yes, provide: AE title: __________________________ Port number: ___________
Being a query/retrieve service class provider allows the Optima XR220amx or Optima XR200amx
with digital upgrade system to query this device and retrieve images stored there.
 Yes
Query/retrieve?
 No
If yes, provide: Query/retrieve AE title:________________________ Port number:__________
The query/retrieve by study or patient controls how much the user is able to retrieve at one time.
For study, the user may retrieve studies, series, images. For patient, the user may retrieve all of the
study attributes plus a patient's entire image collection.
Query/retrieve by:
 Study
 Patient
A storage commitment provider confirms that images sent by the Optima XR220amx or Optima
XR200amx with digital upgrade system to an archival system were received and stored. This option
is available only when the Optima XR220amx or Optima XR200amx with digital upgrade system is
sending DX type images.
Storage commitment?
 Yes
 No
If yes, provide: Storage commitment AE title: ______________________ Port number:________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The MPPS server receives the messages sent by the Optima XR200amx or Optima XR200amx
with digital upgrade system. These messages consist of information such as when the exam started
and closed, how many images were acquired, dose information, etc. This information is then
updated on the facility’s scheduling system.
MPPS server
 Yes
 No
If yes, provide: AE title: _________________________ Port number:___________
Page 40
Section 6.1 Network/workflow information
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Remote host #___
Remote hosts are DICOM devices to which theOptima XR220amx or Optima XR200amx with digital
upgrade system can push an image. Remote hosts can be review workstations, archival devices,
or PACS.
This remote host is a:
 Review workstation
 Archival device
 PACS
 MPPS server
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The host name is the name that appears on the screen, that users will use to identify this device.
Host name: _________________________
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
DICOM supports a number of image types. Indicate if this device supports the DX and/or the CR
image types.
 DX
 Yes
Image types supported:
Supports multi-framing:
 CR
 No
The next four sections address the four services that remote host devices may offer. Each of the
services will have its own AE (application entity) title and port number. The AE title is the name given
to a service or application provided by a DICOM device. The port number is a logical designation
within the device. These pieces of information are available in the device's DICOM Conformance
Statement.
Being a remote host server allows the Optima XR220amx or Optima XR200amx with digital
upgrade system to push images to other devices.
Does the site plan to use this device as a remote host server?
 Yes
 No
If yes, provide: AE title: __________________________ Port number: ___________
Being a query/retrieve service class provider allows the Optima XR220amx or Optima XR200amx
with digital upgrade system to query this device and retrieve images stored there.
 Yes
Query/retrieve?
 No
If yes, provide: Query/retrieve AE title:________________________ Port number:__________
The query/retrieve by study or patient controls how much the user is able to retrieve at one time.
For study, the user may retrieve studies, series, images. For patient, the user may retrieve all of the
study attributes plus a patient's entire image collection.
Query/retrieve by:
 Study
 Patient
A storage commitment provider confirms that images sent by the Optima XR220amx or Optima
XR200amx with digital upgrade system to an archival system were received and stored. This option
Chapter 6 Network / workflow information
Page 41
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
is available only when the Optima XR220amx or Optima XR200amx with digital upgrade system is
sending DX type images.
Storage commitment?
 Yes
 No
If yes, provide: Storage commitment AE title: ______________________ Port number:________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The MPPS server receives the messages sent by the Optima XR200amx or Optima XR200amx
with digital upgrade system. These messages consist of information such as when the exam started
and closed, how many images were acquired, dose information, etc. This information is then
updated on the facility’s scheduling system.
 Yes
MPPS server
 No
If yes, provide: AE title: _________________________ Port number:___________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Printer data
Printer #___
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Prints via spooler:
 Yes
 No
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Look in the DICOM compliance statement for the printer's AE title and port number.
Printer AE title:_________________________
Port number:_________________________
Printer #___
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Prints via spooler:
 Yes
 No
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Look in the DICOM compliance statement for the printer's AE title and port number.
Printer AE title:_________________________
Port number:_________________________
Page 42
Section 6.1 Network/workflow information
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
Printer #___
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Prints via spooler:
 Yes
 No
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Look in the DICOM compliance statement for the printer's AE title and port number.
Printer AE title:_________________________
Port number:_________________________
Printer #___
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Prints via spooler:
 Yes
 No
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Look in the DICOM compliance statement for the printer's AE title and port number.
Printer AE title:_________________________
Port number:_________________________
HIS/RIS data
Manufacturer/model: _______________________ Software/firmware version: ______________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level:
 1.0  2.0  3.0  Not DICOM compliant
Look in the DICOM Compliance Statement for the AE title and port number.
HIS/RIS AE title: _________________________ Port number: __________________
DX and/or CR image type support should also be in the device's DICOM Conformance Statement.
Image types supported:
 DX
 CR
Modality used for scheduling: ________________________
Chapter 6 Network / workflow information
Page 43
GE HEALTHCARE
DIRECTION 5336112-1EN, REVISION 3
Page 44
Section 6.1 Network/workflow information
OPTIMA XR200AMX/XR220AMX
PRE-INSTALLATION MANUAL
© 2011, General Electric Company.
GE Medical Systems, a General Electric Company, going to market as GE Healthcare.
3000 N. Grandview Boulevard
Waukesha, Wisconsin 53188
USA
www.gehealthcare.com
46
Front cover
GE Healthcare
Optima XR200amx/XR220amx
Installation Manual
Direction 5336113-1EN
Revision 10
GE HEALTHCARE
DIRECTION 5336113-1EN REVISION 10
Warning
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR
SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X
représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement
X entraîne des dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les
personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour ellesmêmes. Avant chaque manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se
renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique,
Annales 26: Recommandations de la Commission Internationale sure la Protection Radiologique et les normes
nationales en vigueur.
WARNING
X-RAY EQUIPMENT IS DANGEROUS TO BOTH PATIENT AND OPERATOR UNLESS MEASURES OF
PROTECTION ARE STRICTLY OBSERVED.
Though this equipment is built to the highest standards of electrical and mechanical safety, the useful x-ray beam
becomes a source of danger in the hands of the unauthorized or unqualified operator. Excessive exposure to x-radiation
causes damage to human tissue.
Therefore, adequate precautions must be taken to prevent unauthorized or unqualified persons from operating this
equipment or exposing themselves or others to its radiation.
Before operation, persons qualified and authorized to operate this equipment should be familiar with the
Recommendations of the International Commission on Radiological Protection (ICRP), contained in Annals Number 26
of the ICRP, and with applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS
NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro
al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede
causar daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o
no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán
informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales
No 26: Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE
GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den
Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte
Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden
Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen
Kommission für Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für
Strahlenschutz und anderer nationaler Normenbehörden.
Page 2
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Important information
WARNING
(EN)
ПРЕДУПРЕЖДЕНИЕ
(BG)
警告
(ZH-CN)
警告
(ZH-HK)
警告
(ZH-TW)
This service manual is available in English only.
•
If a customer's service provider requires a language other than English, it is the customer's
responsibility to provide translation services.
•
Do not attempt to service the equipment unless this service manual has been consulted and is
understood.
•
Failure to heed this warning may result in injury to the service provider, operator or patient from
electric shock, mechanical or other hazards.
Tова упътване за работа е налично само на английски език.
•
Ако доставчикът на услугата на клиента изиска друг език, задължение на клиента е да
осигури превод.
•
Не използвайте оборудването, преди да сте се консултирали и разбрали упътването за
работа.
•
неспазването на това предупреждение може да доведе до нараняване на доставчика на
услугата, оператора или пациентa в резултат на токов удар, механична или друга опасност.
本维修手册仅提供英文版本。
•
•
•
如果客户的维修服务人员需要非英文版本，则客户需自行提供翻译服务。
未详细阅读和完全理解本维修手册之前，不得进行维修。
忽略本警告可能对维修服务人员、操作人员或患者造成电击、机械伤害或其他形式的伤
害。
本服務手冊僅提供英文版本。
• 倘若客戶的服務供應商需要英文以外之服務手冊，客戶有責任提供翻譯服務。
• 除非已參閱本服務手冊及明白其內容，否則切勿嘗試維修設備。
• 不遵從本警告或會令服務供應商、網絡供應商或病人受到觸電、機械性或其他的危險。
本維修手冊僅有英文版。
• 若客戶的維修廠商需要英文版以外的語言，應由客戶自行提供翻譯服務。
• 請勿試圖維修本設備，除非 您已查閱並瞭解本維修手冊。
• 若未留意本警告，可能導致維修廠商、操作員或病患因觸電、機械或其他危險而受傷。
UPOZORENJE
(HR)
Ovaj servisni priručnik dostupan je na engleskom jeziku.
•
Ako davatelj usluge klijenta treba neki drugi jezik, klijent je dužan osigurati prijevod.
•
Ne pokušavajte servisirati opremu ako niste u potpunosti pročitali i razumjeli ovaj servisni
priručnik.
•
zanemarite li ovo upozorenje, može doći do ozljede davatelja usluge, operatera ili pacijenta uslijed
strujnog udara, mehaničkih ili drugih rizika.
VÝSTRAHA
(CS)
Tento provozní návod existuje pouze v anglickém jazyce.
• V případě, že externí služba zákazníkům potřebuje návod v jiném jazyce, je zajištění překladu do
odpovídajícího jazyka úkolem zákazníka.
• Nesnažte se o údržbu tohoto zařízení, aniž byste si přečetli tento provozní návod a pochopili jeho
obsah.
• V případě nedodržování této výstrahy může dojít k poranění pracovníka prodejního servisu,
obslužného personálu nebo pacientů vlivem elektrického proudu, respektive vlivem mechanických
či jiných rizik.
Denne servicemanual findes kun på engelsk.
• Hvis en kundes tekniker har brug for et andet sprog end engelsk, er det kundens ansvar at sørge
for oversættelse.
• Forsøg ikke at servicere udstyret uden at læse og forstå denne servicemanual.
• Manglende overholdelse af denne advarsel kan medføre skade på grund af elektrisk stød,
mekanisk eller anden fare for teknikeren, operatøren eller patienten.
ADVARSEL
(DA)
Preface
Page 3
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
WAARSCHUWING
(NL)
HOIATUS
(ET)
VAROITUS
(FI)
ATTENTION
(FR)
WARNUNG
(DE)
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ
(EL)
FIGYELMEZTETÉS
(HU)
AÐVÖRUN
(IS)
Page 4
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.
• Als het onderhoudspersoneel een andere taal vereist, dan is de klant verantwoordelijk voor de
vertaling ervan.
• Probeer de apparatuur niet te onderhouden alvorens deze onderhoudshandleiding werd
geraadpleegd en begrepen is.
• Indien deze waarschuwing niet wordt opgevolgd, zou het onderhoudspersoneel, de operator of
een patiënt gewond kunnen raken als gevolg van een elektrische schok, mechanische of andere
gevaren.
See teenindusjuhend on saadaval ainult inglise keeles
• Kui klienditeeninduse osutaja nõuab juhendit inglise keelest erinevas keeles, vastutab klient
tõlketeenuse osutamise eest.
• Ärge üritage seadmeid teenindada enne eelnevalt käesoleva teenindusjuhendiga tutvumist ja
sellest aru saamist.
• Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja, operaatori või patsiendi vigastamist
elektrilöögi, mehaanilise või muu ohu tagajärjel.
Tämä huolto-ohje on saatavilla vain englanniksi.
• Jos asiakkaan huoltohenkilöstö vaatii muuta kuin englanninkielistä materiaalia, tarvittavan
käännöksen hankkiminen on asiakkaan vastuulla.
• Älä yritä korjata laitteistoa ennen kuin olet varmasti lukenut ja ymmärtänyt tämän huolto-ohjeen.
• Mikäli tätä varoitusta ei noudateta, seurauksena voi olla huoltohenkilöstön, laitteiston käyttäjän tai
potilaan vahingoittuminen sähköiskun, mekaanisen vian tai muun vaaratilanteen vuoksi.
Ce manuel d’installation et de maintenance est disponible uniquement en anglais.
• Si le technicien d'un client a besoin de ce manuel dans une langue autre que l'anglais, il incombe
au client de le faire traduire.
• Ne pas tenter d'intervenir sur les équipements tant que ce manuel d’installation et de maintenance
n'a pas été consulté et compris.
• Le non-respect de cet avertissement peut entraîner chez le technicien, l'opérateur ou le patient
des blessures dues à des dangers électriques, mécaniques ou autres.
Diese Serviceanleitung existiert nur in englischer Sprache.
• Falls ein fremder Kundendienst eine andere Sprache benötigt, ist es Aufgabe des Kunden für eine
entsprechende Übersetzung zu sorgen.
• Versuchen Sie nicht diese Anlage zu warten, ohne diese Serviceanleitung gelesen und
verstanden zu haben.
• Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des Kundendiensttechnikers, des
Bedieners oder des Patienten durch Stromschläge, mechanische oder sonstige Gefahren
kommen.
Το παρόν εγχειρίδιο σέρβις διατίθεται μόνο στα αγγλικά.
• Εάν ο τεχνικός σέρβις ενός πελάτη απαιτεί το παρόν εγχειρίδιο σε γλώσσα εκτός των αγγλικών,
αποτελεί ευθύνη του πελάτη να παρέχει τις υπηρεσίες μετάφρασης.
• Μην επιχειρήσετε την εκτέλεση εργασιών σέρβις στον εξοπλισμό αν δεν έχετε συμβουλευτεί και
κατανοήσει το παρόν εγχειρίδιο σέρβις.
• Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί τραυματισμός στον τεχνικό
σέρβις, στο χειριστή ή στον ασθενή από ηλεκτροπληξία, μηχανικούς ή άλλους κινδύνους.
Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.
• Ha a vevő szolgáltatója angoltól eltérő nyelvre tart igényt, akkor a vevő felelőssége a fordítás
elkészíttetése.
• Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási kézikönyvben leírtakat nem
értelmezték.
• Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető vagy a beteg áramütés,
mechanikai vagy egyéb veszélyhelyzet miatti sérülését eredményezheti.
Þessi þjónustuhandbók er aðeins fáanleg á ensku.
• Ef að þjónustuveitandi viðskiptamanns þarfnast annas tungumáls en ensku, er það skylda
viðskiptamanns að skaffa tungumálaþjónustu.
• Reynið ekki að afgreiða tækið nema að þessi þjónustuhandbók hefur verið skoðuð og skilin.
• Brot á sinna þessari aðvörun getur leitt til meiðsla á þjónustuveitanda, stjórnanda eða sjúklings frá
raflosti, vélrænu eða öðrum áhættum.
Preface
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
AVVERTENZA
(IT)
(JA)
경고
(KO)
BRÎDINÂJUMS
(LV)
ĮSPĖJIMAS
(LT)
ADVARSEL
(NO)
OSTRZEŻENIE
(PL)
AVISO
(PT-BR)
ATENÇÃO
(PT-PT)
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Il presente manuale di manutenzione è disponibile soltanto in lingua inglese.
• Se un addetto alla manutenzione richiede il manuale in una lingua diversa, il cliente è tenuto a
provvedere direttamente alla traduzione.
• Procedere alla manutenzione dell'apparecchiatura solo dopo aver consultato il presente manuale
ed averne compreso il contenuto.
• Il mancato rispetto della presente avvertenza potrebbe causare lesioni all'addetto alla
manutenzione, all'operatore o ai pazienti provocate da scosse elettriche, urti meccanici o altri
rischi.
このサービスマニュアルには英語版しかありません。
 サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業者の責任で行
うものとさせていただきます。
 このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでください。
この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、感電や機械
的又はその他の危険により負傷する可能性があります。
본 서비스 매뉴얼은 영어로만 이용하실 수 있습니다 .
• 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우 , 번역 서비스를 제공하는 것은 고객의
책임입니다 .
• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하려고 시도하지 마십시오 .
• 본 경고 사항에 유의하지 않으면 전기 쇼크 , 기계적 위험 , 또는 기타 위험으로 인해 서비스 제공자
, 사용자 또는 환자에게 부상을 입힐 수 있습니다 .
Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.
• Ja klienta apkopes sniedzējam nepieciešama informācija citā valodā, klienta pienākums ir
nodrošināt tulkojumu.
• Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas un saprašanas.
• Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas trieciena, mehānisku vai
citu faktoru izraisītu traumu risks apkopes sniedzējam, operatoram vai pacientam.
Šis eksploatavimo vadovas yra tik anglų kalba.
• Jei kliento paslaugų tiekėjas reikalauja vadovo kita kalba – ne anglų, suteikti vertimo paslaugas
privalo klientas.
• Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar nesupratote šio
eksploatavimo vadovo.
• Jei nepaisysite šio įspėjimo, galimi paslaugų tiekėjo, operatoriaus ar paciento sužalojimai dėl
elektros šoko, mechaninių ar kitų pavojų.
Denne servicehåndboken finnes bare på engelsk.
• Hvis kundens serviceleverandør har bruk for et annet språk, er det kundens ansvar å sørge for
oversettelse.
• Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest og forstått.
• Manglende hensyn til denne advarselen kan føre til at serviceleverandøren, operatøren eller
pasienten skades på grunn av elektrisk støt, mekaniske eller andre farer.
Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.
• Jeśli serwisant klienta wymaga języka innego niż angielski, zapewnienie usługi tłumaczenia jest
obowiązkiem klienta.
• Nie próbować serwisować urządzenia bez zapoznania się z niniejszym podręcznikiem
serwisowym i zrozumienia go.
• Niezastosowanie się do tego ostrzeżenia może doprowadzić do obrażeń serwisanta, operatora
lub pacjenta w wyniku porażenia prądem elektrycznym, zagrożenia mechanicznego bądź innego.
Este manual de assistência técnica encontra-se disponível unicamente em inglês.
•
Se outro serviço de assistência técnica solicitar a tradução deste manual, caberá ao cliente
fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
A não observância deste aviso pode ocasionar ferimentos no técnico, operador ou paciente
decorrentes de choques elétricos, mecânicos ou outros.
Este manual de assistência técnica só se encontra disponível em inglês.
•
Se qualquer outro serviço de assistência técnica solicitar este manual noutro idioma, é da
responsabilidade do cliente fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
O não cumprimento deste aviso pode colocar em perigo a segurança do técnico, do operador ou
do paciente devido a choques eléctricos, mecânicos ou outros.
Preface
Page 5
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
ATENŢIE
(RO)
ОСТОРОЖНО!
(RU)
UPOZORENJE
(SR)
UPOZORNENIE
(SK)
ATENCION
(ES)
VARNING
(SV)
OPOZORILO
(SL)
DİKKAT
(TR)
Page 6
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Acest manual de service este disponibil doar în limba engleză.
•
Dacă un furnizor de servicii pentru clienţi necesită o altă limbă decât cea engleză, este de datoria
clientului să furnizeze o traducere.
•
Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi înţelegerii acestui manual de
service.
•
Ignorarea acestui avertisment ar putea duce la rănirea depanatorului, operatorului sau pacientului
în urma pericolelor de electrocutare, mecanice sau de altă natură.
Данное руководство по техническому обслуживанию представлено только на английском языке.
•
Если сервисному персоналу клиента необходимо руководство не на английском, а на
каком-то другом языке, клиенту следует самостоятельно обеспечить перевод.
•
Перед техническим обслуживанием оборудования обязательно обратитесь к данному
руководству и поймите изложенные в нем сведения.
•
Несоблюдение требований данного предупреждения может привести к тому, что
специалист по техобслуживанию, оператор или пациент получит удар электрическим током,
механическую травму или другое повреждение
Ovo servisno uputstvo je dostupno samo na engleskom jeziku.
•
Ako klijentov serviser zahteva neki drugi jezik, klijent je dužan da obezbedi prevodilačke usluge.
•
Ne pokušavajte da opravite uređaj ako niste pročitali i razumeli ovo servisno uputstvo.
•
Zanemarivanje ovog upozorenja može dovesti do povređivanja servisera, rukovaoca ili pacijenta
usled strujnog udara ili mehaničkih i drugih opasnosti.
Tento návod na obsluhu je k dispozícii len v angličtine.
•
Ak zákazníkov poskytovateľ služieb vyžaduje iný jazyk ako angličtinu, poskytnutie
prekladateľských služieb je zodpovednosťou zákazníka.
•
Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na obluhu a neporozumiete mu.
•
Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa služieb, obsluhujúcej
osoby alebo pacienta elektrickým prúdom, mechanické alebo iné ohrozenie.
Este manual de servicio sólo existe en inglés.
•
Si el encargado de mantenimiento de un cliente necesita un idioma que no sea el inglés, el cliente
deberá encargarse de la traducción del manual.
•
No se deberá dar servicio técnico al equipo, sin haber consultado y comprendido este manual de
servicio.
•
La no observancia del presente aviso puede dar lugar a que el proveedor de servicios, el
operador o el paciente sufran lesiones provocadas por causas eléctricas, mecánicas o de otra
naturaleza.
Den här servicehandboken finns bara tillgänglig på engelska. .
•
Om en kunds servicetekniker har behov av ett annat språk än engelska, ansvarar kunden för att
tillhandahålla översättningstjänster.
•
Försök inte utföra service på utrustningen om du inte har läst och förstår den här
servicehandboken.
•
Om du inte tar hänsyn till den här varningen kan det resultera i skador på serviceteknikern,
operatören eller patienten till följd av elektriska stötar, mekaniska faror eller andra faror.
Ta servisni priročnik je na voljo samo v angleškem jeziku.
•
Če ponudnik storitve stranke potrebuje priročnik v drugem jeziku, mora stranka zagotoviti prevod.
•
Ne poskušajte servisirati opreme, če tega priročnika niste v celoti prebrali in razumeli.
•
Če tega opozorila ne upoštevate, se lahko zaradi električnega udara, mehanskih ali drugih
nevarnosti poškoduje ponudnik storitev, operater ali bolnik.
Bu servis kılavuzunun sadece ingilizcesi mevcuttur.
•
Eğer müşteri teknisyeni bu kılavuzu ingilizce dışında bir başka lisandan talep ederse, bunu
tercüme ettirmek müşteriye düşer.
•
Servis kılavuzunu okuyup anlamadan ekipmanlara müdahale etmeyiniz.
•
Bu uyarıya uyulmaması, elektrik, mekanik veya diğer tehlikelerden dolayı teknisyen, operatör
veya hastanın yaralanmasına yol açabilir.
Preface
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Legal notes
TRADEMARKS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2
are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of
their respective holders.
COPYRIGHTS
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material
presented and contained herein may not be reproduced in any form or manner, without the written
permission of General Electric Company, Inc.
Preface
Page 7
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation
“damage in shipment” written on all copies of the freight or express bill before delivery is accepted
or “signed for” by a General Electric representative or a hospital receiving agent. Whether noted or
concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event,
within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this
14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and
MIS.” Contact your local service coordinator for more information on this process.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT
All electrical installations that are preliminary to positioning of the equipment at the site prepared
for the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds
into the Power Distribution Unit shall be performed by licensed electrical contractors. Other
connections between pieces of electrical equipment, calibrations and testing shall be performed by
qualified GE Healthcare personnel. The products involved (and the accompanying electrical
installations) are highly sophisticated, and special engineering competence is required. In
performing all electrical work on these products, GE will use its own specially trained field
engineers. All of GE’s electrical work on these products will comply with the requirements of the
applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to
perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein
contained should be thoroughly read and understood by everyone who will use the equipment
before you attempt to place this equipment in operation. GE Healthcare will be glad to assist and
cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the
useful beam, no practical design of equipment can provide complete protection. Nor can any
practical design compel the operator to take adequate precautions to prevent the possibility of any
persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully
acquainted with the recommendations of the National Council on Radiation Protection and
Measurements (NCRP) as published in NCRP Reports available from NCRP Publications, 7910
Woodmont Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission
on Radiation Protection, and take adequate steps to protect against injury.
The equipment is sold with the understanding that GE Healthcare, its agents, and representatives
have no responsibility for injury or damage which may result from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be
used.
Page 8
Preface
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
LITHIUM BATTERY CAUTIONARY STATEMENT
DANGER - Risk of Explosion
Danger of explosion if battery is incorrectly replaced.
Replace only with the same or equivalent type recommended by the
manufacturer. Discard used batteries according to the manufacturer’s
instructions.
ATTENTION - Danger d’Explosion
Il y a danger d’explosion s’il y a replacement incorrect de la batterie.
Remplacer uniquement avec une batterie du même type ou d’un type
recommandé par le constructeur. Mettre au rébut les batteries
usagées conformément aux instructions du fabricant.
TECHNICAL MANUAL UPDATES
When operating or servicing GE Healthcare products, please contact your GE representative for
the latest revision of product documentation. Product documentation may also be available on-line
at the GE Healthcare support documentation library.
OMISSIONS AND ERRORS
Customers, please contact your GE Healthcare sales or service representatives.
GE personnel, please use the GE Healthcare complaint handling process to report all omissions,
errors, and defects in this publication.
Preface
Page 9
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Revision history
Revision
Date
Reason for change
1
26SEP2011
Initial release of document.
2
26OCT2011
SPR HCSDM00103773 - Table 3-3 and Table 3-5 removing drive handle
SPR HCSDM00103774 - DAP installation
SPR HCSDM00103780 - Xray tube rating plate in wrong position
3
14NOV2011
Validation updates. Refer to SPRs: HCSDM00108057, HCSDM00108062,
HCSDM00108063, HCSDM00108064
4
17OCT2011
Validation updates. Refer to SPRs: HCSDM00109082 - Importing IP looks procedural
issue
5
28SEP2012
Updated Chapter 4, Section 4.2.6.1 - Adding certificates and Section 4.2.6.2 - Configuring
broadcast SSID networks per FMI 10861A (see PR#7646877).
In Chapter 3, Section 3.5.2.1, step 1, changed text from "External" to "Enclosure
Leakage". Changed text instances from "probe" to "clamp" in Chapter 3, Sections 3.5.2.1
(step 5), 3.5.2.2 (step 3), 3.5.2.3 (step 3), 3.5.3.4 (step 3) and 3.5.3.5 (step 3).
Added text to front material on how to obtain most recent revisions of technical manuals.
Satisfies FDA recommendation.
Added ’Detector firmware download’ procedure to Chapter 3, Section 3.6.4. Refer to SPR
HCSDM00157822.
6
02AUG2013
Chapter 3, Section 3.5.2, added Notice about potential test equipment damage. Refer to
HCSDM00188252.
Chapter 4, Sections 4.10.3.1 and 4.10.3.2, added Notice regarding reset of system after
DAP is reconnected. Refer to HCSDM00188256.
Chapter 3, Section 3.6.3, added Caution message regarding wall plug. Refer to
TrackWise 10831134.
7
12NOV2013
Chapter 4, Sections 4.10.3.1 and 4.10.3.2, added new steps 6 and 14 (respectively)
regarding DAP calibration reference to the System Manual. Refer to HCSDM00159583.
8
29APR2014
Chapter 2, Section 2.1, added Wireless Hand Switch (optional, Optima XR220amx and
Optima XR200amx) under "shipped separately". Refer to ECO 2162103.
Chapter 3, Section 3.5.1.5, changed bin measurement point in Table 3-3 to "Screw used
for mounting strain relief of wired handswitch cable". Changed picture for Fig 3-15 to show
new measurement point. Refer to ECO 2148874.
Chapter 4, Section 4.10.3, changed Figures 4-9 and 4-10 to show DAP meter in lower set
of collimator rails. Refer to HCSDM00264083.
Chapter 4, Section 4.10.3.2, added steps to remove cable cover and then put back on at
end of procedure. Refer to ECO 2160317.
Chapter 4, Section 4.10.4, added wireless exposure switch installation procedure. Refer
to ECO 2162103.
Page 10
Preface
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Revision
Date
9
03DEC2014
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Reason for change
Chapter 2, Section 2.1, added Tablet holder assembly (optional, Optima XR220amx and
Optima XR200amx) under “shipped with the Optima XR200amx/Optima XR220amx
system”.
Chapter 4, Section 4.2.6, added “FIPS ON” column in table 4-7 and table 4-8 for wireless
Authentication requirement.
Chapter 4, Section 4.8, Section 4.9, Section 4.13, added notes regarding consulting your
administrator for Account and Password information.
Chapter 4, Section 4.10.4, added tablet holder assembly installation procedure.
Chapter 8, added task regarding special login and user management account and
password creation to system administrator, added task regarding providing account and
password information to system administrator.
10
06FEB2015
Chapter 4, Section 10.4, revised Tablet holder installation procedure by following ECR/O
2186522
Preface
Page 11
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Page 12
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Preface
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Preface - Publica-
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Preface Publication Conventions
Standardized conventions for representing information is a uniform way of communicating
information to a reader in a consistent manner. Conventions are used so that the reader can easily
recognize the actions or decisions that must be made. There are a number of character and
paragraph styles used in this publication to accomplish this task. Please become familiar with them
before proceeding forward.
It is important that you read and understand hazard statements, and not just ignore them.
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and
style for safety communications reflected in this publication represents the harmonization of IEC/
ISO 3864 and ANSI Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential
hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify
important safety information. Text (Hazard) styles are applied to the paragraph contents that are
applicable to each specific safety statement.
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert
symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation
mark within it. It Is always used next to the signal word to indicate the severity of the hazard.
Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert
symbol and signal word are placed immediately before any paragraph they affect. Safety
information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Text Format of Signal Words
DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH, IF
NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS SIGNAL
WORD IS LIMITED TO THE MOST EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT
AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Caution - Indicates a potentially hazardous situation which, if not avoided, may result in
minor or moderate injury. It may also be used to alert against unsafe practices.
NOTICE - Indicates information or a company policy that relates directly or indirectly to the
safety of personnel or protection of property. This signal word is associated directly with a
hazard or hazardous situation and is used in place of 'DANGER,' 'WARNING,' or 'CAUTION.'
It can include:
Preface
Page 13
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
•
Destruction of a disk drive
•
Potential for internal mechanical damage, such as to a X-ray tube
Symbols and Pictorials Used
The following Symbols and Pictorials are be used in this publication. These graphical icons
(symbols) may be used to make you aware of specific types of hazards that could possibly cause
harm.
Page 14
keep_up
magnetic
biohazard
compressgas
ppe-hearing
fragile
impact
corrosive
heavyobject
ppe-2people
static_elec
heat
general
laser
ppe-respitory
keep_dry
pinch
radiation
poisongas
ppe-loto
general
explosive
electrical
flammable
ppe-eye
torque
crush/mechanical
tipping
Read Manual
ppe-gloves
ce
instuction
poisonmatl
entanglement
instuction
Preface
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such
as Purpose, Example, Comment or Note) are used to identify important but non-safety related
information. Text styles are also applied to text within each paragraph modified by the specific
prefix.
EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:
Purpose: Introduces and provides meaning as to the information contained within the chapter,
section or subsection (such as used at the beginning this chapter, for example).
Note:
Example:
Comment:
Conveys information that should be considered important to the reader.
Used to make the reader aware that the paragraph(s) that follow are examples of information
possibly stated previously.
Represents “additional” information that may or may not be relevant to your situation.
Page Layout
Publication Part Number & Revision Number
The current section and its title
are always shown in the footer of
the left (even) page.
An exclamation point in a triangle is used
to indicate important information to the user.
Paragraphs preceeded by Alphanumeric
characters (e.g. numbers) contain information that must be followed in a specific order.
Publication Title
The current chapter and its title
are always shown in the footer of
the right (odd) page.
Paragraphs preceeded by a symbol
(e.g. bullets) contain information that
has no specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location.
The document part number and revision number appears in every header on every page. Odd
numbered page footers indicate the current chapter, its title and current page number. Even page
footers show the current section and its title, as well as the current page number.
Preface
Page 15
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text
that’s either screen input and output. Mono-spaced fonts, such courier, are used to indicated text
direction. When you type at your keyboard, you are generating computer input. Occasionally you
will see the math operator “greater-than” and “less-than” symbols used to indicate the start and
finish of variable output. When reading text generated by the computer, you are reading it as
computer generated output. In addition to direction, characters are italicized (e.g. italics) to indicate
information specific to your system or site.
Example: Fixed
Output
This paragraph’s font represents computer generated screen “fixed” output.
Its output is fixed from the sense that it does not vary from application
to application. It is the most commonly used style used to indicate
filenames, paths and text that do not change from system to system. The
character style used is a fixed width such as courier.
Example:
Variable Output
This paragraph’s font represents computer screen output that is
“variable”. It is used to represent output that varies from application
to application or system to system. Variable output is sometimes found
placed between greater-than and less-than operators for clarification. For
example: <variable_ouput> or <3.45.120.3>. In both cases, the < and >
operators are not part of the actual input.
Example: Fixed
Input
This paragraph’s font represents fixed input. It is computer input that
is typed-in via the keyboard. Typed input that does not vary from
application to application or system to system. Fixed text the user is
required to supply as input. For example: cd /usr/3p
Example:
Variable Input
This paragraph’s font represents computer input that can vary from
application to application or system to system. With variable text, the
user is required to supply system dependent input or information. Variable
input sometimes is placed between greater-than and less-than operators.
For example: <variable_input>. In these cases, the (<>) operators would
be dropped prior to input. For example: ypcat hosts | grep <3.45.120.3>
would be typed into the computer as:
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or
soft button, switch or key. Physical hardware, such as buttons and switches, are called hard keys
because they are hard wired or mechanical in nature. A keyboard or on/off switch would be a hard
key. Software or computer generated buttons are called soft keys because they are software
generated. Software driven menu buttons are an example of such keys. Soft and hard keys are
represented differently in this publication.
Example: Hard
Keys
A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style
that uses both over and under-lined bold text that is bold. This is a hard key.
Example: Soft
Keys
Whereas the computer MENU button that you would click with your mouse or touch with your hand
uses over and under-lined regular text. This is a soft key.
Page 16
Preface
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Table of contents
Chapter 1
Safety............................................................................................... 21
Section 1.1 Energy sources........................................................................... 21
Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power ..... 22
1.2.1
1.2.2
1.2.3
Preparing for LOTO................................................................................................... 22
Performing LOTO ...................................................................................................... 24
Returning system to service ...................................................................................... 27
Section 1.3 Electrostatic discharge (ESD) ................................................... 28
1.3.1 Important ESD considerations when working on a mobile system............................
1.3.2 Generating static .......................................................................................................
1.3.3 Personal grounding methods and equipment ...........................................................
1.3.3.1 Static shielding protection levels ......................................................................
1.3.4 Grounding the work area...........................................................................................
1.3.5 Recommended materials and equipment .................................................................
Chapter 2
28
28
29
29
29
30
System overview ............................................................................ 31
Section 2.1 System components .................................................................. 31
Chapter 3
Installation....................................................................................... 33
Section 3.1 Installation process.................................................................... 33
Section 3.2 Unpacking the system ............................................................... 34
Section 3.3 Replacing the electrical plug..................................................... 35
Section 3.4 Turning on the system ............................................................... 35
Section 3.5 Ground and leakage testing ...................................................... 37
3.5.1 Performing ground resistance testing .......................................................................
3.5.1.1 Gathering test equipment.................................................................................
3.5.1.2 Attaching test cables ........................................................................................
3.5.1.3 Setting test parameters ....................................................................................
3.5.1.4 Performing zero adjustment .............................................................................
3.5.1.5 Taking ground measurements .........................................................................
3.5.2 Performing leakage current testing ...........................................................................
3.5.2.1 Condition 1: Power off, normal outlet, X-ray off ...............................................
3.5.2.2 Condition 2: Power off, reversed outlet, X-ray off ............................................
3.5.2.3 Condition 3: Power on, normal outlet, X-ray off ...............................................
3.5.2.4 Condition 4: Power on, reversed outlet, X-ray off ............................................
3.5.2.5 Condition 5: Power on, normal outlet, X-ray on ...............................................
37
37
38
40
41
43
47
48
49
50
50
50
Section 3.6 Installing the digital detector..................................................... 50
3.6.1
3.6.2
3.6.3
3.6.4
3.6.5
Unpacking the detector .............................................................................................
Inspecting the detector ..............................................................................................
Charging the detector battery....................................................................................
Connecting the backup tether ...................................................................................
Download detector firmware .....................................................................................
Table of Contents
51
52
52
53
54
Page 17
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
3.6.6 Detector registration .................................................................................................
3.6.7 Applying detector identification shapes ....................................................................
3.6.8 Installing the detector grid.........................................................................................
3.6.8.1 Unpacking and inspecting the grid ..................................................................
3.6.8.2 Grid handling ...................................................................................................
3.6.8.3 Installing the grid .............................................................................................
54
54
55
55
55
56
Section 3.7 Applying local language labels.................................................. 56
Chapter 4
Configuration.................................................................................. 57
Section 4.1 When should I configure the system? ...................................... 57
Section 4.2 Using the System Configuration Tool (SUIF) ........................... 57
4.2.1 Site configuration ......................................................................................................
4.2.2 Networking configuration ..........................................................................................
4.2.3 General configuration ...............................................................................................
4.2.4 Hardware configuration.............................................................................................
4.2.5 Generator configuration ............................................................................................
4.2.6 Wireless configuration ..............................................................................................
4.2.6.1 Adding certificates ...........................................................................................
4.2.6.2 Configuring broadcast SSID networks.............................................................
4.2.6.3 Configuring non-broadcast SSID networks .....................................................
4.2.6.4 Troubleshooting connections...........................................................................
4.2.7 Options configuration................................................................................................
4.2.8 InSite configuration ...................................................................................................
4.2.9 PNF configuration .....................................................................................................
4.2.9.1 PNF GUI Control area .....................................................................................
4.2.9.2 PNF tabs and parameters ...............................................................................
4.2.10 Time Server configuration.........................................................................................
4.2.11 Secure Login configuration .......................................................................................
58
59
59
60
60
61
61
61
62
63
64
64
64
64
65
66
66
Section 4.3 Changing Auto Protocol Assist settings .................................. 67
Section 4.4 DICOM connectivity configuration ............................................ 67
4.4.1 Network host configuration .......................................................................................
4.4.1.1 Adding network hosts ......................................................................................
4.4.1.2 Performing a C-Echo test ................................................................................
4.4.1.3 Removing network hosts .................................................................................
4.4.2 Printer configuration..................................................................................................
4.4.2.1 Adding printers ................................................................................................
4.4.2.2 Removing printers ...........................................................................................
67
67
69
70
70
70
72
Section 4.5 Image management..................................................................... 72
Section 4.6 Image processing........................................................................ 72
4.6.1
Enabling EMI reduction............................................................................................. 72
Section 4.7 Loading demo images ................................................................ 73
4.7.1
Loading images from CD .......................................................................................... 73
Section 4.8 Installing the Operator Manual .................................................. 73
Section 4.9 Login and user management ..................................................... 74
Page 18
Table of Contents
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Section 4.10 Installing hardware options ....................................................... 74
4.10.1 Installing the barcode reader ....................................................................................
4.10.1.1 Installing the barcode reader receiver .............................................................
4.10.1.2 Connecting the barcode reader .......................................................................
4.10.1.3 Barcode reader LED indicators .......................................................................
4.10.1.4 Charging the barcode reader...........................................................................
4.10.2 Configuring the barcode reader ................................................................................
4.10.2.1 Setting to default configuration ........................................................................
4.10.2.2 Verifying the default configuration ...................................................................
4.10.2.3 Optional configuration 1...................................................................................
4.10.2.4 Verifying optional configuration 1 ....................................................................
4.10.2.5 Optional configuration 2...................................................................................
4.10.2.6 Verifying optional configuration 2 ....................................................................
4.10.3 Installing the Dose Area Product (DAP) meter .........................................................
4.10.3.1 DAP installation for Optima XR220amx system ..............................................
4.10.3.2 DAP installation for Optima XR200amx system ..............................................
4.10.4 Installing the tablet holder assembly.........................................................................
4.10.5 Installing the wireless exposure handswitch.............................................................
74
74
77
77
77
78
78
79
79
79
80
80
80
80
81
85
89
Section 4.11 Importing custom IP looks from Definium AMX 700................ 99
Section 4.12 Enabling Advanced Service mode .......................................... 100
Section 4.13 IP Address Change Procedure ................................................ 100
4.13.1 Snapshot Tool Configuration .................................................................................. 101
Chapter 5
Calibration .................................................................................... 111
Section 5.1 Saving changes......................................................................... 111
Section 5.2 Detector calibration .................................................................. 111
Section 5.3 Image quality calibration .......................................................... 111
5.3.1
Calibrating the printer ............................................................................................. 111
Section 5.4 PACS image tests ..................................................................... 112
5.4.1 Comparing PACS test images ................................................................................
5.4.2 Determining PACS burn/no-burn configuration ......................................................
5.4.2.1 Verifying PACS monitor calibration ...............................................................
5.4.2.2 Loading test images ......................................................................................
5.4.2.3 Sending no-burn images to the PACS...........................................................
5.4.2.4 Sending burn-on-send images to the PACS..................................................
5.4.2.5 Reviewing images on PACS..........................................................................
5.4.3 Optional PACS tests ...............................................................................................
5.4.3.1 Sending all PACS test images.......................................................................
5.4.3.2 Verifying DICOM header tags........................................................................
5.4.3.3 Verifying WC and WW values .......................................................................
>
No-Burn Mode (PACS Test Image #1) .......................................................
>
Burn-on-Send Mode (PACS Test Image #6) ..............................................
5.4.3.4 Checking for image saturation .......................................................................
5.4.3.5 Testing reduced dynamic range with Burn-on-Send .....................................
5.4.4 PACS image comparison results ............................................................................
Table of Contents
112
112
112
113
113
114
114
116
116
116
117
117
117
117
117
118
Page 19
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Chapter 6
Detector checks and QAP ........................................................... 119
6.0.1
6.0.2
Chapter 7
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Detector check........................................................................................................ 119
QAP checkout......................................................................................................... 119
Certified components .................................................................. 121
Section 7.1 Component rating plates.......................................................... 121
Chapter 8
Final tasks..................................................................................... 127
Section 8.1 Final tasks.................................................................................. 127
Page 20
Table of Contents
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Chapter 1 Safety
Section 1.1 Energy sources
Table 1-1
Energy source
Yes/No
Location of energy
isolating means
Magnitude of energy
Electrical
Yes
AC power plug
120 VAC/60Hz
220 VAC/50Hz
Electrical
Yes
Circuit breaker
156VDC
Electrical (batteries)
Yes
Battery board
connector J1
156VDC
Pneumatic
No
n/a
n/a
Hydraulic
No
n/a
n/a
Gas/water/steam
No
n/a
n/a
Chemical
No
n/a
n/a
Mechanical motion
No
n/a
n/a
Gravity
No
n/a
n/a
Rear suspension spring
No
n/a
n/a
Column spring
Yes
Scroll lock at
610 N-m (5400 in-lbs)
top of column
Thermal
No
n/a
n/a
Stored energy (generator
capacitors)
Yes
Time discharge and
DVM verification
15kW generator: 2200J
Air under pressure
No
n/a
n/a
Oil under pressure
No
n/a
n/a
Water under pressure
No
n/a
n/a
Gas under pressure
No
n/a
n/a
Steam
No
n/a
n/a
Other
No
n/a
n/a
30kW generator: 8800J
Type of equipment and/or method selected to dissipate or isolate stored energy:
-
Allow three minutes for stored energy to dissipate. Stored energy is indicated by safety
lamps on the generator Aux boxes.
-
After waiting period, verify dissipation with volt meter.
Type of equipment and/or method used to ensure disconnections:
-
One lock and tag for each electrical power source
-
Multiple locking device
Chapter 1 Safety
Page 21
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical
power
Name of equipment: Optima XR200amx/Optima XR220amx
Number of locks: 3
Title of employees authorized to perform LOTO: Those trained in LOTO
Title of affected employees and how to notify: Hospital personnel, notified by verbal communication
1.2.1 Preparing for LOTO
1.
Have this equipment on hand:
-
Safety glasses
-
Voltage meter
-
LOTO kit 5421892, contains (see Figure 1-1):
*
3 brass padlocks and identification labels
*
3 LOTO tag packages (25 tags per package)
*
1 electrical plug lockout device 110V - for AC power plug
*
2 electrical plug lockout devices 160VDC - for battery connectors
*
1 nylon carry bag
Figure 1-1 LOTO kit contents
Page 22
Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
2.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Locate the AC power plug (E1), system circuit breaker (E2), and battery connectors (E3). See
Figure 1-2.
E2
E1
E3
Figure 1-2 Electrical energy lockout locations
Chapter 1 Safety
Page 23
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
1.2.2 Performing LOTO
1.
Notify all affected personnel working in the area that LOTO is being performed.
2.
Exit all system software.
3.
Turn off the Optima XR200amx/Optima XR220amx system by pressing the power button and
holding it for several seconds until the power button light ring turns blue, indicating that the
system is shutting down.
4.
When the power light ring begins to blink blue, indicating that the system is in standby, switch
the circuit breaker (E2) to the OFF position. See Figure 1-3.
Figure 1-3 Circuit breaker (E2) in OFF position
5.
Unplug the power cord from the wall outlet.
6.
Apply an approved AC power plug locking device to the AC power plug (E1), then apply your
personal red lock and tag. See Figure 1-4.
Figure 1-4 AC power plug with locking device applied
7.
Page 24
Wait three minutes for discharge of stored energy.
Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
8.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Disconnect the two green battery power connectors J3 and J4 and the two sense connectors
J13 and J14 from the Cricket board. Apply a locking device, then apply your personal red lock
and tag. See Figure 1-5.
1
2
Item
Description
1
Battery power connectors (J3, J4)
2
Battery sense connectors (J13, J14)
Figure 1-5 Battery connectors J3/J4/J13/J14 and locking device
Chapter 1 Safety
Page 25
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
9.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Disconnect the two green battery power connectors J1 and J2 and the two sense connectors
J11 and J12 from the Cricket board. Apply a locking device, then apply your personal red lock
and tag. See Figure 1-6.
1
2
Item
Description
1
Battery power connectors (J1, J2)
2
Battery sense connectors (J11, J12)
Figure 1-6 Battery connectors J1/J2/J11/J12 and locking device
10. Press the power button and verify that the system does not turn on.
11. Verify that the voltage meter is working properly by testing it on a known live voltage source
(such as a wall outlet).
Page 26
Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
12.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
See Figure 1-7. Verify that electrical power has been removed from the system by applying
the DC voltmeter (+) lead to connector J5 pin 1 (Item 1, left-side screw terminal) on the Cricket
board and the meter (-) lead to chassis ground (Item 2).
1
2
Item
Description
1
Connect DC voltmeter (+) to J5 pin 1 (left-side screw terminal)
2
Connect DC voltmeter (-) to chassis ground
Figure 1-7 Cricket board test points
ELECTRICAL SHOCK HAZARD
IF THE SYSTEM CANNOT BE LOCKED OUT, OR IF THE SYSTEM FAILS
VERIFICATION, CONTACT YOUR SUPERVISOR.
13. Perform the necessary service or repair.
1.2.3 Returning system to service
1.
Notify affected personnel that LOTO devices are being removed and equipment is being reenergized.
2.
Verify that the area is safe to re-energize the equipment.
3.
Verify that any safety guards or devices have been reinstalled, and replace all guards and
covers as necessary.
4.
Remove tools and all non-essential equipment.
5.
Verify that all personnel are clear and in a safe position.
6.
Verify that all controls and switches are in the off or neutral position.
7.
Remove locks and tags as appropriate.
Chapter 1 Safety
Page 27
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
8.
Re-energize equipment and follow safe startup procedures.
9.
Notify affected persons that energy has been restored.
Section 1.3 Electrostatic discharge (ESD)
A sudden discharge of static electricity from your finger or other conductor can destroy static
sensitive devices or microcircuitry. Often the spark is neither felt nor heard, but damage occurs. An
electronic device exposed to electrostatic discharge (ESD) might not appear to be affected at all
and can work perfectly throughout a normal cycle. The device can function normally for a while, but
it has been degraded in the internal layers, reducing its life expectancy.
Networks built into many integrated circuits provide some protection, but in many cases, the
discharge contains enough power to alter device parameters or melt silicon junctions.
1.3.1 Important ESD considerations when working on a mobile system
Static Discharge Risk to Components
If you are using a static mat or wrist strap, be sure to connect the mat and strap to machine ground,
not earth ground. This is necessary to isolate yourself from earth ground and equalize your potential
with the machine.
ESD damage prevention includes these steps:
1.
Perform LOTO.
2.
Verify that the AC plug is not connected to an energy source/outlet.
3.
Connect ground mat and wrist strap assembly to frame connection point of the mobile unit.
1.3.2 Generating static
The following table shows that different activities generate different amounts of static electricity, and
that static electricity increases as humidity decreases.
Table 1-2
Event
Relative humidity
55%
40%
10%
Walking across carpet
7,500 V
15,000 V
35,000 V
Walking across vinyl floor
3,000 V
5,000 V
12,000 V
Motions of bench worker
400 V
800 V
6,000 V
Removing bubble pack from PCB
7,000 V
20,000 V
26,500 V
Packing PCBs in foam-lined box
5,000 V
11,000 V
21,000 V
Many electronic components are sensitive to ESD. Circuitry design and structure determine the
degree of sensitivity. The following packaging and grounding precautions are necessary to prevent
damage to electric components and accessories.
•
Page 28
Transport products in static-safe containers to avoid hand contact.
Section 1.3 Electrostatic discharge (ESD)
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
•
Protect all electrostatic parts and assemblies with conductive or approved containers or
packaging.
•
Keep electrostatic sensitive parts in their containers until they arrive at static-free stations.
•
Place items on a grounded surface before removing them from their container.
•
When handling or touching a sensitive component or assembly, ground yourself by touching
the chassis.
•
Avoid contact with pins, leads, or circuitry.
•
Place reusable electrostatic-sensitive parts from assemblies in protective packaging or
conductive foam.
1.3.3 Personal grounding methods and equipment
ELECTRICAL SHOCK HAZARD
This section defines a workzone that is not connected to the system under service. The mobile
system is a battery powered unit that can deliver lethal current. Ensure you are not providing an
earth ground path when practicing ESD procedures.
Use the following equipment to prevent static electricity damage to equipment:
•
Wrist straps are flexible straps with a maximum of one-megohm +/- 10% resistance in the
ground cords. To provide a proper ground, wear the strap against bare skin. The ground cord
must connect snugly into the banana plug connector on the grounding mat or workstation.
•
Heel, toe, and boot straps can be used at standing workstations and are compatible with most
types of shoes or boots. On conductive floors or dissipative floor mats, use them on both feet
with a maximum of one-megohm +/- 10% resistance between the operator and ground.
1.3.3.1 Static shielding protection levels
Table 1-3
Method
Voltage
Antistatic plastic
1,500
Carbon-loaded plastic
7,500
Metalized laminate
15,000
1.3.4 Grounding the work area
ELECTRICAL SHOCK HAZARD
This section defines a workzone that is not connected to the system under service. The mobile
system is a battery powered unit that can deliver lethal current. Ensure you are not providing an
earth ground path when practicing ESD procedures.
To prevent static damage of components and parts in the work area:
Chapter 1 Safety
Page 29
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
•
Cover the work surface with approved static-dissipative material. Provide a wrist strap
connected to the work surface and properly grounded tools and equipment.
•
Use static-dissipative mats, foot straps, or air ionizers to give added protection.
•
Handle electrostatic sensitive components, parts, and assemblies by case or PCB laminate.
•
Handle components only at static-free work areas.
•
Turn off power and input signals before inserting and removing connectors or test equipment.
•
Use static-safe fixtures when fixtures must directly contact dissipative surfaces.
•
Keep work area free of non-conductive materials, like plastic assembly aids and Styrofoam.
1.3.5 Recommended materials and equipment
ELECTRICAL SHOCK HAZARD
This section defines a workzone that is not connected to the system under service. The mobile
system is a battery powered unit that can deliver lethal current. Ensure you are not providing an
earth ground path when practicing ESD procedures.
Materials and equipment that are recommended for use in preventing static electricity include:
•
Anti-static tape, smocks, aprons, or sleeve protectors
•
Conductive bins, foam, tabletop workstations with ground cord of one-megohm +/-10%
resistance, and other assembly or soldering aids
•
Static-dissipative table or floor mats with hard tie to ground
•
ESD field service kits
•
Static awareness labels
•
Wrist straps and footwear straps providing one-megohm +/-10% resistance
•
Material handling packages:
-
Conductive plastic bags, plastic tubes and tote boxes
-
Opaque shielding bags
-
Transparent metalized shielding bags and shielding tubes
Chapter 1 Safety
Page 30
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Chapter 2 System overview
Section 2.1 System components
Available components of the Optima XR200amx/Optima XR220amx system are listed below.
Shipped with the Optima XR200amx/Optima XR220amx system:
•
Optima XR200amx/Optima XR220amx
•
Backup tether for digital detector (Optima XR220amx only)
•
Service keyboard
•
Software CD
•
External CD/DVD-ROM drive
•
Operating System firmware USB drive
•
Tablet holder assembly (optional, Optima XR220amx and Optima XR200amx)
Shipped separately:
•
DAP meter (standard with Optima XR220amx, optional for Optima XR200amx)
•
Digital detector (Optima XR220amx only)
•
Detector batteries (Optima XR220amx only)
•
Detector battery charger (Optima XR220amx only)
•
6:1 grid (Optima XR220amx only)
•
Barcode reader (optional, Optima XR220amx only)
•
Wireless Hand Switch (optional, Optima XR220amx and Optima XR200amx)
Chapter 2 System overview
Page 31
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Optima XR200amx
Figure 2-1 Optima systems
Page 32
Section 2.1 System components
Optima XR220amx
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Chapter 3 Installation
Section 3.1 Installation process
1.
Unpack the system (Section 3.2 Unpacking the system on page 34).
2.
Replace the electrical plug, if necessary (Section 3.3 Replacing the electrical plug on
page 35).
3.
Perform leakage and ground testing as required (Section 3.5 Ground and leakage testing on
page 37).
4.
Power on and plug in the system (Section 3.4 Turning on the system on page 35).
5.
Install the digital detector (Section 3.6 Installing the digital detector on page 50) (Optima
XR220amx only).
6.
Install hardware options, such as the DAP meter or barcode reader (Section 4.10 Installing
hardware options on page 74).
7.
Apply local language labels (Section 3.7 Applying local language labels on page 56).
See Figure 3-1 for the installation workflow.
After installation, configure the system according to the site’s requirements, as described in Chapter
4 Configuration. Perform necessary calibration, as described in Chapter 5 Calibration.
Chapter 3 Installation
Page 33
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
SYSTEM INSTALLATION WORKFLOW
Upack
the system
Does the
power plug meet
requirements? No
Replace the
power plug
Yes
Perform
ground and
leakage
testing
Is the
system an
Optima
XR220amx?
Plug in and
turn on
system power
Yes
Install the
detector
No
Install
optional
hardware
Ready for
configuration
and
calibration
Figure 3-1 Optima XR200amx/Optima XR220amx installation workflow
Section 3.2 Unpacking the system
Within the United States, the Optima XR200amx/Optima XR220amx is shipped on its own wheels,
with minimal packaging. External to the United States, the Optima XR200amx/Optima XR220amx
is shipped in a packing crate.
To prepare the unit for installation, follow these steps:
Page 34
Section 3.2 Unpacking the system
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
1.
Unpack the unit and remove all packaging materials.
2.
Remove and unpack any components shipped in the system package, such as the service
keyboard and external CD/DVD drive.
3.
Visually inspect the system and components for any damage that might have occurred during
shipping.
-
If no damage is observed, continue with the installation.
-
If damage is found, contact GE Service or the installation specialist.
Section 3.3 Replacing the electrical plug
In regions that use an electrical plug other than the style used in the United States, remove the
electrical plug and replace it with the appropriate hospital-grade plug as dictated by local
regulations.
The replacement electrical plug must meet the following electrical specifications:
-
Hospital-grade plug
-
100-240 VAC
-
1440 VA
-
50/60 Hz
To replace the plug:
1.
Remove the three cross-recessed screws that hold the plug together.
2.
Remove the plug.
3.
Remove the cross-recessed screw holding the wires to the plug.
4.
Attach the wires to the new plug as required:
-
Pin 1, 120/220VAC, hot wire, brown
-
Pin 2, 120 neutral (220 hot) wire, blue
-
Pin 3, earth ground wire, green/yellow
5.
Assemble the new plug.
6.
Test the plug operation.
Section 3.4 Turning on the system
The lighted ring around the power button on the console indicates the system’s power state:
•
Green means the system is on.
•
Solid blue means the system is in a power transition state.
•
Blinking blue means the system is in standby.
•
No light means the system is off.
Chapter 3 Installation
Page 35
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
1.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
If the circuit breaker is OFF, flip it to the ON position.
Item
Description
1
ON position
2
OFF position
3
Trip lever
Figure 3-2 Circuit breaker in ON position
2.
Press and release the power button to turn on the Optima XR200amx/XR220amx system.
3.
Check the battery level, indicated by the battery symbol on the interface.
In the figure below, the battery shows 25% capacity and discharging status.
Figure 3-3 Battery icon - discharging
4.
If battery charging is needed, plug the system in to an electrical outlet.
5.
The icon changes to indicate that the battery is charging.
In the figure below, the battery shows 40% capacity and charging status.
Figure 3-4 Battery icon - charging
Page 36
Section 3.4 Turning on the system
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Section 3.5 Ground and leakage testing
Perform ground resistance testing & leakage testing only in the cases outlined in Table 3-1.
Site location
Perform ground testing?
Perform leakage testing?
Within the United States
Yes, if you replace a damaged plug
or power cord or incoming AC
circuitry.
Yes
Outside of the United States
Yes, if you replace the standard
U.S. style plug with a regionally
compliant plug, or if you replace a
damaged plug or power cord or
incoming AC circuitry.
Yes
Table 3-1 Test requirements
3.5.1 Performing ground resistance testing
Ground resistance testing must be performed if the AC power plug has been replaced or disturbed.
RISK OF ELECTRIC SHOCK
Voltage present!
Disconnect the AC charging plug from any wall outlet power source.
3.5.1.1 Gathering test equipment
Obtain a Hioki 3157 grounding tester or equivalent. For sites in Europe, use the cables that are
provided with the Hioki tester. For sites outside of Europe, obtain the following:
•
Two green/yellow ground stranded wire cables:
-
Cable A = 2.5 mm² (12 AWG), 3 m (9.8 ft)
-
Cable B = 2.5 mm² (12 AWG), 5 m (16.4 ft)
•
Two lugs to fit 0.64 cm (0.25 in) terminals to the meter end of each cable (Figure 3-5).
•
Two clamps to fit onto the other end of the cables (Figure 3-5).
Chapter 3 Installation
Page 37
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 3-5 Lug and clamp on ground wire
3.5.1.2 Attaching test cables
1.
On the tester, loosen both the current output (Source) terminal knob (top right) and the voltage
measurement (Sense) terminal knob (bottom right) by turning them counterclockwise.
2.
Connect Cable B to the current output knob.
3.
Connect the short bar between the current output and voltage measurement knobs as shown
in Figure 3-6.
Figure 3-6 Test Cable B and short bar installation
4.
Turn the two knobs clockwise to tighten.
5.
Loosen the other current output (Source) terminal (top left), attach Cable A, and retighten the
knob.
The resulting connections should look as shown in Figure 3-7.
Page 38
Section 3.5 Ground and leakage testing
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 3-7 Cable A, Cable B, and short bar connections
Chapter 3 Installation
Page 39
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
3.5.1.3 Setting test parameters
1.
Turn on the tester by pressing the POWER button.
The tester enters the ready state five seconds after startup (the model name and version
display during startup).
2.
Verify that the tester displays the test parameters specified in Table 3-2.
Test parameters
Values
Canada: 30.0 A
Current
All other countries: 25.0 A
Test value
0.100 Ohms
Timer
5.0 sec
Table 3-2 Ground resistance test parameters
If it does not, perform the following steps to change the parameters as needed (the system will
save the settings even after system power is turned off). See Figure 3-8.
A. While in the ready state, press the
begins flashing.
B. Press the
or
or
button until the output current display
button to change the output current. The value changes in
0.1-A increments. To change the value by 1.0-A increments, press
+
or
button.
C. Press the
button again to move to each of the other settings (Maximum Test
Value, Timer, and Frequency).
D. Use the
E. Press
or
+
buttons as needed to adjust the values.
.
Figure 3-8 Test parameter value settings
3.
While in the ready state, press the
setting screen.
+
buttons to display the Optional function
The Output Current Frequency is the first digit displayed, where the value is 0 for 50 Hz or 1
for 60 Hz. The Pass/Fail hold function is represented by the second digit.
Page 40
4.
Press the
or
button until the second digit begins flashing.
5.
Press the
button to change the value to 1 (Figure 3-9).
6.
Press the
+
buttons to save this setting and return to the ready state. The unit will
display and hold the measured resistance value after the test.
Section 3.5 Ground and leakage testing
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 3-9 Current setting on the tester
3.5.1.4 Performing zero adjustment
Ground measurements may be affected by a voltage drop in the A and B cables. To account for the
voltage drop, perform the zero adjustment procedure before taking ground measurements.
1.
Confirm that the unit is in the ready state.
2.
Short circuit cable A with cable B.
Figure 3-10 Cable A and cable B short-circuited
3.
Press the
button.
The orange test indicator is displayed, the 0ADJ indicator begins flashing below the resistance
value, and the zero adjustment begins. During the zero adjustment, a preset current is output
through the shorted leads. When zero adjustment is complete (about three seconds), the unit
enters the ready state, and the 0ADJ lamp lights.
If the test cables are too resistive, the offset cannot be set. Use less-resistive cables and try to
set the offset again. The zero adjustment function is automatically disabled if the output current
value is changed or if data settings are changed.
Zero adjustment is possible within a range equivalent to a resistance between 0.000 Ohms and
0.100 Ohms on the resistor indicator. If the measured value falls outside this range, the
resistance value flashes, and the unit enters the ready state.
Chapter 3 Installation
Page 41
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Figure 3-11 Tester during and after zero adjustment
Page 42
Section 3.5 Ground and leakage testing
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
3.5.1.5 Taking ground measurements
1.
Turn off system power and main circuit breaker.
2.
Connect cable A to the grounding pin on the electrical plug.
3.
Connect cable B to the first measurement point listed in Table 3-3.
4.
On the tester, press the green START button.
The orange indicator is displayed, the Test Current display value quickly increases from 0.0 to
the preset output current (25.0 A or 30.0 A), and the timer value decreases from 5.0 seconds
to 0.0 seconds.
If the test passes, the green Pass indicator is displayed. Record the displayed resistance value
in Table 3-3.
5.
Press Stop.
6.
Move cable B to the next measurement (Table 3-3), then repeat steps 4 and 5.
The voltage must not exceed 2.5 V (0.1 ohms).
Component
Tube
Collimator
Column
Bin
Tube latch
Measurement point
Measured
resistance
Tube endcap screws or HV cable nuts
See Figure 3-12
Skin guards
See Figure 3-13
Scroll support rivets
See Figure 3-14
Screw used for mounting strain relief of wired handswitch cable
See Figure 3-15
Tube latch on top cover
See Figure 3-16
Table 3-3 Ground measurement test points
Chapter 3 Installation
Page 43
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Figure 3-12 Tube test points
Figure 3-13 Collimator test points
Page 44
Section 3.5 Ground and leakage testing
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 3-14 Column test point
Figure 3-15 Rear bin accessory access cover test point
Chapter 3 Installation
Page 45
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Figure 3-16 Tube latch test point
Page 46
Section 3.5 Ground and leakage testing
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
3.5.2 Performing leakage current testing
If ground testing is required for this system, verify that the ground testing results (see Table 3-3) are
< 0.1 Ohms before conducting leakage testing.
Leakage testing must be performed if the AC power plug has been replaced or disturbed.
The leakage current must not exceed 300 uA.
Before you begin, verify these steps:
1.
Complete ground testing, if required (see 3.5.1 Performing ground resistance testing on
page 37).
2.
Ensure that all system covers are installed.
3.
Obtain a Dale 601/601E test meter or equivalent.
Perform leakage testing under the five specific conditions outlined in Table 3-4:
Condition
Power
Test meter
outlet
X-ray on
Section reference
1
Off
Normal
No
3.5.2.1 Condition 1: Power off, normal outlet,
X-ray off
2
Off
Reversed
No
3.5.2.2 Condition 2: Power off, reversed
outlet, X-ray off
3
On
Normal
No
3.5.2.3 Condition 3: Power on, normal outlet,
X-ray off
4
On
Reversed
No
3.5.2.4 Condition 4: Power on, reversed
outlet, X-ray off
5
On
Normal
Yes
3.5.2.5 Condition 5: Power on, normal outlet,
X-ray on
Table 3-4 Leakage current test conditions
Chapter 3 Installation
Page 47
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Potential test equipment damage. Always pause in the OFF position when moving the OUTLET
switch from NORMAL to REVERSED or REVERSED to NORMAL. Failure to do so can result in the
internal test meter failure and tripping of facilities circuit breakers.
3.5.2.1 Condition 1: Power off, normal outlet, X-ray off
1.
Turn off the system power, main circuit breaker ON.
On the test meter, set the Function switch to ENCLOSURE LEAKAGE, the L2 switch to
CLOSED, the Outlet switch to Normal and the M.A.P/Lift Gnd to OFF (Figure 3-17).
Figure 3-17 Dale 601 meter
Page 48
Section 3.5 Ground and leakage testing
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
2.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Insert the black coil cord with clamp into the CHASSIS connection located on the top of the
test meter (Figure 3-18).
Figure 3-18 Dale 601 meter, top view
3.
Connect the Dale 601 test meter to a wall outlet.
4.
Important! Connect the System AC power cord to the receptacle on the test meter.
5.
Using the clamp, connect to all conductive surfaces listed in Table 3-5. Record the readings.
Readings should be close to 0.0. Address high readings by checking for damaged ground wire
or internal system wiring that could be causing current to flow to the tested component or
chassis.
Conductive surface
Condition 1:
Condition 2:
Condition 3:
Condition 4:
Condition 5:
Power off,
Power off,
Power on,
Power on,
Power on,
normal outlet, reversed outlet, normal outlet, reversed outlet, normal outlet,
X-ray off
X-ray off
X-ray off
X-ray off
X-ray on
Leakage current
Tube
Collimator
Column
Bin
Tube latch
Table 3-5 Leakage current test results
3.5.2.2 Condition 2: Power off, reversed outlet, X-ray off
1.
On the test meter, set the Outlet switch to Reversed.
2.
Verify the system power is OFF, main circuit breaker ON.
3.
Using the clamp, connect to all conductive surfaces.
4.
Record the readings in Table 3-5.
Chapter 3 Installation
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GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
3.5.2.3 Condition 3: Power on, normal outlet, X-ray off
1.
Turn on the system power.
2.
On the test meter, set the Outlet switch to Normal.
3.
Using the clamp, connect to all conductive surfaces.
4.
Record the readings in Table 3-5.
3.5.2.4 Condition 4: Power on, reversed outlet, X-ray off
1.
On the test meter, set the Outlet switch to Reversed.
2.
Verify that system power is on.
3.
Using the clamp, connect to all conductive surfaces.
4.
Record the readings in Table 3-5.
3.5.2.5 Condition 5: Power on, normal outlet, X-ray on
EXPOSURE TO RADIATION
Wear a lead vest to protect yourself from radiation.
1.
On the test meter, set the Outlet switch to Normal.
2.
Verify that system power is on.
3.
Make an exposure (see Table 3-6) while using the clamp to connect to all conductive surfaces.
Generator power
kVp
mAs
15 kW
125
100
30 kW
125
100
Table 3-6 Exposure technique
4.
Record the readings in Table 3-5.
Section 3.6 Installing the digital detector
The digital detector is for use only with the Optima XR220amx or Optima XR200amx with digital
upgrade.
The digital detector uses a wireless signal to communicate with the system. The detector contains
a docking mechanism that provides charging power when the detector is in the digital bin.
Because the detector does not have to be physically connected to the system to function, the
system needs a method of identifying which of the wireless detectors in the area to communicate
with. The detector that is actively communicating with the system is called the active detector, and
is the one that will generate digital images when the system performs an exposure. This detector is
registered with the system and it is defined as the main detector at that time. Multiple detectors can
be registered with the system, but only one can be the active detector at a given time.
Page 50
Section 3.6 Installing the digital detector
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
The detector also has a backup tether that can be attached, if needed, to provide input power and
wired communication. The backup tether must be attached to the detector to register the detector
with the system, and can then be removed and stored.
3.6.1 Unpacking the detector
The detector packing is designed to protect the detector during shipping and handling. There are
three boxes inside each other to give maximum detector protection.
1.
Locate the detector shipping box. See Figure 3-19.
Figure 3-19 Detector shipping box
2.
Inspect the box for physical or water damage. If present, document the damage.
3.
Remove all four clips and lift top of outer box from bottom. Instructions are printed on the
outside of the box.
4.
Lift the plastic bag and inner box out of the outer box. See Figure 3-20. More instructions are
printed on the outside of the inner box.
Figure 3-20 Inner box
5.
Unfasten the bag straps and box straps.
6.
Remove the box end and pull out the black inner box. See Figure 3-21.
Figure 3-21 Detector box
7.
Using the box flaps, open the box.
Chapter 3 Installation
Page 51
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
3.6.2 Inspecting the detector
Visually inspect the detector for any signs of physical damage that might have occurred during
shipping. Check the corners for any signs of sharp edges or damage. Check all surfaces for any
signs of scratches or abrasions.
•
If no damage is observed, proceed to the next step.
•
If damage is found, contact GE Service.
3.6.3 Charging the detector battery
For all customers that do not support the USA style wall plugs, locally obtain and install a computer
style power cord with a CE approved, IEC 60320-1 C13 style connector on one end and the locally
appropriate wall plug connector on the other. The cord must meet or exceed the following electrical
specification, AC 120-240V 50/60 Hz 130VA - 168VA 1.4 Amps. Do not modify the shipped US style
cord as this can present a shock hazard to the user.
The detector is delivered with two batteries and a desktop charger, which can be used to charge
the batteries when disconnected from the detector. The battery can also be charged by inserting it
into the detector, then docking the detector in the bin.
It can take up to eight hours to charge the detector battery, depending on remaining charge. The
battery LEDs (labeled with 1 in Figure 3-22) on the detector indicate remaining power.
Page 52
Section 3.6 Installing the digital detector
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Battery LED status
Meaning
Green, green
Battery more than 75% remaining
Off, green
Battery remaining between 25% and 75%
Off, yellow
Battery remaining between 10% and 25%
Off, red
Battery less than 10% remaining
Off, off
Detector in sleep mode
Figure 3-22 Detector LEDs
3.6.4 Connecting the backup tether
1.
Unpack and inspect the tether. Verify that there is no damage.
2.
Remove the battery, if present.
3.
Connect the backup tether to the detector. Figure 3-23.
Figure 3-23 Connecting the tether to the detector
Chapter 3 Installation
Page 53
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
The tether connector will only fit one way, as shown.
3.6.5 Download detector firmware
This section applies to Optima XR200amx with digital upgrade and Optima XR220amx systems
only.
Note:
The first time a new detector is used with an Optima XR220amx or Optima XR200amx with digital
upgrade system, detector firmware must downloaded because the existing firmware present on the
detector may not be compatible with the system. If you attempt to use a detector that does not have
the correct firmware, an error message will be displayed stating The detector is not
compatible with this system. or Digital cassette firmware is incorrect.
1.
Ensure the system has booted to applications without error.
2.
Connect the detector to the system using the tether and ensure the detector is on, Detector
Status Led illuminated.
3.
Power on the detector.
4.
On the Applications desktop, press the UTILITIES button.
5.
On the Utilities desktop, press LAUNCH.
6.
On the Service Home tab, press the UTILITIES tab button.
7.
In the left navigation frame, expand the SUBSYSTEM SOFTWARE folder.
8.
Select DET DATA DOWNLOAD folder.
9.
Select DET DATA DOWNLOAD link.
10. Select the appropriate detector.
11. Follow the on-screen instructions.
3.6.6 Detector registration
The first time a detector is used with an Optima XR220amx or Optima XR200amx with digital
upgrade, it must be registered with that system. During registration, the detector must be connected
to the system using the backup tether (3.6.4 Connecting the backup tether on page 53).
The system automatically retrieves the detector’s calibration information, and checks whether there
has been a drop or impact.
For instructions on registering a detector, see the Optima XR220amx Operator Manual, Chapter 14
Set Preferences (Detector Registration).
Note these guidelines:
•
There can be only one active detector at a time on each system.
•
There can be a maximum of 10 detectors registered on a system.
•
A detector can be registered on a maximum of 20 systems.
3.6.7 Applying detector identification shapes
Instead of affixing a label with alphanumeric characters, the site may choose to identify the detector
with plastic tags. These circular plastic tags are designed to snap into a matching recess in the
detector handle. A set of tags are delivered with the detector. Each one has a different color and/or
shape, which match the selections available in the detector registration Add/Edit Detector lists.
•
Page 54
To insert, rotate the plastic tag until the notch in the tag aligns with the tab in the recess. Press
until it snaps into place.
Section 3.6 Installing the digital detector
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
•
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
To remove, use a small flat-blade screwdriver. Insert the screwdriver tip under the slot in the
side of the tag, and pry until the tag pops out.
For more information about detector identification shapes,see the Optima XR220amx Operator
Manual, Chapter 14 Set Preferences (Detector Registration).
3.6.8 Installing the detector grid
The digital detector grid is integrated with a holder that fits the detector exactly. The grid fits over
the detector handle and has raised edges to fit around the detector. See Figure 3-24.
Item
Description
1
Grid (6:1 grid is a standard component, 8:1 grid is a purchasable option)
2
Detector
Figure 3-24 Detector grid
3.6.8.1 Unpacking and inspecting the grid
Inspect the surface of the grid (inside surface of the grid holder) for any signs of damage incurred
during shipment. Look for signs of scuffing, abrasions, or dents. The patient contact side of the grid
holder is covered with a padded overlay. Inspect it for any signs of scrapes or tears. Check the
perimeter of the grid holder for signs of sharp edges or damage/fraying to the carbon fiber structure.
3.6.8.2 Grid handling
Sensitive Device
The grid is manufactured with a delicate mechanical structure of thin lead strips, inter-spaced with
strips of aluminum. Do not subject it to drops, impacts or crushing conditions.
Chapter 3 Installation
Page 55
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
3.6.8.3 Installing the grid
Pinch Hazard
Attach the grid holder according to Figure 3-24, being careful not to pinch fingers or clothing.
1.
The grid clips onto the detector. Make sure you attach it to the imaging side of the detector.
2.
With the system switched ON, verify that the grid detection operates correctly.
Each time the grid is attached, removed, or attached improperly the system alerts the user with
a double beep and displays a message on the status bar.
Section 3.7 Applying local language labels
Each Optima XR200amx/XR220amx system must be labeled with the appropriate X-ray warning
label in the local language. The system is delivered with an English label applied.
Figure 3-25 English X-ray warning label
If the system is located at a site where the primary language is not English, follow these steps.
Page 56
1.
In the installation kit, locate the X-ray warning label for the local language.
2.
Clean the surface of the English label with alcohol.
3.
Allow at least two minutes for the area to dry.
4.
Apply the local language label on top of the English label.
Section 3.7 Applying local language labels
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Chapter 4 Configuration
Potential for Data Loss
•
Always create an up-to-date backup of system data after changing the configuration.
•
For configuration changes to take effect, restart the system after exiting the Service User
Interface (SUIF). You must restart the system before using it for patient acquisitions.
Section 4.1 When should I configure the system?
•
During system installation. The system is delivered with pre-configured information from the
manufacturing process. However, many parameters are specific to the customer and location.
These parameters need to be configured. Other parameters should be confirmed and/or
modified per the customers preference.
Table 4-1
Configuration
Comments
SUIF (Site parameters, Generator See Section 4.2 Using the System Configuration Tool (SUIF)
parameters, etc.)
on page 57
DICOM
See Section 4.4 DICOM connectivity configuration on
page 67
Demo images
See Section 4.7 Loading demo images on page 73
Operator manual
See Section 4.8 Installing the Operator Manual on page 73
Hardware options such as the
barcode reader
See Section 4.10 Installing hardware options on page 74
System login
See Section 4.9 Login and user management on page 74
•
If system backups are lost or missing. If the software is re-installed but system configuration
files are not restored, configure the system again. GE service may need to be contacted to
enable purchased options. A software install resets all configuration data. If the system
configuration files are restored, you do not need to re-configure the system.
•
After adding purchased options. Installation of purchased options can only be performed by
an authorized GE Healthcare service representative. If you add purchased options to the
system, update the system configuration files immediately and create and save a new backup.
Purchased option configurations are described in 4.2.7 Options configuration on page 64.
Section 4.2 Using the System Configuration Tool (SUIF)
1.
Turn on the system.
2.
Log on to the system with administrator privileges.
3.
On the Applications desktop, press the UTILITIES button.
Chapter 4 Configuration
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GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
4.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
On the Utilities desktop, next to Service, press LAUNCH.
The Service Home tab is displayed. The Home tab contains summary information including
site identification, connectivity parameters, and enabled options.
5.
Press the CONFIGURATION tab button.
6.
On the Configuration page, in the left folder tree, select the parameter group to change.
7.
Configure the system according to site preferences.
An overview of the configurable system attributes is given in the tables below.
Contact a GE service representative for items marked “Editable by GE Healthcare personnel
only.”
8.
On each page, after making changes, press COMMIT to put the changes into effect.
4.2.1 Site configuration
The following information can be viewed regardless of service mode. However, some fields are
editable only by sites with Advanced Service mode enabled (Section 4.12 Enabling Advanced
Service mode on page 100), and some are editable only by GE Healthcare personnel.
Table 4-2 Site tab parameters
Parameter
Definition
Site Name
Name of specific site where system is installed.
Street Address 1
Street address of site where system is installed.
Street Address 2
Street address, continued, of site where system is installed.
City
City where system is installed.
State/Province
State or province where system is installed.
Postal Code
Postal or ZIP code where system is installed.
Department Name
Department name (for example, Radiology) responsible for system
maintenance.
Telephone
Phone number of department responsible for system.
Fax
Fax number of department responsible for system.
Contact Person Name
Person responsible for system maintenance.
Contact Person Phone
Phone number of person responsible for system maintenance.
Editable by GE Healthcare personnel only.
System identifier assigned by GE Healthcare following system
installation and prior to customer turnover.
System ID
Installation Date
Service Contract Number
This field is a GE proprietary field and cannot be used for any purpose
other than the System ID. Violation of this mandate will result in Insite
and/or other features not working. Customer IT personnel need to use
other means for DICOM filtering on their DICOM machines.
Editable by GE Healthcare personnel only.
Date system installation is completed, created by GE Healthcare.
Editable by GE Healthcare personnel only.
Customer’s Service Contract number, created by GE Healthcare.
Editable by GE Healthcare personnel only.
Contract Expiration
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Customer’s Service Contract expiration date, created by GE
Healthcare.
Section 4.2 Using the System Configuration Tool (SUIF)
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
4.2.2 Networking configuration
The following information can be viewed regardless of service mode.
Table 4-3 Networking tab parameters
Parameter
Definition
Options: DHCP or Static.
Determines whether the IP address is assigned, or acquired
dynamically. If Static is selected, enter associated information in IP
Address, Subnet Mask, and DNS fields.
DHCP Configuration
System IP address.
IP Address Fixed Only
Enabled only if Wired IP Settings is set to Static.
System subnet mask.
Subnet Mask Fixed Only
Enabled only if Wired IP Settings is set to Static.
Default Gateway Fixed Only
Default gateway.
Enabled only if Wired IP Settings is set to Static.
Site domain name server.
Static DNS Server 1
Enabled only if Wired IP Settings is set to Static.
Site domain name server.
Static DNS Server 2
Enabled only if Wired IP Settings is set to Static.
AE Title Fixed Only
Application Entity Title for DICOM.
Fixed value.
Port Number Fixed Only
Software port used for network communications.
Fixed value.
4.2.3 General configuration
If the site is using a master time server (see 4.2.10 Time Server configuration on page 66), some
settings in this section are superceded by the master clock server data.
Table 4-4 General tab parameters
Parameter
Definition
Timezone
Time zone of site where system is installed.
System Clock
System time in YYYYMMDD HH:MM:SS format.
Date Display Format
MM-DD-YYYY or DD-MM-YYYY.
Time Display Format
Military (24-hour) or AM/PM (12-hour).
Country Code
Country where system is installed.
A list of selectable countries. The system auto configures to the
correct regulatory approved formats and frequencies for all wireless
Wireless Regulatory Code communications. If a country does not allow a specific wireless
communication technology then the feature is disabled, Flashpad
wireless for example.
Measurement System
English or Metric.
Chapter 4 Configuration
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DIRECTION 5336113-1EN, REVISION 10
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INSTALLATION MANUAL
Table 4-4 General tab parameters
Parameter
Definition
Application Language
Language used for application screens.
QAP Timeout (Optima
XR220amx or Optima
XR200amx with digital
upgrade)
Interval between QAP tests, in days. When time-out is reached,
system users see a warning flag indicating that a QAP test should be
performed.
Editable by GE Healthcare personnel only.
Applies to USA Veterans Affairs facilities.
VA Site
Yes or No.
Screen Blank Timeout
Period of inactivity (no user input or processing activity) after which
the screen will go blank, in minutes.
Image Mask Adjustment
(Optima XR220amx or
Optima XR200amx with
digital upgrade)
Adjust the mask that is applied to the acquired image from the
detector. Options: 3mm, 2mm, 1mm, 0, -1mm, -2mm, -3mm.
4.2.4 Hardware configuration
Table 4-5 Hardware tab parameters
Parameter
Definition
Collimator Light Maximum
Time, in seconds, that the collimator light will remain on.
On Time
Collimator Lamp Install
Date
Date the collimator lamp was installed. YYYY-MM-DD format.
4.2.5 Generator configuration
Table 4-6 Generator tab parameters
Parameter
Page 60
Definition
Tube HUR Alarm
Percentage of the tube thermal capacity limit, from 0 to 100. When this
limit is reached, X-ray exposure is inhibited and an alarm sounds.
Tube ID
Tube ID. Not editable.
Tube Serial
Serial number of the tube. Confirm the serial number matches that of
the attached tube.
Tube Install Date and
Time
Date and time the tube was installed. YYYYMMDD HH:MM:SS
format.
Section 4.2 Using the System Configuration Tool (SUIF)
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
4.2.6 Wireless configuration
Before configuring the wireless settings, verify that the Wireless Hospital Network option is enabled
on the Options screen (see 4.2.7 Options configuration on page 64). If the site doesn’t require for
authentication certificates and keys, go directly to 4.2.6.2 Configuring broadcast SSID networks or
4.2.6.3 Configuring non-broadcast SSID networks to configure the wireless network.
4.2.6.1 Adding certificates
If your customer uses site-specific network security certificates, contact the IT administrator to
obtain a copy of the certficate(s) on a USB flashdrive.
1.
Ensure that the restoration of all configuration parameters has been completed and the system
has been reset.
2.
Launch the SUIF and navigate to CONFIGURATION > WIRELESS.
3.
Launch the wireless configuration utility as instructed on the screen.
4.
Connect the USB flashdrive containing the site-specific certificates to a left-side USB port.
5.
Click on the Certificates tab.
a.
Observe the USB flashdrive-resident certificates in the pull-down list next to the ADD
button.
b.
If there is more than one certificate, you will need to select each certificate individually.
c.
Click ADD to install the displayed certificate from the drop-down list.
6.
Continue with the site-specific configurations as defined by the IT administrator.
7.
Exit the Configuration utility.
8.
Remove the USB flashdrive.
9.
Reset the system.
4.2.6.2 Configuring broadcast SSID networks
1.
On the Wireless configuration screen, confirm that the "adapter" is ON or ENABLED.
2.
Select the Current Status tab.
3.
Click SCAN to find the network.
Note: Some customers may have their network access in a non-broadcast mode. This may
result in strange naming conventions for the scan results. Confirm with your IT contact.
4.
In the Scan Results window, double-click the network to which you want to connect.
5.
In the Network Config window, some fields are auto-populated. Depending on the type of
authentication used by the network, complete the other required information, as described in
the table below:
Table 4-7
Authentication type
Static WEP (Shared Key
authentication)
WPATM-Personal (PSK)
Required fields
•
WEP keys
•
Encryption (if different than TKIP)
•
PSK
Chapter 4 Configuration
No FIPS
FIPS ON
Y
N
Y
N
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DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Table 4-7
Authentication type
WPATM-Enterprise (EAP)
WPA2TM-Personal (PSK)
WPA2TM-Enterprise (EAP)
WPA2TM-Enterprise (EAP)
Required fields
•
Encryption (if different than TKIP)
•
Identity
•
Password
•
Client certificate
•
Inner Auth
•
Private key file
•
Private key password
•
PEAP version (only if EAP method is set to PEAP)
•
Encryption (if different than TKIP)
•
PSK
•
Encryption (if different than CCMP)
•
Identity
•
Password
•
Client certificate
•
Inner Auth
•
Private key file
•
Private key password
•
PEAP version (only if EAP method is set to PEAP)
•
EAP-TLS
No FIPS
FIPS ON
Y
N
Y
Y
Y
N
N
Y
6.
Click ADD.
7.
Select the Current Status tab, and click CONNECT. Verify successful connection message.
8.
To verify connectivity:
a.
Select FILE menu > TOOLS.
b.
Enter the IP of the machine you want to ping.
c.
Press START PING and check for messages verifying connectivity.
d.
Press STOP PING.
4.2.6.3 Configuring non-broadcast SSID networks
1.
2.
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On the Wireless configuration screen, select NETWORK menu > ADD.
Select IP settings:
-
If the system will be identified on the network by a static IP address, select STATIC IP,
and enter the IP address, netmask, and gateway. If no gateway is used, you must enter
0.0.0.0.
-
If the system will be identified on the network using DHCP, select DHCP.
3.
Enter the network SSID.
4.
Choose the authentication type.
Section 4.2 Using the System Configuration Tool (SUIF)
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Some fields are auto-populated. Depending on the type of authentication, complete the other
required information, as described in the table below:
Table 4-8
Authentication type
Required fields
No FIPS
FIPS ON
Static WEP (Shared Key
authentication)
•
WEP keys
Y
N
WPATM-Personal (PSK)
•
Encryption (if different than TKIP)
Y
N
•
PSK
•
Encryption (if different than TKIP)
Y
N
•
Identity
•
Password
•
Client certificate
•
Inner Auth
•
Private key file
•
Private key password
•
PEAP version (only if EAP method is set to PEAP)
•
Encryption (if different than TKIP)
Y
Y
•
PSK
•
Encryption (if different than CCMP)
Y
N
•
Identity
•
Password
•
Client certificate
•
Inner Auth
N
Y
WPATM-Enterprise (EAP)
WPA2TM-Personal
(PSK)
WPA2TM-Enterprise (EAP)
WPA2TM-Enterprise (EAP)
•
Private key file
•
Private key password
•
PEAP version (only if EAP method is set to PEAP)
•
EAP-TLS
5.
Click ADD.
6.
Select the Networks tab, and verify that the network is listed.
7.
Select the Current Status tab, and click CONNECT. Verify successful connection message.
8.
To verify connectivity:
a.
Select FILE > TOOLS.
b.
Enter the IP of the machine you want to ping.
c.
Press START PING and check for messages verifying connectivity.
d.
Press STOP PING.
4.2.6.4 Troubleshooting connections
If you try to connect in an enterprise situation, it will continue to try to connect until you tell it to stop
by selecting DISCONNECT.
Chapter 4 Configuration
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GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
4.2.7 Options configuration
The Optima XR200amx/XR220amx systems are delivered with a base set of operating software
that is configured for immediate operation.
Optional software and hardware purchased by the site must be enabled by GE Healthcare service
personnel, such as:
•
Wireless network connectivity
•
DAP (Dose Area Product) meter (standard with Optima XR220amx, optional for Optima
XR200amx)
•
Repeat Reject Analysis (RRA) (Optima XR220amx or Optima XR200amx with digital upgrade
only)
•
Auto Protocol Assist (APA) (Optima XR220amx or Optima XR200amx with digital upgrade
only)
•
Generator Power - 30kW
4.2.8 InSite configuration
Contact a GE service representative to configure InSite ExC settings.
4.2.9 PNF configuration
The Firewall option at the top of the PNF area must be set to On. If it is set to Off, select TURN
FIREWALL ON.
•
When the firewall is off, all network traffic in both directions is allowed. This setting is used
primarily for troubleshooting.
•
When the firewall is on, it allows only the network communications that are specified by its
configuration and rejects all the rest.
After modifying any PNF options, select RESTART FIREWALL to apply the changes.
4.2.9.1 PNF GUI Control area
The PNF GUI Control area, near the top of the screen, contains these options:
Table 4-9 PNF GUI Control options
Option
Filter Settings
Action
Configure filter settings that allow access through the firewall by
adding allowed services and IP addresses, and removing filters.
Options:
BACKUP CURRENT FILTERS: Create a backup of the current filters.
Backup/Restore
RESTORE FROM BACKUP FILTERS: Restore the filters to a
previously backed up set.
RESTORE TO FACTORY DEFAULTS: Reset all filter settings to
those originally installed.
REMOVE BACKUP FILTERS:
Page 64
Network Tools
Show the firewall rules that are currently in effect on this system.
Select REFRESH to refresh the list of rules.
Configure PNF
Select which red interfaces the filter settings should be applied to.
Select UPDATE RED INTERFACES to apply the changes.
Section 4.2 Using the System Configuration Tool (SUIF)
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
4.2.9.2 PNF tabs and parameters
Table 4-10 PNF parameters
Option
Description
Named Services tab
Used to set up filters to allow traffic to common network services (such as telnet or ftp) by
name, without needing to know the port and protocol.
Services/Allowed IPs
Lists current filters by name and IP.
Remove Existing Filters
Select the Delete box checkbox next to the filter to delete, then
select DELETE EXISTING FILTERS.
From the Service Name drop-down list, select the service to be
allowed (such as telnet, ssh, ftp).
Add New Filter
In the Allowed IPs field, specify a particular IP address, a range
of IP addresses, or a masked subnet.
Select ADD FILTER to apply your changes.
Allowed Nodes tab
Used to set up filters to allow all traffic from specified nodes. You can specify a particular IP
address, a range of IP addresses, or a masked subnet.
Allowed IPs
Lists current filters by IP.
Remove Existing Filters
Select the Delete box checkbox next to the filter to delete, then
select DELETE EXISTING FILTERS.
Add New Filter
In the Allowed IPs field, specify a particular IP address, a range
of IP addresses, or a masked subnet.
Select ADD FILTER to apply your changes.
DICOM tab
Used to add DICOM port numbers (all IP addresses are allowed DICOM access; the DICOM
application may limit access by IP). You can add multiple DICOM ports.
Allowed DICOM Ports
Lists current DICOM ports by number.
Remove Existing Filters
Select the Delete box checkbox next to the port to delete, then
select DELETE EXISTING FILTERS.
Add New Filter
In the Allowed Port field, specify a particular DICOM port.
Select ADD FILTER to apply your changes.
Expert tab
Used to set up detailed filters by port, protocol, and node-lock (source).
Used only by advanced IT users.
Name/Port/Protocol
Lists current filters by name, port number, protocol, and IP.
Remove Existing Filters
Select the Delete box checkbox next to the filter to delete, then
select DELETE EXISTING FILTERS.
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DIRECTION 5336113-1EN, REVISION 10
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INSTALLATION MANUAL
Table 4-10 PNF parameters
Option
Description
In the Name field, specify the filter name.
In the Allowed IPs field, specify a particular IP address, a range
of IP addresses, or a masked subnet.
Add New Filter
In the Allowed Port field, specify a particular port.
From the Protocol drop-down list, select the protocol to be
allowed (TCP, UDP, Any).
Select ADD FILTER to apply your changes.
NAT tab
Used to define NAT (Network Address Translation) rules.
Name/Source IP/Dest. IP
Lists current filters by name, source IP, destination IP,
destination port, and protocol.
Remove Existing Filters
Select the Delete box checkbox next to the filter to delete, then
select DELETE EXISTING FILTERS.
In the Name field, specify the filter name.
In the Source IP field, specify the source IP.
In the Destination IP field, specify the destination IP.
Add New Filter
In the Destination Port field, specify the destination port.
From the Protocol drop-down list, select the protocol to be
allowed (TCP, UDP, Any).
Select ADD FILTER to apply your changes.
GE Service tab
Used to set IIP node-lock IP address and DICOM port. This page is limited to GE service
personnel.
4.2.10 Time Server configuration
Contact a GE service representative to configure Time Server settings.
4.2.11 Secure Login configuration
Select SAVE to apply your changes, or CANCEL to cancel them.
Use the arrow buttons to move through the pages.
Table 4-11 Secure Login options
Option
Description
Audit Message Settings tab
Audit Source ID
IP address of audit message source.
Patient Name
Anonymized
On or Off.
Enterprise Repository tab
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Enterprise Repository 1
On or Off.
Host Name/IP
Primary audit server name or IP.
Section 4.2 Using the System Configuration Tool (SUIF)
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Table 4-11 Secure Login options
Option
Description
Port Number
Port number used to communicate with primary audit server.
Protocol
Protocol used to communicate with primary audit server (TCP,
UDP).
Send Test Message
Test connection with primary audit server.
Enterprise Repository 2
On or Off.
Host Name/IP
Secondary audit server name or IP.
Port Number
Port number used to communicate with secondary audit server.
Protocol
Protocol used to communicate with secondary audit server.
Send Test Message
Test connection with secondary audit server.
Local Repository tab
On/Off
Radio buttons.
Refresh
Button to refresh the list.
Event ID / Time / Event
Outcome
Headers for list of messages.
Display Raw XML
Display the raw data file to the user.
Section 4.3 Changing Auto Protocol Assist settings
Contact a GE service representative to change Auto Protocol Assist settings.
Section 4.4 DICOM connectivity configuration
Follow the procedures in this section to configure DICOM connectivity to network hosts and printers.
After successful configuration, use the tables below to capture the system’s DICOM connectivity
configuration for future reference. Store the worksheets in a secure location at the site.
4.4.1 Network host configuration
4.4.1.1 Adding network hosts
This section provides instructions for setting the system preferences for network host connections.
1.
Turn on the system.
2.
On the Applications desktop, press the UTILITIES button.
3.
On the Utilities desktop, next to Network Connections, press EDIT.
4.
On the Network Connections window, in the Network Hosts section, press ADD.
The Add Network Host screen appears.
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DIRECTION 5336113-1EN, REVISION 10
5.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
On the Add Network Host window, on the Host tab, enter the appropriate values in the fields
listed below. Some fields are available only on the Optima XR220amx or Optima XR200amx
with digital upgrade system.
Table 4-12 Add Network Host – Hosts tab description
Function
Description
Host Label
Name of the host that appears in the Network Hosts lists and
on the Image Management screen. Host labels cannot
contain spaces; use underscores ( _ ) to separate words.
Application Entry Title
DICOM application title.
IP/Network Address
IP address of the network host.
Port Number
Port number for the network host.
Query Retrieve
Storage Commitment
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Type of information the host will provide upon query from
another host. Options are No provider, Study, and Patient.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Designates whether the host will store image data.
Storage Commitment Application Entry Title (if
Storage Commitment is
Yes)
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
DICOM application title.
Available only on the Optima XR220amx or Optima
Storage Commitment Network Address (if Storage XR200amx with digital upgrade system.
Commitment is Yes)
IP address of the storage database.
Storage Commitment - Port Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Number (if Storage
Commitment is Yes)
Port number for the storage database.
Comments
Area for notes about the network host or configuration.
6.
Press SAVE.
7.
Select the PREFERENCES tab.
8.
On the Add Network Host window, on the Preferences tab, select the appropriate options as
described below. All options except "Make this network host the HIS/RIS source" are available
only on the Optima XR220amx or Optima XR200amx with digital upgrade system.
Table 4-13 Add Network Host – Preferences tab description
Function
Allow this network host to query the
(system name)
Description
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Allows this host to search and filter the system.
Available only on the Optima XR220amx or Optima
Allow this network host to retrieve from XR200amx with digital upgrade system.
the (system name)
Allows this host to open and display exams from the
system.
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Section 4.4 DICOM connectivity configuration
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Table 4-13 Add Network Host – Preferences tab description
Function
Description
Available only on the Optima XR220amx or Optima
Allow this network host to send images XR200amx with digital upgrade system.
to the (system name)
Allows the host to send images to the system.
This network host accepts multiple
frame image.
Perform de-identification (anonymous
patient images) when sending to this
network host.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Allows multiple frame images to be sent to this
network host.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Automatically de-identifies (anonymizes) any
images that the system sends to this host.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Burns the VOI LUT (Look-Up Tables) into the
Apply “Burn-On-Send” to images when DICOM header to be displayed by PACS. Leaving
this option unselected sends all available VOI LUTs
sending to this network host.
to the DICOM header for PACS to query and apply.
Note: PACS should be configured to read the first
VOI LUT for proper display of images on the
Acquisition workstation.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Send MPPS N-Create and N-Set
notification to this network host.
Make this network host the HIS/RIS
source. (Only one host can be
designated as the HIS/RIS source.)
DR Images sent as CR Modality
This node acts as the Destination for receiving the
MPPS NCreate & N-Set Notification. When
configured for MPPS, the System sends information
like which exam is in progress, when a Study is
completed, how many images were acquired, and
what was the radiation dose to which the patient
was exposed during that session, etc.
Designates the host as the DICOM Worklist
provider. Defining the Radiology Information
System (RIS) and Hospital Information System
(HIS) host allows patient worklists to be downloaded
from those networks to the system.
Note: Only one HIS/RIS source may be designated
on the system. Selecting this option will de-select
any other hosts as the HIS/RIS source.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Options are Yes or No.
9.
Press SAVE.
10. Repeat this process for each network host device the site wants to add.
4.4.1.2 Performing a C-Echo test
Use this function to determine if the system is communicating with a particular network host.
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INSTALLATION MANUAL
On the Applications desktop, press the UTILITIES button.
2.
On the Utilities desktop, next to Network Connections, press EDIT.
3.
On the Network Connections window, in the Network Hosts section, select the network host
connection to test, and press C-ECHO TEST.
A message appears saying whether the test passed or failed.
-
A “passed” message means that the network host is working and that exams can be
retrieved from or transferred to it.
-
A “failed” message means that the system could not contact the network host. Perform
the following tasks to resolve the problem:
*
Re-try the test at a later time. The host may be temporarily unavailable.
*
Confirm the host configuration on the Edit screen. (On the Network Connections
window, in the Network Hosts section, select the network host connection to verify,
and press EDIT.
If the problem persists, contact the technical support group or system administrator.
4.4.1.3 Removing network hosts
Follow these instructions to remove a network host.
1.
On the Applications desktop, press the UTILITIES button.
2.
On the Utilities desktop, next to Network Connections, press EDIT.
3.
On the Network Connections window, in the Network Hosts section, select the network host
connection to delete, and press REMOVE.
A message appears saying “Are you sure you want to remove (host name)?”
4.
Press YES to remove the network host connection.
4.4.2 Printer configuration
Printer connections are available only on the Optima XR220amx or Optima XR200amx with digital
upgrade system.
4.4.2.1 Adding printers
This section provides instructions for setting the system preferences for printer connections.
1.
Turn on the system.
2.
On the Applications desktop, press the UTILITIES button.
3.
On the Utilities desktop, next to Network Connections, press EDIT.
4.
On the Network Connections window, in the DICOM Printers section, press ADD.
The Add Printer screen appears.
5.
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On the Add Printer window, on the Printer tab, enter the appropriate values in the fields listed
below.
Section 4.4 DICOM connectivity configuration
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
For suggested parameter values for specific printer brands and models, refer to the System
Manual, Appendix A Printer configuration.
Table 4-14 Add Printer screen parameter descriptions
Attribute
Value
Printer tab
DICOM Printer Label
Name of the printer that appears in the DICOM Printers list
and on the print setup screens. DICOM printer labels
cannot contain spaces in the name. Use underscores ( _ )
to separate words.
Application Entry Title
DICOM application title, provided by the site’s network
administrator.
Network Address
IP address of the printer, provided by the site’s network
administrator.
Port Number
Port number of the printer. May be site-specific; check with
site.
Pixel Depth
Resolution of the printer. Options are 10 or 12.
Printer Pixel Size (micron)
Designates the pixel size the printer uses. This is specified
by the printer manufacturer.
Configuration Information
Area for notes about the printer or configuration.
Density Min
Minimum density range.
Density Max
Maximum density range.
Magnification Type
Options are Replicate, Bilinear, Cubic, None.
Smooth Factor
Image smoothing factor.
Trim
Designates whether there is to be trim. Yes or No.
Polarity
Options are Normal, Reverse.
Border Density
Color of the image border. Options are Black, White.
Empty Image Density
Color of areas that have no image printed. Options are
Black, White.
Printer Memory Size
Designates the memory size of the printer, in Mbytes. This
is specified by the printer manufacturer.
Layouts tab
Select the desired layouts
allowed for this printer
Slide formats
Number and layout of images that may be printed on a
single sheet of film or paper.
Some selections control the orientation of the images on
the page. For example, two images per page may be side
by side, or one above the other.
Slide formats available for the printer, if any. Options are 35
or 40 mm.
Film Sizes tab
Select the sizes of film available for this printer, and enter the pixel width (W) and pixel height
(H). Pixel width and height values are provided by the printer manufacturer based on what
the printer supports.
Printer Settings tab
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Table 4-14 Add Printer screen parameter descriptions
Attribute
Value
# Of Copies
Print Mode
Magnification
Format
Orientation
Media Type
Destination
Media Size
6.
Press SAVE.
7.
Repeat this process for each printer the site wants to add.
4.4.2.2 Removing printers
Follow these instructions to remove a printer.
1.
On the Applications desktop, press the UTILITIES button.
2.
On the Utilities desktop, next to Network Connections, press EDIT.
3.
On the Network Connections window, in the DICOM Printers section, select the printer
connection to delete, and press REMOVE.
A message appears: “Are you sure you want to remove (printer name)?”
4.
Press YES to remove the printer connection.
Section 4.5 Image management
Image management parameters let the site control how images will be handled after acquisition,
including printing, archiving, and deleting. For more information about image management
parameters, including Auto Print, Auto Send (sometimes called Auto Push), and Auto Delete, refer
to the Optima XR220amx or Optima XR200amx with digital upgrade Operator Manual.
Section 4.6 Image processing
4.6.1 Enabling EMI reduction
The EMI Reduction algorithm is designed to reduce artifacts resulting from electromagnetic
interference from other equipment in the area during image acquisition.
Administrative users can enable or disable EMI reduction using the UTILITIES > PREFERENCES
> IMAGE PROCESSING screen.
Contact a GE service representative to configure EMI reduction factors.
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Section 4.5 Image management
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INSTALLATION MANUAL
Section 4.7 Loading demo images
Load demo images from the CD-ROM provided with the system into the image database. This is
applicable only to Optima XR220amx or Optima XR200amx with digital upgrade systems.
Refer to the Optima XR220amx Operator Manual’s chapter on Image Management for more details.
4.7.1 Loading images from CD
Follow this process to access images stored on a CD.
1.
Attach the external CD/DVD drive, and insert the disk with images into the CD/DVD drive.
2.
On the Image Management screen, press Source CD1.
3.
Select the exams to copy.
4.
Copy the exams to the Local database.
5.
Press the LOCAL Destination button.
The exam list is updated to show the images stored on the CD.
A message appears: “Selected images will be copied to (destination name).
Select OK to confirm.“
6.
Press OK.
7.
Open the exams from the Local database.
If the exams are being viewed on a computer that has the DICOM viewer installed, images may
be viewed directly from the disk.
Section 4.8 Installing the Operator Manual
Optima XR220amx and Optima XR200amx with digital upgrade systems only.
Note:
To install the Operator Manual (OM), you need the Account and Password information. Please
consult your administrator for them.
To install the Operator Manual (OM), follow these steps:
1.
Attach the external CD/DVD drive.
2.
Exit all service applications, and close the SUIF.
3.
Connect the service keyboard to a USB port.
4.
Press these keys simultaneously:
CTRL+ALT+F2
5.
At the login prompt, type the Account: xruser.
Note: Please consult your administrator for the Account.
Press ENTER.
6.
Enter the password: 4$xray
Note: Please consult your administrator for the Password.
Press ENTER.
7.
Insert the Operator Manual CD into the external CD/DVD drive.
8.
To run the interactive script, at the prompt, type:
./xrdinstall.om
Press ENTER.
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9.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
At the prompt, type Y.
10. Type the number of the language to install, then press ENTER.
11. When the installation is complete, at the prompt, type:
exit
Press ENTER.
12. To return to the applications screen, at the login prompt, press these keys simultaneously:
CTRL+ALT+F7
Section 4.9 Login and user management
GE service engineers must create a specified Account and Password for system administrator.
System administrators can perform a number of tasks that affect what users can do or will see. The
administrative options are described in the Optima XR200amx or Optima XR220amx Operator
Manual, Appendix A Login Administration.
Note:
If you meet any question about the Account and Password information, please consult your
administrator.
Note:
Except the login and user management account and password created specially to the system
administrator, GE field engineers also need to provide the related account and password
information to system administrator for the below configuration:
•
Installing the Operator Manual.(Account:xruser/Password:4$xray)
•
IP Address Change Procedure.(Account:su/Password:#superxr)
Section 4.10 Installing hardware options
4.10.1 Installing the barcode reader
Applies to Optima XR220amx or Optima XR200 with digital upgrade systems only
Unpack the OPI-4002 barcode reader and associated components.
Note: The USB cable is packaged and shipped in a separate box than the barcode reader
assembly.
4.10.1.1 Installing the barcode reader receiver
1.
Plug the USB cable into the barcode reader receiver. See Figure 4-1.
Note: If the position of the label makes the barcode unreadable, move the label so the barcode
can be read. A sample label similar to the one on the USB receiver is shown in Figure 4-1
below.
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INSTALLATION MANUAL
Figure 4-1 Sample barcode label
2.
Remove the system side covers and the top cover. See the System manual, Replacement
Procedures, Top cover removal.
3.
Remove the two screws from the inside of the left drive handle support, then remove the cover.
See Figure 4-2.
Figure 4-2 Left drive handle screws and cover
4.
Route the USB cable through the opening in the bottom of the left drive handle support. See
Figure 4-3.
Note: You may need to loosen the detector bin mounting screws to provide clearance for
routing the cable.
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Cable
access
hole
Figure 4-3 Cable access hole and receiver placement on system
Page 76
5.
Attach the USB receiver to the plastic clip with the barcode facing out as shown in Figure 4-3.
6.
Plug the USB cable into a USB port on the PC. See Figure 4-4.
Section 4.10 Installing hardware options
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Item
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Description
1
Host PC
2
Detector power supply (Optima XR220amx and Optima XR200amx with digital
upgrade only)
Figure 4-4 Connect USB cable to PC
The Windows standard device driver will be installed automatically when you connect the
barcode reader receiver to the USB port and the system is powered up.
During initialization, the LED is orange. When the receiver LED turns green, the initialization
is complete and a connection has been made.
4.10.1.2 Connecting the barcode reader
1.
Turn on system power.
2.
Verify that the USB receiver is connected and that the green LED is blinking.
3.
On the barcode reader, press the trigger key to start scanning.
4.
Scan the barcode label on the USB receiver (Figure 4-1) to register the barcode reader.
The connection is complete and the barcode reader is ready for use.
Do not replace the covers at this point. You will need to scan the barcode receiver label
during configuration.
5.
Each time the system is rebooted, a message saying, “Do you want to connect to a
bluetooth SPP?" appears. The user needs to select YES or the barcode reader functionality
will not be enabled.
4.10.1.3 Barcode reader LED indicators
By default, the OPI-4002 scanner is in power saving mode. To turn it on, press the trigger key for a
few seconds. If the scanner is not in use for a while, it will go into sleep mode and the trigger key
must be pressed for a few seconds to reactivate the unit before scanning.
The table below lists the state of the scanner based on the scanner LEDs.
Table 4-15 LED indicator state
Color
Description
Green
Barcode was successfully read.
Red Blinking
Data transmission error. The battery may need to be charged.
Red Solid
Charging on the cradle. The LED changes from red to green when the battery
is fully charged.
4.10.1.4 Charging the barcode reader
The barcode reader will not start up if the battery is empty. Use the charging cradle to charge the
battery. It takes about three hours to fully charge a battery. Adapters are provided to connect the
AC/DC converter to various power outlet configurations.
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INSTALLATION MANUAL
Figure 4-5 OPI-4002 barcode reader charging cradle and power adapters
4.10.2 Configuring the barcode reader
Applies to Optima XR220amx or Optima XR200 with digital upgrade systems only
The following section provides instructions for the default configuration and two optional settings.
Have a printed copy of these pages on hand so you can scan the necessary barcodes. Refer to the
OPI-4002 User’s Guide for additional configuration options.
4.10.2.1 Setting to default configuration
1.
Turn on the system. Wait until the green LED on the barcode reader receiver starts flashing.
2.
Press the barcode reader trigger to start the scan.
3.
Scan the Reset To Default barcode.
Figure 4-6 Reset to Default barcode
You will hear three quick sets of high-low-high beeps.
Whenever you scan the Reset To Default barcode, rescan the barcode label (on the barcode
reader receiver) and re-program any optional configuration.
4.
Scan the barcode label (Figure 4-1) on the barcode reader receiver to register the barcode
reader.
You will hear one set of high-low beeps, a short pause, and then one long high beep.
The connection is complete and the barcode reader is ready for verification.
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Section 4.10 Installing hardware options
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INSTALLATION MANUAL
4.10.2.2 Verifying the default configuration
1.
Turn on the system. Wait until the login screen appears.
2.
Verify that a green LED is blinking on the barcode reader receiver.
3.
Scan any barcode.
You will hear one set of high-low beeps. The scanned barcode characters appear in the Login
ID field on the login screen, and the cursor remains at the end of the scanned barcode.
The configuration is successful and the barcode reader is ready for use.
4.
Replace the system covers.
4.10.2.3 Optional configuration 1
Optional configuration 1 is to add a Tab at the end instead of Return.
This configuration sets the barcode reader to add a Tab at the end of the scan instead of a Return.
Have a printed copy of these pages on hand so you can scan the necessary barcodes. If you make
a mistake during this configuration, start over at step 1.
1.
Power up the system. Wait until the green LED on the receiver starts flashing.
2.
Perform 4.10.2.1 Setting to default configuration on page 78.
3.
Scan the barcodes shown in Figure 4-7, top to bottom.
After scanning each barcode you will hear one set of high-low-high beeps. The scanner will
beep at a one-second interval, and the LED will alternate green and red.
After scanning the last barcode, the scanner beam will turn off.
SET
RZ
TAB
END
Figure 4-7 Set Tab at the end instead of Return
4.10.2.4 Verifying optional configuration 1
1.
Turn on the system. Wait until the login screen appears.
2.
Verify that a green LED is blinking on the barcode reader receiver.
3.
Scan any barcode.
You will hear one set of high-low beeps. The scanned barcode characters appear in the Login
ID field on the login screen, and the cursor moves to the Password field.
The configuration is successful and the barcode reader is ready for use.
4.
Replace the system covers.
Chapter 4 Configuration
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INSTALLATION MANUAL
4.10.2.5 Optional configuration 2
Optional configuration 2 is to strip first two and last four characters, and add a Tab suffix.
This configuration sets the barcode reader to strip the first two and last four characters, and add a
Tab at the end of the scan. Have a printed copy of these pages on hand so you can scan the
necessary barcodes. If you make a mistake during this configuration, start over at step 1.
1.
Power up the system. Wait until the green LED on the receiver starts flashing.
2.
Perform 4.10.2.2 Verifying the default configuration on page 79.
3.
Scan the barcode shown in Figure 4-8.
After scanning the barcode you will hear three sets of high-low-high beeps.
Figure 4-8 Strip first two and last four characters, and add a Tab suffix
4.10.2.6 Verifying optional configuration 2
1.
Turn on the system. Wait until the login screen appears.
2.
Verify that a green LED is blinking on the barcode reader receiver.
3.
Scan any barcode.
You will hear one set of high-low beeps. The scanned barcode characters appear in the Login
ID field on the login screen, with the first two and last four characters stripped. The cursor
moves to the Password field.
The configuration is successful and the barcode reader is ready for use.
4.
Replace the system covers.
4.10.3 Installing the Dose Area Product (DAP) meter
4.10.3.1 DAP installation for Optima XR220amx system
Page 80
1.
Shut down the system and turn off the main circuit breaker.
2.
Unpack the DAP meter.
3.
Slide the meter into the lower set of collimator rails (the set further from the collimator). The
meter must be installed with the cable exiting toward the rear.
4.
Connect the DAP cable to the existing connector in the cable drape. See Figure 4-9.
Section 4.10 Installing hardware options
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 4-9 DAP meter cable attached
5.
For Optima XR220amx systems, the DAP meter option is a standard option and has already
been enabled. It can be turned on/off at the Applications level.
a.
On the Applications desktop, click the UTILITIES button.
b.
On the Utilities desktop, select PREFERENCES > OPTIONS.
c.
Turn the DAP function ON.
d.
Refer to the system Operator Manual for instructions on DAP usage.
Notice: The system must be reset using the power button each time the DAP meter is
disconnected and then reconnected with system power on. The DAP meter does not support "Hot
Swapping". Failure to reset the system in this occurrence can result in an inaccurate dose value
reported by the DAP meter.
6.
Perform DAP calibration. See the System Manual, Calibration Chapter, Hardware Calibration/
DAP Calibration section, for calibration procedure.
4.10.3.2 DAP installation for Optima XR200amx system
1.
Shut down the system and turn off the main circuit breaker.
2.
Remove the side covers, top cover and front bin. See the System manual, Replacement
Procedures chapter, Front Bin Removal section.
3.
Remove the cable cover from the vertical column cable bundle:
a.
Cut the cable ties at the ends of the cable cover.
b.
Unzip and remove the cable cover.
4.
Unpack the DAP meter and cable.
5.
Slide the meter into the lower set of collimator rails (the set further from the collimator).The
meter must be installed with the cable exiting toward the rear.
6.
Install the DAP cable:
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a.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Connect the round cable connector to the DAP meter. See Figure 4-10.
Figure 4-10 DAP meter cable attached
b.
Route the long DAP cable through the cable drape along the horizontal arm and vertical
column.
Loosely attach cable ties to hold the cable in position, but do not tighten them until range
of motion is confirmed.
Leave enough extra cable length at the DAP meter so that the tube/collimator assembly
can be moved through the normal range of motion without unplugging the cable.
c.
Route the DAP cable through the cable access opening in the right-front cover. See
Figure 4-11.
d.
Remove the HV cable clamp mounting screws. See Figure 4-11.
1
Item
1
Description
HV cable clamp mounting screws (2)
Figure 4-11 HV cable clamp mounting screws
e.
Page 82
Remove the clamp from the HV cable bundle. See Figure 4-12.
Section 4.10 Installing hardware options
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DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 4-12 HV cable clamp
f.
Plug the other end of the DAP cable into the J6 bulkhead connector. See Figure 4-13.
Install cable ties as necessary to secure cable within the bulkhead area.
J6
Figure 4-13 DAP meter cable attached to J6 on bulkhead
7.
Confirm that there is sufficient slack in the DAP cable at the tube/collimator assembly:
a.
Move the tube/collimator assembly through the full range of motion and verify that the
DAP cable remains connected to the DAP meter.
b.
Once sufficient cable slack is confirmed, tighten down the cable ties to secure the DAP
cable to the existing cable drape.
8.
Arrange the cable bundle as shown in Figure 4-14, use a cable tie to maintain cable positions.
9.
Install the clamp onto the cable bundle. DO NOT TIGHTEN THE CLAMP YET.
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10. Mount the clamp to the Thorax chassis. Slide the clamp to the rear of the mounting screw slots.
11. Tighten the clamp around the cable bundle, ensuring that the cables are not pinched by the
clamp.
C
Item
1
2
4
3
Description
1
DAP cable (optional for Brivo XR285amxOptima XR200amx systems)
2
Wireless cable (only valid for Optima XR220amx systems)
3
Vertical brake cable
4
Horizontal arm lock cable
Figure 4-14 Correct cable bundle arrangement
12. Install the front bin, top cover and side covers.
13. Re-install the cable cover on the vertical column cable bundle. See the System manual,
Replacement Procedures chapter, Cable Cover Installation section.
14. Configure the system to enable the DAP meter option. See 4.2.7 Options configuration on
page 64.
15. Once the DAP meter option has been enabled, it must be ’switched on’ at the Applications
level:
Page 84
a.
On the Applications desktop, click the UTILITIES button.
b.
On the Utilities desktop, select PREFERENCES > OPTIONS.
c.
Turn the DAP function ON.
d.
Refer to the system Operator Manual for instructions on DAP usage.
Section 4.10 Installing hardware options
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
The system must be reset using the power button each time the DAP meter is disconnected and
then reconnected with system power on. The DAP meter does not support "Hot Swapping". Failure
to reset the system in this occurrence can result in an inaccurate dose value reported by the DAP
meter.
16. Perform DAP calibration. See the System Manual, Calibration Chapter, Hardware Calibration/
DAP Calibration section, for calibration procedure.
4.10.4 Installing the tablet holder assembly
When the tablet holder is on hand, contact a GE service representative to install the tablet holder
assembly.
1.
Shut down the system and turn off the main circuit breaker.
2.
Unpack the tablet holder assembly.
3.
Remove the 4 screws on the lead apron hanger, and then remove the lead apron hanger from
the column.
4.
Hang on the whole tablet holder assembly (item 2) on the column. Put the lead apron hanger
(item 3) on the tablet holder assembly in order to install the lead apron hanger and the tablet
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holder assembly on the column.Apply thread locker (i.e. Loctite 243 ) to the 4 tablet holder
assembly mounting screws (new item 1), and tighten the screws. Torque to 3.2 N-m (2.36 lbft).
3
1
2
Item
Description
1
Tablet holder assembly mounting screws (4)
2
Tablet holder assembly
3
Lead apron hanger
Figure 4-15 Installing the tablet holder assembly
5.
Unlock the tablet clamp assembly with the key.
lock
6.
Page 86
Lift up the top cover of the tablet holder clamp.
Section 4.10 Installing hardware options
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
7.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Put the tablet on the tablet holder and make sure the tablet is clamped well.
After you turn the key to lock the clamp, please check the back of the tablet clamp assembly to make
sure the tablet is well fixed by the clamp without any possibility to fall down from the holder. (See
below figures)
Front
Back
Not Clamped
8.
Well Clamped
Lock the tablet clamp assembly with the key and remove the key.
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Lock
Tablet
9.
Page 88
Tablet holder assembly functional check.
a.
Tilt the tablet holder from 10° to -10°.
b.
Rotate the tablet holder from 0° to 90°
c.
Pull the handle on the tablet holder assembly to relax it from the column.
Section 4.10 Installing hardware options
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
d.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Rotate the tablet holder arm around the column from 0° to 180°.
10. Hand over the keys to site administrator.
4.10.5 Installing the wireless exposure handswitch
Contact a GE service representative to install the wireless handswitch.
Leave the wired handswitch on the system as a backup.
1.
Remove both side covers and the top cover. See System manual 5336122-1EN, Chapter 8,
Section 8.1.2 - Top cover removal.
2.
Identify the components of the kit shown below (Table 4-16, Figure 4-16, Figure 4-17):
Table 4-16 Wireless handswitch kit 5503600
Part Number
5503600:
5503601
Description
Wireless Handswitch kit, contains the following items:
Wireless Handswitch Collector (see Figure 4-16):
PCB Module (with cable)
Spare transmitter
Remote Finder/Transmitter
Cradle
Receiver (with cable)
5486733
Receiver Mount (see Figure 4-17)
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Table 4-16 Wireless handswitch kit 5503600
Part Number
Description
5497064
Self-tapping Screw, KA35 X 10mm, Phillips Pan Head (not
shown)
5497362
Drill Bit, 0.5 inch with 0.375 inch shank (not shown)
5497364
Drill Bit, #22 (not shown)
5498227-1EN
Wireless Handswitch Installation Manual (this document)
46-302200P7
Rating Plate (not shown)
PCB Module
Spare Transmitter
Cradle
Remote Finder/Transmitter
Receiver
Figure 4-16 Wireless Handswitch Collector - 5503601
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OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 4-17 Receiver mount
3.
Remove the existing nut and washer located behind where the PCB Module is to be placed,
then attach the ground wire from the PCB Module to the system chassis stud and re-install the
washer and nut. See Figure 4-18.
Figure 4-18 Attach ground wire
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4.
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Mount the PCB Module in the bottom of the Thorax as shown below (Figure 4-19) by removing
the adhesive liner and applying pressure to activate the adhesive.
Figure 4-19 Mount PCB module in bottom of Thorax
5.
Route the cable attached to the PCB Module up along the main cable bundle between the
Spyder and Locust boards. See Figure 4-20.
Figure 4-20 Route cable
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Disconnect the J5 plug from the Spyder board and plug into End C of the main cable from the
PCB Module.
Plug End B of the main cable into Spyder J5.
See Figure 4-21 to see how connections appear after re-wiring is complete.
End B
J5 Connector
J5 Plug
End C
Spyder Board
Figure 4-21 Cable connection to Spyder board
7.
Remove the top-left mounting fastener on the Spyder board and mount the ground terminal,
End D, of the main cable underneath the head of the fastener. See Figure 4-22.
End D
Ground Fastener
Figure 4-22 Ground connection
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Continue routing the main cable (twisted black and red wires) up through the Thorax (Figure 423) to the LVLE2 and plug End A of the main cable into J6 on the LVLE2 (Figure 4-24).
Route red/black wires
up through opening in
top of Thorax
Figure 4-23 Route red/black wires
Connect to J6
Figure 4-24 Connect cable to LVLE2 J6
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Position the Receiver Mount on the top cover. The mount is curved and will fit the contour of
the top cover when it is located in the proper position. See Figure 4-25 for approximate
location.
Figure 4-25 Receiver mount location
10. While holding the Receiver Mount securely in position, mark the locations for the 3 mounting
holes and the cable access hole. See Figure 4-26.
Figure 4-26 Mark holes
11. Drill the holes in the top cover using the drill bits provided in the kit. See Figure 4-27.
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Figure 4-27 Drill holes
12. Temporarily remove the two nylon nuts from the standoffs on the Receiver. Run the cable of
the Receiver through the ½" diameter hole in the Receiver Mount, then place the Receiver onto
the Receiver Mount and reinstall the nylon nuts to secure it to the mount. Do not over-tighten
the plastic nuts. See Figure 4-28.
Figure 4-28 Assemble receiver and receiver mount
13. Use a pair of cutters to remove the excessive length of the standoffs so that they are flush with
the surface of the Receiver Mount. See Figure 4-29.
Figure 4-29 Trim standoffs
14. Run the cable of the Receiver through the ½" diameter hole in the top cover.
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15. Attach the Receiver/Mount assembly to the top cover using the 3 self-tapping screws provided
in the kit. See Figure 4-30. Do not over-tighten the screws.
Figure 4-30 Attach Receiver/Mount assembly to top cover
16. Route the cable along the power switch cable of the top cover. See Figure 4-31. Zip tie the
cables as necessary.
Figure 4-31 Route the cable
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17. Continue routing the cable along the side of the PC and down through the hole in the sheet
metal of the Thorax and between the Locust and Spyder boards. Plug the cable into the
connector on the PCB Module. See Figure 4-32. Zip tie the cables as necessary.
Figure 4-32 Route cable to PCB Module
18. Re-install the top cover and the side covers.
19. Mount the cradle (in the customer’s desired location) by removing the adhesive liner and
applying pressure to activate the adhesive.
20. Power up the system.
21. Press the collimator light button on the wireless handswitch.
If the collimator light on the system goes on, the wireless handswitch is ready for use.
22. Confirm that the system will take exposures using the wireless handswitch.
23. Apply the rating plate:
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Apply the rating plate label to front cover, next to the power cord area. See Figure 4-33.
Figure 4-33 Apply rating plate
b.
Fill out and submit the product locator card(s).
Section 4.11 Importing custom IP looks from Definium AMX
700
Use the following procedure to back up customized image processing (IP) looks from an Definium
AMX 700 system, and restore them on an Optima XR220amx system or Optima XR200amx with
digital upgrade.
1.
Make a system backup on the Definium AMX 700 system.
2.
On the Optima system, exit the SUIF if it is open.
3.
Insert the Definium AMX 700 system backup CD into the external CD/DVD drive of the system.
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4.
Press CTRL + SHIFT + F5 to open the Engineering User Interface.
5.
On the Engineering User Interface, press the TERMINAL icon.
6.
At the command prompt, type:
mount /media/cdrecorder
Press ENTER.
cd /magichome/xruser/config/restore/
Press ENTER.
7.
At the prompt, type:
chmod 777 restoreCustomIPLooks_F2toF3.sh
Press ENTER.
8.
At the prompt, type:
./restoreCustomIPLooks_F2toF3.sh
Press ENTER. The script takes approximately 20 minutes to run. When completed, the system
returns to the prompt.
9.
At the prompt, type:
umount /media/cdrecorder
Press ENTER.
10. Remove the Definium AMX 700 backup media from the CD/DVD drive and disconnect the
drive from the system.
11. Type exit to close the terminal window.
12. Exit the Engineering User Interface.
13. Reset the system.
Section 4.12 Enabling Advanced Service mode
Advanced Service (sometimes called “in-house service” or “extended service”) is available to
customers that have purchased an Advanced Service package license from GE Healthcare.
Contact a GE service representative to enable Advanced Service.
Advanced Service provides the following functionality:
•
SUIF in Advanced Service mode
•
Detailed error descriptions in the Service Error Log Viewer
•
Advanced diagnostics
•
Extended error log with filtering
The following functionality is never included in an Advanced Service license:
•
InSite ExC configuration
•
Advanced service configuration or entitlement
•
Purchased options configuration
Section 4.13 IP Address Change Procedure
The system uses IP Addresses 192.168.x.x for communication between the PC and the detectors.
If the hospital network to the PC is also 192.168.x.x, issues will occur. Perform the following
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instructions to change the default internal IP Address if an IP Address conflict occurs with the
hospital network.
To change IP address or configure the snapshot tool, you need the Account and Password
information. Please consult your administrator for them.
1.
Plug in the Service Keyboard.
2.
Open a terminal window using CTRL+SHIFT+F5 and click on the terminal window icon.
3.
Change users by entering the account and password at the prompt:
Note: Please consult your administrator for the Account and Password information.
su
#superxr
4.
Run the Change IP script by entering the following text at the prompt:
/magichome/xruser/engg/changeIp.sh
5.
Select 1 of the 5 options of subnet IP addresses. Write down the IP Address you select, you
will need this in a later step.
1.
172.16.x.x
2.
172.17.x.x
3.
172.18.x.x
4.
192.168.x.x (SW LFC default)
5.
192.169.x.x
6.
The PC will reboot automatically, select SHUTDOWN when the system presents the Degraded
mode screen.
7.
Login to system.
8.
Open a terminal window and become root.
Note: Please consult your administrator for the Account and Password information.
xruser@magic: su
Password: #superxr
At prompt, type: ifconfig | more
Confirm the br0 IP Address is XXX.XXX.3.1 (where XXX.XXX equals the address range
selected above).
9.
To test network connectivity, perform a C-Echo test to one or more of the Network Hosts.
10. This step applies to Optima XR220amx or Optima XR200amx with Digital Upgrade only.
Verify that all connected detectors boot successfully. Verify that you can take an exposure on
all available receptors.
11. This step applies to Optima XR220amx or Optima XR200amx with Digital Upgrade only.
Verify the Detector Wireless connection is active by acquiring an image.
12. Perform the Snapshot Tool Configuration.
4.13.1 Snapshot Tool Configuration
To ensure that the Auto-Snapshot Tool works after changing the IP Address.
1.
Open a terminal window using CTRL+SHIFT+F5 and click on the terminal window icon.
2.
Switch to root by entering the following text at the prompt:
Note: Please consult your administrator for the Account and Password information.
su
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#superxr
3.
Open Firefox Browser by typing the following command :
firefox http://localhost/snapshot/Manual_Snapshot.html
4.
Click on SNAPSHOT PREFERENCES. See Figure 4-34.
Figure 4-34 Snapshot Preferences
5.
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Repeat Steps 6 through 17 (below) for the following four Configurations (available under the
drop-down menu):
*
Asnapshot_Lightning
*
ASnapshot_BKP
*
Snapshot_ResetTimeOut
*
QuickSnapshot
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6.
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In the Configuration drop-down menu, select ASNAPSHOT_LIGHTNING. See Figure 4-35.
Figure 4-35 Select Configuration
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In Server Names section, click on EDIT. See Figure 4-36.
Figure 4-36 Edit Server Name - Magic
7.
In the IP Address data entry text box, change 192.168.3.1 to “xxx.xxx.3.1” (where
xxx.xxx.3.1 is the same IP Address range used in Section 4.13 IP Address Change
Procedure and 3.1 is the specific address assignment for the host pc port). See Figure 437.
Figure 4-37 Change IP Address
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Click on SUBMIT. See Figure 4-38.
Figure 4-38 Submit New IP Address
9.
Under Target Names - Magic, click EDIT. See Figure 4-39.
Figure 4-39 Edit Magic Target Name
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10. In the IP Address data entry text box, change 192.168.3.1 to “xxx.xxx.3.1” (where
xxx.xxx.3.1 is the same IP Address range used in Section 4.13 IP Address Change
Procedure and 3.1 is the specific address assignment for the host pc port). See Figure 440.
Figure 4-40 Edit Magic IP Address
11. Click on SUBMIT. See Figure 4-41.
Figure 4-41 Submit New Magic IP Address
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12. Back on Snapshot Preferences main screen, click on Target Names – Table_IDC –
DELETE. See Figure 4-42.
Figure 4-42 Delete Target Name “Table_IDC”
13. You will get a popup like below, select OK. See Figure 4-43.
Figure 4-43 Table_IDC Popup Message
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14. Under Target Names – WallStand_IDC click on DELETE. See Figure 4-44.
Figure 4-44 Delete Target Name “WallStand_IDC”
15. You will get a popup like below, select OK. See Figure 4-45.
Figure 4-45 WallStand_IDC Popup Message
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16. Under Manage Preferences section, click on SAVE AS.... See Figure 4-46.
Figure 4-46 Save Changes
17. Go to Step 5 until all four configurations are completed.
18. Press CTRL+F4 at the same time to close the html interface.
19. Success Check Steps:
If everything is fine you should be able to see Auto Snapshots getting generated after
reset:
a.
Perform a system reset.
b.
After system is booted up, login and wait for 5 minutes.
(Snapshot is being created in a temp location)
c.
While you are waiting, open a terminal window using CTRL+SHIFT+F5 and click
on the terminal window icon.
d.
Run following command:
ls –ltr /enggdata/Snapshots/*3400017*.zip
e.
Note the date/time stamp of the most recently created file.
f.
After 5 minutes reset and reboot the system, login.
(Snapshot from temp location is written to Snapshots directory and a new
snapshot is being created in a temp location)
g.
Open a terminal window using CTRL+SHIFT+F5 and click on the terminal
window icon.
h.
Run following command:
ls –ltr /enggdata/Snapshots/*3400017*.zip
i.
The output of (c) above should show a snapshot file, having the string 3400017
embedded in the snapshot filename, created after the most recent system boot
(in Step b above).
j.
Type date to see the current system time.
The latest snapshot file should have been created a few minutes before the date
command output.
k.
Verify the file size is greater than 400,000:
-rw–rw-r- - 1 xruser xruser file size date time /path/filename
20. Close all windows.
21. Complete all system configurations and customer settings.
22. Create a new System Backup on DVD media.
Note: Do not use backup media from any other system. The result will be that half of the
system is configured for 172.x.x.x and other half is configured for 192.x.x.x
The system will then boot into Degraded Mode only.
Also, when performing a Software Load, you must perform this procedure first before
doing a System Restore.
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Chapter 5 Calibration
This chapter explains how to calibrate the printer and configure PACS features. No other
calibrations are required during system installation. The unit has been fully calibrated and tested
during the manufacturing process. If desired, please reference the System manual for instructions
of the various calibration processes.
Section 5.1 Saving changes
After changing, creating, or restoring calibration files, be sure to reboot the system so that the
application software can detect the file changes.
After completing the steps in this chapter, save the changes by performing a system backup. See
Chapter 3 System data and software in the Optima XR200amx/XR220amx System Manual for
the backup procedure.
Section 5.2 Detector calibration
The detector contains a complete set of calibration files. These files are uploaded to the system
upon first tether connection. There is no need to perform any detector calibrations unless QAP fails
or the system reports incompatible detector firmware. See the System Service manual for details
related to detector calibrations.
Section 5.3 Image quality calibration
Image quality calibrations apply only to Optima XR220amx or Optima XR200amx with digital
upgrade systems.
5.3.1 Calibrating the printer
Follow this procedure to send grayscale output to the printer and to calculate compensation LUT
(look up table) for compatibility.
1.
On the Applications desktop, press the UTILITIES button.
2.
On the Utilities desktop, press LAUNCH.
3.
On the SUIF home page, press the CALIBRATION tab button.
4.
On the Calibration page, in the left folder tree, select IMAGE QUALITY > PRINTER.
5.
Press the CALIBRATION icon.
6.
In the left frame, select IMAGE QUALITY > PRINTER.
7.
Select the correct printer from the Printer Label drop-down list.
8.
Press START and follow the on-screen instructions.
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Section 5.4 PACS image tests
PACS image tests apply only to Optima XR220amx or Optima XR200amx with digital upgrade
systems.
Follow these procedures to test image display characteristics and determine the burn configuration
for PACS images for each destination host.
5.4.1 Comparing PACS test images
In the following tests, use the nine PACS test images to test image display characteristics and
determine image display configuration.
Each PACS test image consists of two aspects:
•
On the right, a clinical chest image with image number and GE logo watermark (Figure 5-1).
•
On the left, a series of 12 vertical bands. The top six bands are dark and the bottom six are
bright.
Inside each band are five small squares with different intensities (like the 5%/95% squares in
a SMPTE pattern). The squares provide a quantitative way to compare two images.
The pixel data in every test image is identical. Only the DICOM headers, annotations, and window
center (WC) and window width (WW) values are slightly different for each pattern.
Figure 5-1 PACS/image display test image
5.4.2 Determining PACS burn/no-burn configuration
5.4.2.1 Verifying PACS monitor calibration
1.
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Verify that the PACS monitor is calibrated according to DICOM Standard Part 14. Each site is
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responsible for providing evidence of PACS monitor calibration.
2.
At the application desktop, press IMAGE TOOLS.
3.
Click SMPTE to load the SMPTE pattern into the Patient List.
4.
Send the SMPTE pattern to the PACS review workstation
5.
Verify that 5% and 95% squares are equally visible on PACS (Figure 5-2).
Figure 5-2 SMPTE pattern
5.4.2.2 Loading test images
1.
2.
Load the PACS test images onto the acquisition workstation. Use either:
-
A DICOM-formatted CD-ROM with images.
-
Images that are stored on the system in Image Tools.
Verify that the patient name is GE_DX_Image_Display_Test, GEHC and the patient ID is
2000002.
5.4.2.3 Sending no-burn images to the PACS
1.
In the SUIF, press the UTILITIES tab button.
2.
Next to Network Connections, press EDIT.
3.
Select the appropriate network host and press EDIT.
4.
On the Preferences tab, verify that the following parameter is NOT checked:
Apply Burn-on-Send to images when sending to this network host.
5.
In the Images list, highlight PACS Test Image #1.
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In the Destination icon list, press the appropriate PACS network host.
5.4.2.4 Sending burn-on-send images to the PACS
1.
In the SUIF, press the UTILITIES tab button.
2.
Next to Network Connections, press EDIT.
3.
Select the appropriate network host and press EDIT.
4.
On the Preferences tab, check Apply Burn-on-Send to images when sending to
this network host.
5.
In the Images list, highlight PACS Test Image #6.
6.
In the Destination icon list, press the appropriate PACS network host.
5.4.2.5 Reviewing images on PACS
1.
On the PACS review workstation, display PACS test images #1 and #6. To identify an image,
look in the chest image region for the watermark image number next to the GE logo.
2.
Verify that image #1 is displayed with a Value-of-Interest Look-Up Table (VOI-LUT).
3.
Verify that image #6 is displayed with a Linear Look-Up Table (Linear LUT).
4.
Compare PACS Test Images #1 and #6 and note the following items:
a.
The number of distinct bright and dark bands (based on the band intensity)
b.
The number of squares visible in each band
Count bands that have distinct gray levels, not simply the number of bands with visible
squares. For example, in Figure 5-3, there are two squares in band #4, three squares in
band #5, and three squares in band #11. There are three distinct dark bands and six
distinct bright bands. This is because the top three dark bands are indistinguishable.
Figure 5-3 Example showing distinct bands and visible squares
5.
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-
If PACS test images #1 and #6 appear visually identical (with an equal number of bright
and dark bands), the PACS supports VOI-LUT. Configure the PACS as No-Burn for this
host.
-
If PACS Test Images #1 and #6 appear visually different (with a different number of bright
and dark bands), or if you can see saturation in the lung or abdomen of the chest region
(saturation appears as a completely flat dark or white area), the PACS does not support
VOI-LUT or applies it incorrectly. Configure the PACS as Burn-on-Send for this host.
Repeat sections 5.4.2.3 Sending no-burn images to the PACS and 5.4.2.4 Sending burn-onsend images to the PACS for each PACS destination host.
Section 5.4 PACS image tests
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Record the results in the table below.
Example
Distinct dark
bands
3
1
0
2
0
3
0
4
2
5
3
6
4
7
5
8
4
9
4
10
3
11
3
12
0
Distinct bright
bands
6
Test 1
Test 2
Test 3
Test 4
Test 5
Test 6
Test 7
Table 5-1 PACS image test results
In addition to the test results above, use Table 5-2 as a guideline to determine if a PACS should be
configured as Burn-on-Send. This table considers only whether a PACS supports VOI-LUT
No-Burn
Burn-on-Send
GE Centricity RA1000 v1.0, v2.0, v2.1
GE Pathspeed v7.12, 8.0
GE Centricity RA600 v6.1, 7.0
GE AW v3.1, 4.0
GE Radworks v5.1
Kodak DirectView v4.3
GE Pathspeed v8.1 or later
Kodak DirectView v5.1, 5.2
McKesson HRS v3.3, 3.3.2
Kodak Directview(CEMAX ICON), v4.3
Fuji Synapse v3.0, 3.1
Merge eFilm, v2.0
Agfa IMPAX v4.5, 5.2
Stentor iSite v3.0, v3.3.1
Philips
Siemens Magic View 300
RealTime iPACS Viewer v5.0
VA Vista
-
Picker
-
Neusoft v3.0
-
Thinking Systems
Table 5-2 PACS support of VOI-LUT
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5.4.3 Optional PACS tests
Perform the following tests to obtain further information for troubleshooting.
5.4.3.1 Sending all PACS test images
1.
2.
Send all nine images to PACS and follow the test instructions in Table 5-3:
-
Send images #1-5 as No-Burn
-
Send images #6-8 as Burn-on-Send
If the site is interested in exploring CR-Fallback as an option, configure the PACS for CRfallback with help from the local IT team. Then send image #9 as No-Burn.
Image #
Platform
Send
Annotation notes
1
All No-Burn
None
Test No-Burn mode
2
All No-Burn
None
Identical to #1
3
All No-Burn
None
Identical to #1
4
All No-Burn
Text
Test annotations
5
All No-Burn
L
Test annotations
6
All Burn-on-Send
None
Test Burn-on-Send mode
7
All Burn-on-Send
Text
Test annotations
8
All Burn-on-Send
L
Test annotations
9
All No-Burn None
Test TEXT?
CR-Fallback
Table 5-3 Test instructions for all PACS images
5.4.3.2 Verifying DICOM header tags
1.
On the PACS review workstation, open PACS test image #1 (Patient ID 2000002).
2.
Access the DICOM header information through a drop-down list, a button, or by right-clicking
the image and then selecting an option such as “information,” “i,” or “header.” For help, contact
local IT support.
3.
Verify Burn-on-Send mode by verifying that:
4.
a.
The WC tag is 0028x1050 and the WW tag is 0028x1051
b.
The values are WC=5226\5226\5226 and WW=2654\1990\3981
Verify VOI-LUT tags as follows:
a.
Search the DICOM header for tag 0028x3010VOILUTSequence.
b.
Below that tag, verify that there are three additional tags:
c.
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*
0028x3002LUTDescriptor
*
0028x3003LUTExplanation
*
0028x3006LUTData
Verify that each VOILUTSequence has a LUTExplanation set to either Normal, Harder,
or Softer.
5.
Record the results in Table 5-4.
6.
Open PACS test image #6 and view the DICOM header.
7.
Verify No-Burn mode by ensuring that:
Section 5.4 PACS image tests
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a.
The WC tag is 0028x1050 and the WW tag is 0028x1051
b.
The values are WC=8192\8192\8192 and WW=16383\12288\24575
Verify VOI-LUT tags as follows:
a.
Search the DICOM header for tag 0028x3010VOILUTSequence.
b.
No VOILUTSequence tag should be present. If a VOILUTSequence is present, the image
was not sent correctly. Resend the image as Burn-on-Send.
Record the results in Table 5-4.
5.4.3.3 Verifying WC and WW values
No-Burn Mode (PACS Test Image #1)
The DICOM header of each PACS Test Image is always sent with WC/WW=5226/2654. The values
displayed on the PACS may appear differently. This is acceptable according to DICOM standards.
The values can show up as 8192/16384, 5226/2654, or something else. The most common and
preferred implementation is to show values of 8192/16384 on the PACS.
1.
Open PACS test image #1.
2.
Verify that the WC/WW values are 8192/16384.
If the values do not appear as 8192/16384, check that the VOI-LUT is enabled on the PACS.
The VOI-LUT often can be enabled with a drop-down list on the image or through hanging
protocols.
Note: This does not indicate that the PACS does not support VOI-LUTs. Support for VOI-LUTs
is strictly determined by the visual appearance of PACS test images #1 and #6.
3.
Record the results in Table 5-4 (see 5.4.4 PACS image comparison results on page 118).
Burn-on-Send Mode (PACS Test Image #6)
1.
Open PACS test image #6.
2.
Verify that the WC/WW values are 8192/16384.
If the values do not appear as 8192/16384, check that the VOI-LUT is enabled on the PACS.
The VOI-LUT often can be enabled with a drop-down list on the image or through hanging
protocols.
3.
Record the results in Table 5-4 (see 5.4.4 PACS image comparison results on page 118).
5.4.3.4 Checking for image saturation
1.
Open PACS test image #1.
2.
Check that the clinical chest area appears with no saturation in the lung or abdomen region.
3.
Record the results in Table 5-4.
5.4.3.5 Testing reduced dynamic range with Burn-on-Send
The Burn-on-Send configuration causes a reduced dynamic range in the image if you change the
window level of the image on the PACS.
1.
Open PACS test image #6.
2.
Change the window level on the PACS to attempt to see the five squares in all twelve bands.
Start by changing the WC value to 0 and the WW value to 500 (the appropriate values may
vary among different PACS workstations).
Chapter 5 Calibration
Page 117
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INSTALLATION MANUAL
The loss of dynamic range is most common in the top dark band. If reduced dynamic range
occurs, the five squares will not be visible in the top dark band (band #1).
3.
Record the results in Table 5-4.
5.4.4 PACS image comparison results
Use the values in Table 5-4 to quantitatively compare images. For example, to determine if a PACS
supports GE VOI-LUTs, compare PACS test images #1 and #6. If the number of distinct bands and
visible squares are equal, then the PACS correctly supports VOI-LUTs.
Tests
Results
WC = __________
DICOM header on PACS (image #1 No-Burn)
WW = __________
VOI-LUT (Yes/No)
WC = __________
DICOM header on PACS (image #6 Burn-on-Send)
WW = __________
VOI-LUT (Yes/No)
Values displayed on PACS viewer (image #1)
Values displayed on PACS viewer (image #6)
WC = __________
WW = __________
WC = __________
WW = __________
Saturation visible in lung or abdomen region
Able to see all five squares in top band of image #6
Able to see all five squares in top band of image #1
Images #1, 4, 5 appear visually identical
Images #6, 7, 8 appear visually identical
PACS able to select Normal/Harder/Softer
DICOM header on PACS (image #9 CR-Fallback).
Table 5-4 PACS image comparison results
Page 118
Section 5.4 PACS image tests
VOI-LUT not present;
correct WW/WC
GE HEALTHCARE
DIRECTION 5336113-1EN REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Chapter 6 Detector checks and QAP
Perform QAP every time you calibrate the detector, and as the final step in calibrations during
installation.
For more information about performing QAP and viewing QAP results, see the Optima XR200amx
or Optima XR220amx Operator Manual, Quality Assurance and Maintenance.
6.0.1 Detector check
This procedure applies only to the Optima XR220amx and Optima XR200amx with digital upgrade
systems.
1.
On the Application screen, press the WORKLIST icon.
2.
On the Worklist screen, at the bottom, press the QAP button.
3.
On the Image Quality screen, in the left folder tree, select Quality Control Tools >
Acquisition.
4.
On the Quality Assurance Program screen, press DETECTOR CHECK, and then press
START.
The test takes about one minute. While the test is running, the status bar at the bottom of the
screen says “Performing Dark Image Tests.”
When the test is complete, the results screen is displayed.
5.
Scroll to the right side of the screen to see the pass/fail results.
All tests should pass. If there are any failures, contact GE Service.
6.
To quit the QAP session and return to Applications, press EXIT. Or, to return to the previous
QAP screen, press BACKUP.
6.0.2 QAP checkout
This procedure applies only to the Optima XR220amx and Optima XR200amx with digital upgrade
systems.
1.
On the Application screen, press the WORKLIST icon.
2.
On the Worklist screen, at the bottom, press the QAP button.
3.
On the Image Quality screen, in the left folder tree, select Quality Control Tools >
Acquisition.
4.
On the Quality Assurance Program screen, press QAP, and then press START.
The test takes about ten minutes, and is made up of three parts. After completing each part,
the program automatically advances to the next part, but you must press START to initiate the
testing for each part.
1. Detector Check.
2. Detector QC Checks:
>
User ID is required to take an exposure.
>
Flat field phantom must inserted in collimator rails.
>
QC Check must pass to proceed to Flat Field Tests.
3. Flat Field Tests:
>
Follow the instructions on the screen.
>
Remove the DAP meter, if present.
Chapter 6 Detector checks and QAP
Page 119
GE HEALTHCARE
DIRECTION 5336113-1EN REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
>
Insert the flat field phantom in the collimator rails.
>
Set SID to the on-screen instructions.
>
Make an X-ray exposure.
>
When image appears, touch anywhere on the image to return to the previous
screen.
>
Make another X-ray exposure.
>
When image appears, touch anywhere on the image to return to the previous
screen.
>
Remove the flat field phantom, and replace the DAP meter if applicable.
While the test is running, the status bar at the bottom of the screen will display status
messages.
When the tests are complete, the results screen will be displayed.
5.
Scroll to the right side of the screen to see the pass/fail results.
All tests should pass. If there are any failures, contact GE Service.
6.
Page 120
To quit the QAP session and return to Applications, press EXIT. Or, to return to the previous
QAP screen, press BACKUP.
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Chapter 7 Certified components
Section 7.1 Component rating plates
The following components will be certified (FDA 21CFR) and will have rating plates:
Table 7-1
Item
System component
Model number
Location
1
X-ray control
5555000-x
On the outside of the system,
above the main breaker switch
2
Generator
5140761-2
On the outside of the system
above the main breaker switch
and on the generator itself
3
X-ray tube housing (casing)
5508800
On the outside of the system
above the main breaker switch
and on rear of X-ray tube
4
Beam limiting device
(collimator)
5129498
Side of collimator
Rating plates are provided with certified system components.
Also, when an option is purchased, rating plates are supplied with the option. Rating plates for these
options must be placed on the Optima XR200amx/XR220amx system. Be sure to properly attach
rating plates so they can be checked for accuracy and compliance.
Rating plates for certified components need to be visible on the system. For the generator, a copy
of the rating plate will be placed on the outside of the system in addition to the rating plate on the
generator itself.
Chapter 7 Certified components
Page 121
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DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Rating plate locations are shown in Figure 7-1.
4
1
2
3
Table 7-1
Item
Description
1
Primary rating plate location, located on cover above main circuit breaker. Consists of:
•
System rating plate
•
Generator rating plate
•
X-ray tube rating plates
See Figure 7-2 on page 123, Figure 7-3 on page 123.
2
Generator rating plate, also located inside unit on generator module. See Figure 7-4
on page 124.
3
X-ray tube/casing rating plates, also located on bottom of X-ray tube casing. See
Figure 7-5 on page 124.
4
Collimator rating plate, located on side of collimator. See Figure 7-6 on page 125.
Figure 7-1 Rating plate locations
Page 122
Section 7.1 Component rating plates
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 7-2 Primary rating plate location
5555000-x
123456789
January 201x
Optima XR220amx
Figure 7-3 Optima system rating plate
Chapter 7 Certified components
Page 123
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 7-4 X-ray generator rating plate
Figure 7-5 X-ray tube/casing rating plates
Page 124
Section 7.1 Component rating plates
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Figure 7-6 Collimator rating plate
Chapter 7 Certified components
Page 125
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Page 126
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Section 7.1 Component rating plates
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Chapter 8 Final tasks
Section 8.1 Final tasks
•
Ready the system for normal customer operation.
•
It is recommended to plug in the system and allow it to reach full charge.
•
Remove trash, remove installation equipment and tools, clean up the installation area, and
store the service manuals.
•
Complete product locator cards and return them.
•
Record the installation time in the Service database.
•
Create specified login and user management account and password information to system
administrator. The account must be satisfied with all of the three roles: Administrator/Standard
User/Limited User.
•
Provide the below account and password information to system administrator.
-
Login and user management (Specially created account and password for system
administrator)
-
Installing the operator manual
-
IP change procedure
Chapter 8 Final tasks
Page 127
GE HEALTHCARE
DIRECTION 5336113-1EN, REVISION 10
Page 128
OPTIMA XR200AMX/XR220AMX
INSTALLATION MANUAL
Section 8.1 Final tasks
© 2011 General Electric Company.
GE Medical Systems, a General Electric Company, going to market as GE Healthcare.
3000 N. Grandview Boulevard
Waukesha, Wisconsin 53188
USA
www.gehealthcare.com
130
Front cover
GE Healthcare
Optima XR200amx/XR220amx
System Parts List
Direction 5336115-1EN
Revision 6
GE HEALTHCARE
Warning
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement X entraîne des
dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour elles-mêmes. Avant chaque
manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique, Annales 26: Recommandations de la
Commission Internationale sure la Protection Radiologique et les normes nationales en vigueur.
WARNING
X-RAY EQUIPMENT IS DANGEROUS TO BOTH PATIENT AND OPERATOR UNLESS MEASURES OF PROTECTION ARE STRICTLY OBSERVED.
Though this equipment is built to the highest standards of electrical and mechanical safety, the useful x-ray beam becomes a source of danger in the hands of the unauthorized or unqualified operator. Excessive exposure to x-radiation causes
damage to human tissue.
Therefore, adequate precautions must be taken to prevent unauthorized or unqualified persons from operating this equipment or exposing themselves or others to its radiation.
Before operation, persons qualified and authorized to operate this equipment should be familiar with the Recommendations of the International Commission on Radiological Protection (ICRP), contained in Annals Number 26 of the ICRP, and with
applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede causar
daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales No 26:
Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen Kommission für
Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für Strahlenschutz und anderer nationaler Normenbehörden.
Page 2
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Important information
WARNING
(EN)
ПРЕДУПРЕЖДЕНИЕ
(BG)
警告
(ZH-CN)
警告
(ZH-HK)
警告
(ZH-TW)
This service manual is available in English only.
•
If a customer's service provider requires a language other than English, it is the customer's
responsibility to provide translation services.
•
Do not attempt to service the equipment unless this service manual has been consulted and is
understood.
•
Failure to heed this warning may result in injury to the service provider, operator or patient from
electric shock, mechanical or other hazards.
Tова упътване за работа е налично само на английски език.
•
Ако доставчикът на услугата на клиента изиска друг език, задължение на клиента е да
осигури превод.
•
Не използвайте оборудването, преди да сте се консултирали и разбрали упътването за
работа.
•
неспазването на това предупреждение може да доведе до нараняване на доставчика на
услугата, оператора или пациентa в резултат на токов удар, механична или друга опасност.
本维修手册仅提供英文版本。
•
•
•
如果客户的维修服务人员需要非英文版本，则客户需自行提供翻译服务。
未详细阅读和完全理解本维修手册之前，不得进行维修。
忽略本警告可能对维修服务人员、操作人员或患者造成电击、机械伤害或其他形式的伤
害。
本服務手冊僅提供英文版本。
• 倘若客戶的服務供應商需要英文以外之服務手冊，客戶有責任提供翻譯服務。
• 除非已參閱本服務手冊及明白其內容，否則切勿嘗試維修設備。
• 不遵從本警告或會令服務供應商、網絡供應商或病人受到觸電、機械性或其他的危險。
本維修手冊僅有英文版。
• 若客戶的維修廠商需要英文版以外的語言，應由客戶自行提供翻譯服務。
• 請勿試圖維修本設備，除非 您已查閱並瞭解本維修手冊。
• 若未留意本警告，可能導致維修廠商、操作員或病患因觸電、機械或其他危險而受傷。
UPOZORENJE
(HR)
Ovaj servisni priručnik dostupan je na engleskom jeziku.
•
Ako davatelj usluge klijenta treba neki drugi jezik, klijent je dužan osigurati prijevod.
•
Ne pokušavajte servisirati opremu ako niste u potpunosti pročitali i razumjeli ovaj servisni
priručnik.
•
zanemarite li ovo upozorenje, može doći do ozljede davatelja usluge, operatera ili pacijenta uslijed
strujnog udara, mehaničkih ili drugih rizika.
VÝSTRAHA
(CS)
Tento provozní návod existuje pouze v anglickém jazyce.
• V případě, že externí služba zákazníkům potřebuje návod v jiném jazyce, je zajištění překladu do
odpovídajícího jazyka úkolem zákazníka.
• Nesnažte se o údržbu tohoto zařízení, aniž byste si přečetli tento provozní návod a pochopili jeho
obsah.
• V případě nedodržování této výstrahy může dojít k poranění pracovníka prodejního servisu,
obslužného personálu nebo pacientů vlivem elektrického proudu, respektive vlivem mechanických
či jiných rizik.
Denne servicemanual findes kun på engelsk.
• Hvis en kundes tekniker har brug for et andet sprog end engelsk, er det kundens ansvar at sørge
for oversættelse.
• Forsøg ikke at servicere udstyret uden at læse og forstå denne servicemanual.
• Manglende overholdelse af denne advarsel kan medføre skade på grund af elektrisk stød,
mekanisk eller anden fare for teknikeren, operatøren eller patienten.
ADVARSEL
(DA)
Preface
Page 3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
WAARSCHUWING
(NL)
HOIATUS
(ET)
VAROITUS
(FI)
ATTENTION
(FR)
WARNUNG
(DE)
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ
(EL)
FIGYELMEZTETÉS
(HU)
AÐVÖRUN
(IS)
Page 4
SYSTEM PARTS LIST
Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.
• Als het onderhoudspersoneel een andere taal vereist, dan is de klant verantwoordelijk voor de
vertaling ervan.
• Probeer de apparatuur niet te onderhouden alvorens deze onderhoudshandleiding werd
geraadpleegd en begrepen is.
• Indien deze waarschuwing niet wordt opgevolgd, zou het onderhoudspersoneel, de operator of
een patiënt gewond kunnen raken als gevolg van een elektrische schok, mechanische of andere
gevaren.
See teenindusjuhend on saadaval ainult inglise keeles
• Kui klienditeeninduse osutaja nõuab juhendit inglise keelest erinevas keeles, vastutab klient
tõlketeenuse osutamise eest.
• Ärge üritage seadmeid teenindada enne eelnevalt käesoleva teenindusjuhendiga tutvumist ja
sellest aru saamist.
• Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja, operaatori või patsiendi vigastamist
elektrilöögi, mehaanilise või muu ohu tagajärjel.
Tämä huolto-ohje on saatavilla vain englanniksi.
• Jos asiakkaan huoltohenkilöstö vaatii muuta kuin englanninkielistä materiaalia, tarvittavan
käännöksen hankkiminen on asiakkaan vastuulla.
• Älä yritä korjata laitteistoa ennen kuin olet varmasti lukenut ja ymmärtänyt tämän huolto-ohjeen.
• Mikäli tätä varoitusta ei noudateta, seurauksena voi olla huoltohenkilöstön, laitteiston käyttäjän tai
potilaan vahingoittuminen sähköiskun, mekaanisen vian tai muun vaaratilanteen vuoksi.
Ce manuel d’installation et de maintenance est disponible uniquement en anglais.
• Si le technicien d'un client a besoin de ce manuel dans une langue autre que l'anglais, il incombe
au client de le faire traduire.
• Ne pas tenter d'intervenir sur les équipements tant que ce manuel d’installation et de maintenance
n'a pas été consulté et compris.
• Le non-respect de cet avertissement peut entraîner chez le technicien, l'opérateur ou le patient
des blessures dues à des dangers électriques, mécaniques ou autres.
Diese Serviceanleitung existiert nur in englischer Sprache.
• Falls ein fremder Kundendienst eine andere Sprache benötigt, ist es Aufgabe des Kunden für eine
entsprechende Übersetzung zu sorgen.
• Versuchen Sie nicht diese Anlage zu warten, ohne diese Serviceanleitung gelesen und
verstanden zu haben.
• Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des Kundendiensttechnikers, des
Bedieners oder des Patienten durch Stromschläge, mechanische oder sonstige Gefahren
kommen.
Το παρόν εγχειρίδιο σέρβις διατίθεται μόνο στα αγγλικά.
• Εάν ο τεχνικός σέρβις ενός πελάτη απαιτεί το παρόν εγχειρίδιο σε γλώσσα εκτός των αγγλικών,
αποτελεί ευθύνη του πελάτη να παρέχει τις υπηρεσίες μετάφρασης.
• Μην επιχειρήσετε την εκτέλεση εργασιών σέρβις στον εξοπλισμό αν δεν έχετε συμβουλευτεί και
κατανοήσει το παρόν εγχειρίδιο σέρβις.
• Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί τραυματισμός στον τεχνικό
σέρβις, στο χειριστή ή στον ασθενή από ηλεκτροπληξία, μηχανικούς ή άλλους κινδύνους.
Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.
• Ha a vevő szolgáltatója angoltól eltérő nyelvre tart igényt, akkor a vevő felelőssége a fordítás
elkészíttetése.
• Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási kézikönyvben leírtakat nem
értelmezték.
• Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető vagy a beteg áramütés,
mechanikai vagy egyéb veszélyhelyzet miatti sérülését eredményezheti.
Þessi þjónustuhandbók er aðeins fáanleg á ensku.
• Ef að þjónustuveitandi viðskiptamanns þarfnast annas tungumáls en ensku, er það skylda
viðskiptamanns að skaffa tungumálaþjónustu.
• Reynið ekki að afgreiða tækið nema að þessi þjónustuhandbók hefur verið skoðuð og skilin.
• Brot á sinna þessari aðvörun getur leitt til meiðsla á þjónustuveitanda, stjórnanda eða sjúklings frá
raflosti, vélrænu eða öðrum áhættum.
Preface
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
AVVERTENZA
(IT)
(JA)
경고
(KO)
BRÎDINÂJUMS
(LV)
ĮSPĖJIMAS
(LT)
ADVARSEL
(NO)
OSTRZEŻENIE
(PL)
AVISO
(PT-BR)
ATENÇÃO
(PT-PT)
SYSTEM PARTS LIST
Il presente manuale di manutenzione è disponibile soltanto in lingua inglese.
• Se un addetto alla manutenzione richiede il manuale in una lingua diversa, il cliente è tenuto a
provvedere direttamente alla traduzione.
• Procedere alla manutenzione dell'apparecchiatura solo dopo aver consultato il presente manuale
ed averne compreso il contenuto.
• Il mancato rispetto della presente avvertenza potrebbe causare lesioni all'addetto alla
manutenzione, all'operatore o ai pazienti provocate da scosse elettriche, urti meccanici o altri
rischi.
このサービスマニュアルには英語版しかありません。
 サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業者の責任で行
うものとさせていただきます。
 このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでください。
この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、感電や機械
的又はその他の危険により負傷する可能性があります。
본 서비스 매뉴얼은 영어로만 이용하실 수 있습니다 .
• 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우 , 번역 서비스를 제공하는 것은 고객의
책임입니다 .
• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하려고 시도하지 마십시오 .
• 본 경고 사항에 유의하지 않으면 전기 쇼크 , 기계적 위험 , 또는 기타 위험으로 인해 서비스 제공자
, 사용자 또는 환자에게 부상을 입힐 수 있습니다 .
Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.
• Ja klienta apkopes sniedzējam nepieciešama informācija citā valodā, klienta pienākums ir
nodrošināt tulkojumu.
• Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas un saprašanas.
• Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas trieciena, mehānisku vai
citu faktoru izraisītu traumu risks apkopes sniedzējam, operatoram vai pacientam.
Šis eksploatavimo vadovas yra tik anglų kalba.
• Jei kliento paslaugų tiekėjas reikalauja vadovo kita kalba – ne anglų, suteikti vertimo paslaugas
privalo klientas.
• Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar nesupratote šio
eksploatavimo vadovo.
• Jei nepaisysite šio įspėjimo, galimi paslaugų tiekėjo, operatoriaus ar paciento sužalojimai dėl
elektros šoko, mechaninių ar kitų pavojų.
Denne servicehåndboken finnes bare på engelsk.
• Hvis kundens serviceleverandør har bruk for et annet språk, er det kundens ansvar å sørge for
oversettelse.
• Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest og forstått.
• Manglende hensyn til denne advarselen kan føre til at serviceleverandøren, operatøren eller
pasienten skades på grunn av elektrisk støt, mekaniske eller andre farer.
Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.
• Jeśli serwisant klienta wymaga języka innego niż angielski, zapewnienie usługi tłumaczenia jest
obowiązkiem klienta.
• Nie próbować serwisować urządzenia bez zapoznania się z niniejszym podręcznikiem
serwisowym i zrozumienia go.
• Niezastosowanie się do tego ostrzeżenia może doprowadzić do obrażeń serwisanta, operatora
lub pacjenta w wyniku porażenia prądem elektrycznym, zagrożenia mechanicznego bądź innego.
Este manual de assistência técnica encontra-se disponível unicamente em inglês.
•
Se outro serviço de assistência técnica solicitar a tradução deste manual, caberá ao cliente
fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
A não observância deste aviso pode ocasionar ferimentos no técnico, operador ou paciente
decorrentes de choques elétricos, mecânicos ou outros.
Este manual de assistência técnica só se encontra disponível em inglês.
•
Se qualquer outro serviço de assistência técnica solicitar este manual noutro idioma, é da
responsabilidade do cliente fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
O não cumprimento deste aviso pode colocar em perigo a segurança do técnico, do operador ou
do paciente devido a choques eléctricos, mecânicos ou outros.
Preface
Page 5
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
ATENŢIE
(RO)
ОСТОРОЖНО!
(RU)
UPOZORENJE
(SR)
UPOZORNENIE
(SK)
ATENCION
(ES)
VARNING
(SV)
OPOZORILO
(SL)
DİKKAT
(TR)
Page 6
SYSTEM PARTS LIST
Acest manual de service este disponibil doar în limba engleză.
•
Dacă un furnizor de servicii pentru clienţi necesită o altă limbă decât cea engleză, este de datoria
clientului să furnizeze o traducere.
•
Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi înţelegerii acestui manual de
service.
•
Ignorarea acestui avertisment ar putea duce la rănirea depanatorului, operatorului sau pacientului
în urma pericolelor de electrocutare, mecanice sau de altă natură.
Данное руководство по техническому обслуживанию представлено только на английском языке.
•
Если сервисному персоналу клиента необходимо руководство не на английском, а на
каком-то другом языке, клиенту следует самостоятельно обеспечить перевод.
•
Перед техническим обслуживанием оборудования обязательно обратитесь к данному
руководству и поймите изложенные в нем сведения.
•
Несоблюдение требований данного предупреждения может привести к тому, что
специалист по техобслуживанию, оператор или пациент получит удар электрическим током,
механическую травму или другое повреждение
Ovo servisno uputstvo je dostupno samo na engleskom jeziku.
•
Ako klijentov serviser zahteva neki drugi jezik, klijent je dužan da obezbedi prevodilačke usluge.
•
Ne pokušavajte da opravite uređaj ako niste pročitali i razumeli ovo servisno uputstvo.
•
Zanemarivanje ovog upozorenja može dovesti do povređivanja servisera, rukovaoca ili pacijenta
usled strujnog udara ili mehaničkih i drugih opasnosti.
Tento návod na obsluhu je k dispozícii len v angličtine.
•
Ak zákazníkov poskytovateľ služieb vyžaduje iný jazyk ako angličtinu, poskytnutie
prekladateľských služieb je zodpovednosťou zákazníka.
•
Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na obluhu a neporozumiete mu.
•
Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa služieb, obsluhujúcej
osoby alebo pacienta elektrickým prúdom, mechanické alebo iné ohrozenie.
Este manual de servicio sólo existe en inglés.
•
Si el encargado de mantenimiento de un cliente necesita un idioma que no sea el inglés, el cliente
deberá encargarse de la traducción del manual.
•
No se deberá dar servicio técnico al equipo, sin haber consultado y comprendido este manual de
servicio.
•
La no observancia del presente aviso puede dar lugar a que el proveedor de servicios, el
operador o el paciente sufran lesiones provocadas por causas eléctricas, mecánicas o de otra
naturaleza.
Den här servicehandboken finns bara tillgänglig på engelska. .
•
Om en kunds servicetekniker har behov av ett annat språk än engelska, ansvarar kunden för att
tillhandahålla översättningstjänster.
•
Försök inte utföra service på utrustningen om du inte har läst och förstår den här
servicehandboken.
•
Om du inte tar hänsyn till den här varningen kan det resultera i skador på serviceteknikern,
operatören eller patienten till följd av elektriska stötar, mekaniska faror eller andra faror.
Ta servisni priročnik je na voljo samo v angleškem jeziku.
•
Če ponudnik storitve stranke potrebuje priročnik v drugem jeziku, mora stranka zagotoviti prevod.
•
Ne poskušajte servisirati opreme, če tega priročnika niste v celoti prebrali in razumeli.
•
Če tega opozorila ne upoštevate, se lahko zaradi električnega udara, mehanskih ali drugih
nevarnosti poškoduje ponudnik storitev, operater ali bolnik.
Bu servis kılavuzunun sadece ingilizcesi mevcuttur.
•
Eğer müşteri teknisyeni bu kılavuzu ingilizce dışında bir başka lisandan talep ederse, bunu
tercüme ettirmek müşteriye düşer.
•
Servis kılavuzunu okuyup anlamadan ekipmanlara müdahale etmeyiniz.
•
Bu uyarıya uyulmaması, elektrik, mekanik veya diğer tehlikelerden dolayı teknisyen, operatör
veya hastanın yaralanmasına yol açabilir.
Preface
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Legal notes
TRADEMARKS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2 are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material presented and contained herein may not be reproduced in any form or manner, without the written permission of General Electric Company, Inc.
Preface
Page 7
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation “damage in shipment” written on all copies of the freight or express bill before delivery is accepted or “signed for” by a General Electric representative
or a hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and MIS.” Contact your local service coordinator for more information on this process.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT
All electrical installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds into the Power Distribution Unit shall be performed
by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE Healthcare personnel. The products involved (and the accompanying electrical installations)
are highly sophisticated, and special engineering competence is required. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GE’s electrical work on these products will comply with the
requirements of the applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein contained should be thoroughly read and understood by everyone who will use the equipment before you attempt to place this equipment in operation. GE
Healthcare will be glad to assist and cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the useful beam, no practical design of equipment can provide complete protection. Nor can any practical design compel the operator to take adequate
precautions to prevent the possibility of any persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully acquainted with the recommendations of the National Council on Radiation Protection and Measurements (NCRP) as published in NCRP Reports available
from NCRP Publications, 7910 Woodmont Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission on Radiation Protection, and take adequate steps to protect against injury.
The equipment is sold with the understanding that GE Healthcare, its agents, and representatives have no responsibility for injury or damage which may result from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be used.
LITHIUM BATTERY CAUTIONARY STATEMENT
DANGER - Risk of Explosion
Danger of explosion if battery is incorrectly replaced.
Replace only with the same or equivalent type recommended by the
manufacturer. Discard used batteries according to the manufacturer’s
instructions.
ATTENTION - Danger d’Explosion
Il y a danger d’explosion s’il y a replacement incorrect de la batterie.
Remplacer uniquement avec une batterie du même type ou d’un type
recommandé par le constructeur. Mettre au rébut les batteries
usagées conformément aux instructions du fabricant.
TECHNICAL MANUAL UPDATES
When operating or servicing GE Healthcare products, please contact your GE representative for the latest revision of product documentation. Product documentation may also be available on-line at the GE Healthcare support documentation library.
OMISSIONS AND ERRORS
Customers, please contact your GE Healthcare sales or service representatives.
GE personnel, please use the GE Healthcare complaint handling process to report all omissions, errors, and defects in this publication.
Page 8
Preface
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Revision history
Revision
Date
Reason for change
1
15NOV2011
Initial release of document
2
09FEB2012
Refer to SPR HCSDM00120703:
Removed part 5451000 - SuperBee Firmware Collector.
Changed digital bin part number from 5555004-2 to 5555004-3, updated ADW drawing and BOM.
Added “Chapter 4 - FlashPad detector and related components”.
Added detector part numbers 5399000-3, -4, -5 and -6 to Chapter 4.
Added UWB dongle part numbers 5390144, -2 and -3.
Added part numbers 5436002 (FlashPad docking interface board) and 5394471 (FlashPad battery charger).
Updated firmware part number from 5451000-2 to 5451000-3.
Updated software part number from 5409779 to 5409779-3.
3
28SEP2012
DAP cable FRU changed from 5557046 to 5557046-2 in Table 5-8. See ECO 2131197.
New Cathode Side Tube Mount: Changed old part 5507701 to FRU = No in Table 5-16 and added new part 5450136 and new Section 5.2.1. See ECO 2122380.
New Anode Side Tube Mount: Changed from old part 5507702 to FRU = No in Table 5-16 and added new part 5450136-2 and new Section 5.2.1. See ECO 2122380.
Added text to front material on how to obtain most recent revisions of technical manuals. Satisfies FDA recommendation.
Updated Locust part number to 5350006-2 per FMI 10867 (see PR# 7792277).
Replaced Top Cover part number (including drawings & BOMs) with 5555005-8 in Table 1-1, Figures 2-5 through 2-9, Table 2-1, Figures 3-52 through 3-56 and Table 3-9 per FMI 10869 (see PR# 8915068).
Changed Hornet UIF board part number from 5350004 to 5350004-2 as a result of FMI 10869 (see PR# 8915068).
Updated Firmware part number with 5451000-6 per FMI 10867 (see PR# 7792277).
Changed SW Collector part numbers from 5409778 (XR200) and 5409779-3 (XR220) to 5409778-4 (XR200) and 5409779-6 (XR220) per FMI 10865 (see PR#7886856 & PR#8630581).
Added FlashPad Detector Battery part number 5382000 to Chapter 4, Table 4-17.
Preface
Page 9
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Revision
Date
4
17SEP2013
SYSTEM PARTS LIST
Reason for change
Chapter 2, Section 2.3, removed handswitch drawings and BOM. Refer to ECR 2145562.
Table 5-1, changed Mark 1 to 5509900-3. Refer to ECO 2145141.
Chapter 5, Section 5.1, changed 5509900 to 5509900-3. Refer to ECO 2145141.
Figure 5-2, replaced with correct 5509900ADW Rev 9 drawing. Refer to ECO 2136310.
Figure 5-8, updated 5370111ADW to Rev 4. Refer to ECO 2137062.
Figure 5-15, updated 5392386ADW to Rev 3. Refer to ECO 2137636.
Table 1-1, updated Mark 1 to 5555001-2. Refer to ECO 2143108.
Chapter 5, Section 5.1, changed all 5555001 to 5555001-2. Refer to ECO 2143108.
Table 5-1, updated entire BOM. Refer to ECO 2143108.
Chapter 5, Section 5.1, changed all 5509900 to 5509900-3. Refer to ECO 2145141.
Table 5-2, updated entire BOM. Refer to ECO 2145141.
Chapter 5, Section 5.1.2, changed all 5507000 to 5507000-3 and updated Figure 5-10 drawing. Refer to ECO 2145141.
Table 5-8, updated entire BOM. Refer to ECO 2145141.
Chapter 5, Section 5.1.2, changed all 5350000 to 5350000-2 and updated Figure 5-14 drawing to Rev 6. Refer to ECO 2145141.
Table 5-9, updated 5350000 to 5350000-2. Refer to ECO 2145141.
Table 5-8, updated Mark 149 to 5557049-2. Refer to ECO 2144452.
Table 5-13, updated entire BOM. Refer to ECO 2144957.
Figure 5-18, updated with 5504000ADW Rev 12. Refer to ECO 2144957.
Table 1-1, Mark 91 changed to 5421994-2, Mark 75 changed to 5407019-5 and 5407019-4. Refer to ECO 2134034.
Table 1-1, added Mark 202 part 5449450. Refer to ECO 2145626.
Table 1-1, Mark 47 changed to 5409779-9, refer to ECO 2151611. Mark 200 changed to 5451000-12, refer to ECO 2146540.
Figure 3-77, updated 5555004-3 drawing to Rev 4. Refer to ECO 2148874.
Table 3-14, replaced 5555004-3 BOM. Refer to ECO 2148874.
Table 5-3, Mark 3 changed to FRU Yes, Mark 7 changed to 5449164, changed Mark 7 to 5449164 and FRU Yes. Refer to ECO 2147940.
Table 1-1, added 5479307 and added note to Mark 97 description. Refer to ECO 2147940.
Table 1-1, changed Mark 97 to 5503017-2. Refer to ECR 2149565.
Table 1-1, changed Mark 47 to 5409778-6. Refer to ECR 2150530.
Table 5-4, changed Mark 16, 5413926 to FRU Yes. Refer to ECR 2147940.
5
27FEB2014
Chapter 5, Section 5.1, Table 5-2, added new column assembly part number 5505000-2 (short column). Refer to ECO 2158872.
Chapter 5, Section 5.1.2, Table 5-8, changed LVLE2 part number from 5192958 to 5192958-2. Refer to ECO 2155385.
Chapter 5, Section 5.6, Table 5-26, added Wireless Hand Switch kit part number 5503600. Refer to ECO 2162103.
Chapter 1, updated top level drawing 5555000ADW to Rev 14 (affects Figures 1-1 through 1-6). Added cable cover part number 5453234 as Mark 205 in Table 1-1. Refer to ECO 2160317.
6
15JAN2015
Chapter 1, add 5409779-11 in table 1-4.
Chapter 1, add 5451000-15 in table 1-4.
Chapter 5, add 5570321 in table 5-26.
Page 10
Preface
GE HEALTHCARE
DIRECTION 5336115-1EN, REVISION 6
Preface - Publication conventions
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
Preface Publication Conventions
Standardized conventions for representing information is a uniform way of communicating information to a reader in a consistent manner. Conventions are used so that the reader can easily recognize the actions or decisions that must be made.
There are a number of character and paragraph styles used in this publication to accomplish this task. Please become familiar with them before proceeding forward.
It is important that you read and understand hazard statements, and not just ignore them.
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and style for safety communications reflected in this publication represents the harmonization of IEC/ISO 3864 and ANSI Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify important safety information. Text (Hazard) styles are
applied to the paragraph contents that are applicable to each specific safety statement.
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation mark within it. It Is always used next to the signal
word to indicate the severity of the hazard. Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert symbol and signal word are placed immediately before any paragraph they affect. Safety information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Text Format of Signal Words
DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH, IF NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS SIGNAL WORD IS LIMITED TO THE MOST
EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Caution - Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury. It may also be used to alert against unsafe practices.
NOTICE - Indicates information or a company policy that relates directly or indirectly to the safety of personnel or protection of property. This signal word is associated directly with a hazard or hazardous situation and is used in
place of 'DANGER,' 'WARNING,' or 'CAUTION.' It can include:
•
Destruction of a disk drive
•
Potential for internal mechanical damage, such as to a X-ray tube
Preface
Page 11
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Symbols and Pictorials Used
The following Symbols and Pictorials are be used in this publication. These graphical icons (symbols) may be used to make you aware of specific types of hazards that could possibly cause harm.
keep_up
magnetic
biohazard
compressgas
ppe-hearing
fragile
impact
corrosive
heavyobject
ppe-2people
static_elec
heat
general
laser
ppe-respitory
keep_dry
pinch
radiation
poisongas
ppe-loto
general
explosive
electrical
flammable
ppe-eye
torque
crush/mechanical
tipping
Read Manual
ppe-gloves
ce
instuction
poisonmatl
entanglement
instuction
Page 12
Preface
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such as Purpose, Example, Comment or Note) are used to identify important but non-safety related information. Text styles are also applied to text within
each paragraph modified by the specific prefix.
EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:
Purpose:
Introduces and provides meaning as to the information contained within the chapter, section or subsection (such as used at the beginning this chapter, for example).
Note:
Conveys information that should be considered important to the reader.
Example:
Used to make the reader aware that the paragraph(s) that follow are examples of information possibly stated previously.
Comment:
Represents “additional” information that may or may not be relevant to your situation.
Page Layout
Publication Part Number & Revision Number
The current section and its title
are always shown in the footer of
the left (even) page.
An exclamation point in a triangle is used
to indicate important information to the user.
Paragraphs preceeded by Alphanumeric
characters (e.g. numbers) contain information that must be followed in a specific order.
Publication Title
The current chapter and its title
are always shown in the footer of
the right (odd) page.
Paragraphs preceeded by a symbol
(e.g. bullets) contain information that
has no specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location. The document part number and revision number appears in every header on every page. Odd numbered page footers indicate the current chapter,
its title and current page number. Even page footers show the current section and its title, as well as the current page number.
Preface
Page 13
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text that’s either screen input and output. Mono-spaced fonts, such courier, are used to indicated text direction. When you type at your keyboard, you are
generating computer input. Occasionally you will see the math operator “greater-than” and “less-than” symbols used to indicate the start and finish of variable output. When reading text generated by the computer, you are reading it as computer
generated output. In addition to direction, characters are italicized (e.g. italics) to indicate information specific to your system or site.
Example: Fixed Output
This paragraph’s font represents computer generated screen “fixed” output. Its output is fixed from the sense that it does not vary from application to application. It is the most
commonly used style used to indicate filenames, paths and text that do not change from system to system. The character style used is a fixed width such as courier.
Example:
Variable Output
This paragraph’s font represents computer screen output that is “variable”. It is used to represent output that varies from application to application or system to system. Variable
output is sometimes found placed between greater-than and less-than operators for clarification. For example: <variable_ouput> or <3.45.120.3>. In both cases, the < and > operators
are not part of the actual input.
Example:
Fixed Input
This paragraph’s font represents fixed input. It is computer input that is typed-in via the keyboard. Typed input that does not vary from application to application or system to
system. Fixed text the user is required to supply as input. For example: cd /usr/3p
Example:
Variable Input
This paragraph’s font represents computer input that can vary from application to application or system to system. With variable text, the user is required to supply system dependent
input or information. Variable input sometimes is placed between greater-than and less-than operators. For example: <variable_input>. In these cases, the (<>) operators would be
dropped prior to input. For example: ypcat hosts | grep <3.45.120.3> would be typed into the computer as:
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or soft button, switch or key. Physical hardware, such as buttons and switches, are called hard keys because they are hard wired or mechanical in
nature. A keyboard or on/off switch would be a hard key. Software or computer generated buttons are called soft keys because they are software generated. Software driven menu buttons are an example of such keys. Soft and hard keys are
represented differently in this publication.
Example: Hard Keys
A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style that uses both over and under-lined bold text that is bold. This is a hard key.
Example: Soft Keys
Whereas the computer MENU button that you would click with your mouse or touch with your hand uses over and under-lined regular text. This is a soft key.
Page 14
Preface
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table of contents
Chapter 1
Optima Top Level Assembly....................................................................... 19
Chapter 2
Optima XR200amx Drawings ...................................................................... 31
Section 2.1 Base .............................................................................................................................. 31
2.1.1 Breaker tray - 5555008 ..................................................................................................................... 31
2.1.2 USB Bulkhead, Analog - 5399422-2 ................................................................................................ 32
2.1.3 Cord Reel Plug, US - 5409524 ......................................................................................................... 33
2.1.4 Wipes Hold Down Support - 5555015 ............................................................................................. 34
Section 2.2 Covers .......................................................................................................................... 35
2.2.1 Top Cover HLA, Optima, United States - 5555005-8 ..................................................................... 35
2.2.1.1 Top Cover - 5368309................................................................................................................................
2.2.1.2 Power Switch Assembly - 5391117 ........................................................................................................
2.2.1.3 Overlay Board Assembly - 5391109 .......................................................................................................
2.2.1.4 Hornet Display Module Board PWA - 5350004-2...................................................................................
2.2.1.5 Drive Login Active Board Collector - 5394459 ......................................................................................
2.2.1.5.1 Drive Login Active Board PWA - 5378850 .......................................................................................
2.2.1.6 Display and Inverter Collector - 5394460...............................................................................................
42
43
44
45
46
47
48
2.2.2 Hold Down Strap - 5406840 ............................................................................................................. 50
2.2.3 Right Side Cover - 5555002 ............................................................................................................. 51
2.2.4 Left Side Cover - 5555003................................................................................................................ 52
2.2.5 Front Cover Right - 5555006 ........................................................................................................... 53
2.2.6 Front Cover Left - 5555007 .............................................................................................................. 55
2.2.7 Top External Cabling Exit Cover - 5555017 ................................................................................... 57
2.2.8 Bottom External Cabling Exit Cover - 5555018 ............................................................................. 58
2.2.9 Column Skirt Front - 5555022 ......................................................................................................... 59
2.2.10 Column Skirt Rear - 5555023......................................................................................................... 60
2.2.11 Kick Plate - 5555016....................................................................................................................... 61
2.2.12 Access Cover, Docking Connector - 5393547 ............................................................................. 62
Section 2.3 Tube .............................................................................................................................. 63
2.3.1 Tube cover assembly - 5505500 ..................................................................................................... 63
Section 2.4 Bin................................................................................................................................. 64
2.4.1 Analog Bin Assembly - 5555004-1.................................................................................................. 64
2.4.2 Front Bin - 5555011 .......................................................................................................................... 65
Table of Contents
Page 15
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
2.4.3 Front Bin Window - 5555012 ........................................................................................................... 67
2.4.4 Front Bin Hold Down Right - 5555013 ............................................................................................ 68
2.4.5 Front Bin Hold Down Left - 5555014............................................................................................... 69
2.4.6 Wipes Hold Down Support - 5555015 ............................................................................................. 70
2.4.7 Front Bin Filler Blank - 5406506...................................................................................................... 71
2.4.8 Back-up Tether Filler Blank - 5406507 ........................................................................................... 72
2.4.9 Storage Bin Assembly - 5399160.................................................................................................... 73
2.4.9.1 Door Assy, Storage Compartment - 5402020........................................................................................ 75
2.4.10 Rear bin mounting bracket Analog - 5406430 ............................................................................. 76
2.4.11 Access Cover, Docking Connector - 5393547 ............................................................................. 77
Section 2.5 PC.................................................................................................................................. 78
2.5.1 Whip antenna for 802.11abgn wireless/SMA coaxial connector with swivel mount - 5367724 78
2.5.2 Reverse Polarity SMA coaxial RF cable - 5367723........................................................................ 79
Chapter 3
Optima XR220amx Drawings ...................................................................... 81
Section 3.1 Base .............................................................................................................................. 81
3.1.1 Breaker tray - 5555008 ..................................................................................................................... 81
3.1.2 USB Bulkhead - 5399422 ................................................................................................................. 83
3.1.3 Cord Reel Plug, US - 5409524 ......................................................................................................... 84
3.1.4 Wipes Hold Down Support - 5555015 ............................................................................................. 85
Section 3.2 Covers .......................................................................................................................... 86
3.2.1 Top Cover HLA, Optima, United States - 5555005-8 ..................................................................... 86
3.2.1.1
3.2.1.2
3.2.1.3
3.2.1.4
3.2.1.5
3.2.1.6
Top Cover - 5368309................................................................................................................................
Power Switch Assembly - 5391117 ........................................................................................................
Overlay Board Assembly - 5391109 .......................................................................................................
Hornet Display Module Board PWA - 5350004-2...................................................................................
Drive Login Active Board Collector - 5394459 ......................................................................................
Display and Inverter Collector - 5394460...............................................................................................
93
94
95
96
97
99
3.2.2 Hold Down Strap - 5406840 ........................................................................................................... 100
3.2.3 Right Side Cover - 5555002 ........................................................................................................... 101
3.2.4 Left Side Cover - 5555003.............................................................................................................. 102
3.2.5 Front Cover Right - 5555006 ......................................................................................................... 103
3.2.6 Front Cover Left - 5555007 ............................................................................................................ 105
3.2.7 Top External Cabling Exit Cover - 5555017 ................................................................................. 107
3.2.8 Bottom External Cabling Exit Cover - 5555018 ........................................................................... 108
3.2.9 Column Skirt Front - 5555022 ....................................................................................................... 109
Page 16
Table of Contents
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
3.2.10 Column Skirt Rear - 5555023....................................................................................................... 110
3.2.11 Kick Plate - 5555016..................................................................................................................... 111
3.2.12 Access Cover, Docking Connector - 5393547 ........................................................................... 112
Section 3.3 Tube ............................................................................................................................ 113
3.3.1 Tube cover assembly - 5505500 ................................................................................................... 113
Section 3.4 Bin............................................................................................................................... 114
3.4.1 Digital Bin Assembly - 5555004-3 ................................................................................................. 114
3.4.2 Front Bin - 5555011 ........................................................................................................................ 116
3.4.3 Front Bin Window - 5555012 ......................................................................................................... 118
3.4.4 Front Bin Hold Down Right - 5555013 .......................................................................................... 119
3.4.5 Front Bin Hold Down Left - 5555014............................................................................................. 120
3.4.6 Front Bin Filler Blank - 5406506.................................................................................................... 121
3.4.7 Back-up Tether Filler Blank - 5406507 ......................................................................................... 122
3.4.8 Storage Bin Assembly - 5399160.................................................................................................. 123
3.4.8.1 Door Assy, Storage Compartment - 5402020...................................................................................... 125
3.4.9 Access Cover, Docking Connector - 5393547 ............................................................................. 126
Section 3.5 PC................................................................................................................................ 127
3.5.1 Whip antenna/SMA coaxial connector ......................................................................................... 127
3.5.2 Reverse Polarity SMA coaxial RF cable - 5367723...................................................................... 128
Chapter 4
FlashPad detector and related components ........................................... 129
Chapter 5
Common SuperBee VHLA - 5555001-2 .................................................... 133
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3 ....................... 135
5.1.1 Base - 5508000 ............................................................................................................................... 140
5.1.1.1
5.1.1.2
5.1.1.3
5.1.1.4
Drive assembly - 5370437 .....................................................................................................................
Column support assembly - 5368482 ..................................................................................................
Bumper - 5370111 ..................................................................................................................................
Cricket Battery Board - 5350008 ..........................................................................................................
143
145
148
150
5.1.2 Thorax HLA - 5507000-3 ............................................................................................................... 151
5.1.2.1
5.1.2.2
5.1.2.3
5.1.2.4
Firefly Charger Board - 5350000-2 .......................................................................................................
Tube park latch - 5392386 .....................................................................................................................
Locust Drive Board - 5350006-2 ...........................................................................................................
Fuse holder assembly, thorax Superbee - 5394888 ...........................................................................
158
159
161
162
5.1.3 Drive Handle HLA - 5504000.......................................................................................................... 163
5.1.4 Horizontal Arm Assembly - 5506700 ............................................................................................ 168
5.1.5 DJINN 15R DC 2P - 5341550 .......................................................................................................... 171
Table of Contents
Page 17
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 5.2 Tube and Tube Mount - 5507700 .............................................................................. 175
5.2.1 Anode/Cathode Side Tube Mount Identification and FRUs........................................................ 176
Section 5.3 SuperBee Manual Collimator - 5129498 .................................................................. 177
5.3.1 RoHS-SuperBee Collimator - 5396306 ......................................................................................... 179
5.3.1.1 Collimator knob set - 5397014 .............................................................................................................. 185
5.3.1.2 RoHS-Mechanical Interface - 5396643 ................................................................................................. 186
Section 5.4 HV Cable Collector - 5503011 ................................................................................... 192
Section 5.5 Hardware Kit for SuperBee - 5399683...................................................................... 192
Section 5.6 Other ........................................................................................................................... 193
Page 18
Table of Contents
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Chapter 1 Optima Top Level Assembly
Figure 1-1 5555000ADW_s1_r14
Chapter 1 Optima Top Level Assembly
Page 19
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 1-2 5555000ADW_s2_r2
Page 20
Chapter 1 Optima Top Level Assembly
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 1-3 5555000ADW_s3_r4
Chapter 1 Optima Top Level Assembly
Page 21
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 1-4 5555000ADW_s4_r4
Page 22
Chapter 1 Optima Top Level Assembly
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 1-5 5555000ADW_s5_r8
Chapter 1 Optima Top Level Assembly
Page 23
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 1-6 5555000ADW_s6_r10
Page 24
Chapter 1 Optima Top Level Assembly
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 1-1 Optima XR200amx/XR220amx, US and International, 15kW (5555000-3, -5) & 30kW (5555000-4, -6)
Mark No.
Part No.
FRU
Description
1
5555001-2
No
Common SuperBee VHLA Sys Comm
2
5555005-8
Yes
Top Cover HLA - Optima (see 3.2.1 Top Cover HLA, Optima, United States - 5555005-8 on page 86)
3
5503015
No
Upper External Cable Clamp
4
5503015-2
No
Lower External Cable Clamp
5
5503500
Yes
SUPERBEE WIRED HANDSWITCH
6
2188371-2
Yes
Handswitch Cable - N9 Color
7
1000-M4C010-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
8
2000-M4-02
Yes
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
9
1000-M4C020-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X20mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
10
3002-M4C-04
No
Hexagon Prevailing Torque Nut, ISO7040, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
11
5555008
Yes
Breaker Tray (see 3.1.1 Breaker tray - 5555008 on page 81)
12
5555002
Yes
Right Side Cover (see 3.2.3 Right Side Cover - 5555002 on page 101)
13
5555003
Yes
Left Side Cover (see 3.2.4 Left Side Cover - 5555003 on page 102)
14
5555006
Yes
Front Cover Right (see 3.2.5 Front Cover Right - 5555006 on page 103)
15
5555007
Yes
Front Cover Left (see 3.2.6 Front Cover Left - 5555007 on page 105)
16
5555011
Yes
Front Bin (see 3.4.2 Front Bin - 5555011 on page 116)
17
5555012
Yes
Front Bin Window (see 3.4.3 Front Bin Window - 5555012 on page 118)
18
5555013
Yes
Front bin hold down Right (see 3.4.4 Front Bin Hold Down Right - 5555013 on page 119)
19
5555014
Yes
Front Bin Hold Down Left (see 3.4.5 Front Bin Hold Down Left - 5555014 on page 120)
20
5555015
Yes
Wipes Hold Down Support (see 3.1.4 Wipes Hold Down Support - 5555015 on page 85)
21
5555017
Yes
Top External Cabling Exit Cover (see 3.2.7 Top External Cabling Exit Cover - 5555017 on page 107)
22
5555018
Yes
Bottom External Cabling Exit Cover (see 3.2.8 Bottom External Cabling Exit Cover - 5555018 on page 108)
23
5555022
Yes
Column Skirt Front (see 3.2.9 Column Skirt Front - 5555022 on page 109)
24
5555023
Yes
Column Skirt Rear (see 3.2.10 Column Skirt Rear - 5555023 on page 110)
26
5406506
Yes
Front bin filler blank (see 3.4.6 Front Bin Filler Blank - 5406506 on page 121)
27
5406507
Yes
Back-up tether filler blank - Optima XR200amx only (see 3.4.7 Back-up Tether Filler Blank - 5406507 on page 122)
28
5505500
Yes
Tube Cover Assembly (see 3.3.1 Tube cover assembly - 5505500 on page 113)
29
5555004-1
5555004-3
Yes
Yes
Analog Bin Assembly - Optima XR200amx only (see 2.4.1 Analog Bin Assembly - 5555004-1 on page 64)
Digital Bin Assembly - Optima XR220amx only (see 3.4.1 Digital Bin Assembly - 5555004-3 on page 114)
30
5331287
Yes
PC - Single Board Computer for X-Ray Mobile with six USB ports, two 1000Mbps Ethernet ports, LVDS display output, 802.11n miniPCI card
31
5426915
Yes
Ethernet Jack
34
5390144-3
Yes
Wireless USB Host Radio Board - Optima XR220amx only
35
5419392
Yes
Detector Power Supply Assembly - Optima XR220amx only
36
3002-M2P5C-04
No
Hexagon Prevailing Torque Nut, ISO7040, M2.5-0.45, Grade 8 Steel, Zinc Plated, RoHS Fastener - Optima XR220amx only
37
5389155
Yes
FlashPad Tether with Plug Asm, 4m - Optima XR220amx only
38
5136461
Yes
USB External DVD, CD- RW device
See Chapter 5 Common SuperBee VHLA - 5555001-2 on page 133
Chapter 1 Optima Top Level Assembly
Page 25
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 1-1 Optima XR200amx/XR220amx, US and International, 15kW (5555000-3, -5) & 30kW (5555000-4, -6)
Mark No.
Part No.
FRU
40
5486036-5
No
Clamp - cable, 9.5 dia, P type, steel with zinc finish, RoHS compliant
41
5503013
Yes
Cable Clamp
42
1000-M5C020-07
Yes
Hexagon Socket Head Cap Screw, M5-0.8, X20mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
43
1000-M5C025-07
No
Hexagon Socket Head Cap Screw, M5-0.8, X25mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
44
5367724
Yes
Whip antenna for hospital wireless 802.11 (see 3.5.1 Whip antenna/SMA coaxial connector on page 127)
45
5367723
Yes
Reverse Polarity SMA coaxial RF cable (see 3.5.2 Reverse Polarity SMA coaxial RF cable - 5367723 on page 128)
46
5409599
Yes
USB Keyboard
47
5409778-6
5409779-9
Yes
Yes
SW Collector for the Optima XR200amx, the Digital Ready configuration available through the SuperBee Program - Optima XR200amx only
SW Collector for the Optima XR220amx, the Digital configuration available through the SuperBee Program - Optima XR220amx only
50
5399422
No
USB Bulkhead (see 3.1.2 USB Bulkhead - 5399422 on page 83)
51
5406430
Yes
Rear bin mounting bracket Analog - Optima XR200amx only
52
5555016
Yes
Kick Plate (see 3.2.11 Kick Plate - 5555016 on page 111)
53
5406840
Yes
Hold Down Strap (see 3.2.2 Hold Down Strap - 5406840 on page 100)
54
5406217
No
kickplate bracket
55
5412632
No
HV Cable Ferrite
56
5429442
No
M5x20 socket head cap screw, low head
57
5411614
No
ANTENNA BOARD BRACKET - Optima XR220amx only
58
5395666
No
UWB bd spacer - Optima XR220amx only
60
1008-M4P8C016-29
1008-M4P8C019-29
No
No
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 19mm Long, Steel, Zinc Plated, RoHS Fastener - Optima XR200amx only
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 16mm Long, Steel, Zinc Plated, RoHS Fastener - Optima XR220amx only
61
1000-M6C012-04
Yes
Hexagon Socket Head Cap Screw, M6-1, X12mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
62
3000-M6C-04
No
Hexagon Nut, ISO4032, M6-1.0, Grade 8 Steel, Zinc Plated, RoHS Fastener
63
2000-M6-03
No
Flat Washer, ISO7089, M6, Steel 200HV, Zinc Plated, RoHS Fastener (30kW systems only)
64
2203-M6-07
No
Curved Lock Washer, DIN 128A, M6, Spring Steel, Zinc Plated, RoHS Fastener (30kW systems only)
65
1000-M4C008-04
No
Hexagon Socket Head Cap Screw, M4-0.7, X8mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
66
2000-M4-02
Yes
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
67
5375925
Yes
FRU AUX MODULE 30kW (30kW systems only)
68
5150675
Yes
Flat Field Phantom - Optima XR220amx only
69
1008-M4P8C013-29
No
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 13mm Long, Steel, Zinc Plated, RoHS Fastener - Optima XR220amx only
70
46-279773P1
Yes
IEC ON SYMBOL
71
46-279772P1
Yes
IEC OFF SYMBOL
72
46-302200P9
No
BLANK RATING PLATE FOR SERIAL NO ETC
73
5409936
No
Tip Warning Label
74
5410372
No
Voltage Warning Label
75
5407019-5
5407019-4
No
No
Optima XR200amx System Label
Optima XR220amx System Label
76
5407387
No
washer, tether button - Optima XR200amx only
78
5419764
No
Flange socket button head screw - M5 X 12 long
Page 26
Description
Chapter 1 Optima Top Level Assembly
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 1-1 Optima XR200amx/XR220amx, US and International, 15kW (5555000-3, -5) & 30kW (5555000-4, -6)
Mark No.
Part No.
FRU
Description
79
46-252635P7
Yes
.25 NOM., PLAIN WASHER
80
5421364
No
Ferrite 46 ROUND CABLE CORE ASSEMBLY - Optima XR220amx only
81
5486035-8
Yes
Cushioned cable clamp, 15.9mm diameter, RoHS Compliant
90
5503002
Yes
Aux Box to Rotor Jumper Cable
91
5421994-2
No
UWB System Label - Optima XR220amx only
92
5503005
Yes
Col Bulkhead to DAP Cable Assembly - Optima XR220amx only
93
5423408
No
Security Torx M4x10 Buttonhead Fastener
94
5406517
No
front cover thimble
95
5423674
No
M6x10 Lo-head SHCS A2 SS
96
5503011
No
HV Cable Collector (see Section 5.4 HV Cable Collector - 5503011 on page 192)
97
5503017-2
No
External cabling tie wrap (see FRU part number = 5479307 Qty 100)
98
5414029
Yes
gimp seal - left hand
99
5414030
Yes
gimp seal - right hand
100
46-220312P1
Yes
LOCTITE SUPERBONDER 416, 1 OZ (28.4G) BOTTLE, 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER. (REV, TK, 1/92).
101
5557001
Yes
Cable Assy- Spyder to Hornet
111
5557011
Yes
Cable Assy - LVLE2 to DPM-PC
112
5557012
Yes
Cable Assy- Spyder to PC
141
5557041
Yes
Cable Assy - DPM to PC-Backup Tether - Optima XR220amx only
150
5557050
Yes
Cable Assy - Spyder to PC USB
151
5557051
Yes
Cable Assy - PC to Ethernet Bulkhead
152
5557052
Yes
Cable Assy - PC to USB Bulkhead
154
5557054
Yes
Cable Assy - PC to UWB Antenna - Optima XR220amx only
155
5557055
Yes
Cable Assy- Caterpillar to Detector Park Switch - Optima XR220amx only
165
5557065
Yes
Ground cable Top Cover to Chassis
166
5557066
Yes
Cable Asm - Detector Power Supply to Detector charge - Optima XR220amx only
172
5557072
Yes
Cable Asm - DPS to 5557066 - Optima XR220amx only
200
5451000-12
Yes
Firmware USB Dongle for OptimaXR220amx and OptimaXR200amx
201
5434448
Yes
Label- Optima Spyder Board
202
5449450
No
eIFU Label
203
5410372-2
Yes
Voltage Warning Label - French
204
5492661
No
Optima XR200amx LATAM Label
205
5453234
Yes
Superbee Cable Cover with Zippers
None
5393547
Yes
ACCESS COVER, DOCKING CONNECTOR
None
5399683
Yes
HARDWARE KIT FOR SUPERBEE
None
5409524
Yes
Cord Reel Plug US (see 3.1.3 Cord Reel Plug, US - 5409524 on page 84)
None
5409712
Yes
Fuse - Filter Kit
None
5557058
Yes
Cable Assy- Spyder Dose Reporting to USB Bulkhead
See Table 1-2 5399683, HARDWARE KIT FOR SUPERBEE on page 28 for kit contents
See Table 1-3 5409712, Fuse - Filter Kit on page 29 for kit contents
Chapter 1 Optima Top Level Assembly
Page 27
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 1-1 Optima XR200amx/XR220amx, US and International, 15kW (5555000-3, -5) & 30kW (5555000-4, -6)
Mark No.
Part No.
FRU
Description
None
5150092
Yes
USB wireless bar code reader - Optima XR220amx and Optima XR200amx with digital upgrade only
None
5443804
Yes
USB cable for bar code reader - Optima XR220amx and Optima XR200amx with digital upgrade only
None
5479307
Yes
Collector of cable ties (Qty. 100)
Table 1-2 5399683, HARDWARE KIT FOR SUPERBEE
Part No.
Qty
Description
1000-M4C008-04
24
Hexagon Socket Head Cap Screw, M4-0.7, X8mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
1000-M4C030-07
2
Hexagon Socket Head Cap Screw, M4-0.7, X30mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
1000-M4C035-07
4
Hexagon Socket Head Cap Screw, M4-0.7, X35mm Long, Grade12.9 Steel, Black Oxide RoHS Fastener
1000-M4C010-07
34
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
1000-M5C016-07
16
Hexagon Socket Head Cap Screw, M5-0.8, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
1000-M6C016-07
16
Hexagon Socket Head Cap Screw, M6-1, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
1000-M6C020-04
6
Hexagon Socket Head Cap Screw, M6-1, X20mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
1004-M6C020-31
3
Hexagon Socket C-Sunk Head Screw, M6-1, X20mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
1040-M10C025-27
1
Hexagon Set Screw with Cup Point, M10-1.5, X25mm Long, Grade 45H Steel, Black Oxide, RoHS Fastener
1000-M12C025-07
1
Hexagon Socket Head Cap Screw, M12-1.75, X25mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
2000-M4-02
2
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
2000-M5-02
2
Flat Washer, ISO7089, M5, Steel 140HV, Zinc Plated, RoHS Fastener
2000-M6-02
6
Flat Washer, ISO7089, M6, Steel 140HV, Zinc Plated, RoHS Fastener
2203-M4-07
5
Curved Lock Washer, DIN 128A, M4, Spring Steel, Zinc Plated, RoHS Fastener
2203-M6-07
2
Curved Lock Washer, DIN 128A, M6, Spring Steel, Zinc Plated, RoHS Fastener
2106-M5-14
8
Spring Lock Washer with Flat Ends JIS B1251, M5, Spring Stainless Steel, Rohs Fastener
3000-M10C-04
10
Hexagon Nut, ISO4032, M10-1.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
3000-M4C-04
13
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
3000-M5C-04
4
Hexagon Nut, ISO4032, M5-0.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
3000-M6C-04
6
Hexagon Nut, ISO4032, M6-1.0, Grade 8 Steel, Zinc Plated, RoHS Fastener
5370272
6
hex standoff, m-f, 20 mm long, m4
5384944
2
M2.5 X 0.45 X 4mm flat socket, 18-8 stainless, McMaster-Carr 92125A082
2108663-4
1
CLAMP,CLOSED/CABL D9.5X9.5 METAL M4
2193201
1
SCREW DIN7991 M4X8/6 A4-70
1007-M3C016-31
4
Phillips Pan Head Screw, ISO 7045, M3-0.5, X16mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
1003-M3C008-31
4
Hexagon Socket Button Head Screw, M3-0.5, X8mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
1003-M3C006-31
4
Hexagon Socket Button Head Screw, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
1000-M5C020-07
2
Hexagon Socket Head Cap Screw, M5-0.8, X20mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
1000-M5C025-07
2
Hexagon Socket Head Cap Screw, M5-0.8, X25mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
1003-M4C006-31
4
Hexagon Socket Button Head Screw, M4-0.7, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
Page 28
Chapter 1 Optima Top Level Assembly
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 1-2 5399683, HARDWARE KIT FOR SUPERBEE
Part No.
Qty
Description
5423408
4
Security Torx M4x10 Buttonhead Fastener
5423674
2
M6x10 Lo-head SHCS A2 SS
5419764
10
Flange socket button head screw - M5 X 12 long
1004-M6C016-22
3
Hexagon Socket C-Sunk Head Screw, M6-1, X16mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
5406517
2
front cover thimble
5486036-5
1
Clamp - cable, 9.5 dia, P type, steel with zinc finish,
5427920
1
Torx Bit
1004-M8C016-22
1
M8 x 16 Flat head
1008-M4P8C013-29
2
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 13mm Long, Steel, Zinc Plated, RoHS Fastener
5429442
8
M5x20 socket head cap screw, low head
46-252635P7
8
.25 NOM., PLAIN WASHER
1008-M4P8C016-29
10
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 16mm Long, Steel, Zinc Plated, RoHS Fastener
Table 1-3 5409712, Fuse - Filter Kit
Part No.
Qty
Description
5351707
1
Single Phase AC Line EMI Filter
5392168
2
3AG fuse holder, 250V rated, 20A rated, 2000V dielectric strength min, UL94V0 rated
5392167
4
Ceramic Fuse, 250VAC, 15A, Fast Action, 6.3mm x 32mm
5341181
2
PROTECTION FUSE, 3A, TIME DELAY, 300VDC, 600VAC, CARTRIDGE
5306477
4
PROTECTION FUSE, 8A, TIME DELAY, 300VDC, 600VAC, CARTRIDGE
5306477-3
3
PROTECTION FUSE, 15A, TIME DELAY, 300VDC, 600VAC, CARTRIDGE
5184715-3
2
FUSE, TIME DELAY, 5X20MM, 3.15A IEC, 250V, 1.5KA INTERRUPT, CERAMIC, UL REC
Table 1-4 Software Collector and Firmware dongle for Optima XR220amx for VA
Part No.
FRU
Description
5409779-11
Yes
Software Collector for Optima XR220amx for VA
5451000-15
Yes
Firmware USB Dongle for Optima XR220amx and XR200amx
Chapter 1 Optima Top Level Assembly
Page 29
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Page 30
SYSTEM PARTS LIST
Chapter 1 Optima Top Level Assembly
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Chapter 2 Optima XR200amx Drawings
Section 2.1 Base
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.1.1 Breaker tray - 5555008
Approved Document - 5555008DDW_r8.pdf Page 2 of 3
Figure 2-1 Breaker tray - 5555008
Chapter 2 Optima XR200amx Drawings
Page 31
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.1.2 USB Bulkhead, Analog - 5399422-2
Approved Document - 5399422DDW_r3.pdf Page 2 of 2
Figure 2-2 USB Bulkhead, Analog - 5399422-2
Page 32
Section 2.1 Base
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
2.1.3 Cord Reel Plug, US - 5409524
Figure 2-3 Cord Reel Plug, US - 5409524
Chapter 2 Optima XR200amx Drawings
Page 33
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.1.4 Wipes Hold Down Support - 5555015
Figure 2-4 Wipes Hold Down Support - 5555015
Page 34
Section 2.1 Base
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 2.2 Covers
2.2.1 Top Cover HLA, Optima, United States - 5555005-8
Figure 2-5 Top Cover HLA, Optima, United States - 5555005-8ADW_r2_s1
Chapter 2 Optima XR200amx Drawings
Page 35
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 2-6 Top Cover HLA, Optima, United States - 5555005-8ADW_r2_s2
Page 36
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 2-7 Top Cover HLA, Optima, United States - 5555005-8ADW_r2_s3
Chapter 2 Optima XR200amx Drawings
Page 37
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 2-8 Top Cover HLA, Optima, United States - 5555005-8ADW_r2_s4
Page 38
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 2-9 Top Cover HLA, Optima, United States - 5555005-8ADW_r2_s5
Chapter 2 Optima XR200amx Drawings
Page 39
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Table 2-1
SYSTEM PARTS LIST
Top Cover HLA, Optima, United States - 5555005-8
Mark No.
Part No.
FRU?
Description
1
1000-M4C010-31
No
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
2
1000-M3C006-31
No
Hexagon Socket Head Cap Screw, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
3
5404040
No
Display Inverter
4
5412745
No
Sheet metal display bracket left
5
5412744
No
Sheet Metal Display Bracket Right
6
5411274
No
Bar Graph Seal
7
5412785
No
Drive login sheet metal bracket
8
5412786
No
Drive login electrode retainer
9
5412787
No
Window glass adhesive film
10
5412746
No
Sheet metal bracket pcb
12
5368309
Yes
Top Cover (see 2.2.1.1 Top Cover - 5368309 on page 42)
13
5391117
Yes
Power Switch Assembly (see 2.2.1.2 Power Switch Assembly - 5391117 on page 43)
14
5391109
Yes
Overlay Board Assembly
15
5404038
No
TFT Color LCD Module 38cm 15.0 type XGA LVDS Interface 1port
16
5390076
No
Overlay Touchscreen Assembly - Optima - United States
17
2000-M4-16
No
External Toothed Lock Washer, DIN 6797A, M4, A2 Stainless Steel, RoHS Fastener
18
2204-M3-16
No
External Toothed Lock Washer, DIN 6797A, M3, A2 Stainless Steel, RoHS Fastener
19
5412754
No
Screw CBLX M3x6
20
2000-M3-10
No
Flat Washer, ISO7089, M3, Stainless Steel 140HV, RoHS Fastener
21
5350004-2
Yes
Hornet Display Module Board -2 variation
22
5378852
No
Drive Login Electrode Board PWA
23
5390080
No
Drive Login Lightpipe Assembly - Glass Windows
24
5378850
Yes
Drive Login Active Board PWA (see 2.2.1.5.1 Drive Login Active Board PWA - 5378850 on page 47)
25
5412994
No
Adhesive Electrode Board + 2 Liner
26
5557018
Yes
Cable Assy - Hornet to Display
28
5557028
Yes
Cable Assy - Hornet to Inverter
29
5557029
Yes
Cable Assy - Hornet to Overlay Board
30
5557034
Yes
Cable Assy - Drive Login to Overlay Board
31
5413000
No
CABLE GROUND
32
5416426
No
Hornet EMC Sheet Metal Enclosure
33
3003-M4C-04
Yes
Hexagon Nut with Lock Washer, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
34
5417868
No
Cable clamp
35
5417873
No
Flat cable clamp
36
5417896
No
flat tie holder
37
1000-M4C012-04
Yes
Hexagon Socket Head Cap Screw, M4-0.7, X12mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener.
Page 40
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Table 2-1
SYSTEM PARTS LIST
Top Cover HLA, Optima, United States - 5555005-8
Mark No.
Part No.
FRU?
Description
38
46-220312P1
Yes
LOCTITE SUPERBONDER 416, 1 OZ (28.4G) BOTTLE
39
5420683
No
Ferrite
40
5421209
No
Ferrite
60
5423145
No
gasket
5394460
Yes
Display and Inverter Collector (see 2.2.1.6 Display and Inverter Collector - 5394460 on page 48)
5394459
Yes
Drive Login Active Board Collector (see 2.2.1.5 Drive Login Active Board Collector - 5394459 on page 46)
Chapter 2 Optima XR200amx Drawings
Page 41
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.1.1 Top Cover - 5368309
Approved Document - 5368309DDW_r6.pdf Page 4 of 4
Figure 2-10 Top Cover - 5368309
Page 42
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
2.2.1.2 Power Switch Assembly - 5391117
Figure 2-11 Power Switch Assembly - 5391117
Table 2-2
Power Switch Assembly - 5391117
Mark No.
Part No.
FRU?
Description
1
5391118
No
Power Switch Diffuser
2
5391119
No
Power Switch Pushbutton Cover
3
5391120
No
Power Switch Locknut
4
5404004
No
Power Switch
5
5557044
Yes
Cable Assy - Power Switch Pigtail
Chapter 2 Optima XR200amx Drawings
Page 43
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.1.3 Overlay Board Assembly - 5391109
5391109
THIS DRAWING WAS MADE
BY DELTATECH CONTROLS
FOR GE HEALTHCARE.
Approved Document - 5391109ADW_r2.pdf Page 2 of 2
Figure 2-12 Overlay Board Assembly - 5391109
Page 44
Section 2.2 Covers
Overlay Board Assembly
02
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
2.2.1.4 Hornet Display Module Board PWA - 5350004-2
Figure 2-13 Hornet Display Module Board PWA - 5350004ADW
Chapter 2 Optima XR200amx Drawings
Page 45
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
2.2.1.5 Drive Login Active Board Collector - 5394459
Table 2-3
Drive Login Active Board Collector - 5394459
Mark No. Part No.
FRU
Description
1
5378850
No
Drive Login Active Board PWA, see 2.2.1.5.1 Drive Login Active Board PWA - 5378850 on page 47
2
5557034
Yes
Cable Assy - Drive Login to Overlay Board
3
5412785
No
Drive login sheet metal bracket
4
1000-M3C006-31
No
Hexagon Socket Head Cap Screw, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
5
2000-M3-10
No
Flat Washer, ISO7089, M3, Stainless Steel 140HV, RoHS Fastener
Page 46
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
2.2.1.5.1 Drive Login Active Board PWA - 5378850
Figure 2-14 Drive Login Active Board PWA - 5378850 (1/2)
Chapter 2 Optima XR200amx Drawings
Page 47
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 2-15 Drive Login Active Board PWA - 5378850 (2/2)
2.2.1.6 Display and Inverter Collector - 5394460
Table 2-4
Display and Inverter Collector - 5394460
Mark No. Part No.
FRU
Description
1
5404038
No
TFT Color LCD Module 38cm 15.0 type XGA LVDS Interface 1port
2
5404040
No
Display Inverter
3
5412745
No
Sheet metal display bracket left
4
5412744
No
Sheet Metal Display Bracket Right
Page 48
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Table 2-4
SYSTEM PARTS LIST
Display and Inverter Collector - 5394460
Mark No. Part No.
FRU
Description
5
1000-M3C006-04
No
Hexagon Socket Head Cap Screw, M3-0.5, X6mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
6
2000-M3-02
No
Flat Washer, ISO7089, M3, Steel 140HV, Zinc Plated, RoHS Fastener
Chapter 2 Optima XR200amx Drawings
Page 49
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.2 Hold Down Strap - 5406840
Approved Document - 5406840DDW_r4.pdf Page 2 of 2
Figure 2-16 Hold Down Strap - 5406840
Page 50
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.3 Right Side Cover - 5555002
Approved Document - 5555002ADW_r9.pdf Page 2 of 2
Figure 2-17 Right Side Cover - 5555002
Chapter 2 Optima XR200amx Drawings
Page 51
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.4 Left Side Cover - 5555003
[
Approved Document - 5555003ADW_r9.pdf Page 2 of 2
Figure 2-18 Left Side Cover - 5555003
Page 52
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.5 Front Cover Right - 5555006
Approved Document - 5555006DDW_r10.pdf Page 2 of 3
Figure 2-19 Front Cover Right - 5555006 (1/2)
Chapter 2 Optima XR200amx Drawings
Page 53
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5555006DDW_r10.pdf Page 3 of 3
Figure 2-20 Front Cover Right - 5555006 (2/2)
Page 54
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.6 Front Cover Left - 5555007
Approved Document - 5555007DDW_r12.pdf Page 2 of 3
Figure 2-21 Front Cover Left - 5555007 (1/2)
Chapter 2 Optima XR200amx Drawings
Page 55
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5555007DDW_r12.pdf Page 3 of 3
Figure 2-22 Front Cover Left - 5555007 (2/2)
Page 56
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.7 Top External Cabling Exit Cover - 5555017
Approved Document - 5555017DDW_r4.pdf Page 2 of 2
Figure 2-23 Top External Cabling Exit Cover - 5555017
Chapter 2 Optima XR200amx Drawings
Page 57
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.8 Bottom External Cabling Exit Cover - 5555018
Approved Document 5555018DDW r3 pdf Page 2 of 2
Figure 2-24 Bottom External Cabling Exit Cover - 5555018
Page 58
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.9 Column Skirt Front - 5555022
Approved Document - 5555022DDW_r6.pdf Page 2 of 2
Figure 2-25 Column Skirt Front - 5555022 (1/2)
Chapter 2 Optima XR200amx Drawings
Page 59
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.10 Column Skirt Rear - 5555023
Approved Document - 5555023DDW_r5.pdf Page 2 of 2
Figure 2-26 Column Skirt Rear - 5555023
Page 60
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.11 Kick Plate - 5555016
Approved Document - 5555016DDW_r5.pdf Page 2 of 2
Figure 2-27 Kick Plate - 5555016
Chapter 2 Optima XR200amx Drawings
Page 61
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.2.12 Access Cover, Docking Connector - 5393547
Approved Document - 5393547DDW_r6.pdf Page 2 of 2
Figure 2-28 Access Cover, Docking Connector - 5393547
Page 62
Section 2.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 2.3 Tube
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.3.1 Tube cover assembly - 5505500
Approved Document - 5505500ADW_r1.pdf Page 2 of 2
Figure 2-29 Tube cover assembly - 5505500
Table 2-5
Tube cover assembly - 5505500
Mark No.
Part No.
FRU?
Description
3
5507721
No
Angle Indicator Assembly
9
1008-M4P8C016-29 No
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 16mm Long, Steel, Zinc Plated, RoHS Fastener
10
1000-M4C010-07
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
No
Chapter 2 Optima XR200amx Drawings
Page 63
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 2.4 Bin
2.4.1 Analog Bin Assembly - 5555004-1
Figure 2-30 Analog Bin Assembly - 5555004-1
Table 2-6
Analog Bin Assembly - 5555004-1
Mark No.
Part No.
FRU?
Description
1
5394404
No
Analog Bin Weldment
2
5396888
No
Analog Bin Cover
3
5398416
No
Analog Bin Cushion
4
5398418
No
Analog Bin Mat
5
1004-M4C008-22
No
Hexagon Socket C-Sunk Head Screw, M4-0.7, X8mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
6
1000-M4C020-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X20mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
7
46-270240P1
Yes
AMX 4 - Spacer Plastic
8
5399160
No
Storage Bin Assembly (see 2.4.9 Storage Bin Assembly - 5399160 on page 73)
9
2000-M4-02
No
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
10
3000-M4C-04
No
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
Page 64
Section 2.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.2 Front Bin - 5555011
Approved Document - 5555011DDW_r8.pdf Page 2 of 3
Figure 2-31 Front Bin - 5555011 (1/2)
Chapter 2 Optima XR200amx Drawings
Page 65
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5555011DDW_r8.pdf Page 3 of 3
Figure 2-32 Front Bin - 5555011 (2/2)
Page 66
Section 2.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.3 Front Bin Window - 5555012
Approved Document - 5555012DDW_r7.pdf Page 2 of 2
Figure 2-33 Front Bin Window - 5555012
Chapter 2 Optima XR200amx Drawings
Page 67
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.4 Front Bin Hold Down Right - 5555013
Approved Document - 5555013DDW_r5.pdf Page 2 of 2
Figure 2-34 Front Bin Hold Down Right - 5555013
Page 68
Section 2.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.5 Front Bin Hold Down Left - 5555014
Approved Document - 5555014DDW_r5.pdf Page 2 of 2
Figure 2-35 Front Bin Hold Down Left - 5555014
Chapter 2 Optima XR200amx Drawings
Page 69
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.6 Wipes Hold Down Support - 5555015
Approved Document - 5555015DDW_r10.pdf Page 2 of 2
Figure 2-36 Wipes Hold Down Support - 5555015
Page 70
Section 2.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.7 Front Bin Filler Blank - 5406506
Approved Document - 5406506DDW_r6.pdf Page 2 of 2
Figure 2-37 Front Bin Filler Blank - 5406506
Chapter 2 Optima XR200amx Drawings
Page 71
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.8 Back-up Tether Filler Blank - 5406507
Approved Document - 5406507DDW_r6.pdf Page 2 of 2
Figure 2-38 Back-up Tether Filler Blank - 5406507
Page 72
Section 2.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
2.4.9 Storage Bin Assembly - 5399160
Figure 2-39 Storage Bin Assembly - 5399160
Chapter 2 Optima XR200amx Drawings
Page 73
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Table 2-7
Mark No.
Page 74
SYSTEM PARTS LIST
Storage Bin Assembly - 5399160
Part No.
FRU?
Description
5399180
No
Storage Bin
5402020
Yes
Door Assy, Storage Compartment (see 2.4.9.1 Door Assy, Storage Compartment - 5402020 on page 75)
5402021
Yes
Storage Compartment Latch
5402022
Yes
Storage Compartment Hinge
1000-M5C012-04
No
Hexagon Socket Head Cap Screw, M5-0.8, X12mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
3000-M4C-04
No
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
3000-M5C-04
No
Hexagon Nut, ISO4032, M5-0.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
46-170686P1
Yes
Loctite 242, 0.5CC tube 12 month shelf life from date of shipment from manufacturer
Section 2.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.9.1 Door Assy, Storage Compartment - 5402020
Approved Document - 5402020ADW_r3.pdf Page 2 of 2
Figure 2-40 Door Assy, Storage Compartment - 5402020
Chapter 2 Optima XR200amx Drawings
Page 75
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
2.4.10 Rear bin mounting bracket Analog - 5406430
Figure 2-41 Rear bin mounting bracket, Analog - 5406430
Page 76
Section 2.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.4.11 Access Cover, Docking Connector - 5393547
Approved Document - 5393547DDW_r6.pdf Page 2 of 2
Figure 2-42 Access Cover, Docking Connector - 5393547
Chapter 2 Optima XR200amx Drawings
Page 77
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 2.5 PC
2.5.1 Whip antenna for 802.11abgn wireless/SMA coaxial connector with swivel mount - 5367724
Figure 2-43 Whip antenna for 802.11abgn wireless/SMA coaxial connector with swivel mount - 5367724
Page 78
Section 2.5 PC
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
2.5.2 Reverse Polarity SMA coaxial RF cable - 5367723
Approved Document - 5367723DDW_r1.pdf Page 2 of 2
Figure 2-44 Reverse Polarity SMA coaxial RF cable - 5367723
Chapter 2 Optima XR200amx Drawings
Page 79
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Page 80
SYSTEM PARTS LIST
Section 2.5 PC
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Chapter 3 Optima XR220amx Drawings
Section 3.1 Base
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.1.1 Breaker tray - 5555008
Approved Document - 5555008DDW_r8.pdf Page 2 of 3
Figure 3-1 Breaker tray - 5555008 (1/2)
Chapter 3 Optima XR220amx Drawings
Page 81
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5555008DDW_r8.pdf Page 3 of 3
Figure 3-2 Breaker tray - 5555008 (2/2)
Page 82
Section 3.1 Base
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.1.2 USB Bulkhead - 5399422
Approved Document - 5399422DDW_r3.pdf Page 2 of 2
Figure 3-3 USB Bulkhead - 5399422
Chapter 3 Optima XR220amx Drawings
Page 83
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
3.1.3 Cord Reel Plug, US - 5409524
Figure 3-4 Cord Reel Plug, US - 5409524
Page 84
Section 3.1 Base
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.1.4 Wipes Hold Down Support - 5555015
Figure 3-5 Wipes Hold Down Support - 5555015
Chapter 3 Optima XR220amx Drawings
Page 85
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 3.2 Covers
3.2.1 Top Cover HLA, Optima, United States - 5555005-8
Figure 3-6 Top Cover HLA, Optima, United States - 5555005-8_r1_s1
Page 86
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 3-7 Top Cover HLA, Optima, United States - 5555005-8_r1_s2
Chapter 3 Optima XR220amx Drawings
Page 87
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 3-8 Top Cover HLA, Optima, United States - 5555005-8_r1_s3
Page 88
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 3-9 Top Cover HLA, Optima, United States - 5555005-8_r1_s4
Chapter 3 Optima XR220amx Drawings
Page 89
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 3-10 Top Cover HLA, Optima, United States - 5555005-8_r1_s5
Page 90
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Table 3-1
SYSTEM PARTS LIST
Top Cover HLA, Optima, United States - 5555005-8
Mark No.
Part No.
FRU?
Description
1
1000-M4C010-31
No
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
2
1000-M3C006-31
No
Hexagon Socket Head Cap Screw, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
3
5404040
No
Display Inverter
4
5412745
No
Sheet metal display bracket left
5
5412744
No
Sheet Metal Display Bracket Right
6
5411274
No
Bar Graph Seal
7
5412785
No
Drive login sheet metal bracket
8
5412786
No
Drive login electrode retainer
9
5412787
No
Window glass adhesive film
10
5412746
No
Sheet metal bracket pcb
12
5368309
Yes
Top Cover (see 3.2.1.1 Top Cover - 5368309 on page 93)
13
5391117
Yes
Power Switch Assembly (see 3.2.1.2 Power Switch Assembly - 5391117 on page 94)
14
5391109
Yes
Overlay Board Assembly
15
5404038
No
TFT Color LCD Module 38cm 15.0 type XGA LVDS Interface 1port
16
5390076
No
Overlay Touchscreen Assembly - Optima - United States
17
2204-M4-16
No
External Toothed Lock Washer, DIN 6797A, M4, A2 Stainless Steel, RoHS Fastener
18
2204-M3-16
No
External Toothed Lock Washer, DIN 6797A, M3, A2 Stainless Steel, RoHS Fastener
19
5412754
No
Screw CBLX M3x6
20
2000-M3-10
No
Flat Washer, ISO7089, M3, Stainless Steel 140HV, RoHS Fastener
21
5350004-2
Yes
Hornet Display Module Board -2 variation (see 3.2.1.4 Hornet Display Module Board PWA - 5350004-2 on page 96)
22
5378852
No
Drive Login Electrode Board PWA
23
5390080
No
Drive Login Lightpipe Assembly - Glass Windows
24
5378850
No
Drive Login Active Board PWA (see 3.2.1.5 Drive Login Active Board Collector - 5394459 on page 97)
25
5412994
No
Adhesive Electrode Board + 2 Liner
27
5557018
Yes
Cable Assy - Hornet to Display
28
5557028
Yes
Cable Assy - Hornet to Inverter
29
5557029
Yes
Cable Assy - Hornet to Overlay Board
30
5557034
Yes
Cable Assy - Drive Login to Overlay Board
31
5413000
No
Cable Ground
32
5416426
No
Hornet EMC Sheet Metal Enclosure
33
3003-M4C-04
Yes
Hexagon Nut with Lock Washer, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
34
5417868
No
Cable clamp
35
5417873
No
Flat cable clamp
36
5417896
No
Flat tie holder
37
1000-M4C012-04
Yes
Hexagon Socket Head Cap Screw, M4-0.7, X12mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
Chapter 3 Optima XR220amx Drawings
Page 91
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Table 3-1
SYSTEM PARTS LIST
Top Cover HLA, Optima, United States - 5555005-8
Mark No.
Part No.
FRU?
Description
38
46-220312P1
Yes
"LOCTITE SUPERBONDER 416, 1 OZ (28.4G) BOTTLE 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE
MANUFACTURER. (REV, TK, 1/92)."
39
5420683
No
Ferrite
40
5421209
No
Ferrite
60
5423145
No
gasket
-
5394459
Yes
Drive Login Active Board Collector (see 3.2.1.5 Drive Login Active Board Collector - 5394459 on page 97)
-
5394460
Yes
Display and Inverter Collector (see 3.2.1.6 Display and Inverter Collector - 5394460 on page 99)
Page 92
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.2.1.1 Top Cover - 5368309
Approved Document - 5368309DDW_r6.pdf Page 4 of 4
Figure 3-11 Top Cover - 5368309
Chapter 3 Optima XR220amx Drawings
Page 93
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
3.2.1.2 Power Switch Assembly - 5391117
Figure 3-12 Power Switch Assembly - 5391117
Table 3-2
Power Switch Assembly - 5391117
Mark No.
Part No.
FRU?
Description
1
5391118
No
Power Switch Diffuser
2
5391119
No
Power Switch Pushbutton Cover
3
5391120
No
Power Switch Locknut
4
5404004
No
Power Switch
5
5557044
Yes
Cable Assy - Power Switch Pigtail
Page 94
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.2.1.3 Overlay Board Assembly - 5391109
5391109
THIS DRAWING WAS MADE
BY DELTATECH CONTROLS
FOR GE HEALTHCARE.
02
Overlay Board Assembly
Approved Document - 5391109ADW_r2.pdf Page 2 of 2
Figure 3-13 Overlay Board Assembly - 5391109
Chapter 3 Optima XR220amx Drawings
Page 95
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
3.2.1.4 Hornet Display Module Board PWA - 5350004-2
o
Figure 3-14 Hornet Display Module Board PWA - 5350004-2
Page 96
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
3.2.1.5 Drive Login Active Board Collector - 5394459
Table 3-3
Drive Login Active Board Collector - 5394459
Mark No. Part No.
FRU
Description
1
5378850
No
Drive Login Active Board PWA, see 3.2.1.5 Drive Login Active Board Collector - 5394459 on page 97
2
5557034
Yes
Cable Assy - Drive Login to Overlay Board
3
5412785
No
Drive login sheet metal bracket
4
1000-M3C006-31
No
Hexagon Socket Head Cap Screw, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
5
2000-M3-10
No
Flat Washer, ISO7089, M3, Stainless Steel 140HV, RoHS Fastener
Figure 3-15 Drive Login Active Board PWA - 5378850 (1/2)
Chapter 3 Optima XR220amx Drawings
Page 97
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 3-16 Drive Login Active Board PWA - 5378850 (2/2)
Page 98
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
3.2.1.6 Display and Inverter Collector - 5394460
Table 3-4
Display and Inverter Collector - 5394460
Mark No. Part No.
FRU
Description
1
5404038
No
TFT Color LCD Module 38cm 15.0 type XGA LVDS Interface 1port
2
5404040
No
Display Inverter
3
5412745
No
Sheet metal display bracket left
4
5412744
No
Sheet Metal Display Bracket Right
5
1000-M3C006-04
No
Hexagon Socket Head Cap Screw, M3-0.5, X6mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
6
2000-M3-02
No
Flat Washer, ISO7089, M3, Steel 140HV, Zinc Plated, RoHS Fastener
Chapter 3 Optima XR220amx Drawings
Page 99
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.2.2 Hold Down Strap - 5406840
Approved Document - 5406840DDW_r4.pdf Page 2 of 2
Figure 3-17 Hold Down Strap - 5406840
Page 100
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.2.3 Right Side Cover - 5555002
Approved Document - 5555002ADW_r9.pdf Page 2 of 2
Figure 3-18 Right Side Cover - 5555002
Chapter 3 Optima XR220amx Drawings
Page 101
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.2.4 Left Side Cover - 5555003
Approved Document - 5555003ADW_r9.pdf Page 2 of 2
Figure 3-19 Left Side Cover - 5555003
Page 102
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.2.5 Front Cover Right - 5555006
Figure 3-20 Front Cover Right - 5555006 (1/2)
Chapter 3 Optima XR220amx Drawings
Page 103
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5555006DDW_r10.pdf Page 3 of 3
Figure 3-21 Front Cover Right - 5555006 (2/2)
Page 104
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.2.6 Front Cover Left - 5555007
Figure 3-22 Front Cover Left - 5555007 (1/2)
Chapter 3 Optima XR220amx Drawings
Page 105
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5555007DDW_r12.pdf Page 3 of 3
Figure 3-23 Front Cover Left - 5555007 (2/2)
Page 106
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.2.7 Top External Cabling Exit Cover - 5555017
Approved Document - 5555017DDW_r4.pdf Page 2 of 2
Figure 3-24 Top External Cabling Exit Cover - 5555017
Chapter 3 Optima XR220amx Drawings
Page 107
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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3.2.8 Bottom External Cabling Exit Cover - 5555018
Figure 3-25 Bottom External Cabling Exit Cover - 5555018
Page 108
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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3.2.9 Column Skirt Front - 5555022
Approved Document - 5555022DDW_r6.pdf Page 2 of 2
Figure 3-26 Column Skirt Front - 5555022
Chapter 3 Optima XR220amx Drawings
Page 109
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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3.2.10 Column Skirt Rear - 5555023
Figure 3-27 Column Skirt Rear - 5555023
Page 110
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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3.2.11 Kick Plate - 5555016
Approved Document - 5555016DDW_r5.pdf Page 2 of 2
Figure 3-28 Kick Plate - 5555016
Chapter 3 Optima XR220amx Drawings
Page 111
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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3.2.12 Access Cover, Docking Connector - 5393547
Figure 3-29 Access Cover, Docking Connector - 5393547
Page 112
Section 3.2 Covers
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 3.3 Tube
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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3.3.1 Tube cover assembly - 5505500
Approved Document - 5505500ADW_r1.pdf Page 2 of 2
Figure 3-30 Tube cover assembly - 5505500
Table 3-5
Tube cover assembly - 5505500
Mark No.
Part No.
FRU?
Description
3
5507721
No
Angle Indicator Assembly
9
1008-M4P8C016-29 No
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 16mm Long, Steel, Zinc Plated, RoHS Fastener
10
1000-M4C010-07
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
No
Chapter 3 Optima XR220amx Drawings
Page 113
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 3.4 Bin
3.4.1 Digital Bin Assembly - 5555004-3
For Optima XR220amx and Optima XR200amx with digital upgrade systems only.
Figure 3-31 Digital Bin Assembly - 5555004-3
Page 114
Section 3.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Table 3-6
SYSTEM PARTS LIST
Digital Bin Assembly - 5555004-3
Mark No.
Part No.
FRU?
Description
1
5393540
No
Digital Bin Weldment
2
5393543-2
No
Injection Molded Bin Lower Rail
3
5393542-3
No
Injection Molded Bin Side Rails
4
5454666
Yes
Charging Connector Assembly
5
5557056
Yes
Cable Assy- Detector Park Switch to Bulkhead
6
5397273
Yes
Detector Bin Park Switch
7
5443673
No
Divider Plate
8
5393545
No
COVER, DIGITAL BIN
9
5393547
Yes
ACCESS COVER, DOCKING CONNECTOR
10
5396367
Yes
Shock Absorber
11
5398416-2
No
Digital Bin Cushion
12
5398418-2
No
Digital Bin Mat
13
1004-M4C008-22
No
Hexagon Socket C-Sunk Head Screw, M4-0.7, X8mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
15
5398402
No
Rubber Bumper
16
1004-M4C020-22
No
Hexagon Socket C-Sunk Head Screw, M4-0.7, X20mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
17
3000-M4C-04
Yes
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
18
5399160
No
STORAGE BIN ASSEMBLY
19
2000-M4-02
Yes
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
24
5460146
No
M14 THIN FINE THREAD NUT - 22MM ACROSS FLATS - 1.5 MM PITCH
25
5462412
No
4 MM PLAS-TITE SCREW 8 MM LONG BINDING HEAD PHILLIPS TYPE WN1412PT10 SAME AS BN13577 EXACT PART
Article No. 2000474
26
5449321
No
4 MM PLAS-TITE SCREW 8 MM LONG FLAT HEAD PHILLIPS TYPE WN1413PT10 SAME AS BN13576 EXACT PART Article
No. 2001365
Chapter 3 Optima XR220amx Drawings
Page 115
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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GE HEALTHCARE
DIRECTION 5336115-1EN, REVISION 6
Page 116
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
3.4.2 Front Bin - 5555011
Figure 3-32 Front Bin - 5555011 (1/2)
Section 3.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5555011DDW_r8.pdf Page 3 of 3
Figure 3-33 Front Bin - 5555011 (2/2)
Chapter 3 Optima XR220amx Drawings
Page 117
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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GE HEALTHCARE
DIRECTION 5336115-1EN, REVISION 6
Page 118
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
3.4.3 Front Bin Window - 5555012
Figure 3-34 Front Bin Window - 5555012
Section 3.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.4.4 Front Bin Hold Down Right - 5555013
Figure 3-35 Front Bin Hold Down Right - 5555013
Chapter 3 Optima XR220amx Drawings
Page 119
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.4.5 Front Bin Hold Down Left - 5555014
Figure 3-36 Front Bin Hold Down Left - 5555014
Page 120
Section 3.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.4.6 Front Bin Filler Blank - 5406506
Figure 3-37 Front Bin Filler Blank - 5406506
Chapter 3 Optima XR220amx Drawings
Page 121
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.4.7 Back-up Tether Filler Blank - 5406507
Approved Document - 5406507DDW_r6.pdf Page 2 of 2
Figure 3-38 Back-up Tether Filler Blank - 5406507
Page 122
Section 3.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
3.4.8 Storage Bin Assembly - 5399160
Figure 3-39 Storage Bin Assembly - 5399160
Chapter 3 Optima XR220amx Drawings
Page 123
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Table 3-7
SYSTEM PARTS LIST
Storage Bin Assembly - 5399160
Mark No.
Part No.
FRU?
Description
1
5399180
No
Storage Bin
2
5402020
Yes
Door Assy, Storage Compartment (see 3.4.8.1 Door Assy, Storage Compartment - 5402020 on page 125)
3
5402021
Yes
Storage Compartment Latch
4
5402022
Yes
Storage Compartment Hinge
5
1000-M5C012-04
No
Hexagon Socket Head Cap Screw, M5-0.8, X12mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
6
3000-M4C-04
Yes
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
7
3000-M5C-04
No
Hexagon Nut, ISO4032, M5-0.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
8
46-170686P1
Yes
Loctite 242, 0.5CC tube 12 month shelf life from date of shipment from manufacturer
Page 124
Section 3.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.4.8.1 Door Assy, Storage Compartment - 5402020
Figure 3-40 Door Assy, Storage Compartment - 5402020
Chapter 3 Optima XR220amx Drawings
Page 125
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3.4.9 Access Cover, Docking Connector - 5393547
Figure 3-41 Access Cover, Docking Connector - 5393547
Page 126
Section 3.4 Bin
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 3.5 PC
3.5.1 Whip antenna/SMA coaxial connector
Figure 3-42 Whip antenna for 802.11abgn wireless/SMA coaxial connector with swivel mount - 5367724
Chapter 3 Optima XR220amx Drawings
Page 127
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
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3.5.2 Reverse Polarity SMA coaxial RF cable - 5367723
Approved Document - 5367723DDW_r1.pdf Page 2 of 2
Figure 3-43 Reverse Polarity SMA coaxial RF cable - 5367723
Page 128
Section 3.5 PC
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Chapter 4 FlashPad detector and related components
Table 4-1
FlashPad detector and related components
Part No.
FRU
Description
5399000-3
Yes
FlashPad detector - New (Rev 1 US, Canada, EU) See Figure 4-88.
5399000-4
Yes
FlashPad detector - service (Rev 1 US, Canada, EU) See Figure 4-88.
5339900-5
Yes
FlashPad detector - new (Rev 2 US, Canada, EU, Japan, Australia) See Figure 4-88.
5339900-6
Yes
Flashpad detector - service (Rev 2 US, Canada, EU, Japan, Australia) See Figure 4-88.
5363606
Yes
FlashPad Grid Holder Asm, 6:1 Ratio See Figure 4-89.
5436002
Yes
FlashPad Docking Interface bd. See Figure 4-90.
5394471
Yes
FlashPad Battery Charger See Figure 4-91.
5390144
Yes
UWB Dongle (US Only) See Figure 4-92.
5390144-2
Yes
UWB Dongle (US, Canada, EU) See Figure 4-92.
5390144-3
Yes
UWB Dongle (US, Canada, EU, Japan, Australia) See Figure 4-92.
5389155
Yes
FlashPad Tether with Plug Asm, 4m - Optima XR220amx only
5382000
Yes
FlashPad Battery with cap
Figure 4-1 FlashPad detector, 5399000-3, -4, -5, -6
Chapter 4 FlashPad detector and related components
Page 129
GE HEALTHCARE
DIRECTION 5336115-1EN, REVISION 6
Figure 4-2 FlashPad Grid Holder Asm, 6:1 Ratio, 5363606
Figure 4-3 FlashPad docking interface board, 5436002
Page 130
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 4-4 FlashPad Battery Charger, 5394471
Figure 4-5 UWB Dongle, 5390144, -2, -3
Chapter 4 FlashPad detector and related components
Page 131
GE HEALTHCARE
DIRECTION 5336115-1EN, REVISION 6
Page 132
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Chapter 5 Common SuperBee VHLA - 5555001-2
Figure 5-1 5555001ADW_r5_s1
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 133
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-1 Common SuperBee VHLA - 5555001-2
Mark No.
Part No.
FRU
1
5509900-3
No
Base, Column, Arm, Drive Handle, Thorax Assembly
Thorax Assembly - 5509900-3 on page 135
2
5507700
No
Tube and Tube Mount
4
5129498
Yes
Superbee manual Collimator
5
1004-M6C016-22
No
Hexagon Socket C-Sunk Head Screw, M6-1, X16mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
6
5503012
No
Cable Mount Bracket at Tube Head
7
1004-M3C008-22
No
Hexagon Socket C-Sunk Head Screw, M3-0.5, X8mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
8
1004-M8C016-22
No
Hexagon Socket C-Sunk Head Screw, M8-1.25, X16mm Long, Grade 10.9 Steel, Black Oxide, RoHS
Fastener
9
5505065
No
Carriage Cover Plate
10
5505044
No
Column Top Cover
11
1003-M4C008-22
Yes
Hexagon Socket Button Head Screw, M4-0.7, X8mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
12
2000-M4-02
Yes
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
13
5505116
No
Safety Spring Spacer
14
1000-M4C016-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
16
5410374
No
Column Pawl Warning Label
18
46-170684P1
Yes
"LOCTITE 271, 0.5CC VIAL 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE
MANUFACTURER"
19
5341550
No
DJINN 15R DC 2P
20
1000-M6C012-04
Yes
Hexagon Socket Head Cap Screw, M6-1, X12mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
21
2000-M6-03
Yes
Flat Washer, ISO7089, M6, Steel 200HV, Zinc Plated, RoHS Fastener
22
2203-M6-07
Yes
Curved Lock Washer, DIN 128A, M6, Spring Steel, Zinc Plated, RoHS Fastener
23
5394300
No
Note:
Page 134
Description
See Section 5.1 Base, Column, Arm, Drive Handle,
See Section 5.2 Tube and Tube Mount - 5507700 on page 175
See Section 5.3 SuperBee Manual Collimator - 5129498 on page 177
Nylon Cable Tie, 140mm Long, 3.70mm Wide, RoHS Compliant
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
Figure 5-2 5509900ADW_s1_r9
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 135
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 5-3 5509900ADW_s2_r8
Page 136
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 5-4 5509900ADW_s3_r8
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 137
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-2 2.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
Mark No.
Part No.
FRU
1
5508000
No
Base
2
5507000-3
No
Thorax HLA
3
5504000
Yes
Drive Handle HLA
4
5505000
or
5505000-2
Yes
Standard Column Assembly
or
Short Column Assembly
5
5506700
Yes
Horizontal Arm Assembly
6
2000-M6-03
Yes
Flat Washer, ISO7089, M6, Steel 200HV, Zinc Plated, RoHS Fastener
7
5366186
No
front clamp plate
8
1000-M6C016-07
No
Hexagon Socket Head Cap Screw, M6-1, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
9
1000-M12C025-07
No
Hexagon Socket Head Cap Screw, M12-1.75, X25mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
10
5505083
No
Arm Carriage Joint
11
1000-M6C020-04
Yes
Hexagon Socket Head Cap Screw, M6-1, X20mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
12
3000-M6C-04
No
Hexagon Nut, ISO4032, M6-1.0, Grade 8 Steel, Zinc Plated, RoHS Fastener
14
5394300
No
Nylon Cable Tie, 140mm Long, 3.70mm Wide, RoHS Compliant
15
5402092
No
left side barrier
16
5402094
No
right side barrier
17
1000-M4C010-04
Yes
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
18
2203-M4-07
Yes
Curved Lock Washer, DIN 128A, M4, Spring Steel, Zinc Plated, RoHS Fastener
19
2203-M6-07
Yes
Curved Lock Washer, DIN 128A, M6, Spring Steel, Zinc Plated, RoHS Fastener
35
5486072
No
Label - IEC Protective Earth ground, 19,05mm square, RoHS compliant, Dayton
36
5407230
No
rubber grommet
37
5413302
No
BULKHEAD FERRITE SUPPORT
38
5415344
No
wheel weight
103
5557003
Yes
Cable Assy- Spyder to Djinn
110
5557010
Yes
Cable Assy- LVLE2 to Djinn
113
5557013
Yes
Cable Assy- Locust to Caterpillar
114
5557014
Yes
Cable Assy- Locust to Caterpillar
116
5557016
Yes
Cable Assy- Locust to Cricket
121
5557021
Yes
Cable Assy- Cricket to Firefly
122
5557022
Yes
Cable Assy- Cricket to Djinn
126
5557026
Yes
Cable Assy- Caterpillar to Bumper
127
5557027
Yes
Cable Assy- Caterpillar to Rot Brake
130
5557030
Yes
Cable Assy- Firefly to Cricket
Page 138
Description
See 5.1.1 Base - 5508000 on page 140
See 5.1.2 Thorax HLA - 5507000-3 on page 151
See 5.1.3 Drive Handle HLA - 5504000 on page 163
See 5.1.4 Horizontal Arm Assembly - 5506700 on page 168
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-2 2.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
Mark No.
Part No.
FRU
Description
161
5557061
No
Ground Cable Caterpillar to Base
242
46-170686P1
Yes
LOCTITE 242, 0.5CC TUBE 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER
271
46-170684P1
Yes
LOCTITE 271, 0.5CC VIAL 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 139
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.1 Base - 5508000
Figure 5-5 5508000ADW_r5
Page 140
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-3 2.1 Base - 5508000
Mark No.
Part No.
FRU
Description
2
5370437
No
Drive assembly
3
5368482
Yes
column support assembly
4
5368545
Yes
Battery Pack Assembly
5
5370111
Yes
bumper
6
5344583
No
Base weldment
7
5449164
Yes
battery compartment cover
8
5392487
Yes
caster
9
5350010
Yes
Caterpillar Base Board
10
5341866
No
Column mount trap spacer
11
5350008
Yes
Cricket Battery Board
12
5370271
Yes
fuse shield
13
5343843
No
Spring Rod Pivot
14
5370186
No
EXTENSION SPRING, .5 INCH OD, 2.5 INCH FREE LENGTH, 0.075 INCH WIRE DIAMETER
16
5346286
No
isolation mount backup washer
17
5367885
No
Caterpillar support
18
5370272
No
hex standoff, m-f, 20 mm long, m4
19
1006-M12C050-04
No
Hexagon Head Screw, ISO 4017, M12-1.75, X50mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
20
3000-M12C-04
No
Hexagon Nut, ISO4032, M12-1.75, Grade 8 Steel, Zinc Plated, RoHS Fastener
21
3000-M10C-04
No
Hexagon Nut, ISO4032, M10-1.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
22
1040-M10C025-27
No
Hexagon Set Screw with Cup Point, M10-1.5, X25mm Long, Grade 45H Steel, Black Oxide, RoHS Fastener
23
3000-M4C-04
Yes
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
24
1000-M4C010-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
25
1000-M4C030-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X30mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
26
1000-M6C010-07
No
Hexagon Socket Head Cap Screw, M6-1, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
27
1000-M8C020-07
No
Hexagon Socket Head Cap Screw, M8-1.25, X20mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
28
3000-M16C-04
No
Hexagon Nut, ISO4032, M16-2.0, Grade 8 Steel, Zinc Plated, RoHS Fastener
29
46-170260P2
Yes
LUBRICATING GREASE USED ON BEARINGS. LITHIUM BASED MINERAL OIL GREASE. BEIGE COLOR, 1 LB. CAN. EXTREME
PRESSURE AND WATERPROOF FEATURES.
30
46-170686P3
Yes
LOCTITE 242, 50CC 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER.
31
5401728
No
cricket insulating shield
33
5394277
No
lower front cover
34
5394278
No
front bumper slot closure
35
3000-M6C-04
No
Hexagon Nut, ISO4032, M6-1.0, Grade 8 Steel, Zinc Plated, RoHS Fastener
See 5.1.1.1 Drive assembly - 5370437 on page 143
See 5.1.1.2 Column support assembly - 5368482 on page 145
See 5.1.1.3 Bumper - 5370111 on page 148
See 5.1.1.4 Cricket Battery Board - 5350008 on page 150
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 141
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-3 2.1 Base - 5508000
Mark No.
Part No.
FRU
36
5410206
No
motor shield
37
2000-M6-03
Yes
Flat Washer, ISO7089, M6, Steel 200HV, Zinc Plated, RoHS Fastener
38
1000-M4C016-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
Page 142
Description
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.1.1 Drive assembly - 5370437
Figure 5-6 5370437ADW_r4
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 143
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-4 2.1 Drive assembly - 5370437
Mark No.
Part No.
FRU
2
5370432
Yes
motor reducer assembly
3
5343348
Yes
drive wheel
5
5342648
No
drive support machining
6
5351887
Yes
motor brake, 30 in-lb
7
1000-M4C010-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
8
1000-M5C016-07
No
Hexagon Socket Head Cap Screw, M5-0.8, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
10
5344390
No
center bonded isolation mount
11
5344349
No
spring, 5.5 free length 2.95 solid 343 lb per inch. Lee Spring LHL 2000AB 07
12
5399178
No
M20 FLANGE NUT, Zinc Plated, With Nylon Insert
13
5343844
No
Rubber Washer
14
5343842
No
Suspension Upper Link
16
5413926
Yes
GROUND STRAP
17
E61-HC-30
No
HEXAGON MACHINE SCREW NUT, ASME B18.6.3, 1_4th - 20, STAINLESS STEEL 18-8, RoHS FASTENER
19
46-170686P3
Yes
LOCTITE 242, 50CC 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER.
20
5389103
No
Guide bushing
21
46-170260P1
Yes
LUBRICATING GREASE USED ON BEARINGS.LITHIUM BASED MINERAL OIL GREASE. BEIGE COLOR, 6 LB. CAN. EXTREME
PRESSURE AND WATERPROOF FEATURES. (DWG REV 4/92, JFK - OK).
Page 144
Description
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.1.2 Column support assembly - 5368482
Figure 5-7 5368482ADW_r5
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 145
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-5 2.1 Column support assembly - 5368482
Mark No.
Part No.
FRU
2
5414808
No
idler sprocket
3
5413866
No
BEARING SUPPORT STUD
4
5413867
No
STEPPED SPACER
5
5125180
No
snap ring, TRU-ARC N5000-86
6
5413925
No
BEARING - 6900ZZ
7
5341976
No
Cam follower, .75 inch OD, .25 inch ID, .5625 overall length. with seals
8
5341978
No
detent roller shaft
9
4000-M8L020-02
No
Parallel Pin, ISO 8734, 8mm Diameter X 20mm Long, Steel, RoHS Fastener
10
5370673
No
roller chain number 25, 94 total links including one master link
11
5341871
No
column brake shaft
12
5341981
No
column rotation lock drive sprocket
13
5341950
No
column inner sleeve
15
5341875
No
column rotation sprocket #25 72 teeth
16
5340762
No
COLUMN SUPPORT MACHINED CASTING
18
5413919
No
ball bearing - 6203ZZ
19
5346815
No
double row angular contact bearing, 72 od 35 id 27 wide
20
5341869
No
eccentric stud
21
5346816
No
deep groove ball bearing, ISO number 6009, 75 OD, 45 ID, 16 wide
22
3000-M10C-04
No
Hexagon Nut, ISO4032, M10-1.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
23
3000-M12C-04
No
Hexagon Nut, ISO4032, M12-1.75, Grade 8 Steel, Zinc Plated, RoHS Fastener
24
3000-M4C-04
Yes
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
25
1000-M4C012-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X12mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
26
1000-M4C035-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X35mm Long, Grade12.9 Steel, Black Oxide RoHS Fastener
27
1000-M4C008-07
Yes
Hexagon Socket Head Cap Screw, M4-0.7, X8mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
28
1000-M6C016-07
No
Hexagon Socket Head Cap Screw, M6-1, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
29
3000-M8C-04
No
Hexagon Nut, ISO4032, M8-1.25, Grade 8 Steel, Zinc Plated, RoHS Fastener
30
1000-M8C035-07
No
Hexagon Socket Head Cap Screw, M8-1.25, X35mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
31
2000-M8-02
No
Flat Washer, ISO7089, M8, Steel 140HV, Zinc Plated, RoHS Fastener
32
1000-M8C020-07
No
Hexagon Socket Head Cap Screw, M8-1.25, X20mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
33
5340767
No
ROTATION STOP UPPER
34
5340770
No
ROTATION STOP LOWER
35
5340769
No
ROTATION STOP MIDDLE
36
5340774
No
ROTATION STOP SPACER
Page 146
Description
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-5 2.1 Column support assembly - 5368482
Mark No.
Part No.
FRU
Description
37
5336828
Yes
spring applied brake - 90 inch pound
38
2000-M6-03
Yes
Flat Washer, ISO7089, M6, Steel 200HV, Zinc Plated, RoHS Fastener
39
5370186
No
EXTENSION SPRING, .5 INCH OD, 2.5 INCH FREE LENGTH, 0.075 INCH WIRE DIAMETER
40
5343839
No
tensioner block
41
5370173
No
detent lever upper, offset
42
5370172
No
lower detent lever, offset
43
46-170684P3
Yes
LOCTITE 271, 50ML BOTTLE. 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER. REV, TK, Jan 92
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 147
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.1.3 Bumper - 5370111
Figure 5-8 5370111ADW_r4
Page 148
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-6 2.1 Bumper - 5370111
Mark No.
Part No.
FRU
Description
2
5352060
No
Bumper Pivot
4
5357139
No
left pivoting base
5
5357256
No
left switch arm
6
3000-M6C-04
No
Hexagon Nut, ISO4032, M6-1.0, Grade 8 Steel, Zinc Plated, RoHS Fastener
8
5352908
No
right pivot base
9
5357579
No
right switch arm
10
5413864
No
SPRING
11
5392470
Yes
Switch, SPDT, 0,1A, gold contacts Micro Switch part V7-1S10D8
12
46-170684P3
Yes
LOCTITE 271, 50ML BOTTLE. 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER. REV, TK, Jan 92
13
1000-M3C008-07
No
Hexagon Socket Head Cap Screw, M3-0.5, X8mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
14
2001-M3-02
No
Large Flat Washer, ISO7093, M3, Steel 140HV, Zinc Plated, RoHS Fastener
15
5392096
No
Left Pivot Bracket
16
5392095
No
Right Pivot Bracket
17
5392204
Yes
bumper
18
3000-M3C-04
No
Hexagon Nut, ISO4032, M3-0.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
19
2000-M10-02
No
Flat Washer, ISO7089, M10, Steel 140HV, Zinc Plated, RoHS Fastener
20
1008-M4P8C022-29
No
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 22mm Long, Steel, Zinc Plated, RoHS Fastener
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 149
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.1.4 Cricket Battery Board - 5350008
Figure 5-9 5350008ADW_r3
Table 5-7 2.1 Cricket Battery Board - 5350008
Mark No.
Part No.
FRU
-
5350008
Yes
Cricket battery board
-
5306477-3
Yes
PROTECTION FUSE, 15A, TIME DELAY, 300VDC, 600VAC, CARTRIDGE
Page 150
Description
Also see Table 1-3 5409712, Fuse - Filter Kit on page 29 for kit contents
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.2 Thorax HLA - 5507000-3
Figure 5-10 5507000-2ADW_s1_r3
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 151
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 5-11 5507000-2ADW_s2_r2
Page 152
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 5-12 5507000-2ADW_s3_r2
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 153
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 5-13 5507000-2ADW_s4_r2
Page 154
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-8 Thorax HLA - 5507000-3
Mark No.
Part No.
FRU
Description
1
5350000-2
Yes
Firefly Charger Board
2
5392386
Yes
tube park latch
3
5350006-2
Yes
Locust Board with Drive Improvement
4
5350002-3
Yes
Spyder System Controller with Sys Comm FW Brivo
5
5311985
Yes
Mantis AC-DC Converter
6
5192958-2
Yes
LVLE2 Power Supply
7
5395516
No
Insulating Film, Thorax-Firefly
8
5351707
Yes
Single Phase AC Line EMI Filter
9
5395518
No
Insulating Film Thorax-CLS
None
5444444
Yes
Superbee cord reel without Plug
11
5444444-2
Yes
Cord reel with plug
12
5394888
No
fuse holder assembly, thorax Superbee
13
5447564
No
Thorax Weldment with Nyloc PEMS
14
1000-M4C008-04
Yes
Hexagon Socket Head Cap Screw, M4-0.7, X8mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
15
3000-M5C-04
No
Hexagon Nut, ISO4032, M5-0.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
16
2106-M5-14
No
Spring Lock Washer with Flat Ends JIS B1251, M5, Spring Stainless Steel, Rohs Fastener
17
3000-M6C-04
No
Hexagon Nut, ISO4032, M6-1.0, Grade 8 Steel, Zinc Plated, RoHS Fastener
18
2203-M6-07
Yes
Curved Lock Washer, DIN 128A, M6, Spring Steel, Zinc Plated, RoHS Fastener
19
2000-M6-02
No
Flat Washer, ISO7089, M6, Steel 140HV, Zinc Plated, RoHS Fastener
21
2000-M4-02
Yes
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
23
3000-M4C-04
Yes
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
24
2000-M5-02
No
Flat Washer, ISO7089, M5, Steel 140HV, Zinc Plated, RoHS Fastener
26
1000-M6C020-04
Yes
Hexagon Socket Head Cap Screw, M6-1, X20mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
27
5350038
Yes
Board Data Module
28
5450200
Yes
Collimator Lamp Supply
29
5395517
No
Insulating Film, Thorax-Locust
31
5394640
No
Thorax Bulkhead for Column Cables
33
5396295
No
Speaker Bracket
34
1000-M3C008-04
No
Hexagon Socket Head Cap Screw, M3-0.5, X8mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
36
5394300
No
Nylon Cable Tie, 140mm Long, 3.70mm Wide, RoHS Compliant
37
46-220178P10
Yes
GROMMET, 12.75~ LONG GROMMET STRIP, OFF WHITE, FOR 0.090~ THICK APPLICATIONS
38
5503599
No
RJ11 BRACKET
40
5399514
Yes
L-COM RJ11 RECEPTACLE
See 5.1.2.1 Firefly Charger Board - 5350000-2 on page 158
See 5.1.2.2 Tube park latch - 5392386 on page 159
See 5.1.2.3 Locust Drive Board - 5350006-2 on page 161
Also see Table 1-3 5409712, Fuse - Filter Kit on page 29
See 5.1.2.4 Fuse holder assembly, thorax Superbee - 5394888 on page 162
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 155
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-8 Thorax HLA - 5507000-3
Mark No.
Part No.
FRU
41
3002-M4C-04
No
Hexagon Prevailing Torque Nut, ISO7040, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
42
1000-M3C010-04
No
Hexagon Socket Head Cap Screw, ISO 4762, M3-0.5, X10mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
43
2000-M3-03
Yes
WASHER PLAIN - LARGE 3.2 MM 7 MM , HV200, Steel, Zinc plate RoHS Washer
44
2203-M3-07
Yes
Curved Lock Washer, DIN 128A, M3, Spring Steel, Zinc Plated, RoHS Fastener
45
5406825
No
Insulating Film - Spyder
46
2203-M4-07
Yes
Curved Lock Washer, DIN 128A, M4, Spring Steel, Zinc Plated, RoHS Fastener
47
5406823
No
Fuse Holder Insulating Film
48
5486072
No
Label - IEC Protective Earth ground, 19,05mm square, RoHS compliant, Dayton
49
1008-M4P8C016-29
No
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 16mm Long, Steel, Zinc Plated, RoHS Fastener
53
3000-M3C-04
No
Hexagon Nut, ISO4032, M3-0.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
54
5418302
No
HEX STANDOFF MALE FEMALE M4 X 60MM
55
5417354
No
emc shield, firefly superbee
102
5557002
Yes
Cable Assy- Spyder to Locust
104
5557004
Yes
Cable Assy- Spyder to LVLE2
105
5557005
Yes
Cable Assy- Spyder to Firefly
106
5557006
Yes
Cable Assy - Spyder to Wired Handswitch
107
5557007
Yes
Cable Assy- LVLE2 to Firefly
108
5557008
Yes
Cable Assy- Locust to LVLE2
109
5557009
Yes
Cable Assy- LVLE2 to Firefly
119
5557019
Yes
Cable Assy- Mantis to Firefly
120
5557020
Yes
Cable Assy- Mantis to Firefly
123
5557023
Yes
Cable Assy- Cricket to Breaker
124
5557024
No
Cable Assy- Firefly to AC Present Lamp
125
5557025
Yes
Cable Assy- Locust to Park Latch
135
5557035
Yes
Cable Assy - Firefly to Power Switch
136
5557036
Yes
Cable Assy - Firefly to CLS J1
137
5557037
Yes
Cable Assy - Mantis to Filter
138
5557038
Yes
Cable Assy - Fuse to Filter
140
5557040
Yes
Cable Assy- Firefly to CLS
143
5557043
Yes
Cable Assy - Locust to Thorax Column Bulkhead
145
5557045
Yes
Cable Assy - Spyder to Speaker
146
5557046-2
Yes
Cable Assy - Sypder to Thorax Column Bulkhead - DAP
147
5557047
Yes
Cable Assy - CLS to Thorax Column Bulkhead - Collimator
149
5557049-2
Yes
Shielded BDM to Spyder Cable Assembly
Page 156
Description
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-8 Thorax HLA - 5507000-3
Mark No.
Part No.
FRU
Description
158
5557058
Yes
Cable Assy- Spyder Dose Reporting to USB Bulkhead
159
5557059
No
Cable Assy - Firefly to AC Present Lamp terminals
None
5557062
Yes
Collector for AC-present Cables
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 157
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.2.1 Firefly Charger Board - 5350000-2
Figure 5-14 5350000ADW_r6
Table 5-9 Firefly Charger Board - 5350000-2
Mark No.
Part No.
FRU
-
5350000-2
Yes
Firefly charger board
-
5306477-3
Yes
PROTECTION FUSE, 15A, TIME DELAY, 300VDC, 600VAC, CARTRIDGEr
Page 158
Description
Also see Table 1-3 5409712, Fuse - Filter Kit on page 29
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.2.2 Tube park latch - 5392386
Figure 5-15 5392386ADW_r3
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 159
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
.
Table 5-10 Tube park latch - 5392386
Mark No.
Part No.
FRU
1
5390750
Yes
SOLENOID
2
5380946
No
latch base machining
3
5380949
No
latch pawl machining
4
5380947
No
switch actuator
5
5392470
Yes
Switch, SPDT, 0,1A, gold contacts Micro Switch part V7-1S10D8
6
5392389
No
latch release spring
7
5392388
No
latch park switch spring
8
5392391
No
round bumper
9
5392390
No
rectangular bumper
10
46-220312P1
Yes
LOCTITE SUPERBONDER 416, 1 OZ (28.4G) BOTTLE 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER. (REV, TK, 1/92).
11
1003-M3C006-22
No
Hexagon Socket Button Head Screw, M3-0.5, X6mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
12
46-170684P3
Yes
LOCTITE 271, 50ML BOTTLE. 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER. REV, TK, Jan 92
13
5392392
No
roll pin
14
1000-M3C016-02
No
Hexagon Socket Head Cap Screw, M3-0.5, X16mm Long, Grade 8.8 Steel, Black Oxide RoHS Fastener
Page 160
Description
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.2.3 Locust Drive Board - 5350006-2
Figure 5-16 5350006ADW_r7
Table 5-11 Locust Drive Board - 5350006-2
Mark No.
Part No.
FRU
Description
-
5350006-2
Yes
Locust drive board with Drive Improvement
-
5306477
Yes
PROTECTION FUSE, 8A, TIME DELAY, 300VDC, 600VAC, CARTRIDGE. Also see Table 1-3 5409712, Fuse - Filter Kit on page 29 for kit contents
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 161
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.2.4 Fuse holder assembly, thorax Superbee - 5394888
Figure 5-17 5394888ADW_r4
Table 5-12 Fuse holder assembly, thorax Superbee - 5394888
Mark No.
Part No.
FRU
1
5394887
No
thorax fuse box, superbee
2
5392168
Yes
3AG fuse holder, 250V rated, 20A rated, 2000V dielectric strength min, UL94V0 rated
3
5392167
Yes
Ceramic Fuse, 250VAC, 15A, Fast Action, 6.3mm x 32mm
Page 162
Description
Also see Table 1-3 5409712, Fuse - Filter Kit on page 29 for kit contents
Also see Table 1-3 5409712, Fuse - Filter Kit on page 29 for kit contents
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.1.3 Drive Handle HLA - 5504000
%3
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30%#)&)#!4)/. 434 4(% -!.5&!#452%2 3(!,, 02/6)$% !. ).$)6)$5!,
-!2+).' /& #/-0,)!.#% 0%2 $/#5-%.4 '30 7)4( %6%29 5.)4 3()00%$
4/ '%(# 34!4).' 4(% 5.)4 (!3 35##%33&5,,9 0!33%$ 4%34).' )& ,!"%,%$ 0,!#%
). 3!-% !002/8)-!4% ,/#!4)/. !3 0!24 ,!"%,
4()3 $2!7).' 7!3 #2%!4%$
"9 $%,4!4%#( #/.42/,3
&/2 '% (%!,4(#!2%
!$7
Figure 5-18 5504000ADW_s1_r12
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 163
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
4()3 $2!7).' 7!3 #2%!4%$
"9 $%,4!4%#( #/.42/,3
&/2 '% (%!,4(#!2%
!$7
Figure 5-19 5504000ADW_s2_r12
Page 164
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
4()3 $2!7).' 7!3 #2%!4%$
"9 $%,4!4%#( #/.42/,3
&/2 '% (%!,4(#!2%
!$7
Figure 5-20 5504000ADW_s3_r12
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 165
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-13 Drive Handle HLA - 5504000
Mark No.
Part No.
FRU
1
5418209
No
Epoxy
2
5418084
No
Grease
3
5426344
No
ura-bond 24n adhesive
4
5452873
No
Delta PT Thread Forming Torx Flat-head Fastener - K30-10-WN1423
5
1000-M3C008-02
No
Hexagon Socket Head Cap Screw, M3-0.5, X8mm Long, Grade 8.8 Steel, Black Oxide RoHS Fastener
6
2000-M5-02
No
Flat Washer, ISO7089, M5, Steel 140HV, Zinc Plated, RoHS Fastener
7
3002-M5C-31
No
Hexagon Prevailing Torque Nut, ISO7040, M5-0.8, A2-70, Stainless Steel, Passivate, RoHS Fastener
8
1000-M5C012-02
No
Hexagon Socket Head Cap Screw, M5-0.8, X12mm Long, Grade 8.8 Steel, Black Oxide RoHS Fastener
9
1000-M5C016-02
No
Hexagon Socket Head Cap Screw, M5-0.8, X16mm Long, Grade 8.8 Steel, Black Oxide RoHS Fastener
10
1000-M5C025-02
No
Hexagon Socket Head Cap Screw, M5-0.8, X25mm Long, Grade 8.8 Steel, Black Oxide RoHS Fastener
11
1000-M2P5C006-07
No
Hexagon Socket Head Cap Screw, M2.5-0.45, X6mm Long, Grade 12.9 Steel, Black Oxide, RoHS Fastener
12
1000-M4C010-02
No
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade 8.8 Steel, Black Oxide RoHS Fastener
13
2001-M3-02
No
Large Flat Washer, ISO7093, M3, Steel 140HV, Zinc Plated, RoHS Fastener
14
2204-M3-16
No
External Toothed Lock Washer, DIN 6797A, M3, A2 Stainless Steel, RoHS Fastener
15
1000-M2P5C008-07
No
Hexagon Socket Head Cap Screw, M2.5-0.45, X8mm Long, Grade 12.9 Steel, Black Oxide, RoHS Fastener
16
5476247
No
Self-tapping Fastener K50 x 25mm, PT
18
4000-M3L016-02
No
Parallel Pin, ISO 8734, 3mm Diameter X 16mm Long, Steel, RoHS Fastener
19
5400380
No
Magnet
20
5423145
No
gasket
21
5392202
No
Magnet Support Bracket - Right
22
5392203
No
Magnet Support Bracket - Left
23
5392197
No
Handle Boot_Bellow
24
5410465
No
Spring Blade Support Right
25
5410468
No
Spring Blade Support Left
26
5399713
No
Steel Plate - in handle bar for cable
27
5392198
No
Hinge Support Bracket - Right
28
5392199
No
Hinge Support Bracket - Left
29
5395451
No
Engage Bar Compression Spring
30
5392190
Yes
Wired Handswitch Holder
31
5410463
No
Handle Bar Ring Bellow
32
5391519
No
Outer Cover Assembly - Right
33
5391517
No
Inner Cover Assembly - Right
34
5391520
No
Outer Cover Assembly - Left
35
5391518
No
Inner Cover Assembly - Left
36
5416161
No
Overmoulded bar assembly
Page 166
Description
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-13 Drive Handle HLA - 5504000
Mark No.
Part No.
FRU
Description
37
5391521-2
No
Rear Tray without Inserts
38
5392193
No
Spring Steel Clamp Plate
39
5392192
No
Spring Steel
40
5400717
No
SINGLE POLE, 6 AMP, MOMENTARY PUSHBUTTON SWITCH, MOMENTARY ON PUSHBUTTON WITH 0.250 TAB TERMINATION
41
5416167
No
Engage Bar EQ Assembly
42
5457739
No
Tie Holder Richco FTH-5-01
43
5461547
No
Ty-wrap Panduit part number PLT.7M-M
44
5418083
No
Housing connector 2 pts
45
5418081
No
Housing connector 3 pts
46
5451899
No
Drive handle harness
47
5557015
Yes
Cable Assy - Locust to Drive Handle
48
5557039
Yes
Cable Assy - Locust to Hard Brake Release
49
5416172
No
PCB Switch
50
5395457
No
Drive Handle Board - Left PWA
51
5395455
No
Drive Handle Board - Right PWA
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 167
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
5.1.4 Horizontal Arm Assembly - 5506700
Approved Document - 5506700ADW_r5.pdf Page 2 of 3
Figure 5-21 5506700ADW
Page 168
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-14 Horizontal Arm Assembly - 5506700
Mark No.
Part No.
FRU
Description
1
5506670
No
OUTER TUBE ASSEMBLY MACHINING
2
5506602
No
Center Extrusion Assembly
3
5506628
No
Inner Arm Section
4
5506604
No
Pulley Mtg Bar
6
5506606
No
Rear Stop Block
7
5506607
No
#25 Roller Chain - 53 Links
8
5506609
No
20mm Linear Bearing
9
5506617
No
Bar Cable Support
10
5506672
No
Cable Block Mount to Inner Section
11
5506619
No
Horizontal Arm Aircraft Cable
12
5506632
No
Horizontal Arm Brake
13
5506633
No
Cable Connector Bracket
16
5506654
No
Sprocket Bearing
17
5506655
No
Pulley Bearing
18
5506656
No
Set Screw
19
5506645
No
Cable Anchor
20
5506646
No
Chain Shaft
21
5506647
No
Pulley Shaft
22
5506648
No
Pulley
23
5506649
No
16 Tooth Sprocket
24
5506662
Yes
Brake Cable Assembly with Track
25
5506651
Yes
Park Latch Pin Assembly
26
5506657
No
Arm Stop Bumper
27
5506658
No
Pulley Spacer
28
5506661
No
Park Latch Bracket
29
5505091-2
No
Heyco Bushing part number 1140
30
5506671
No
Arm Park Latch Spacer
34
1000-M5C012-04
No
Hexagon Socket Head Cap Screw, M5-0.8, X12mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
35
2000-M5-02
No
Flat Washer, ISO7089, M5, Steel 140HV, Zinc Plated, RoHS Fastener
36
1000-M4C006-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X6mm Long, Grade12.9 Steel, Black Oxide RoHS Fastener
37
1000-M4C010-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
38
1000-M4C012-07
No
Hexagon Socket Head Cap Screw, M4-0.7, X12mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
40
1000-M6C035-07
No
Hexagon Socket Head Cap Screw, M6-1, X35mm Long, Grade12.9 Steel, Black Oxide RoHS Fastener
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 169
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-14 Horizontal Arm Assembly - 5506700
Mark No.
Part No.
FRU
42
1004-M4C008-22
No
Hexagon Socket C-Sunk Head Screw, M4-0.7, X8mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
43
1004-M4C012-22
No
Hexagon Socket C-Sunk Head Screw, M4-0.7, X12mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
44
1004-M5C012-22
No
Hexagon Socket C-Sunk Head Screw, M5-0.8, X12mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
45
1004-M6C012-22
No
Hexagon Socket C-Sunk Head Screw, M6-1, X12mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
46
2000-M4-02
Yes
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
47
2000-M6-02
No
Flat Washer, ISO7089, M6, Steel 140HV, Zinc Plated, RoHS Fastener
49
2204-M4-06
No
External Toothed Lock Washer, DIN 6797A, M4, Spring Steel, Zinc Plated, RoHS Fastener
50
3003-M4C-04
No
Hexagon Nut with Lock Washer, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
51
5506673
No
M6 x 5 Set Screw Cup Point
52
1004-M8C016-22
No
Hexagon Socket C-Sunk Head Screw, M8-1.25, X16mm Long, Grade 10.9 Steel, Black Oxide, RoHS Fastener
54
46-170684P1
Yes
LOCTITE 271, 0.5CC VIAL 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER
55
46-220312P1
Yes
LOCTITE SUPERBONDER 416, 1 OZ (28.4G) BOTTLE 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER. (REV, TK, 1/92).
Page 170
Description
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
5.1.5 DJINN 15R DC 2P - 5341550
Approved Document - 5341550ADW_r5.pdf Page 2 of 4
Figure 5-22 5341550ADW_s1_r5
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 171
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5341550ADW_r5.pdf Page 3 of 4
Figure 5-23 5341550ADW_s2_r5
Page 172
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
DIRECTION 5336115-1EN, REVISION 6
Approved Document - 5341550ADW_r5.pdf Page 4 of 4
Figure 5-24 5341550ADW_s3_r5
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 173
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-15 DJINN 15R DC 2P - 5341550
Mark No.
Part No.
FRU
5397083
No
BEETLE DJINN Set of cables
5399675
No
Packing Box for 15kW Configuration with Brackets
1
5140761-2
No
Djinn Bipolar HVTank
2
5341549
No
BEETLE DJINN POWER MODULE
3
5338768
No
BEETLE DJINN AUX MAIN BOX
None
5375925
Yes
FRU AUX MODULE 30kW (30kW systems only)
4
5389106
No
Bracket, HV Tank And Power Mod
5
5389026
No
Bracket- Main Aux Box
8
5342196
No
Beetle Djinn generator 15kw labeling
11
2193201-50
No
SCREW DIN7991 M4X8by6 A4-70
12
46-170686P3
Yes
LOCTITE 242, 50CC 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER.
17
5264409
No
Grounding label
18
5454841
No
Djinn Beetle SW Package D429B
19
46-303268P1
Yes
PRODUCT LOCATOR CARD FORM FOR RATING PLATES, PRINTED BY DUPLITECH
None
5341553
Yes
FRU BEETLE DJINN Set of cables
None
5351748
Yes
FRU Djinn Bipolar HV Tank
None
5375923
Yes
FRU Power Module
None
5375924
Yes
FRU Aux module 15kW
Page 174
Description
See 5341553 (FRU BEETLE DJINN Set of cables) in this table
See 5351748 (FRU Djinn Bipolar HV Tank) in this table
See 5375923 (FRU Power Module) in this table
See 5375924 (FRU Aux module 15kW) in this table
Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 5.2 Tube and Tube Mount - 5507700
Approved Document - 5507700ADW_r3.pdf Page 2 of 2
Figure 5-25 5507700ADW_r3
Table 5-16 Tube and Tube Mount - 5507700
Mark No.
Part No.
FRU
Description
1
5507701
No
Cathode Side Tube Mount with Detent. See 5.2.1 Anode/Cathode Side Tube Mount Identification and FRUs for FRU information.
2
5507702
No
Anode Side Tube Mount with Friction. See 5.2.1 Anode/Cathode Side Tube Mount Identification and FRUs for FRU information.
3
5507703
Yes
Tube Yoke Assembly
4
5508800-2
Yes
X-Ray Tube
8
1000-M6C020-07
No
Hexagon Socket Head Cap Screw, M6-1, X20mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
9
1000-M5C010-04
No
Hexagon Socket Head Cap Screw, M5-0.8, X10mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
10
2000-M5-02
No
Flat Washer, ISO7089, M5, Steel 140HV, Zinc Plated, RoHS Fastener
11
46-170684P1
Yes
LOCTITE 271, 0.5CC VIAL 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER
12
5503001
Yes
Aux Box to Rotor Cable Assembly
13
2000-M6-03
Yes
Flat Washer, ISO7089, M6, Steel 200HV, Zinc Plated, RoHS Fastener
14
46-170686P1
Yes
"LOCTITE 242, 0.5CC TUBE 12 MONTH SHELF LIFE FROM DATE OF SHIPMENT FROM THE MANUFACTURER."
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 175
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.2.1 Anode/Cathode Side Tube Mount Identification and FRUs
A newer version of this part has been introduced. It is not backward-compatible with the original version.
If replacing the original version, you must replace BOTH sides with the newer version.
The newer version is physically longer.
Mixing old and new versions results in tube attachment mis-alignment.
The newer version part requires longer bolts at the tube yoke. These bolts will come with the replacement FRU.
See Figure 5-26 for identification of mounts and Table 5-17 for FRU part numbers.
1
Item
1
Description
A thickness notch in this location identifies a newer version tube mount
Figure 5-26 Tube mount identification
Table 5-17 Anode/Cathode Side Tube Mount
Page 176
Mark No.
Part No.
FRU
Description
-
5450136
Yes
Newer version Cathode Side Tube Mount with Detent (includes longer bolts) - replaces 5507701
-
5450136-2
Yes
Newer version Anode Side Tube Mount with Friction (includes longer bolts) - replaces 5507702
Section 5.2 Tube and Tube Mount - 5507700
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 5.3 SuperBee Manual Collimator - 5129498
Figure 5-27 5129498ADW_r3
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 177
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-18 SuperBee Manual Collimator - 5129498
Mark No.
Part No.
FRU
-
5129498
Yes
SuperBee Manual Collimator
1
5396306
No
RoHS-SuperBee Collimator See 5.3.1 RoHS-SuperBee Collimator - 5396306 on page 179
2
5396307
No
RoHS-ETL Label
3
5396614
No
RoHS-Rating plate
4
46-303268P1
Yes
PRODUCT LOCATOR CARD FORM FOR RATING PLATES, PRINTED BY DUPLITECH
5
5129246
No
Grease
Page 178
Description
Section 5.3 SuperBee Manual Collimator - 5129498
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.3.1 RoHS-SuperBee Collimator - 5396306
Figure 5-28 5396306ADW_r7_s1
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 179
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Figure 5-29 5396306ADW_r7_s2
Page 180
Section 5.3 SuperBee Manual Collimator - 5129498
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-19 RoHS-SuperBee Collimator - 5396306
Mark No.
Part No.
FRU
Description
1
5396640
No
RoHS-Accessory Rail-2
2
5396588
No
RoHS-Holding Plate
3
5396589
No
RoHS-Cross Mark Plate
4
5396639
No
RoHS-Accessory Rail-1
5
5396638
Yes
Plate Spring
6
5396587
No
RoHS-Handle
7
1003-M3C008-31
No
Hexagon Socket Button Head Screw, M3-0.5, X8mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
8
2204-M3-06
No
External Toothed Lock Washer, DIN 6797A, M3, Spring Steel, Zinc Plated, RoHS Fastener
9
5396485
No
RoHS-Bearing DR-30
10
5396486
No
RoHS-Bearing DR-22
11
3000-M5C-04
No
Hexagon Nut, ISO4032, M5-0.8, Grade 8 Steel, Zinc Plated, RoHS Fastener
12
5412675
No
Dust proof washer
13
C2006-M6-02
No
Flat Washer, 6X12-1, Steel, Zinc Plated, RoHS Fastener
14
5398367
No
RoHS-Waved washer WW-6
15
2002-M8-02
No
Flat Washer, Small OD Series, ISO7092, M8, Steel 140HV, Zinc Plated, RoHS Fastener
16
5396630
No
RoHS-Knob Support
17
5396599
No
RoHS-Screw Shaft
18
5396424
No
RoHS-Bushing
19
5396624
No
RoHS-Knob washer See 5.3.1.1 Collimator knob set - 5397014 on page 185
20
1040-M4C004-27
No
Hexagon Set Screw with Cup Point, M4-0.7, X4mm Long, Grade 45H Steel, Black Oxide, RoHS Fastener
21
5396617
No
RoHS-Knob See 5.3.1.1 Collimator knob set - 5397014 on page 185
22
5396643
No
RoHS-Mechanical Interface See 5.3.1.2 RoHS-Mechanical Interface - 5396643 on page 186
23
5396616
No
RoHS-Blade Stopper
24
5396451
No
RoHS-Frame 2
25
C2000-M3-80
No
Flat Washer, ISO7089, Steel 140HV,Black Oxide RoHS Fastener
26
C2106-M3-80
No
Spring Lock Washer, M3, Black Oxide, Rohs Fastener
27
C1007-M3C006-80
No
Pan Head Screw,GB-T818, M3X6, Black Oxide, RoHS Fastener
28
1010-M3C006-31
No
Phillips Flat Head Screw, ISO 7046, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
29
5396612
No
RoHS-Angle Plate 1
30
5396591
No
RoHS-Angle plate 3
31
5396602
No
RoHS-Shielding Plate Support
32
5396593
No
RoHS-Knob Shaft
33
5396629
No
RoHS-Driving Wheel D
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 181
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-19 RoHS-SuperBee Collimator - 5396306
Mark No.
Part No.
FRU
34
5396632
No
RoHS-Connection Plate L
35
5396594
No
RoHS-Stop Plate
36
5396414
No
RoHS-Button Cable
37
5396442
No
RoHS-Driving Wheel-A Riveting
38
5396423
No
RoHS-Front Panel
39
5396452
No
RoHS-Front Cover
40
1010-M4C016-14
No
Phillips Flat Head Screw, ISO 7046, M4-0.7, X16mm Long, Grade 4.8 Steel, Zinc Plated, RoHS Fastener
41
1010-M4C012-14
No
Phillips Flat Head Screw, ISO 7046, M4-0.7, X12mm Long, Grade 4.8 Steel, Zinc Plated, RoHS Fastener
42
1010-M4C010-14
No
Phillips Flat Head Screw, ISO 7046, M4-0.7, X10mm Long, Grade 4.8 Steel, Zinc Plated, RoHS Fastener
43
5396487
No
RoHS-Back Cover
44
5396583
No
RoHS-Angle Plate
45
5396592
No
RoHS-Frame 1
46
5396585
No
RoHS-Lead Cone
47
5396595
No
RoHS-Base Plate
48
5396374
No
RoHS-Tape Cover
49
5397015
Yes
SID tape assembly
50
5396450
No
RoHS-U-Shape Cover
51
1010-M3C012-14
No
Phillips Flat Head Screw, ISO 7046, M3-0.5, X12mm Long, Grade 4.8 Steel, Zinc Plated, RoHS Fastener
52
2000-M4-02
Yes
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
53
2002-M3-02
No
Flat Washer, Small OD Series, ISO7092, M3, Steel 140HV, Zinc Plated, RoHS Fastener
54
2106-M3-14
No
Spring Lock Washer with Flat Ends JIS B1251, M3, Spring Stainless Steel, Rohs Fastener
55
3000-M3C-04
No
Hexagon Nut, ISO4032, M3-0.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
56
C2204-M4-80
No
Tootthed lock washer GB-T862.2 4, Black Oxide, RoHS fastener
57
C2106-M4-02
No
Spring Lock Washer, M4, Zinc plated, Rohs Fastener
58
C1007-M3C008-80
No
Pan head screw, M3x8, Black Oxide RoHS fastener
59
5396615
No
RoHS-Mask Support
60
C1007-M3C025-80
No
Pan head screw, M3x25, black oxide RoHS fastener
61
1000-M5C012-07
No
Hexagon Socket Head Cap Screw, M5-0.8, X12mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
62
1007-M2P5C006-14
No
Phillips Pan Head Screw, ISO 7045, M2.5-0.45, X6mm Long, Grade 4.8 Steel, Zinc Plated, RoHS Fastener
63
2106-M2P5-14
No
Spring Lock Washer with Flat Ends JIS B1251, M2.5, Spring Stainless Steel, Rohs Fastener
64
2002-M2P5-02
No
Flat Washer, Small OD Series, ISO7092, M2.5, Steel 140HV, Zinc Plated, RoHS Fastener
65
5396484
No
RoHS-Lamp Holder 905-1.0
66
5396421
Yes
Osram Lamp 64642 150W 24V
67
5396604
No
RoHS-Mirror Shaft
Page 182
Description
Section 5.3 SuperBee Manual Collimator - 5129498
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-19 RoHS-SuperBee Collimator - 5396306
Mark No.
Part No.
FRU
Description
68
5396571
No
RoHS-Mirror Shaft Support
69
5396603
No
RoHS-Mirror
70
5396586
No
RoHS-Filter
71
5396596
No
RoHS-Blade Covering
72
5396434
No
RoHS-Adjustable Lamp Support
73
5396634
No
RoHS-Switch Adapter
74
1007-M4C008-14
No
Phillips Pan Head Screw, ISO 7045, M4-0.7, X8mm Long, Grade 4.8 Steel, Zinc Plated, RoHS Fastener
75
5396309
No
RoHS-Wire Clip
76
5396415
No
RoHS-Lock Switch Cable
77
5396590
No
RoHS-Angle Plate 4
78
5396613
No
RoHS-system Cable
79
5396308
No
RoHS-Movable Bushing
80
5396623
No
RoHS-Bushing
81
3001-M6C-27
No
Hexagon Thin Nut, ISO4035, M6-1.0, Grade 04 Steel, Zinc Plated, RoHS Fastener
82
5396600
No
RoHS-Shielding Plate 1
83
5396619
No
RoHS-Lower Layer Blade
84
5396631
No
RoHS-Connection Plate S
85
5396373
No
RoHS-0316 KSS Cable Tie RCV-100
86
5396445
No
RoHS-Driving Wheel-C Riveting
87
5396375
No
RoHS-Cable Holder UC-1.5
88
5412663
No
L shield assembly
89
5396425
No
RoHS-Blade Support Riveting
90
5396622
No
RoHS-Shaft
91
5412673
No
Shield plate assembly
92
5396628
No
RoHS-Lead Plate
93
C2106-M6-02
No
Spring Lock Washer, M6, Zinc plated, Rohs Fastener
94
C2001-M4-80
No
Flat washer, M4, Black Oxide, Rosh Fastener
95
C2001-M3-80
No
Flat washer M3,Black Oxide
96
5396449
No
RoHS-Quicklock washer SE-6
97
C1010-M3C004-14
No
Phillips countersunk flat head screw GB-T819.1 M3x4. Zinc plated RoHS fastener
98
5396417
No
RoHS-Right Handle Plate
99
5396381
No
RoHS-Handle Adapter
100
5396418
No
RoHS-Spring Plate
101
5396420
No
RoHS-Spacer
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 183
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-19 RoHS-SuperBee Collimator - 5396306
Mark No.
Part No.
FRU
102
5396625
No
RoHS-Bearing Shaft
103
5396618
No
RoHS-Stop Angle Plate
104
5396431
No
RoHS-Lamp Support Riveting
105
5396621
No
RoHS-Adjust Screw
106
5396597
No
RoHS-Lamp Mask
107
5396480
No
RoHS-Steel Wire subassembly L
108
5396428
No
RoHS-Blade Base Riveting
109
5396633
No
RoHS-Driving Wheel B
110
5396435
No
RoHS-Crank Wheel Riveting B
111
5396416
No
RoHS-Left Handle Plate
112
C1010-M3C020-80
No
Cross slot flat head machine Screw GB-T819.1 M3x20, Black Oxide, RoHS fastener
113
5396637
No
RoHS-Rail End Cover
114
1107-M4C005-14
Yes
Cross Recessed Pan Head Screw, M4-0.7 X 5mm Long, Grade 4.8 Steel, Zinc plate RoHS Fastener
115
1003-M3C006-31
No
Hexagon Socket Button Head Screw, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
116
5396479
No
RoHS-Angle Plate 2
117
5396627
No
RoHS-Blade Support 3
118
5396620
No
RoHS-Upper Layer Blade
119
5396605
No
RoHS-Blade Support 2
120
5396439
No
RoHS-Crank Wheel Riveting A
121
5396453
No
RoHS-Steel Wire subassembly S
122
5396489
No
RoHS-Driving Shaft
123
1003-M4C006-31
No
Hexagon Socket Button Head Screw, M4-0.7, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
124
5396488
No
RoHS-Blade Bushing
125
3000-M4C-04
Yes
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
126
1003-M3C010-22
No
Hexagon Socket Button Head Screw, M3-0.5, X10mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
127
5395832
No
Super Bee Collimator Switch label
128
5397999
No
HLA label
129
5396376
No
RoHS-Indicator Plate Kit See 5.3.1.1 Collimator knob set - 5397014 on page 185
Page 184
Description
Section 5.3 SuperBee Manual Collimator - 5129498
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.3.1.1 Collimator knob set - 5397014
Table 5-20 Collimator knob set - 5397014
Mark No.
Part No.
FRU
Description
-
5397014
Yes
Collimator knob set
1
5396617
No
RoHS-Knob
2
5396376
No
RoHS-Indicator Plate Kit
3
5396624
No
RoHS-Knob Washer
4
1040-M4C004-27
No
Hexagon Set Screw with Cup Point, M4-0.7, X4mm Long, Grade 45H Steel, Black Oxide, RoHS Fastener
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 185
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
5.3.1.2 RoHS-Mechanical Interface - 5396643
Figure 5-30 5396643ADW_r1
Page 186
Section 5.3 SuperBee Manual Collimator - 5129498
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-21 RoHS-Mechanical Interface - 5396643
Mark No.
Part No.
FRU
Description
1
5396642
No
RoHS-Interface ring
2
1010-M4C010-31
No
Phillips Flat Head Screw, ISO 7046, M4-0.7, X10mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
3
5396644
No
RoHS-Suspending lock set See RoHS-Suspending lock set - 5396644 on page 188
4
5396654
No
RoHS-Rotation lock set See RoHS-Rotation lock set - 5396654 on page 190
5
1007-M3C016-31
No
Phillips Pan Head Screw, ISO 7045, M3-0.5, X16mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 187
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
RoHS-Suspending lock set - 5396644
Figure 5-31 5396644ADW_r1
Page 188
Section 5.3 SuperBee Manual Collimator - 5129498
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-22 RoHS-Suspending lock set - 5396644
Mark No.
Part No.
FRU
Description
1
5396645
No
RoHS-Finger end
2
5396646
No
RoHS-Suspending Finger
3
5396647
No
RoHS-Push pin
4
5396648
No
RoHS-Push pin block
5
5396649
No
RoHS-Cover
6
5396650
No
RoHS-block plate1
7
5396651
Yes
Block plate2
8
5396652
No
RoHS-Push pin spring
9
5396653
No
RoHS-Finger spring
10
C1003-M3C004-31
No
Hexagon Socket Button Head Screw, M3-0.5, X4mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
11
1003-M3C006-31
No
Hexagon Socket Button Head Screw, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 189
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
RoHS-Rotation lock set - 5396654
Figure 5-32 5396654ADW_r1
Page 190
Section 5.3 SuperBee Manual Collimator - 5129498
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-23 RoHS-Rotation lock set - 5396654
Mark No.
Part No.
FRU
Description
1
5396655
Yes
Rotation lock Finger
2
5396656
No
RoHS-Rotation lock block
3
5396657
No
RoHS-Rotation lock shaft
4
5396658
No
RoHS-Rotation lock base1
5
5396659
No
RoHS-Rotation lock base2
6
5396660
No
RoHS-Rotation lock handle
7
5396661
No
RoHS-Cover plate
8
5396662
No
RoHS-Rotation lock spring
9
1000-M3C020-04
No
Hexagon Socket Head Cap Screw, M3-0.5, X20mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
11
1040-M3C006-27
No
Hexagon Set Screw with Cup Point, M3-0.5, X6mm Long, Grade 45H Steel, Black Oxide RoHS Fastener
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 191
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Section 5.4 HV Cable Collector - 5503011
Table 5-24 HV Cable Collector - 5503011
Mark No.
Part No.
FRU
Description
1
5503010
Yes
HV Cable - Cathode
2
5503010-2
Yes
HV Cable - Anode
Section 5.5 Hardware Kit for SuperBee - 5399683
Table 5-25 Hardware Kit for SuperBee - 5399683
Mark No. Part No.
Qty. Description
1
1000-M4C008-04
24
Hexagon Socket Head Cap Screw, ISO 4762, M4-0.7, X8mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
3
1000-M4C030-07
2
Hexagon Socket Head Cap Screw, M4-0.7, X30mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
4
1000-M4C035-07
4
Hexagon Socket Head Cap Screw, M4-0.7, X35mm Long, Grade12.9 Steel, Black Oxide RoHS Fastener
5
1000-M4C010-07
34
Hexagon Socket Head Cap Screw, M4-0.7, X10mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
6
1000-M5C016-07
16
Hexagon Socket Head Cap Screw, M5-0.8, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
8
1000-M6C016-07
16
Hexagon Socket Head Cap Screw, M6-1, X16mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
9
1000-M6C020-04
6
Hexagon Socket Head Cap Screw, M6-1, X20mm Long, Grade 8.8 Steel, Zinc Plated, RoHS Fastener
11
1004-M6C020-31
3
Hexagon Socket C-Sunk Head Screw, M6-1, X20mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
12
1040-M10C025-27
1
Hexagon Set Screw with Cup Point, M10-1.5, X25mm Long, Grade 45H Steel, Black Oxide, RoHS Fastener
13
1000-M12C025-07
1
Hexagon Socket Head Cap Screw, M12-1.75, X25mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
21
2000-M4-02
2
Flat Washer, ISO7089, M4, Steel 140HV, Zinc Plated, RoHS Fastener
22
2000-M5-02
2
Flat Washer, ISO7089, M5, Steel 140HV, Zinc Plated, RoHS Fastener
23
2000-M6-02
6
Flat Washer, ISO7089, M6, Steel 140HV, Zinc Plated, RoHS Fastener
24
2203-M4-07
5
Curved Lock Washer, DIN 128A, M4, Spring Steel, Zinc Plated, RoHS Fastener
25
2203-M6-07
2
Curved Lock Washer, DIN 128A, M6, Spring Steel, Zinc Plated, RoHS Fastener
26
2106-M5-14
8
Spring Lock Washer with Flat Ends JIS B1251, M5, Spring Stainless Steel, Rohs Fastener
32
3000-M10C-04
10
Hexagon Nut, ISO4032, M10-1.5, Grade 8 Steel, Zinc Plated, RoHS Fastener
33
3000-M4C-04
13
Hexagon Nut, ISO4032, M4-0.7, Grade 8 Steel, Zinc Plated, RoHS Fastener
34
3000-M5C-04
4
Hexagon Nut, ISO4032, M5-0.8, Grade 8 Steel, Zinc Plated, RoHS Fastener
35
3000-M6C-04
6
Hexagon Nut, ISO4032, M6-1.0, Grade 8 Steel, Zinc Plated, RoHS Fastener
41
5370272
6
hex standoff, m-f, 20 mm long, m4
42
5384944
2
M2.5 X 0.45 X 4mm flat socket, 18-8 stainless, McMaster-Carr 92125A082
43
2108663-4
1
CLAMP,CLOSED/CABL D9.5X9.5 METAL M4
44
2193201
1
SCREW DIN7991 M4X8/6 A4-70
45
1007-M3C016-31
4
Phillips Pan Head Screw, ISO 7045, M3-0.5, X16mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
Page 192
Section 5.4 HV Cable Collector - 5503011
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
SYSTEM PARTS LIST
Table 5-25 Hardware Kit for SuperBee - 5399683
Mark No. Part No.
Qty. Description
46
1003-M3C008-31
4
Hexagon Socket Button Head Screw, M3-0.5, X8mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
47
1003-M3C006-31
4
Hexagon Socket Button Head Screw, M3-0.5, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
48
1000-M5C020-07
2
Hexagon Socket Head Cap Screw, M5-0.8, X20mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
49
1000-M5C025-07
2
Hexagon Socket Head Cap Screw, M5-0.8, X25mm Long, Grade12.9 Steel, Black Oxide, RoHS Fastener
50
1003-M4C006-31
4
Hexagon Socket Button Head Screw, M4-0.7, X6mm Long, A2-70 Stainless Steel, Passivate, RoHS Fastener
51
5423408
4
Security Torx M4x10 Buttonhead Fastener
52
5423674
2
M6x10 Lo-head SHCS A2 SS
53
5419764
10
Flange socket button head screw - M5 X 12 long
55
1004-M6C016-22
3
Hexagon Socket C-Sunk Head Screw, M6-1, X16mm Long, Grade10.9 Steel, Black Oxide, RoHS Fastener
57
5406517
2
front cover thimble
58
5486036-5
1
"Clamp - cable, 9.5 dia, P type, steel with zinc finish, RoHS compliant"
59
5427920
1
Security Torx Bit, T-15
60
1004-M8C016-22
1
Hexagon Socket C-Sunk Head Screw, M8-1.25, X16mm Long, Grade 10.9 Steel, Black Oxide, RoHS Fastener
61
1008-M4P8C013-29
2
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 13mm Long, Steel, Zinc Plated, RoHS Fastener
62
5429442
8
M5x20 socket head cap screw, low head
63
46-252635P7
8
.25 NOM., PLAIN WASHER
64
1008-M4P8C016-29
10
Hexagon Head Tapping Screw, ISO 1479, ST 4,8 X 16mm Long, Steel, Zinc Plated, RoHS Fastener
Section 5.6 Other
Table 5-26 Other
Mark No.
Part No.
FRU
Description
None
5423551
Yes
Blank USB memory stick with Label
None
5400481
Yes
Dose Area Product (DAP) option
None
5503005
Yes
Col Bulkhead to DAP Cable Assembly
None
5421892
Yes
LockOut TagOut (LOTO) kit collector:
•
46-194427P320
Qty = 3
PADLOCK,BRASS WITH BRASS SHACKLE MASTER LOCK #4B
•
46-194427P322
Qty = 3
LOCKOUT TAG,BLACK &amp; WHITE ON RED. PKG OF 25
•
2393068
Qty = 3
DANGER LOTO DO NOT REMOVE (for the LOTO locks)
•
5421889
Qty = 1
Nylon Lockout Cinch Bag
•
5421891
Qty = 3
Electrical Plug Lockout 220-550 volt
None
5503600
Yes
Wireless Hand Switch kit
None
5570321
Yes
Tablet Holder
Chapter 5 Common SuperBee VHLA - 5555001-2
Page 193
GE HEALTHCARE
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
Page 194
SYSTEM PARTS LIST
Section 5.6 Other
© 2011 General Electric Company.
GE Medical Systems, a General Electric Company, going to market as GE Healthcare.
3000 N. Grandview Boulevard
Waukesha, Wisconsin 53188
USA
www.gehealthcare.com
196
Front cover
GE HEALTHCARE
gehealthcare.com
Technical
Publication
Direction 5336116-1EN
Revision 3
GE Healthcare
Optima XR200amx/XR220amx System Schematics and Drawings
Copyright 2011 by General Electric Company, Inc.
All Rights Reserved
GE HEALTHCARE
REVISION 3
Warning
OPTIMA XR200AMX/XR220AMX
DIRECTION 5336116-1EN
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement X entraîne des
dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour elles-mêmes. Avant chaque
manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique, Annales 26: Recommandations de la
Commission Internationale sure la Protection Radiologique et les normes nationales en vigueur.
WARNING
X-RAY EQUIPMENT IS DANGEROUS TO BOTH PATIENT AND OPERATOR UNLESS MEASURES OF PROTECTION ARE STRICTLY OBSERVED.
Though this equipment is built to the highest standards of electrical and mechanical safety, the useful x-ray beam becomes a source of danger in the hands of the unauthorized or unqualified operator. Excessive exposure to x-radiation causes
damage to human tissue.
Therefore, adequate precautions must be taken to prevent unauthorized or unqualified persons from operating this equipment or exposing themselves or others to its radiation.
Before operation, persons qualified and authorized to operate this equipment should be familiar with the Recommendations of the International Commission on Radiological Protection (ICRP), contained in Annals Number 26 of the ICRP, and with
applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede causar
daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales No 26:
Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen Kommission für
Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für Strahlenschutz und anderer nationaler Normenbehörden.
Page 2
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Important information
WARNING
(EN)
ПРЕДУПРЕЖДЕНИЕ
(BG)
警告
(ZH-CN)
警告
(ZH-HK)
警告
(ZH-TW)
This service manual is available in English only.
•
If a customer's service provider requires a language other than English, it is the customer's
responsibility to provide translation services.
•
Do not attempt to service the equipment unless this service manual has been consulted and is
understood.
•
Failure to heed this warning may result in injury to the service provider, operator or patient from
electric shock, mechanical or other hazards.
Tова упътване за работа е налично само на английски език.
•
Ако доставчикът на услугата на клиента изиска друг език, задължение на клиента е да
осигури превод.
•
Не използвайте оборудването, преди да сте се консултирали и разбрали упътването за
работа.
•
неспазването на това предупреждение може да доведе до нараняване на доставчика на
услугата, оператора или пациентa в резултат на токов удар, механична или друга опасност.
本维修手册仅提供英文版本。
•
•
•
如果客户的维修服务人员需要非英文版本，则客户需自行提供翻译服务。
未详细阅读和完全理解本维修手册之前，不得进行维修。
忽略本警告可能对维修服务人员、操作人员或患者造成电击、机械伤害或其他形式的伤
害。
本服務手冊僅提供英文版本。
• 倘若客戶的服務供應商需要英文以外之服務手冊，客戶有責任提供翻譯服務。
• 除非已參閱本服務手冊及明白其內容，否則切勿嘗試維修設備。
• 不遵從本警告或會令服務供應商、網絡供應商或病人受到觸電、機械性或其他的危險。
本維修手冊僅有英文版。
• 若客戶的維修廠商需要英文版以外的語言，應由客戶自行提供翻譯服務。
• 請勿試圖維修本設備，除非 您已查閱並瞭解本維修手冊。
• 若未留意本警告，可能導致維修廠商、操作員或病患因觸電、機械或其他危險而受傷。
UPOZORENJE
(HR)
Ovaj servisni priručnik dostupan je na engleskom jeziku.
•
Ako davatelj usluge klijenta treba neki drugi jezik, klijent je dužan osigurati prijevod.
•
Ne pokušavajte servisirati opremu ako niste u potpunosti pročitali i razumjeli ovaj servisni
priručnik.
•
zanemarite li ovo upozorenje, može doći do ozljede davatelja usluge, operatera ili pacijenta uslijed
strujnog udara, mehaničkih ili drugih rizika.
VÝSTRAHA
(CS)
Tento provozní návod existuje pouze v anglickém jazyce.
• V případě, že externí služba zákazníkům potřebuje návod v jiném jazyce, je zajištění překladu do
odpovídajícího jazyka úkolem zákazníka.
• Nesnažte se o údržbu tohoto zařízení, aniž byste si přečetli tento provozní návod a pochopili jeho
obsah.
• V případě nedodržování této výstrahy může dojít k poranění pracovníka prodejního servisu,
obslužného personálu nebo pacientů vlivem elektrického proudu, respektive vlivem mechanických
či jiných rizik.
Denne servicemanual findes kun på engelsk.
• Hvis en kundes tekniker har brug for et andet sprog end engelsk, er det kundens ansvar at sørge
for oversættelse.
• Forsøg ikke at servicere udstyret uden at læse og forstå denne servicemanual.
• Manglende overholdelse af denne advarsel kan medføre skade på grund af elektrisk stød,
mekanisk eller anden fare for teknikeren, operatøren eller patienten.
ADVARSEL
(DA)
Preface
Page 3
GE HEALTHCARE
REVISION 3
WAARSCHUWING
(NL)
HOIATUS
(ET)
VAROITUS
(FI)
ATTENTION
(FR)
WARNUNG
(DE)
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ
(EL)
FIGYELMEZTETÉS
(HU)
AÐVÖRUN
(IS)
Page 4
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.
• Als het onderhoudspersoneel een andere taal vereist, dan is de klant verantwoordelijk voor de
vertaling ervan.
• Probeer de apparatuur niet te onderhouden alvorens deze onderhoudshandleiding werd
geraadpleegd en begrepen is.
• Indien deze waarschuwing niet wordt opgevolgd, zou het onderhoudspersoneel, de operator of
een patiënt gewond kunnen raken als gevolg van een elektrische schok, mechanische of andere
gevaren.
See teenindusjuhend on saadaval ainult inglise keeles
• Kui klienditeeninduse osutaja nõuab juhendit inglise keelest erinevas keeles, vastutab klient
tõlketeenuse osutamise eest.
• Ärge üritage seadmeid teenindada enne eelnevalt käesoleva teenindusjuhendiga tutvumist ja
sellest aru saamist.
• Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja, operaatori või patsiendi vigastamist
elektrilöögi, mehaanilise või muu ohu tagajärjel.
Tämä huolto-ohje on saatavilla vain englanniksi.
• Jos asiakkaan huoltohenkilöstö vaatii muuta kuin englanninkielistä materiaalia, tarvittavan
käännöksen hankkiminen on asiakkaan vastuulla.
• Älä yritä korjata laitteistoa ennen kuin olet varmasti lukenut ja ymmärtänyt tämän huolto-ohjeen.
• Mikäli tätä varoitusta ei noudateta, seurauksena voi olla huoltohenkilöstön, laitteiston käyttäjän tai
potilaan vahingoittuminen sähköiskun, mekaanisen vian tai muun vaaratilanteen vuoksi.
Ce manuel d’installation et de maintenance est disponible uniquement en anglais.
• Si le technicien d'un client a besoin de ce manuel dans une langue autre que l'anglais, il incombe
au client de le faire traduire.
• Ne pas tenter d'intervenir sur les équipements tant que ce manuel d’installation et de maintenance
n'a pas été consulté et compris.
• Le non-respect de cet avertissement peut entraîner chez le technicien, l'opérateur ou le patient
des blessures dues à des dangers électriques, mécaniques ou autres.
Diese Serviceanleitung existiert nur in englischer Sprache.
• Falls ein fremder Kundendienst eine andere Sprache benötigt, ist es Aufgabe des Kunden für eine
entsprechende Übersetzung zu sorgen.
• Versuchen Sie nicht diese Anlage zu warten, ohne diese Serviceanleitung gelesen und
verstanden zu haben.
• Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des Kundendiensttechnikers, des
Bedieners oder des Patienten durch Stromschläge, mechanische oder sonstige Gefahren
kommen.
Το παρόν εγχειρίδιο σέρβις διατίθεται μόνο στα αγγλικά.
• Εάν ο τεχνικός σέρβις ενός πελάτη απαιτεί το παρόν εγχειρίδιο σε γλώσσα εκτός των αγγλικών,
αποτελεί ευθύνη του πελάτη να παρέχει τις υπηρεσίες μετάφρασης.
• Μην επιχειρήσετε την εκτέλεση εργασιών σέρβις στον εξοπλισμό αν δεν έχετε συμβουλευτεί και
κατανοήσει το παρόν εγχειρίδιο σέρβις.
• Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί τραυματισμός στον τεχνικό
σέρβις, στο χειριστή ή στον ασθενή από ηλεκτροπληξία, μηχανικούς ή άλλους κινδύνους.
Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.
• Ha a vevő szolgáltatója angoltól eltérő nyelvre tart igényt, akkor a vevő felelőssége a fordítás
elkészíttetése.
• Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási kézikönyvben leírtakat nem
értelmezték.
• Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető vagy a beteg áramütés,
mechanikai vagy egyéb veszélyhelyzet miatti sérülését eredményezheti.
Þessi þjónustuhandbók er aðeins fáanleg á ensku.
• Ef að þjónustuveitandi viðskiptamanns þarfnast annas tungumáls en ensku, er það skylda
viðskiptamanns að skaffa tungumálaþjónustu.
• Reynið ekki að afgreiða tækið nema að þessi þjónustuhandbók hefur verið skoðuð og skilin.
• Brot á sinna þessari aðvörun getur leitt til meiðsla á þjónustuveitanda, stjórnanda eða sjúklings frá
raflosti, vélrænu eða öðrum áhættum.
Preface
GE HEALTHCARE
REVISION 3
AVVERTENZA
(IT)
(JA)
경고
(KO)
BRÎDINÂJUMS
(LV)
ĮSPĖJIMAS
(LT)
ADVARSEL
(NO)
OSTRZEŻENIE
(PL)
AVISO
(PT-BR)
ATENÇÃO
(PT-PT)
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Il presente manuale di manutenzione è disponibile soltanto in lingua inglese.
• Se un addetto alla manutenzione richiede il manuale in una lingua diversa, il cliente è tenuto a
provvedere direttamente alla traduzione.
• Procedere alla manutenzione dell'apparecchiatura solo dopo aver consultato il presente manuale
ed averne compreso il contenuto.
• Il mancato rispetto della presente avvertenza potrebbe causare lesioni all'addetto alla
manutenzione, all'operatore o ai pazienti provocate da scosse elettriche, urti meccanici o altri
rischi.
このサービスマニュアルには英語版しかありません。
 サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業者の責任で行
うものとさせていただきます。
 このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでください。
この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、感電や機械
的又はその他の危険により負傷する可能性があります。
본 서비스 매뉴얼은 영어로만 이용하실 수 있습니다 .
• 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우 , 번역 서비스를 제공하는 것은 고객의
책임입니다 .
• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하려고 시도하지 마십시오 .
• 본 경고 사항에 유의하지 않으면 전기 쇼크 , 기계적 위험 , 또는 기타 위험으로 인해 서비스 제공자
, 사용자 또는 환자에게 부상을 입힐 수 있습니다 .
Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.
• Ja klienta apkopes sniedzējam nepieciešama informācija citā valodā, klienta pienākums ir
nodrošināt tulkojumu.
• Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas un saprašanas.
• Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas trieciena, mehānisku vai
citu faktoru izraisītu traumu risks apkopes sniedzējam, operatoram vai pacientam.
Šis eksploatavimo vadovas yra tik anglų kalba.
• Jei kliento paslaugų tiekėjas reikalauja vadovo kita kalba – ne anglų, suteikti vertimo paslaugas
privalo klientas.
• Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar nesupratote šio
eksploatavimo vadovo.
• Jei nepaisysite šio įspėjimo, galimi paslaugų tiekėjo, operatoriaus ar paciento sužalojimai dėl
elektros šoko, mechaninių ar kitų pavojų.
Denne servicehåndboken finnes bare på engelsk.
• Hvis kundens serviceleverandør har bruk for et annet språk, er det kundens ansvar å sørge for
oversettelse.
• Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest og forstått.
• Manglende hensyn til denne advarselen kan føre til at serviceleverandøren, operatøren eller
pasienten skades på grunn av elektrisk støt, mekaniske eller andre farer.
Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.
• Jeśli serwisant klienta wymaga języka innego niż angielski, zapewnienie usługi tłumaczenia jest
obowiązkiem klienta.
• Nie próbować serwisować urządzenia bez zapoznania się z niniejszym podręcznikiem
serwisowym i zrozumienia go.
• Niezastosowanie się do tego ostrzeżenia może doprowadzić do obrażeń serwisanta, operatora
lub pacjenta w wyniku porażenia prądem elektrycznym, zagrożenia mechanicznego bądź innego.
Este manual de assistência técnica encontra-se disponível unicamente em inglês.
•
Se outro serviço de assistência técnica solicitar a tradução deste manual, caberá ao cliente
fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
A não observância deste aviso pode ocasionar ferimentos no técnico, operador ou paciente
decorrentes de choques elétricos, mecânicos ou outros.
Este manual de assistência técnica só se encontra disponível em inglês.
•
Se qualquer outro serviço de assistência técnica solicitar este manual noutro idioma, é da
responsabilidade do cliente fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
O não cumprimento deste aviso pode colocar em perigo a segurança do técnico, do operador ou
do paciente devido a choques eléctricos, mecânicos ou outros.
Preface
Page 5
GE HEALTHCARE
REVISION 3
ATENŢIE
(RO)
ОСТОРОЖНО!
(RU)
UPOZORENJE
(SR)
UPOZORNENIE
(SK)
ATENCION
(ES)
VARNING
(SV)
OPOZORILO
(SL)
DİKKAT
(TR)
Page 6
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Acest manual de service este disponibil doar în limba engleză.
•
Dacă un furnizor de servicii pentru clienţi necesită o altă limbă decât cea engleză, este de datoria
clientului să furnizeze o traducere.
•
Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi înţelegerii acestui manual de
service.
•
Ignorarea acestui avertisment ar putea duce la rănirea depanatorului, operatorului sau pacientului
în urma pericolelor de electrocutare, mecanice sau de altă natură.
Данное руководство по техническому обслуживанию представлено только на английском языке.
•
Если сервисному персоналу клиента необходимо руководство не на английском, а на
каком-то другом языке, клиенту следует самостоятельно обеспечить перевод.
•
Перед техническим обслуживанием оборудования обязательно обратитесь к данному
руководству и поймите изложенные в нем сведения.
•
Несоблюдение требований данного предупреждения может привести к тому, что
специалист по техобслуживанию, оператор или пациент получит удар электрическим током,
механическую травму или другое повреждение
Ovo servisno uputstvo je dostupno samo na engleskom jeziku.
•
Ako klijentov serviser zahteva neki drugi jezik, klijent je dužan da obezbedi prevodilačke usluge.
•
Ne pokušavajte da opravite uređaj ako niste pročitali i razumeli ovo servisno uputstvo.
•
Zanemarivanje ovog upozorenja može dovesti do povređivanja servisera, rukovaoca ili pacijenta
usled strujnog udara ili mehaničkih i drugih opasnosti.
Tento návod na obsluhu je k dispozícii len v angličtine.
•
Ak zákazníkov poskytovateľ služieb vyžaduje iný jazyk ako angličtinu, poskytnutie
prekladateľských služieb je zodpovednosťou zákazníka.
•
Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na obluhu a neporozumiete mu.
•
Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa služieb, obsluhujúcej
osoby alebo pacienta elektrickým prúdom, mechanické alebo iné ohrozenie.
Este manual de servicio sólo existe en inglés.
•
Si el encargado de mantenimiento de un cliente necesita un idioma que no sea el inglés, el cliente
deberá encargarse de la traducción del manual.
•
No se deberá dar servicio técnico al equipo, sin haber consultado y comprendido este manual de
servicio.
•
La no observancia del presente aviso puede dar lugar a que el proveedor de servicios, el
operador o el paciente sufran lesiones provocadas por causas eléctricas, mecánicas o de otra
naturaleza.
Den här servicehandboken finns bara tillgänglig på engelska. .
•
Om en kunds servicetekniker har behov av ett annat språk än engelska, ansvarar kunden för att
tillhandahålla översättningstjänster.
•
Försök inte utföra service på utrustningen om du inte har läst och förstår den här
servicehandboken.
•
Om du inte tar hänsyn till den här varningen kan det resultera i skador på serviceteknikern,
operatören eller patienten till följd av elektriska stötar, mekaniska faror eller andra faror.
Ta servisni priročnik je na voljo samo v angleškem jeziku.
•
Če ponudnik storitve stranke potrebuje priročnik v drugem jeziku, mora stranka zagotoviti prevod.
•
Ne poskušajte servisirati opreme, če tega priročnika niste v celoti prebrali in razumeli.
•
Če tega opozorila ne upoštevate, se lahko zaradi električnega udara, mehanskih ali drugih
nevarnosti poškoduje ponudnik storitev, operater ali bolnik.
Bu servis kılavuzunun sadece ingilizcesi mevcuttur.
•
Eğer müşteri teknisyeni bu kılavuzu ingilizce dışında bir başka lisandan talep ederse, bunu
tercüme ettirmek müşteriye düşer.
•
Servis kılavuzunu okuyup anlamadan ekipmanlara müdahale etmeyiniz.
•
Bu uyarıya uyulmaması, elektrik, mekanik veya diğer tehlikelerden dolayı teknisyen, operatör
veya hastanın yaralanmasına yol açabilir.
Preface
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Legal notes
TRADEMARKS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2 are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material presented and contained herein may not be reproduced in any form or manner, without the written permission of General Electric Company, Inc.
Preface
Page 7
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation “damage in shipment” written on all copies of the freight or express bill before delivery is accepted or “signed for” by a General Electric representative
or a hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and MIS.” Contact your local service coordinator for more information on this process.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT
All electrical installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds into the Power Distribution Unit shall be performed
by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE Healthcare personnel. The products involved (and the accompanying electrical installations)
are highly sophisticated, and special engineering competence is required. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GE’s electrical work on these products will comply with the
requirements of the applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein contained should be thoroughly read and understood by everyone who will use the equipment before you attempt to place this equipment in operation. GE
Healthcare will be glad to assist and cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the useful beam, no practical design of equipment can provide complete protection. Nor can any practical design compel the operator to take adequate
precautions to prevent the possibility of any persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully acquainted with the recommendations of the National Council on Radiation Protection and Measurements (NCRP) as published in NCRP Reports available
from NCRP Publications, 7910 Woodmont Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission on Radiation Protection, and take adequate steps to protect against injury.
The equipment is sold with the understanding that GE Healthcare, its agents, and representatives have no responsibility for injury or damage which may result from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be used.
LITHIUM BATTERY CAUTIONARY STATEMENT
DANGER - Risk of Explosion
Danger of explosion if battery is incorrectly replaced.
Replace only with the same or equivalent type recommended by
the manufacturer. Discard used batteries according to the
manufacturer’s instructions.
ATTENTION - Danger d’Explosion
Il y a danger d’explosion s’il y a replacement incorrect de la
batterie.
Remplacer uniquement avec une batterie du même type ou d’un
type recommandé par le constructeur. Mettre au rébut les
batteries usagées conformément aux instructions du fabricant.
TECHNICAL MANUAL UPDATES
When operating or servicing GE Healthcare products, please contact your GE representative for the latest revision of product documentation. Product documentation may also be available on-line at the GE Healthcare support documentation library.
OMISSIONS AND ERRORS
Customers, please contact your GE Healthcare sales or service representatives.
GE personnel, please use the GE Healthcare complaint handling process to report all omissions, errors, and defects in this publication.
Page 8
Preface
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Revision history
Revision
Date
Reason for change
1
20SEP2011
Initial release of document
2
12SEP2012
Cable ‘5557023 Cricket to breaker’ drawing is incorrect. Instead, 5557032 drawing was shown. Updated Figure 8-8 with the correct drawing. Refer to PR7510828.
Updated Ch 2, Sec 2-1 System Architecture Schematic DOC0645488 to Rev 3.
Updated wiring diagram 5507000WIR to rev 5 in Figure 2-2. Refer to ECO 2131197.
Added text to front material on how to obtain most recent revisions of technical manuals. Satisfies FDA recommendation.
Updated Locust drive board part number and drawings from 5350006 to 5350006-2. Refer to PR# 7792277.
Updated Hornet UIF board part number and drawings from 5350004 to 5350004-2. Refer to PR# 8915068.
3
17SEP2013
Chapter 13, Section 13.1, added drawings 5557070ADW, 5557071ADW, 5557067ADW. Refer to ECR 2150628.
Chapter 5, changed all Spyder board part numbers from 5350002 to 5350002-4 and updated Spyder board schematics to Rev 7. Refer to ECO 2140711.
Chapter 7, changed all Locust board part numbers from 5350006 to 5350006-2 and updated Locust board schematics to Rev 7. Refer to ECO 2143023.
Chapter 4, changed all Firefly board part numbers from 5350000 to 5350000-2 and updated Firefly board ADW drawing and schematics to Rev 6. Refer to ECO 2140711.
Chapter 2, updated Figure 2-2 wiring diagram 5507000WIR to Rev 6. Refer to ECR 2150628.
Preface
Page 9
GE HEALTHCARE
REVISION 3
Page 10
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Preface
GE HEALTHCARE
REVISION 3
Preface - Publi-
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Preface Publication Conventions
Standardized conventions for representing information is a uniform way of communicating information to a reader in a consistent manner. Conventions are used so that the reader can easily recognize the actions or decisions that must be made.
There are a number of character and paragraph styles used in this publication to accomplish this task. Please become familiar with them before proceeding forward.
It is important that you read and understand hazard statements, and not just ignore them.
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and style for safety communications reflected in this publication represents the harmonization of IEC/ISO 3864 and ANSI Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify important safety information. Text (Hazard) styles are
applied to the paragraph contents that are applicable to each specific safety statement.
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation mark within it. It Is always used next to the signal
word to indicate the severity of the hazard. Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert symbol and signal word are placed immediately before any paragraph they affect. Safety information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Text Format of Signal Words
DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH, IF NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS SIGNAL WORD IS LIMITED TO THE MOST
EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Caution - Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury. It may also be used to alert against unsafe practices.
NOTICE - Indicates information or a company policy that relates directly or indirectly to the safety of personnel or protection of property. This signal word is associated directly with a hazard or hazardous situation and is used in
place of 'DANGER,' 'WARNING,' or 'CAUTION.' It can include:
•
Destruction of a disk drive
•
Potential for internal mechanical damage, such as to a X-ray tube
Preface
Page 11
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Symbols and Pictorials Used
The following Symbols and Pictorials are be used in this publication. These graphical icons (symbols) may be used to make you aware of specific types of hazards that could possibly cause harm.
keep_up
magnetic
biohazard
compressgas
ppe-hearing
fragile
impact
corrosive
heavyobject
ppe-2people
static_elec
heat
general
laser
ppe-respitory
keep_dry
pinch
radiation
poisongas
ppe-loto
general
explosive
electrical
flammable
ppe-eye
torque
crush/mechanical
tipping
Read Manual
ppe-gloves
ce
instuction
poisonmatl
entanglement
instuction
Page 12
Preface
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such as Purpose, Example, Comment or Note) are used to identify important but non-safety related information. Text styles are also applied to text within
each paragraph modified by the specific prefix.
EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:
Purpose:
Introduces and provides meaning as to the information contained within the chapter, section or subsection (such as used at the beginning this chapter, for example).
Note:
Conveys information that should be considered important to the reader.
Example:
Used to make the reader aware that the paragraph(s) that follow are examples of information possibly stated previously.
Comment:
Represents “additional” information that may or may not be relevant to your situation.
Page Layout
Publication Part Number & Revision Number
The current section and its title
are always shown in the footer of
the left (even) page.
An exclamation point in a triangle is used
to indicate important information to the user.
Paragraphs preceeded by Alphanumeric
characters (e.g. numbers) contain information that must be followed in a specific order.
Publication Title
The current chapter and its title
are always shown in the footer of
the right (odd) page.
Paragraphs preceeded by a symbol
(e.g. bullets) contain information that
has no specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location. The document part number and revision number appears in every header on every page. Odd numbered page footers indicate the current chapter,
its title and current page number. Even page footers show the current section and its title, as well as the current page number.
Preface
Page 13
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text that’s either screen input and output. Mono-spaced fonts, such courier, are used to indicated text direction. When you type at your keyboard, you are
generating computer input. Occasionally you will see the math operator “greater-than” and “less-than” symbols used to indicate the start and finish of variable output. When reading text generated by the computer, you are reading it as computer
generated output. In addition to direction, characters are italicized (e.g. italics) to indicate information specific to your system or site.
Example: Fixed Output
This paragraph’s font represents computer generated screen “fixed” output. Its output is fixed from the sense that it does not vary from application to application. It is the most
commonly used style used to indicate filenames, paths and text that do not change from system to system. The character style used is a fixed width such as courier.
Example:
Variable Output
This paragraph’s font represents computer screen output that is “variable”. It is used to represent output that varies from application to application or system to system. Variable
output is sometimes found placed between greater-than and less-than operators for clarification. For example: <variable_ouput> or <3.45.120.3>. In both cases, the < and > operators
are not part of the actual input.
Example:
Fixed Input
This paragraph’s font represents fixed input. It is computer input that is typed-in via the keyboard. Typed input that does not vary from application to application or system to
system. Fixed text the user is required to supply as input. For example: cd /usr/3p
Example:
Variable Input
This paragraph’s font represents computer input that can vary from application to application or system to system. With variable text, the user is required to supply system dependent
input or information. Variable input sometimes is placed between greater-than and less-than operators. For example: <variable_input>. In these cases, the (<>) operators would be
dropped prior to input. For example: ypcat hosts | grep <3.45.120.3> would be typed into the computer as:
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or soft button, switch or key. Physical hardware, such as buttons and switches, are called hard keys because they are hard wired or mechanical in
nature. A keyboard or on/off switch would be a hard key. Software or computer generated buttons are called soft keys because they are software generated. Software driven menu buttons are an example of such keys. Soft and hard keys are
represented differently in this publication.
Example: Hard Keys
A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style that uses both over and under-lined bold text that is bold. This is a hard key.
Example: Soft Keys
Whereas the computer MENU button that you would click with your mouse or touch with your hand uses over and under-lined regular text. This is a soft key.
Page 14
Preface
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Table of contents
Chapter 1
Introduction to schematics ........................................................... 19
Section 1.1
Content and organization ............................................................................... 19
Section 1.2
Drawing conventions ...................................................................................... 19
Chapter 2
System interconnects .................................................................. 21
Section 2.1
System architecture ........................................................................................ 21
Section 2.2
System wiring .................................................................................................. 22
Chapter 3
Jumpers, switches, LEDs, test points ......................................... 23
Section 3.1
3.1.1
3.1.2
3.1.3
3.1.4
Section 3.2
3.2.1
3.2.2
3.2.3
3.2.4
3.4.1
3.4.2
3.4.3
3.4.4
3.5.1
3.5.2
3.5.3
3.5.4
3.6.1
3.6.2
3.6.3
3.6.4
29
29
30
30
Caterpillar base transition board 5350010 .................................................... 30
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
Section 3.7
27
28
28
28
Cricket battery board 5350008 ....................................................................... 29
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
Section 3.6
26
26
27
27
Locust drive board 5350006-2........................................................................ 27
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
Section 3.5
24
25
25
26
Hornet UIF board 5350004-2........................................................................... 26
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
Section 3.4
23
23
23
24
Spyder system controller board 5350002-4 .................................................. 24
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
Section 3.3
3.3.1
3.3.2
3.3.3
3.3.4
Firefly charger board 5350000-2 .................................................................... 23
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
30
30
30
30
Board data module 5350038........................................................................... 31
Table of Contents
Page 15
GE HEALTHCARE
REVISION 3
3.7.1
3.7.2
3.7.3
3.7.4
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
Section 3.8
3.8.1
3.8.2
3.8.3
3.8.4
3.8.5
31
31
31
31
Collimator lamp supply board 5450200......................................................... 31
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
Potentiometers ...................................................................................................................................
Section 3.9
3.9.1
3.9.2
3.9.3
3.9.4
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
31
31
32
32
32
Mantis power supply 5311985........................................................................ 32
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
32
32
33
33
Section 3.10 LVLE2 power supply 5192958 ........................................................................ 33
3.10.1
3.10.2
3.10.3
3.10.4
Jumpers ..............................................................................................................................................
Switches .............................................................................................................................................
LEDs ...................................................................................................................................................
Test points ..........................................................................................................................................
Chapter 4
33
33
33
33
Firefly charger board 5350000-2................................................... 35
Section 4.1
Firefly schematics ........................................................................................... 36
Section 4.2
Firefly connector cables ................................................................................. 65
Chapter 5
Spyder system controller 5350002-4 ........................................... 75
Section 5.1
Spyder schematics.......................................................................................... 76
Section 5.2
Spyder connector cables.............................................................................. 136
Chapter 6
Hornet UIF board 5350004-2 ....................................................... 147
Section 6.1
Hornet schematics ........................................................................................ 148
Section 6.2
Hornet connector cables .............................................................................. 155
Chapter 7
Locust drive board 5350006-2 .................................................... 159
Section 7.1
Locust schematics ........................................................................................ 160
Section 7.2
Locust connector cables .............................................................................. 184
Chapter 8
Cricket battery board 5350008.................................................... 195
Section 8.1
Cricket schematics........................................................................................ 196
Section 8.2
Cricket connector cables.............................................................................. 199
Page 16
Table of Contents
GE HEALTHCARE
REVISION 3
Chapter 9
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Caterpillar base transition board 5350010 ................................ 205
Section 9.1
Caterpillar schematics .................................................................................. 206
Section 9.2
Caterpillar connector cables ........................................................................ 209
Chapter 10
LVLE2 power supply 5192958 .................................................... 215
Section 10.1 LVLE2 connector cables............................................................................... 216
Chapter 11
Mantis power supply 5311985 .................................................... 223
Section 11.1 Mantis connector cables .............................................................................. 224
Chapter 12
Generator (Djinn) ......................................................................... 229
Section 12.1 Generator Interconnections ......................................................................... 230
Section 12.2 Main auxiliary 15kW module 5338768 ......................................................... 231
12.2.1 Rotor control board 5133326-3......................................................................................................... 233
Section 12.3 Optional auxiliary module 30kW 5338767 ................................................... 246
12.3.1 Beetle CAPA board 5395972 ........................................................................................................... 248
Section 12.4 Power module 5396857................................................................................. 250
12.4.1 Power board 5367800 ...................................................................................................................... 251
12.4.2 Filament board 5394517................................................................................................................... 257
12.4.3 Control board 5305042-2.................................................................................................................. 263
Section 12.5 HV tank 5140761-2......................................................................................... 264
12.5.1 Int measurement board 5309420 ..................................................................................................... 265
12.5.2 HV BIP board 5395639..................................................................................................................... 268
Section 12.6 Generator connector cables......................................................................... 270
Chapter 13
DPS (Detector Power Supply) assembly ................................... 285
Section 13.1 DPS assembly drawing................................................................................. 286
Section 13.2 DPS connector cables .................................................................................. 291
Chapter 14
PC .................................................................................................. 297
Section 14.1 PC connector cables..................................................................................... 298
Chapter 15
Other ............................................................................................. 305
Section 15.1 Drive login board 5378850 and Overlay board 5368325 ............................ 305
15.1.1 Drive login board 5378850 ............................................................................................................... 305
15.1.1.1Drive login board schematics ........................................................................... 306
15.1.1.2Drive login board connector cables .................................................................. 310
15.1.1.3Drive login electrode board 5378852................................................................ 311
15.1.2 Overlay board 5368325 .................................................................................................................... 314
Table of Contents
Page 17
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
15.1.2.1Overlay board connector cables....................................................................... 316
Section 15.2 Cord reel......................................................................................................... 317
15.2.1 Cord reel connector cables............................................................................................................... 318
Section 15.3 Collimator lamp supply (CLS) 5450200 ....................................................... 320
15.3.1 Collimator lamp supply schematics .................................................................................................. 321
15.3.2 Collimator lamp supply connector cables ......................................................................................... 324
Section 15.4 Power switch ................................................................................................. 327
15.4.1 Power switch connector cables ........................................................................................................ 328
Section 15.5 Wireless USB host radio board assembly 5390144-2 ................................ 330
15.5.1 Wireless USB host radio board schematics...................................................................................... 330
15.5.2 Wireless USB host radio board connector cable .............................................................................. 336
Page 18
Table of Contents
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 1 Introduction to schematics
Section 1.1 Content and organization
This service manual contains schematics for the assemblies that make up the Optima XR200amx/Optima XR220amx system. Schematics are arranged in alpha-numeric order, using the reference designators assigned each assembly. Reference
designators are brief codes used to identify and locate the assembly within a system.
Section 1.2 Drawing conventions
Some schematics contained in this document use a hierarchical design philosophy. This hierarchical philosophy allows for easier schematic representation of complex circuitry. To a typical schematic user however, the hierarchical schematics may
seem difficult to follow. So to address this issue, there are listed below, some informative highlights which should help in the understanding of hierarchical design schematics.
•
Hierarchical schematics are structured from a high level (i.e.,complete system) to a low level (i.e., discrete components). In circuit board schematic applications this means that there will typically be a block diagram on the first schematic sheets,
which represents the entire circuit board. Then from this diagram, each of the blocks is broken down into the discrete component circuitry.
•
For individual signal connections, a similar schematic structuring technique is used. At the block diagram schematic level, signals are grouped together into buses, which travel between the blocks. The individual signal connections are first
shown separately when the blocks are broken down into the discrete component circuitry.
•
Buses are drawn thicker than the individual signal lines and they also have two numbers shown in parentheses, immediately following the bus name. These numbers indicate how many individual signals are contained in the bus. For example,
(7:0) indicates that there are eight total signals in the bus, ranging from 0 through 7. If the buses happen to be data or address buses, the numbers in parentheses also indicate the most significant bit and least significant bit as follows, (MSB:LSB).
•
When an individual signal line enters or leaves a bus, it is drawn using a diagonal line called a ripper. Next to the ripper, a number is also drawn. This ripper number is unique to the signal line that it represents. In other words, if a ripper number
is 3 and the signal line name that leaves the bus is XAC, every time XAC leaves or enters that bus, the ripper number, will always be 3.
•
There are some special symbols, called ports and pages, used to link buses and signal lines from one sheet of the schematic to others. Port symbols link signals between different functional blocks, while the page symbols link signals within
the same functional block.
This was just a brief summary of some of the more significant differences associated with hierarchical design schematics. In general, most other schematic guidelines used before the hierarchical applications, still apply. For example; schematic
inputs are still on the left and outputs on the right, and schematic flow is from left-to-right and top-to-bottom. Also, signal names are still consistent throughout an entire schematic design, whenever possible.
Chapter 1 Introduction to schematics
Page 19
GE HEALTHCARE
REVISION 3
Page 20
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 1.2 Drawing conventions
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 2 System interconnects
Section 2.1 System architecture
1
2
802.15.3a
UWB
Detector
3
802.15.4
Zigbee
Zigbee
Barcode
Reader
8 mMNL
PLG
8 mMNL
REC
A
J6
J5
J9
6 Molex Pin
J13
J14
9 Sub-D REC
E
I/O Expander I/F
J16 10 Header 0.1"
FPGA JTAG
5
PCN NO.
CLS
5450200
+Batt
J4
3.15A
Firefly
Charger Board
5350000 - X
J9
J5
DESCRIPTION
J6
MADE
CHECK
APPR
Update to Detector Power Supply
Update to DPM & Board #’s to -X
OTHER
6
APPROVALS
Butzine
DD-MM-YY
J2
J3
G
Collimator Lamp
2MOPP Batt
+Batt
Secondary Isolation Barrier
2000V dielectric
6.1mm cr / 5mm cl
First revision as DOC
Update to connectors
2140711
Field Light Enable
J1
5 MnL Plug
J3
F
Column TS
4
DATE
12 Aug 2009
8 Apr 2010
6 Dec 2011
18 Apr 2013
J7
Unused
4 mMnL
Plug
J12
J15 14 Header 0.1"
AC Present
Lamp
RTN
3 mMnL
Plug
AC Line Filter
MADE BY
Butzine
Butzine
Jablonowski
Sulma
MFG Interface
J11
6 Molex pin
REV
1
2
3
4
15A Fast-Blow
J10
6 Molex Rec
Pack 4
CN2
15 Hsub-D Plug
J2
4 mMnL
Plug
4 mMnL
REC
Pack 3
CN2
15 HSub-D REC
J1
3 mMnL
Plug
3 mMnL
REC
Pack 2
CN2
2 mMnL REC
4 mMnL Rec
Pack 1
CN2
6 Molex Rec
3 Molex Pin
3
6 MicroMatch
REC
6 MicroMatch
Plug
Breaker Trip
15 Hsub-D Rec
3 Molex Rec
2
CN5
Battery Temp Feedback
15 HSub-D Plug
J8
9 SubD Rec
9 SubD Plug
Cord
Reel
802.15.4
Zigbee
Wireless
Handswitch
5350048
5350050
REVISIONS
4mm cr / 2.5mm cl
Line/Gnd and Neutral/Gnd
Battery Temp Feedback
6 MnL Rec
6 MnL Plug
J3
*1MOPP A/C
*
10 MnL Plug
2MOPP 24Vdc
Prep, Exp, Light
2 mMnL Plug
2MOPP Batt
9 MnL Rec
9 MnL Plug
J1
3 Terminal 0.375"
9 SubD Rec
2MOPP A/C
A/C Isolation Barrier
4000V dielectric
8mm cr / 5mm cl
9 SubD Plug
Mantis Supply
(SL Power) J2
5311985
Breaker
J10
10 MnL REC
RJ11-REC
5 MnL Plug
Breaker Trip
Hospital Outlet
85-264 VAC
50/60 Hz
RJ-11 Plug
J1
5 MnL REC
6 MnL Rec
J5
RJ11-REC
Future
6 MnL Plug
J7
2 Phoenix Plug
-Batt
J11, J12,
J13, J14
Cricket
Battery
Board
5350008
2 Phoenix REC
1
4 MnL REC
Battery Temp
150VDC Battery Stack
(12) 17Ah VRLA; (4)
36VDC Packs
15A
D
10A
J6
3A
F1
J1, J2, J3, J4
H
F3
5 MnL Plug
F2
Drive Login
Active Board
5378850
Drive Login
Electrode Board
5378852
15 HSub-D Plug
5 MnL REC
J8
15A
5 MnL REC
2 Phoenix Plug
2 Phoenix REC
G
3 Phoenix REC
J5
I/O
6 MicroMatch
REC
6 MicroMatch
Plug J7
Touch
Screen
15 HSub-D REC
24VDC
4 MnL REC
FPGA JTAG
C
+24VDC
Wireless
Handset
Charge
Receptacle
3 Phoenix Plug
J2
Overlay
Board
5368325
I/O Expander I/F
RJ-11 Plug
J12 10 Header 0.1"
J8
4 MnL REC
4 MnL Plug
J2
J1
HS
5 MnL Plug
F
J7
Board
Data
Module
5350038
J1
I/O
Inverter
CN4
J11 14 Header 0.1"
MFG Interface
10 MicroFit
Plug
10 MicroFit
REC
9 Sub-D Plug
9 Sub-D REC
9 Sub-D REC
J6
J3
2MOPP Batt
J10
2 mMnL Plug
2mMnLREC
J6, J7
LVLE2
5192958
2 mMnL REC
3mMnLPlug
J5
2mMnLPlug
J4
9 Sub-D Rec
1MOPP Batt
9 Sub-D Plug
J2
3mMnLREC
S
P
Y
D
E
R
J9
J9
2mMnLPlug
T
O
J8
2mMnLREC
24 VDC
4 mMnL REC
J7
15“ LCD
CN3
L
O
C
U
S
T
802.15.4
Zigbee
J1
Pwr,
Dim,
On/Off
5 AMPMODU
REC
15 Sub-D REC
J4
J5
8 Bit
LVDS
Power
5 AMPMODU
Plug
2 Phoenix Plug
J1
14 Socket 0.1"
T
O
Spyder
System Controller
5350002 - X
14 Header 0.1"
J3
15 Sub-D Plug
4 mMnL Plug
6 mMnL Plug
15 Hsub-D Plug
J2
15 HSub-D REC
3 mMnL Plug
3 mMnL REC
2MOPP Batt
J3
4 MnL Plug
2 mMnL Plug
J1
2 mMnL REC
12 MiniFit Plug
Locust
Drive Board
5350006 - X
2MOPP Batt
J2
2 Phoenix REC
+48VDC
12 VDC
B
J4
CN2
30kW Optional Aux. Module
Sensor
J8
J11 10 Header 0.1" CPLD JTAG
J12 2 Header 0.1" SPARE PIEZO
J4
2 Phoenix Plug J3
Power Module
6 mMnL REC
J13 20 Header 0.1" SPARE I/O
J10 14 Header 0.1" DSP JTAG
8 MnL Plug
J5
J22
1MOPP Batt
14 Socket 0.1"
12 MnL Plug
12 MnL REC
J6
J23
14 Header 0.1"
15 Sub-D Plug
15 Sub-D REC
J1
USB B REC
USB A REC
J3
J18
15kW Main Aux. Module
Drive
8 MnL REC
9 Sub-D Plug
Column TS
12 MiniFit REC
+Batt
Tube
Park
Latch
Very High Voltage
6 MicroFit
Plug
6 MicroFit
REC
Detector Park
Switch
USB B REC
J19
26 Hsub-D Plug
Rotational
Brake
Speaker
J5
20 MDR Plug
J2
USB B Plug
26 Hsub-D Plug
Bumper
Speaker
USB A Plug
26 Hsub-D REC
12 MnL Plug
Hard Brake
Release
Switch
4 Phoenix Plug
4 Phoenix REC
USB B Plug
4 Microfit
Plug
4 Microfit
REC
15 Sub-D Plug
USB A Plug
20 MDR REC
Mini-75 Plug
120A
20 MDR REC
4 Medi-Snap
PLUG
4 Medi-Snap
REC
BSCAN
(Service
Access)
15 Hsub-D Plug
2 MnL Plug
3 mMnL
REC
3 mMnL
PLG
20 MDR Plug
J10
USB A REC
A
AC Line Voltage
LVDS
15 Hsub-D REC
3 mMnL Plug
J9
Toshiba
E7901X
J3
15 Sub-D Plug
4 mMnL Plug
Arm
Brake
J8
15 Sub-D REC
12 MnL REC
Vertical
Brake
J7
5 SL Plug
15 Sub-D REC
Lock
Release
Switches
J6
J11
5 SL REC
2 MnL REC
Halls, Bar
J9
Mini-75 REC
1MOPP Batt
J1
2 Phoenix Plug
J2
3 mMnL REC
Drive
Handle
E
J10
J7
J12
HV Tank
4 mMnL REC
9 Sub-D REC
D
J11
HV
2 Phoenix REC
J8
Detector
Power
Supply
(DPS 5419392)
USB A REC
PC
HV
Caterpillar
Base Transition Board
5350010
USB A REC
1MOPP 240Vac
2MOPP 60Vdc
1500V
J13
Coil
Power
Relay
Contact
USB A REC
11 Molex REC
J7
USB A Plug
USB A REC
20 Hirose REC
J3
USB A Plug
USB A REC
11 Molex PLUG
J4
USB A Plug
SMA
AC
Battery Voltage
20 Hirose PLUG
2 mMnL REC
USB A Plug
USB A Plug
DC
Mean of Patient Protection
xMOPP = Levels of MOPP
6 MicroFit Plug
4 MnL REC
USB A Plug
Dose Area
Product
Meter
(DAP)
6 MicroFit REC
5 HDR REC
USB Bulkhead
10 Molex Plug
2 mMnL REC
USB A Plug
USB A REC
USB
Thumbdrive
(Service Key)
8
10 Molex REC
4 MnL REC
RJ-45 R
J1
power
data
7
20 Molex Plug
5 HDR REC
RJ-45 R
J2
Keyboard
20 Molex REC
2 mMnL Plug
RJ-45 P
UWB
Adapter
(Detector)
802.15.4
Zigbee
6
DVD/CD
Burner
Hornet UIF Board
5350004 - X 26 Hsub-D REC
4 MnL Plug
Zigbee
Adapter
(Barcode)
802.15.3a
UWB
Ring Term
5 HDR Plug
802.11
WiFi
Screw Term
2 mMnL Plug
24VDC
RJ-45 P
Federal Plug
4 MnL Plug
RJ-45 P
Federal REC
5 HDR Plug
C
12 Microfit
PLG
12 Microfit
REC
M3W3C P
B
R
Hypertronics
5
12VDC
3 mMnL
REC
3 mMnL
PLG
Brake
Brake
L
Hospital
Network
M3W3P R
Halls
Backup
Tether
Hypertronics
3 mMnL
REC
3 mMnL
PLG
Halls
4
Detector
Charge
Receptacle
On / Off Button
TITLE
REV
SuperBee System Architecture Diagram
FIRST MADE FOR:
SuperBee
GE
HEALTHCARE
GE
MEDICALTECHNOLOGIES
SYSTEMS
MILWAUKEE,
WISCONSINWIUSA
MILWAUKEE,
7
MADE USING VISIO PRO 2003
DOC0645488
SHEET
1
4
OF
H
1
8
Figure 2-1 System architecture schematic
Chapter 2 System interconnects
Page 21
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 2.2 System wiring
1
2
802.15.3a
UWB
Detector
3
802.15.4
Zigbee
Zigbee
Barcode
Reader
3 mMnL
REC
3 mMnL
PLG
A
Halls
Halls
5 HDR Plug
4 MnL Plug
2 mMnL Plg
4 MnL REC
2 mMnL REC
J3
J7
J5
802.11
WiFi
802.15.4
Zigbee
UWB
802.15.3a
Adapter
UWB
(Detect
or)
º
RJ-45 P
RJ-45 P
USB A Plug
USB A Plug
USB A Plug
USB A Plug
USB A Plug
RJ-45 R
SMA
USB A REC
USB A REC
USB A REC
USB A REC
USB A REC
J2
J1
J12
J9
J6
J7
J8
J13
3 Phoenix
REC
3 Phoenix
PLG
5 MnL Rec
5 MnL Plug
J8
J14
J12
9 Sub-D REC
J1
J1
J2
2 Microfit 2 Microfit
PLG
REC
2mMnL
PLG
2mMnL
REC
J4
J3
4 Minifit
REC
E
J17 10 Header 0.1"
SPI Programmer
J7
J3
J13
24
AC Present
Lamp
F
Thorax
Bulkhead
36
J1
J3
47
5 MnL
PLG
5 MnL
REC
FPGA JTAG
5 MnL
PLG
5 MnL
Rec
I/O Expander I/F
J16 10 Header 0.1"
59
3 mMnL
Rec
3 mMnL
Plug
J15 14 Header 0.1"
2140711
Update DPM & Bd Part # w/- X
5
Section 2.2 System wiring
6
MADE
CHECK
APPR
OTHER
APPROVALS
A. ALCALA
DD-MM-YY
23-04-10
35
J5
44
On / Off Button
Collimator
TITLE
REV
SuperBee System Wiring Diagram
FIRST MADE FOR:
SuperBee
GE
HEALTHCARE
GE
MEDICALTECHNOLOGIES
SYSTEMS
MILWAUKEE,
WISCONSINWIUSA
MILWAUKEE,
7
G
Field light enable.
Collimator lamp pwr
J2
2MnL PLG
DESCRIPTION
CHANGED TO DET. PWR. SUPPLY
ADDED CABLE 72
46-2 WAS 46
40
2MnL REC
04/08/2013
PCN NO.
2117013
2124431
2131197
2 MnL PLG
J6
2 MnL REC
J4
J5
4 MnL
Rec
4 MnL
Plug
Firefly
Charger Board
5350000 - X
J9
REVISIONS
E.SULMA
MFG Interface
4 MnL
Plug
4 MnL
REC
Pack 4
J10
J11
3 mMnL
Plug
3 mMnL
REC
Pack 3
6 mMnL REC
J2
4 mMnL Rec
Pack 2
6 Micromatch
REC
6 Micromatch
Plug
Thorax Bulkhead
CN2
3 Microfit
REC
CN5
3 Microfit
PLG
CN4
CN2
15 HSub-D REC
Faston Tab
2 mMnL REC
Faston REC
6 mMnL PLG
3 Molex
REC
15 HSub-D Plug
3 Molex plg
9 SubD Rec
Pack 1
CN2
5 AMPMODU REC
RJ-11 Plug
802.15.4
Zigbee
2188371-2
23(b)
2 mMnL Plug
J1
Figure 2-2 System wiring
Page 22
RJ11-REC
9 SubD Plug
4
6 MnL Rec
3
6 MnL Plug
AC Line Filter
10 mMnL PLG
20
REV
MADE BY
DATE
3
A. ALCALA
05/26/2011
4
M.ZIMMERMANN 10/25/2011
5
L.NZUDIE
04/19/2011
6
2
19
37
38
10 mMnL REC
15A Fast-Blow
9 MnL Rec
30
Hospital Outlet
85-264 VAC
50/60 Hz
Drive Login
Electrode
Board
CLS
5450200
3 Terminal 0.375"
23
Cord
Reel
1
9 SubD Rec
J1
9 SubD Plug
10 mMnL PLG
J3
Breaker
6 MnL Rec
10 mMnL REC
2 Phoenix Plug
J10
H
2 Phoenix REC
J5
J2
9 MnL Plug
07
Mantis Supply
(SL Power)
5311985
Breaker Trip
06
RJ11-REC
5 MnL REC
6 MnL Plug
J7
5 MnL Plug
J11, J12,
J13, J14
Cricket
Battery
Board
5350008
5 MnL REC
Battery Temp
J1, J2, J3, J4
4 MnL PLG
J6
4 MnL REC
J8
2 Phoenix REC
3 Phoenix REC
2 Phoenix Plug
G
4 MnL REC
D
Drive Login
Active
Board
HS
RJ-11 Plug
5 MnL Plug
J1
Wireless Hand
Switch Receptacle
6 Micromatch
REC
6 Micromatch
Plug
Wireless
Handswitch
05
09
21
3 Phoenix Plug
14 N4600 Rec
J5
J6
15 HSub-D REC
02
4 MnL Plug
14 N4600 Plug
J9
5 MnL REC
22
16
34
Breaker Trip
2 mMnL Plug
J3
5 MnL Plug
Hard Brake
Release
Switch
Board
Data
Module
5350038
Overlay
Board
C
Touch
Screen
15 HSub-D Plug
J5
J6, J7
49-2
J2
29
Inverter
I/O Expander I/F
10 MicroFit Plug
J4
2 mMnL REC
TBD
2 mMnL Plug
15 Hsub-D Plug
2 mMnL REC
4 MnL PLG
3 mMnL Plug
J2
15 HSub-D REC
3 mMnL REC
39
J3
4 MnL REC
2 mMnL Plug
Vertical
Brake
2 mMnL REC
3 mMnL
REC
3 mMnL
Plug
J1
08
LVLE2
5192958
MFG Interface
10 MicroFit REC
SPARE PIEZO
J2
9 Sub-D REC
J11 14 Header 0.1"
14 N4600 Plug
CPLD JTAG
2 Header 0.1"
J8
04
15 Hsub-D Plug
14 Header 0.1"
J12
J10
J9
15 Hsub-D REC
J11
4 mMnL REC
9 Sub-D PLG
J8
J7
9 Sub-D REC
DSP JTAG
2 mMnL Plug
14 Header 0.1"
2 mMnL REC
J10
25
6 mMnL Plug
SPARE I/O
Locust
Drive Board
5350006 - X
5503004
F
4 mMnL Plug
8 mMnL Plug
20 Header 0.1"
J4
Arm
Brake
J5
J13
J9
5503006
Collimator /
Lock Release
Switches
J6
6 mMnL REC
J7
12 MiniFit Pin
12 MiniFit REC
E
12 MnL Plug
12 MnL REC
8 mMnL REC
43
15 Sub-D Plug
15 Sub-D REC
2 Phoenix PLG
6 mMnL REC
15
9 Sub-D Plug
9 Sub-D REC
Drive
Handle
J8
14 N4600 REC
D
J7
5 AMPMODU Plug
10
2 Phoenix REC
6 mMnL PLG
802.15.4
Zigbee
J1
28
CN3
J1
32
J4
01
J5
CN2
J2
9 Sub-D Plug
11^
15kW Main
Aux.Module
9 Sub-D REC
2MnL PLG
Detector Park
Switch
J2
Spyder
System Controller
5350002 - X
J1
J3
2 MnL REC
Tube Park
Latch
2 Phoenix
REC
2 Phoenix
Plug
46-2º
6 MicroFit
Plug
6 MicroFit
REC
5503002
13
14
56*
15 SubD
REC
15 SubD
PLG
3 Phoenix
PLG
3 Phoenix
REC
03
J22
18
15“ LC D
CN2
4 Microfit PLG
4 Microfit REC
2 MnL Plug
2 Phoenix
Plug
2 Phoenix
REC
J1
J18
J4
11 Molex REC
2 MnL REC
Rotational
Brake
4 Phoenix
Plug
4 Phoenix
REC
Power Module
J6
Thorax
Bulkhead
J23
11 Molex PLUG
55*
60
USB B REC
J3
20 Hirose REC
3 mMnL
REC
3 mMnL
PLG
USB A REC
J19
20 Hirose PLUG
12 MnL Plug
USB B REC
J2
B
6 MicroFit Plug
15 Sub-D Plug
20 MDR Plug
4 Microfit
PLG
4 Microfit
REC
6 MicroFit REC
2 MnL Plug
15 Sub-D
Plug
15 Sub-D
REC
USB B Plug
10 Molex Plug
3 mMnL Plug
HV Tank
USB A Plug
3. DASHED LINES SHOW ALTERNATE CONNECTIONS (DEPENDING ON
DIGITAL OR DIGITAL READY/ANALOG ) (WIRING PART OF DPS ASSEMBLY)
5503005º
10 Molex REC
4 mMnL Plug
30kW Optional
Aux. Module
50^
USB B Plug
A
* - USED IN DIGITAL SYSTEMS ONLY
^ - USED IN DIGITAL AND DIGITAL READY SYSTEMS ONLY
º - USED WITH ACCESSORIES ONLY
~ - USED IN ANALOG SYSTEMS ONLY
20 Molex Plug
12 MnL REC
Mini-75 REC
12^
20 MDR REC
1. ALL CABLES HAVE BASE NUMBER 55570XX EXCEPT
OTHERWISE INDICATED BY A FULL PART NUMBER. FOR
EACH PART NUMBER, REPLACE THE XX WITH THE TWO
DIGITS SHOWN.
2. KEY:
20 Molex REC
15 Sub-D REC
Bumper
USB A Plug
26 Hsub-D Plug
2 MnL REC
27
20 MDR REC
BSCAN
(Service
Access)
26 Hsub-D Plug
3 mMnL REC
26
J10
USB A REC
26 Hsub-D REC
4 mMnL REC
USB A Plug
4Microfit
PLG
4 Microfit
REC
5503001
15 Sub-D Plug
J1
15 Sub-D REC
J2
15 SubD
Plug
15 SubD
REC
C
J10
5 Pin C-Grid Plug
45
5 Pin C-Grid REC
Toshiba
E7901X
Mini-75 Plug
J11
Dose Area
Product
Meter
(DAP)
4 Medi-Snap
PLUG
4 Medi-Snap
REC
58
J3
20 MDR Plug
Speakers
Federal Plug
Federal REC
Ring Term
(DPS 5419392)
USB
Thumbdrive
(Service Key)
PC
Screw Term
Detector
Power
Supply
52^
RJ-45 R
J11
8
NOTES:
52^
52^
54*
J9
Power
Relay
Contact
7
USB Bulkhead
Coil
Caterpillar
Base Transition Board
5350010
J8
6
Hornet UIF Board
5350004 - X 26 Hsub-D REC
B
J6
RJ-45 P
5
Zigbee
Adapter
(Barcode)
51^
12 Microfit
PLG
12 Microfit
REC
3 mMnL
REC
3 mMnL
PLG
2 mMnL REC 5 HDR REC
Hypertronics
Positronic
P
4 MnL Plug
4 MnL REC
Hospital
Network
Positronic
R
2 mMnL Plg
5 HDR Plug
5 HDR REC
J4
R
Hypertronics
Backup
Tether
41*
72*
Brake
Brake
L
8 mMNL
PLG
8 mMNL
REC
66*
4
Detector
Charge
Receptacle
57*
MADE USING VISIO PRO 2003
5507000WIR
8
SHEET
1
6
OF
1
H
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 3 Jumpers, switches, LEDs, test points
Section 3.1 Firefly charger board 5350000-2
3.1.1 Jumpers
Jumper
•
J17 - Mantis
Safe Charge
J20 - Mantis
Heartbeat
Description
Jumper across pins 1 and 2 is the default - Normal operation. The Mantis charger requires the Firefly to be powered and
communicating in order to charge the batteries.(Also true if the Jumper is lost or not connected)
•
Jumper across pins 2 and 3 - Safe Charge Mode. Used if the system batteries are too low to turn the system on, setting this
jumper and plugging in the system will trickle charge the batteries. WARNING: IF the jumper is left in this mode, it is not
possible to charge at full power and will generate Error messages to the user if the jumper is left in this way. This is for recovery
only.
•
Jumper across pins 1 and 2 is the default - Normal operation. Heartbeat communication from Firefly to Mantis is required for
charger operation. (Also true if the Jumper is lost or not connected).
•
Jumper across pins 2 and 3 - Firefly to Mantis Heartbeat communication is not required. Used for troubleshooting ONLY
3.1.2 Switches
Switch
Description
S1
FPGA Reset
S2
Unused
3.1.3 LEDs
LED
Color
Name
Description
DS1
Green
1V2
Regulated power supply status
DS2
Green
5V0
Regulated power supply status
DS3
Green
3V3
Regulated power supply status
DS4
Green
2V5
Regulated power supply status
DS5
Green
NIOS APP
Firmware App
DS6
Yellow
NIOS SAFE
Firmware Safe/Boot
DS7
Green
NIOS HB
Firmware heartbeat
DS8
Green
VHDL HB
VHDL heartbeat
DS9
Green
100%
System batteries 100%
DS10
Green
80%
System batteries 80%
DS11
Green
60%
System batteries 60%
DS12
Yellow
40%
System batteries 40%
DS13
Red
20%
System batteries 20%
DS14
Red
E0
FPGA error E0
DS15
Red
E1
FPGA error E1
DS16
Red
E2
FPGA error E2
Chapter 3 Jumpers, switches, LEDs, test points
Page 23
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
LED
Color
Name
Description
DS17
Red
E3
FPGA error E3
DS18
Green
5V0_ISO
Regulated power supply status
DS19
Yellow
VHDL SAFE
Safe VHDL
DS20
Green
VHDL APP
App VHDL
3.1.4 Test points
Test Point
Name
Description
TP1
LGND
Logic ground (in low voltage area of board)
TP2
24V0
Power In from LVLE2
TP3
1V2
1.2Vdc power supply
TP4
5V0
5.0Vdc power supply
TP5
2V5
2.5Vdc power supply
TP6
3V3
3.3Vdc power supply
TP7
LGND
Logic ground (in low voltage area of board)
TP8
LGND
Logic ground (in low voltage area of board)
TP9
LGND
Logic ground (in low voltage area of board)
TP10
PGND
Power ground (in high voltage area of board)
TP11
On_Off_Switch Status
LVLE2 interface signal
TP12
AC_Present Status
LVLE2 interface signal
TP13
PGND
Power ground (in high voltage area of board)
TP14
PGND
Power ground (in high voltage area of board)
TP15
5V0_ISO
5.0Vdc isolated power supply
TP16
PGND
Power ground (in high voltage area of board)
TP17
PGND
Power ground (in high voltage area of board)
TP18
LGND
Logic ground (in low voltage area of board)
TP19
LGND
Logic ground (in low voltage area of board)
Section 3.2 Spyder system controller board 5350002-4
3.2.1 Jumpers
None
Page 24
Section 3.2 Spyder system controller board 5350002-4
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
3.2.2 Switches
Switch
Name
S1
MODE
S2
TAP
3.2.3 LEDs
LED
Color
Name
DS1
Green
ISO_3V3
DS2
Green
24V0
DS3
Green
12V0
DS4
Green
5V0
DS5
Green
3V3
DS6
Red
USB
DS7
Red
BD_OVRHT
DS8
Green
VHDL_HB
DS9
Red
HEADER
DS10
Red
FPGA_OVRHT
DS11
Green
UP1_HB
DS12
Red
BSCAN
DS13
Red
XR_ON
DS14
Green
UP2_HB
DS15
Red
DEBUG
DS16
Red
EXP_INH
DS17
Red
ERROR_PRES
DS18
Green
2V5
DS19
Green
1V2
DS20
Green
DJINN
DS21
Green
ZBEE HB
DS22
Green
FPGA_NORM
DS23
Yellow
FPGA_SAFE
DS24
Red
BAD TERM
DS25
Red
BAD TERM
DS26
Red
BAD TERM
DS27
Red
BAD TERM
DS30
Green
DRIVE
DS33
Green
CHARGE
DS36
Green
MFG
DS37
Green
RESET
DS38
Green
XR_CMD
Chapter 3 Jumpers, switches, LEDs, test points
Page 25
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
LED
Color
Name
DS41
Green
EXP_EN
DS45
Yellow
XR_ON
3.2.4 Test points
Test Point
Name
Description
TP1
12V
24V --> 12V
TP2
5V
24V --> 5V
TP3
GND
Test points located around board
TP4
GND
Test points located around board
TP5
GND
Test points located around board
TP6
GND
Test points located around board
TP7
GND
Test points located around board
TP8
1V2
5V --> 1.2V
TP9
3V3
12V --> 3.3V
TP10
2V5
3.3V --> 2.5V
TP11
ISO_3V3
ISOLATED: 24V --> ISO_3.3V
TP12
GND
Test point located in isolated region
TP13
TRSTB0_N
"Use TP to disable OE"
TP14
I/O
FPGA I/O
TP15
I/O
FPGA I/O
TP16
I/O
FPGA I/O
TP17
I/O
FPGA I/O
TP18
I/O
FPGA I/O
TP19
I/O
FPGA I/O
TP20
I/O
FPGA I/O
TP21
I/O
FPGA I/O
TP22
DEV_OE
Connected to pin of U35
TP23
DEV_NCLR
Connected to pin of U35
Section 3.3 Hornet UIF board 5350004-2
3.3.1 Jumpers
None
3.3.2 Switches
None
Page 26
Section 3.3 Hornet UIF board 5350004-2
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
3.3.3 LEDs
LED
DS1
Color
Green
Name
5V
DS2
Green
24V
DS3
Green
12V
DS4
Green
3.3V
3.3.4 Test points
Test Point
Name
TP1
5V
TP2
24V
TP3
GND
TP4
12V
TP5
GND
TP6
3.3V
TP7
GND
TP8
GND (rear of board)
Section 3.4 Locust drive board 5350006-2
3.4.1 Jumpers
None
Chapter 3 Jumpers, switches, LEDs, test points
Page 27
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
3.4.2 Switches
Switch
Description
S1
Manual Reset
3.4.3 LEDs
LED
Color
Name
Description
DS1
Red
LMOTOR
Left motor Fuse - Indicates that the left motor fuse is blown
DS2
Red
RMOTOR
Right motor Fuse - Indicates that the right motor fuse is blown
DS3
Red
PERIPH
Peripheral Fuse - Indicates that peripheral power fuse is blown
DS4
Red
BRAKES
Brakes Fuse - Indicates that a Brake fuse is blown
DS5
Red
SYSTEM_RESET
System Reset - Indicates that board has been reset
DS6
Red
E3
IO_B1 activity
DS7
Red
E2
IO_B3 activity
DS8
Red
E1
IO_B4 activity
DS9
Red
E0
IO_B5 activity
DS10
Green
CPLD_HEARTBEAT
Indicates that CPLD is running
DS11
Green
DSP_HEARTBEAT
Indicates that DSP is running
DS12
Red
BUZZER
Indicates status of Buzzer on
DS13
Green
5V0
Indicates that the 5V is present
DS14
Green
3V3
Indicates that the 3.3V is present
DS15
Green
15V0
Indicates that the 15V is present
DS16
Green
1V8
Indicates that the 1.8V is present
DS17
Green
DRIVE_EN_BARr
24V_RETURNS<4>
DS18
Yellow
DSP_SAFEMODE
Indicates that DSP is in safe mode
3.4.4 Test points
Page 28
Test Point
Name
Description
TP1
2V048
Reference
TP2
5V0
Power supply
TP3
3V3
Power supply
TP4
15V0
Power supply
TP5
1V8
Power supply
TP6-TP11
LGND
Ground
TP12
JTAG Mux Enable Low
Tied to OE_N pin of U4
TP13
JTAG Mux Enable High
Through pullup resistor to 3V3
TP14
BATT
Battery power
TP15
BATTSW
Switched Battery Power
Section 3.4 Locust drive board 5350006-2
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Test Point
Name
Description
TP17-TP19
PGND
Power Ground
TP20
VBRAKE
Vertical Brake Output
TP21
ABRAKE
Arm Brake Output
TP22
SOL
Solenoid Output
TP23
ROTBRAKE
Rotational Brake Output
TP24
RBRAKE
Right Motor Brake Output
TP25
LBRAKE
Left Motor Brake Output
Section 3.5 Cricket battery board 5350008
3.5.1 Jumpers
None
3.5.2 Switches
None
Chapter 3 Jumpers, switches, LEDs, test points
Page 29
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
3.5.3 LEDs
LED
Color
Description
DS1
Yellow
Breaker ON
3.5.4 Test points
Test Point
Description
Meaning
Measurement of total battery stack voltage AFTER the system circuit breaker. This
power goes to the Djinn, Locust (through Fuses F2 and F3), and Firefly (through F1).
TP1
Breaker_Out
TP2
Pack 3+
Measurement of voltage sum of battery packs 1, 2, and 3.
TP3
Pack 2+
Measurement of voltage sum of battery packs 1 and 2.
TP4
Charge Fuse Out
Test point for checking battery voltage after the fuse to the Firefly board. This is the
path for recharging the batteries, powering the LVLE2, the On/Off button, and the
Collimator Lamp Supply.
TP5
Pack 1+
Measurement of battery pack 1 voltage.
TP6
GND
Chassis ground, Battery stack (-)
TP7
Pack 4+
Measurement of total battery stack voltage BEFORE the system circuit breaker.
TP8
Drive Fuse1 Out
Test point for checking battery voltage after the main fuse to the Locust board. This
power used for driving, brake/lock releases, solenoid.
TP9
Drive Fuse2 Out
Test point for checking battery voltage after secondary fuse to the Locust board. This
power used for emergency brake release only.
Section 3.6 Caterpillar base transition board 5350010
3.6.1 Jumpers
None
3.6.2 Switches
None
3.6.3 LEDs
None
3.6.4 Test points
None
Page 30
Section 3.6 Caterpillar base transition board 5350010
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 3.7 Board data module 5350038
3.7.1 Jumpers
None
3.7.2 Switches
None
3.7.3 LEDs
None
3.7.4 Test points
None
Section 3.8 Collimator lamp supply board 5450200
3.8.1 Jumpers
None
3.8.2 Switches
None
Chapter 3 Jumpers, switches, LEDs, test points
Page 31
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
3.8.3 LEDs
LED
Color
Name
Description
DS1
Green
24VOUT
Indicates the power supply is ON
3.8.4 Test points
Test Point
Name
Description
TP1
GND_POWER
Chassis Ground Test Point
TP2
GND_LOGIC
Power Supply Output Return Test Point
TP3
BATT
Supply Input (Battery Voltage) Test Point
TP4
VOUT
Power Supply Output Voltage Test Point
TP5
SW_OUT
Collimator Lamp switch signal out (24V when the system is on)
TP6
SW_RTN
Collimator Lamp switch return signal (24V when button is pressed on collimator)
3.8.5 Potentiometers
Pot
R3
Description
10k single-turn potentiometer. Turning clockwise increases the power supply output
voltage. Turning counter-clockwise decreases the power supply output voltage. Adjust as
needed to meet light output requirements.
Section 3.9 Mantis power supply 5311985
3.9.1 Jumpers
None
3.9.2 Switches
None
Page 32
Section 3.9 Mantis power supply 5311985
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
3.9.3 LEDs
LED
Color
Description
Green
AC Detect
Green
Main Output ON
3.9.4 Test points
None
Section 3.10 LVLE2 power supply 5192958
3.10.1 Jumpers
None
3.10.2 Switches
None
3.10.3 LEDs
None
3.10.4 Test points
None
Chapter 3 Jumpers, switches, LEDs, test points
Page 33
GE HEALTHCARE
REVISION 3
Page 34
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 3.10 LVLE2 power supply 5192958
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 4 Firefly charger board 5350000-2
Breaker Trip
05
09
15 HSub-D Plug
6 mMnL PLG
2 mMnL REC
15 HSub-D REC
6 mMnL REC
J2
J10
J1
J8
J11
J12
9 Sub-D REC
MFG Interface
SPI Programmer
J13
J9
J5
36
40
J6
2 MnL PLG
J4
Firefly
Charger Board
5350000 - X
J3
4 MnL
Plug
J17 10 Header 0.1"
3 mMnL
Plug
FPGA JTAG
2 MnL REC
9 SubD Rec
J16 10 Header 0.1"
J7
4 MnL
Plug
4 MnL
REC
6 MnL Rec
9 SubD Plug
I/O Expander I/F
3 mMnL
Plug
3 mMnL
REC
10 mMnL REC
6 MnL Plug
J15 14 Header 0.1"
59
4 mMnL Rec
J14
3 Molex plg
2 mMnL Plug
3 Molex
REC
10 mMnL PLG
20
9 MnL Rec
9 MnL Plug
19
5 MnL REC
5 MnL Plug
07
23(b)
35
Figure 4-1 Firefly portion of wiring diagram
Chapter 4 Firefly charger board 5350000-2
Page 35
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 4.1 Firefly schematics
Figure 4-2 5350000ADW
Page 36
Section 4.1 Firefly schematics
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Figure 4-3 5350000SCH_s1
Chapter 4 Firefly charger board 5350000-2
Page 37
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Figure 4-4 5350000SCH_s2
Page 38
Section 4.1 Firefly schematics
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Figure 4-5 5350000SCH_s3
Chapter 4 Firefly charger board 5350000-2
Page 39
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Figure 4-6 5350000SCH_s4
Page 40
Section 4.1 Firefly schematics
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'
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 4 Firefly charger board 5350000-2
Page 41
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 42
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Chapter 4 Firefly charger board 5350000-2
Page 43
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 44
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Chapter 4 Firefly charger board 5350000-2
Page 45
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 46
Section 4.1 Firefly schematics
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Chapter 4 Firefly charger board 5350000-2
Page 47
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 48
Section 4.1 Firefly schematics
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OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Figure 4-15 5350000SCH_s13
Chapter 4 Firefly charger board 5350000-2
Page 49
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 50
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OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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Chapter 4 Firefly charger board 5350000-2
Page 51
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 4 Firefly charger board 5350000-2
Page 53
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 54
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OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 4 Firefly charger board 5350000-2
Page 55
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 56
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Chapter 4 Firefly charger board 5350000-2
Page 57
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 4 Firefly charger board 5350000-2
Page 59
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 60
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GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 4 Firefly charger board 5350000-2
Page 61
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 62
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 4 Firefly charger board 5350000-2
Page 63
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
27+(5 '(&283/,1*
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Page 64
Section 4.1 Firefly schematics
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GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 4.2 Firefly connector cables
Figure 4-31 5557005, Firefly to Spyder
Chapter 4 Firefly charger board 5350000-2
Page 65
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 4-32 5557024, Firefly to AC present lamp
Page 66
Section 4.2 Firefly connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557036ADW_r2.pdf Page 2 of 2
Figure 4-33 5557036, Firefly to CLS J1
Chapter 4 Firefly charger board 5350000-2
Page 67
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 4-34 5557040, Firefly to CLS J2
Page 68
Section 4.2 Firefly connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 4-35 5557035, Firefly to on/off button
Chapter 4 Firefly charger board 5350000-2
Page 69
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557047ADW_r3.pdf Page 2 of 2
Figure 4-36 5557047, CLS to collimator lamp
Page 70
Section 4.2 Firefly connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 4-37 5557044, Firefly to power switch
Chapter 4 Firefly charger board 5350000-2
Page 71
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 4-38 5557020, Firefly J4 to Mantis J3
Page 72
Section 4.2 Firefly connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 4-39 5557019, Firefly J9 to Mantis J2
Chapter 4 Firefly charger board 5350000-2
Page 73
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557009ADW_r4.pdf Page 2 of 2
Figure 4-40 5557009, Firefly to LVLE2
Page 74
Section 4.2 Firefly connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 5 Spyder system controller 5350002-4
52
52
54*
52
USB A Plug
USB A Plug
USB A Plug
USB A Plug
USB A REC
USB A REC
USB A REC
USB A REC
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J7
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4 Medi-Snap
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Thumbdrive
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USB A Plug
PC
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20 MDR REC
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12^
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USB B Plug
USB A Plug
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5350004 - X
J22
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26 Hsub-D REC
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5350002 - X
J10
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15 HSub-D REC
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J2
J10
J1
Figure 5-1 Spyder portion of wiring diagram
Chapter 5 Spyder system controller 5350002-4
Page 75
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 5.1 Spyder schematics
Figure 5-2 5350002ADW
Page 76
Section 5.1 Spyder schematics
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 77
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 78
Section 5.1 Spyder schematics
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 79
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Section 5.1 Spyder schematics
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OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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Chapter 5 Spyder system controller 5350002-4
Page 81
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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Chapter 5 Spyder system controller 5350002-4
Page 83
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 85
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 87
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 89
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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Chapter 5 Spyder system controller 5350002-4
Page 91
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 93
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 95
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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Chapter 5 Spyder system controller 5350002-4
Page 97
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 98
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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Chapter 5 Spyder system controller 5350002-4
Page 99
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 101
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
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GE HEALTHCARE
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GE HEALTHCARE
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Figure 5-53 5350002SCH_s51
Chapter 5 Spyder system controller 5350002-4
Page 127
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 128
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 129
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 130
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 131
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 132
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 133
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 134
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GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 5 Spyder system controller 5350002-4
Page 135
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 5.2 Spyder connector cables
Approved Document - 5557046ADW_r3.pdf Page 2 of 2
Figure 5-62 5557046, Spyder to DAP
Page 136
Section 5.2 Spyder connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 5-63 5557001, Spyder to Hornet
Chapter 5 Spyder system controller 5350002-4
Page 137
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557049ADW_r4.pdf Page 2 of 2
Figure 5-64 5557049, Spyder to Board Data Module
Page 138
Section 5.2 Spyder connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557006ADW_r7.pdf Page 2 of 2
Figure 5-65 5557006, Spyder to wired handswitch
Chapter 5 Spyder system controller 5350002-4
Page 139
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557005ADW_r3.pdf Page 2 of 2
Figure 5-66 5557005, Spyder to Firefly
Page 140
Section 5.2 Spyder connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557004ADW_r6.pdf Page 2 of 2
Figure 5-67 5557004, Spyder to LVLE2
Chapter 5 Spyder system controller 5350002-4
Page 141
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557003ADW_r4.pdf Page 2 of 2
Figure 5-68 5557003, Spyder to Djinn
Page 142
Section 5.2 Spyder connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557045ADW_r3.pdf Page 2 of 2
Figure 5-69 5557045, Spyder to speakers
Chapter 5 Spyder system controller 5350002-4
Page 143
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 5-70 5557012, Spyder to PC
Page 144
Section 5.2 Spyder connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Figure 5-71 5557050, Spyder J20 to PC
Chapter 5 Spyder system controller 5350002-4
Page 145
GE HEALTHCARE
REVISION 3
Page 146
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 5.2 Spyder connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 6 Hornet UIF board 5350004-2
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Chapter 6 Hornet UIF board 5350004-2
Page 147
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 6.1 Hornet schematics
Figure 6-2 5350004ADW_r4
Page 148
Section 6.1 Hornet schematics
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 149
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Page 158
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
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REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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Chapter 7 Locust drive board 5350006-2
Page 181
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
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See the GEHC Myworkshop System to determine the status of this document.
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Figure 7-25 5350006SCH_s23
Chapter 7 Locust drive board 5350006-2
Page 183
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 7.2 Locust connector cables
Figure 7-26 5557025, Locust to park latch
Page 184
Section 7.2 Locust connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 7-27 5557008, Locust to LVLE2
Chapter 7 Locust drive board 5350006-2
Page 185
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557002ADW_r5.pdf Page 2 of 2
Figure 7-28 5557002, Locust to Spyder
Page 186
Section 7.2 Locust connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557016ADW_r4.pdf Page 2 of 2
Figure 7-29 5557016, Locust to Cricket
Chapter 7 Locust drive board 5350006-2
Page 187
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557039ADW_r3.pdf Page 2 of 2
Figure 7-30 5557039, Locust to hard brake release
Page 188
Section 7.2 Locust connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 7-31 5557043, Locust to col
Chapter 7 Locust drive board 5350006-2
Page 189
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557015ADW_r6.pdf Page 2 of 2
Figure 7-32 5557015, Locust to drive handle
Page 190
Section 7.2 Locust connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557014ADW_r4.pdf Page 2 of 2
Figure 7-33 5557014, Locust J6 to Caterpillar J2
Chapter 7 Locust drive board 5350006-2
Page 191
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 7-34 5557013, Locust J5 to Caterpillar J1
Page 192
Section 7.2 Locust connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Some early production units were shipped with cable assembly 5557068 (see Figure 7-35).
This cable assembly consisted of a bundle of the following individual cables:
•
Locust to LVLE2
•
Locust to Caterpillar
•
Locust to Park Latch
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
The original cable (5557068) is not available as a replacement part and must be replaced with the individual cables as identified above.
Approved Document - 5557068ADW_r3.pdf Page 2 of 2
Figure 7-35 5557068, “Super cable” (obsolete)
Chapter 7 Locust drive board 5350006-2
Page 193
GE HEALTHCARE
REVISION 3
Page 194
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 7.2 Locust connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 8 Cricket battery board 5350008
Vertical
Brake
39
4 MnL PLG
15 Hsub-D Plug
22
Hard Brake
Release
Switch
mMnL REC
3 mMnL
Plug
mMnL Plug
5503004
16
5 MnL P
5 MnL R
3 Phoenix REC
J6
J8
J1, J2, J3, J4
J11, J12,
J13, J14
J10
10 mMnL REC
Cricket
Battery
Board
5350008
J7
J5
2 Phoenix Plug
Pack 4
4 MnL REC
5 MnL Plug
Pack 3
3 Phoenix Plug
2 Phoenix REC
4 MnL REC
4 MnL PLG
Battery Temp
Pack 2
4 MnL Plug
5 MnL REC
2 Phoenix REC
2 Phoenix Plug
Pack 1
02
Breaker Trip
Breaker
23
10 mMnL PLG
Cord
Reel
Figure 8-1 Cricket portion of wiring diagram
Chapter 8 Cricket battery board 5350008
Page 195
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 8.1 Cricket schematics
Figure 8-2 5350008ADW
Page 196
Section 8.1 Cricket schematics
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
4
5
7
6
8
A
A
NOTES:
1. THE VARIATION
PWA IS 5350008
REVISION
ECR/ECO
1
------
2
3
DATE
SIGN OFF
16-OCT-06
---
------
6-NOV-09
---
------
10-AUG-10
---
AND VERSION FOR THIS
C.
2.
THIS COVER SHEET CONTROLS THE REVISION STATUS OF THE ENTIRE DOCUMENT.
THE REVISION OF ALL SHEETS OF THIS
DOCUMENT WILL BE AT THE SAME LEVEL.
3.
THIS SCHEMATIC MEETS THE SPECIFICATIONS OF THE GLOBAL SCHEMATIC STANDARD
GUIDELINES
2299773GSP.
4.
ELECTRONIC SIGNATURES FOR BOTH THE
SCHEMATIC REVIEWER(S) AND APPROVER(S)
CAN BE FOUND WITHIN MY WORKSHOP.
5.
UNLESS OTHERWISE
RESISTORS ARE IN
CAPACITORS ARE IN
INDUCTORS ARE IN
B
SPECIFIED:
OHMS.
FARADS.
HENRIES.
B
C
D
D
Date
C. Jablonowski
Block
Tue Aug 17 10:36:20
Path
2
3
4
CRICKET
Block
cricket_battery
2010
1
Title
10-Aug-2010
5
BATTERY BD
Sheet
1 of
6
Dwg No
2
5350008SCH
7
GE Healthcare
Company
Rev
Restricted
Sheet
3
1 of
2
B Size
Made By
REV
2
01July04
C
8
Figure 8-3 5350008SCH_s1
Chapter 8 Cricket battery board 5350008
Page 197
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
DJINN
4
5
7
6
8
I/F
CHARGE I/F
CHARGE FUSE OUT
TP4
BATT_BRK
J6
RED
1B
1C
DRAIN_ONLY
POWER_GND
A
1A
2A
3A
1
2
3
15A SLOW-BLOW
300VDC FUSE
2B
2C
3B
3C
J7
R4
100K
0.25W
1%
F1
TIME_DELAY
BATT_BRK
PIN
POWER_COMBICON
RIGHT_ANGLE
GND
15A
600VAC_300VDC
BREAKER OUT (LOAD)
TP1
DRIVE
FUSE1 OUT
TP8
RED
BATT_BRK
BATT_RAW
A
R9
100K
0.25W
1%
F2
TIME_DELAY
J5
1
2
3
4
5
PIN
RIGHT_ANGLE
MATE_N_LOK
GND
RED
15A SLOW-BLOW
300VDC FUSE
R1
100K
0.25W
1%
BREAKER I/F
1
2
3
4
5
PACK1
PACK2
PACK3
FUSE_CHRG
FUSE_CHRG
FUSE_DRV
1A
2A
DRIVE
15A
600VAC_300VDC
1
2
DRIVE
BATT_RAW
SOCKET
POWER_COMBICON
RIGHT_ANGLE
FUSE2 OUT
TP9
FUSE_DRV
POWER_GND
DRAIN_ONLY
FUSE_RAW
RED
3A SLOW-BLOW
300VDC FUSE
R10
100K
0.25W
1%
F3
TIME_DELAY
B
I/F
J8
1
2
3
4
B
PIN
RIGHT_ANGLE
MATE_N_LOK
GND
FUSE_RAW
1
2
3
4
3A
600VAC_300VDC
BATTERY FEEDBACK I/F
5V0
J10
PACK 4 I/F
PACK 3 I/F
5V0
PACK 2 I/F
J14
PACK 1 I/F
5V0
5V0
J13
TEMP_SEN_1_POW
TEMP_SEN_2_POW
TEMP_SEN_3_POW
TEMP_SEN_4_POW
DRAIN
2
4
2
4
1
3
1
3
TEMP_SEN_3_RTN
TEMP_SEN_3_POW
2
4
2
4
1
3
1
3
TEMP_SEN_2_RTN
TEMP_SEN_2_POW
2
4
J11
2
4
1
3
1
2
3
4
5
6
7
8
9
10
6
7
8
9
10
TEMP_SEN_1_RTN
TEMP_SEN_2_RTN
TEMP_SEN_3_RTN
TEMP_SEN_4_RTN
5V0
J12
PIN
RIGHT_ANGLE
MATE_N_LOK
C
TEMP_SEN_4_RTN
TEMP_SEN_4_POW
1
2
3
4
5
1
3
TEMP_SEN_1_RTN
TEMP_SEN_1_POW
2
4
C
1
3
1
3
2
4
GND
PIN
STRAIGHT
MATE_N_LOK
PACK 4+
BREAKER IN (LINE)
PIN
STRAIGHT
MATE_N_LOK
GND
PIN
STRAIGHT
MATE_N_LOK
GND
GND
PACK 3+
TP2
PIN
STRAIGHT
MATE_N_LOK
GND
PACK 2+
TP3
TP7
PACK 1+
TP5
RED
RED
BATT_RAW
R8
100K
0.25W
1%
RIGHT_ANGLE
POWER_COMBICON
PIN
2A
1A
RIGHT_ANGLE
POWER_COMBICON
PIN
2A
1A
2B
2C
2
1
RED
RED
R3
100K
0.25W
1%
2B
2C
RIGHT_ANGLE
POWER_COMBICON
PIN
2A
1A
2
1
RIGHT_ANGLE
POWER_COMBICON
PIN
R5
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0.25W
1%
2A
1A
2B
2C
2
1
R11
R12
PACK3
R13
PACK2
100K
0.25W
1%
MHP4_50TB10_00
MH9 MH10
BLACK
NOTE:
J1
PACK1
100K
0.25W
1%
MH8
100K
0.25W
1%
KEEP OUT ON MOUNTING HOLES SHOULD BE
SUFFICIENT
TO ACCEPT A RING TERMINAL.
D
GND
GND
Date
C. Jablonowski
Block
Tue Aug 17 10:52:06
Path
CRICKET
Block
cricket_battery
2010
1
Title
10-Aug-2010
2
3
4
5
Figure 8-4 5350008SCH_s2
Page 198
Sheet
2 of
6
Section 8.1 Cricket schematics
BATTERY BD
Dwg No
2
5350008SCH
7
GE Healthcare
Company
Rev
Restricted
Sheet
3
2 of
8
2
B Size
Made By
REV
2
01July04
D
J2
MH1
2C
2B
1B
1C
1B
1C
1B
1C
J4
J3
== PLATED MOUNTING HOLES ==
GND
CHASSIS
BATTTP6
1B
1C
2
1
R2
100K
0.25W
1%
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 8.2 Cricket connector cables
Approved Document - 5557016ADW_r4.pdf Page 2 of 2
Figure 8-5 5557016, Cricket to Locust
Chapter 8 Cricket battery board 5350008
Page 199
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557022ADW_r6.pdf Page 2 of 2
Figure 8-6 5557022, Cricket to aux box
Page 200
Section 8.2 Cricket connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557021ADW_r5.pdf Page 2 of 2
Figure 8-7 5557021, Cricket J7 to Firefly J12
Chapter 8 Cricket battery board 5350008
Page 201
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557023ADW_r6.pdf Page 2 of 2
Figure 8-8 5557023, Cricket to breaker
Page 202
Section 8.2 Cricket connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557030ADW_r3.pdf Page 2 of 2
Figure 8-9 5557030, Cricket J10 to Firefly J13
Chapter 8 Cricket battery board 5350008
Page 203
GE HEALTHCARE
REVISION 3
Page 204
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 8.2 Cricket connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 9 Caterpillar base transition board 5350010
802.15.4
Zigbee
802.15.3a
UWB
Detector
Zigbee
Barcode
Reader
Halls
Halls
4 MnL Plug
5 HDR REC
4 MnL REC
J4
J3
R
2 mMnL Plg
5 HDR Plug
Brake
Brake
L
5 HDR Plug
4 MnL Plug
2 mMnL Plg
2 mMnL REC 5 HDR REC
4 MnL REC
2 mMnL REC
J5
J9
J7
J6
Caterpillar
Base Transition Board
5350010
J8
J11
J10
J2
J1
4 mMnL REC
3 mMnL REC
2 MnL REC
15 Sub-D REC
12 MnL REC
4 mMnL Plug
3 mMnL Plug
2 MnL Plug
15 Sub-D Plug
12 MnL Plug
14
13
15 Sub-D Plug
12 MnL Plug
26
Bumper
27
Rotational
Brake
55*
2 MnL REC
2 MnL Plug
56*
Detector Park
Switch
6
6
Figure 9-1 Caterpillar portion of wiring diagram
Chapter 9 Caterpillar base transition board 5350010
Page 205
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 9.1 Caterpillar schematics
Approved Document - 5350010ADW_r2.pdf Page 2 of 2
Figure 9-2 5350010ADW
Page 206
Section 9.1 Caterpillar schematics
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
3
5
4
6
7
8
A
A
REVISION
ECR/ECO
1
2
------
DATE
SIGN
NOTES:
1. THE VARIATION
PWA IS 5350010
OFF
23-OCT-06
---
30-NOV-09
---
FOR THIS
2.
THIS COVER SHEET CONTROLS THE REVISION
STATUS OF THE ENTIRE DOCUMENT.
THE REVISION
OF ALL SHEETS OF THIS
DOCUMENT WILL BE AT THE SAME LEVEL.
3.
THIS SCHEMATIC MEETS THE SPECIFICATIONS OF THE GLOBAL SCHEMATIC STANDARD
GUIDELINES
2299773GSP.
4.
ELECTRONIC SIGNATURES FOR BOTH THE
SCHEMATIC REVIEWER(S)
AND APPROVER(S)
CAN BE FOUND WITHIN MY WORKSHOP.
5.
UNLESS OTHERWISE SPECIFIED:
RESISTORS ARE IN OHMS.
CAPACITORS ARE IN FARADS.
INDUCTORS ARE IN HENRIES.
B
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
AND VERSION
B.
B
6.
THIS
7.
ACTIVE LOW SIGNALS ARE INDICATED
TO THE SIGNAL NAME
SCHEMATIC WAS CAPTURED WITH CADENCE CONCEPT HDL
8.
DIFFERENTIAL
SIGNAL PAIRS ARE INDICATED
APPENDED TO THE SIGNAL NAME
WITH A '_N'
APPENDED
WITH A '_H'
& '_L'
C
D
D
By
Date
Casey
Block
Mon Jan
11
15:23:57
Title
10-NOV-2009
Path
2
3
4
CATERPILLAR_BASE
Block
5
Sheet
1 of
caterpillar_base
2010
1
Richmond
6
Dwg
3
No
5350010SCH
7
GE Healthcare
Company
Rev
Restricted
Sheet
2
1 of
3
B Size
Made
REV 2 01July04
C
8
Figure 9-3 5350010SCH_s1
Chapter 9 Caterpillar base transition board 5350010
Page 207
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
3
5
4
BASE SIGNALS
HALL
6
7
SENSORS
8
BUMPER
J2
J4
1
2
3
4
5
6
7
8
A
1
2
3
4
5
6
7
8
HALL_5V0
R_H_CASE_GND
L_H_CASE_GND
R_OUTPUT_H3
R_OUTPUT_H2
R_OUTPUT_H1
L_OUTPUT_H3
L_OUTPUT_H2
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
9
10
11
12
13
14
15
G1
G2
G1
G2
L_OUTPUT_H1
BUMPER_1_RTN
BUMPER_1
BUMPER_2
BUMPER_2_RTN
DETECTOR_P
DETECTOR_P_RTN
9
10
11
12
13
14
15
7
8
9
1
3
1
2
3
4
5
L_OUTPUT_H3
L_OUTPUT_H2
L_OUTPUT_H1
L_H_5V0
L_H_CASE_GND
SILKSCREEN:
LEFT HALL
J8
12
13
1
2
3
4
5
2
BUMPER_2
BUMPER_2_RTN 4
1
3
2
4
1
3
10
11
BUMPER_1
BUMPER_1_RTN
A
PIN
STRAIGHT
MATE_N_LOK
PIN
STRAIGHT
WIRE_TO_BOARD
SOCKET
RIGHT_ANGLE
STD_DENSITY
J6
4
5
6
1
2
GND_CHASSIS
1
2
3
4
5
R_OUTPUT_H3
R_OUTPUT_H2
R_OUTPUT_H1
R_H_5V0
R_H_CASE_GND
SILKSCREEN:
RIGHT HALL
1
2
3
4
5
DETECTOR
PARK
J10
14
15
PIN
STRAIGHT
WIRE_TO_BOARD
DETECTOR_P
DETECTOR_P_RTN
1
2
1
2
PIN
STRAIGHT
MATE_N_LOK
BASE_SIGNALS<15..1>
B
BASE HIGH
VOLTAGE
2
3
5
8
9
11
12
2
ROTBRAKE
ROTBRAKE_RTN 3
5
LBRAKE_REL
6
8
RMOTOR_M2
9
RMOTOR_M3
11
LMOTOR_M2
12
LMOTOR_M3
BRAKES
MOTORS
J1
J3
2
3
5
6
8
9
11
12
1
1
BRAKE_REL_RTN 1
4
4
RBRAKE_REL
4
7
7
RMOTOR_M1
7
10
LMOTOR_M1
10
10
10 LMOTOR_M1
11 LMOTOR_M2
12 LMOTOR_M3
LMOTOR_CASE
1
2
3
4
PIN
STRAIGHT
MATE_N_LOK
1
5
SILKSCREEN:
LEFT MOTOR
BRAKE_REL_RTN
LBRAKE_REL
1
2
1
2
SILKSCREEN:
LEFT BRAKE
ROTATIONAL
PIN
STRAIGHT
MATE_N_LOK
BRAKE
J11
2
3
ROTBRAKE
ROTBRAKE_RTN
1
2
3
1
2
3
C
J5
7 RMOTOR_M1
8 RMOTOR_M2
9 RMOTOR_M3
RMOTOR_CASE
DRAIN
GND_CHASSIS
LAYOUT NOTE:
THIS DRAIN SHOULD BE TIED
CHASSIS GROUND WITH THE
SHORTEST POSSIBLE TRACE.
1
2
3
4
PIN
STRAIGHT
MATE_N_LOK
GND_CHASSIS
C
J7
1
2
3
4
J9
1
2
3
4
SILKSCREEN:
RIGHT MOTOR
1
4
BRAKE_REL_RTN
RBRAKE_REL
1
2
PIN
STRAIGHT
MATE_N_LOK
1
2
SILKSCREEN:
RIGHT BRAKE
TO
GND_CHASSIS
PIN
STRAIGHT
MATE_N_LOK
PIN
STRAIGHT
MATE_N_LOK
BASE_HIGH_VOLTAGE<12..1>
D
Made
By
Date
Casey
Block
Tue
Jan
12
08:28:28
Path
2
3
4
CATERPILLAR_BASE
Block
5
Figure 9-4 5350010SCH_s2
Page 208
Title
10-NOV-2009
Section 9.1 Caterpillar schematics
Sheet
2 of
caterpillar_base
2010
1
Richmond
6
Dwg
3
No
5350010SCH
7
REV 2 01July04
D
GE Healthcare
Company
Rev
Restricted
Sheet
2
2 of
8
3
B Size
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
B
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 9.2 Caterpillar connector cables
Approved Document - 5557026ADW_r4.pdf Page 2 of 2
Figure 9-5 5557026, Caterpillar to bumper
Chapter 9 Caterpillar base transition board 5350010
Page 209
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 9-6 5557027, Caterpillar to rot brake
Page 210
Section 9.2 Caterpillar connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Figure 9-7 5557055, Caterpillar to park sw bulkhead (Optima XR220amx only)
Chapter 9 Caterpillar base transition board 5350010
Page 211
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557056ADW_r3.pdf Page 2 of 2
Figure 9-8 5557056, Caterpillar to det park sw (Optima XR220amx only)
Page 212
Section 9.2 Caterpillar connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557014ADW_r4.pdf Page 2 of 2
Figure 9-9 5557014, Caterpillar J2 to Locust J6
Chapter 9 Caterpillar base transition board 5350010
Page 213
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 9-10 5557013, Caterpillar J1 to Locust J5
Page 214
Section 9.2 Caterpillar connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 10 LVLE2 power supply 5192958
45
Mini-75 Plug
5503001
Grid Plug
11^
Mini-75 REC
4 Microfit REC
5503002
15 SubD
REC
15 SubD
PLG
Power Module
J1
3 Phoenix
PLG
3 Phoenix
REC
2 Phoenix
REC
2 Phoenix
Plug
3 Phoenix
REC
3 Phoenix
PLG
J1
32
10
6 mMnL REC
4 mMnL Plug
4 mMnL REC
J8
J9
2 mMnL Plug
LVLE2
5192958
J5
04
15 Hsub-D REC
9 Sub-D PLG
3 mMnL REC
3 mMnL Plug
J3
2 mMnL REC
2 mMnL REC
2 mMnL Plug
J4
J2
9 Sub-D REC
6 mMnL REC
6 mMnL Plug
2 mMnL REC
2 mMnL Plug
22
J2
2 Phoenix PLG
6 mMnL PLG
08
03
9 Sub-D Plug
2MnL PLG
J2
2 Phoenix REC
25
15 Sub-D
Plug
15 Sub-D
REC
J3
15kW Main
Aux.Module
2 MnL REC
Tube Park
Latch
2 Phoenix
Plug
2 Phoenix
REC
15 SubD
Plug
15 SubD
REC
4 Phoenix
Plug
4 Phoenix
REC
4 Microfit PLG
60
15 Sub-D REC
30kW Optional
Aux. Module
HV Tank
J6, J7
J1
5 MnL REC
5 MnL Plug
5 MnL Plug
5 MnL Rec
07
02
21
Figure 10-1 LVLE2 portion of wiring diagram
Chapter 10 LVLE2 power supply 5192958
Page 215
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 10.1 LVLE2 connector cables
Approved Document - 5557009ADW_r4.pdf Page 2 of 2
Figure 10-2 5557009, LVLE2 to Firefly
Page 216
Section 10.1 LVLE2 connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557010ADW_r7.pdf Page 2 of 2
Figure 10-3 5557010, LVLE2 to Djinn
Chapter 10 LVLE2 power supply 5192958
Page 217
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557004ADW_r6.pdf Page 2 of 2
Figure 10-4 5557004, LVLE2 to Spyder
Page 218
Section 10.1 LVLE2 connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 10-5 5557007, LVLE2 to Firefly
Chapter 10 LVLE2 power supply 5192958
Page 219
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Figure 10-6 5557048, LVLE2 to wireless handswitch cradle
Page 220
Section 10.1 LVLE2 connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 10-7 5557008, LVLE2 to Locust
Chapter 10 LVLE2 power supply 5192958
Page 221
GE HEALTHCARE
REVISION 3
Page 222
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 10.1 LVLE2 connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
10 mM
6 MnL Rec
9 SubD Rec
20
9 SubD Plug
30
19
6 MnL Plug
3 Terminal 0.375"
9 SubD Plug
J3
6 MnL Plug
J1
9 SubD Rec
Mantis Supply
(SL Power)
5311985
6 MnL Rec
J2
10 mM
Chapter 11 Mantis power supply 5311985
J13
J9
J4
37
38
Cord
Reel
Schaffner Filter
FN2030B-16-06
Figure 11-1 Mantis portion of wiring diagram
Chapter 11 Mantis power supply 5311985
Page 223
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 11.1 Mantis connector cables
Figure 11-2 5557019, Mantis J2 to Firefly J9
Page 224
Section 11.1 Mantis connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 11-3 5557020, Mantis J3 to Firefly J4
Chapter 11 Mantis power supply 5311985
Page 225
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 11-4 5557037, Mantis to filter
Page 226
Section 11.1 Mantis connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557038ADW_r4.pdf Page 2 of 2
Figure 11-5 5557038, Filter to fuse
Chapter 11 Mantis power supply 5311985
Page 227
GE HEALTHCARE
REVISION 3
Page 228
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 11.1 Mantis connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 12 Generator (Djinn)
Speakers
Federal Plug
Toshiba
E7901X
Federal REC
11^
Screw Term
Ring Term
3 mMNL
REC
3 mMNL
Plug
45
Mini-75 Plug
5503001
Mini-75 REC
30kW Optional
Aux. Module
4 Microfit PLG
4 Microfit REC
5503002
2 Phoenix
Plug
2 Phoenix
REC
60
15 SubD
Plug
15 SubD
REC
4 Phoenix
Plug
4 Phoenix
REC
HV Tank
15 SubD
REC
15 SubD
PLG
Power Module
3 Phoenix
PLG
3 Phoenix
REC
J1
15 Sub-D
Plug
15 Sub-D
REC
2 Phoenix
REC
2 Phoenix
Plug
0
J2
2 MnL REC
2MnL PLG
15kW Main
Aux.Module
J2
J1
3 Phoenix
REC
3 Phoenix
PLG
J3
32
10
2 Phoenix REC
2 Phoenix PLG
4 mMnL Plug
6
6
J8
4 mMnL REC
J9
Figure 12-1 Generator portion of wiring diagram
Chapter 12 Generator (Djinn)
Page 229
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 12.1 Generator Interconnections
Thermal
2 small wires cable
Shielded wire to tube stator
Rotor
Cathode HV Cable
(-)
X-ray Tube
(+)
Anode HV Cable
+ / Anode
Power Module
HV Tank
- / Cathode
Bipolar
2 small wires
cable
48V
From System
J2
Filament Board
Ribbon
J1
cable
4 wires
cable
J6
J4
J5
J1
Main Auxiliary 15kW
J3
J6
J5
CAN
Rotor Board
Power Board
XJ1
DC Capacitor
XJ2
3 wires
cable
J4
1 very short
wire cable
J4
1 short
wire cable
Diodes
Int
Board
J1
HV BIP
Diodes
XJ3
BB
Inductor
Shielded wire
2 wires cable
J4
DC Capacitor
J1
J3
J6
Control Board
J5
J7
J6
Small
ribbon cable
J6
Opt Auxiliary 30kW
System
Batteries
Communication
= Chassis Ground
Djinn Generator
Interconnect Diagram
Figure 12-2 Generator Interconnections
Page 230
Section 12.1 Generator Interconnections
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 12.2 Main auxiliary 15kW module 5338768
Figure 12-3 Main auxiliary 15kW module 5338768ADW_s1
Chapter 12 Generator (Djinn)
Page 231
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
XJ3
XJ1
XJ2
2 neons
5393151
5351531-3
5351531
Warning : Positive (+)
polarity should be on
the top for capacitor
and printed bord
5351586
3 turns around tore
discharge
+
5357599-2
5 turns
around
tore
5351531-4
+
5351531-2
J8
5352288
+
5352041
+
+
+
5351566
5357599-2
5390129
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
5
5
7
1
3
2
3
5352133
-
Approved Document - 5338768WIR_r2.pdf Page 2 of 2
BEETLE DJINN AUX MAIN BOX 5338768WIR REV 2
Figure 12-4 Main auxiliary 15kW module 5338768WIR_s1
Page 232
Section 12.2 Main auxiliary 15kW module 5338768
1/
GE /
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
12.2.1 Rotor control board 5133326-3
2
3
A
ECR/ECO
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
1
DESCRIPTION
3
DSP PIN
110(VREF2)
DSP CONSTRAINT
SIGN
23-JUNE-08
------
PAGE
OFF
PIN
DC_BUS_SENSE NET ADDED TO PIN
LED RED UPDATED AS PER TO ROHS. RES 108
54
R L
OF DSP.
VALUE CHANGED
TO 1K.
UPDATED AS PER ROHS, FUSE(F2,
CHANGED, C46 & C47 VALUE CHANGED TO 10NF
EURGE 82016
-
F3)
RATING
FROM 22NF.
DC BUS SENSING CKT ADDED AFTER THE FUSES,
CURRENT SENSORS(MT1,MT2,MT3)
LABEL
CHANGED TO LTS15NP
FROM LTS25NP.
& J7
R L
ADDED.
FUSE CHANGED TO ROHS.
R L
R L
R L
ADDED.
EURGE48505
C74
& C75
R L
ADDED.
ECR/ECO
DATE
DESCRIPTION
CKT CHANGED TO INCLUDE
REVISION
OF CHANGE
DATE
DESCRIPTION
CREEPAGE
TABLE
REVISION
UPDATED,
LAYOUT
DESCRIPTION
UPDATED
R126
FROM 2K
TO 1K,R16
13
UPDATED
R107
FROM 10E
TO 33E
10
ADDED
10
UPDATED
RCD SNUBBER
SIGN
ACROSS
R1 FROM 20E
;
CHANGED
Q1:ADDED
TABLE
100E
OFF
TO 270E,R23
BY
FROM 100E
FOR GROUND ISSUE
CONSTRIANTS
UPDATED
TO 10E.
S A
Q3 FROM FZT651
TO FZT851.
S A
IN
D1.
S A
SERIES
WITH
S A
TO 200E.
BRD UPDATED
S A
---
OF CHANGE
FROM 100E
C
BY
AS PER THE CREEPAGE
DATE
13
OFF
---
15-JUL-09
------
PAGE
SIGN
OF CHANGE
MODIFIED
ECR/ECO
4
BY
S A
06-JAN-09
------
PAGE
OFF
---
Q3.
ECR/ECO
3
SIGN
08-AUG-08
------
B
R L
J8
PAGE
AND TRANSFORMER
AS PER IEC
EDTION
T1
SECONDARY
TURNS.
S A
S A
2.
D
Made
By
Date
SANTHOSH
Block
Jul
16
09:46:47
1
UNLESS OTHERWISE SPECIFIED:
RESISTORS
ARE IN OHMS.
CAPACITORS
ARE IN FARADS.
INDUCTORS ARE IN HENRIES
R L
DISCHARGE MECHANISAM CHANGED TO TOP SWITCH CONFIGURATION
2
D
5.
R L
13
2
ELECTRONIC
SIGNATURES
FOR BOTH THE
SCHEMATIC REVIEWER(S)
AND APPROVER(S)
CAN BE FOUND WITHIN
MY WORKSHOP.
A
R L
CONNECTOR CHANGED
REVISION
C
4.
R L
EURGE 64652(D24)
13
THIS SCHEMATIC MEETS THE SPECIFICATIONS OF THE GLOBAL SCHEMATIC STANDARD
GUIDELINES
2299773GSP.
R L
10
14
3.
R L
NEON BULB(DS3)
J2
THIS COVER SHEET CONTROLS THE REVISION
STATUS OF THE ENTIRE DOCUMENT.
THE REVISION
OF ALL SHEETS OF THIS
DOCUMENT WILL BE AT THE SAME LEVEL.
R L
ADDED
5
9
R L
FOR THIS
2.
BY
& TP ADD TO 56TH
8
NOTES:
1. THE VARIATION
AND VERSION
REV 4
PWA IS 5133326-3
OF CHANGE
PULLED TO 3.3V
7
---
4
B
Thu
DATE
6
djin
2009
2
3
4
Title
15-JUL-2009
Path
DJINN
Block
DJINN
5
ROTATION
CONTROL BOARD V3
6
ROTATION
Sheet
1 of
CONTROL
Dwg No
14
5133326-3SCH
7
REV 2 01July04
REVISION
5
4
GE Healthcare
Company
Rev
Restricted
Sheet
4
1 of
13
B Size
1
8
Approved Document - 5133326-3SCH_r4.pdf Page 2 of 14
Figure 12-5 Rotor control board 5133326-3SCH_s1
Chapter 12 Generator (Djinn)
Page 233
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
3V3
C50
A
R120
4.99K
0.1W
1%
R121
4.99K
0.1W
1%
68
110
65
138
156
C60
2.2U
3V3
R113
R110
4.99K
0.1W
4.99K
0.1W
1%
7B4<
DSP_RESET
3A6>
3A6>
XTAL
EXTAL
6A2<
MSCAN_RX
TP8
TP28
TP27
1%
B
3B3<
XTAL
R36
VDD<7-0>
VDDA<2-0>
2.2U
EXTAL
A
U3
DSP56F807
0.1U
16V
10%
C57
0.1U
16V
10%
C62
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3V3
3B3<
A0
A1
A2
A3
A4
A5
A6_GPIOE2
A7_GPIOE3
A8_GPIOA0
A9_GPIOA1
A10_GPIOA2
A11_GPIOA3
A12_GPIOA4
A13_GPIOA5
A14_GPIOA6
A15_GPIOA7
VPP2
VREF2
VCAPC1
VCAPC2
VPP
69
70
98
86
IRQA_N
IRQB_N
RESET_N
EXTBOOT
92
93
XTAL
EXTAL
142
MSCAN_RX
147
148
149
150
PHASEA0_TA0
PHASEB0_TA1
INDEX0_TA2
HOME0_TA3
1MEG
0.1W
1%
1
2
3
4
5
6
7
8
10
11
12
13
14
15
16
17
MSCAN_TX
139
TXD0_GPIOE0
RXD0_GPIOE1
TXD1_GPIOD6
RXD1_GPIOD7
159
160
55
56
C15
C13
1
4
22P
50V
5%
TP3
TP33
22P
50V
5%
Y1
MSCAN_TX
6B2<
RXD0
DISCH_OK
RXD1
13B8>
3V3
B
4.99K
0.1W
1%
5C6>
5C8>
14A8<
7D2<
7D5<
5C3>
TCK
TMS
TDI
TRST
ADC1
ADC2
ADC3
ADC4
ADC5
ADC6
TP14
TP31
TP32
TP30
TP19
TP20
TP26
TP25
TP24
TP22
3V3
0.1U
16V
10%
C65
C
134
135
136
132
102
103
104
105
106
107
108
109
99
113
114
115
116
117
118
119
120
SCLK_GPIOE4
MOSI_GPIOE5
MISO_GPIOE6
SS_GPIOE7_N
TCK
TMS
TDI
TRST_N
RSTO_N
CLKO
TDO
DE_N
97
158
137
121
4.99K
0.1W
1%
SS_N
TP29
TP9
TP13
TP17
RSTO_N
CLKO
TDO
DE_N
D0
D1
D2
D3
D4
D5
D6
D7
D8
D9
D10
D11
D12
D13
D14
D15
23
24
25
26
27
28
29
30
31
32
33
35
36
37
38
39
D0
PS_N
DS_N
RD_N
WR_N
19
20
22
21
PS_N
DS_N
RD_N
WR_N
TD0
TD1
TD2
TD3
TC0
TC1
126
127
128
129
130
131
TD0
TD1
TD2
TD3
TC0
TC1
TCS
GND<8-0>
GNDA<2-0>
133
ANA0
ANA1
ANA2
ANA3
ANA4
ANA5
ANA6
ANA7
VREF
ANB0
ANB1
ANB2
ANB3
ANB4
ANB5
ANB6
ANB7
3V3
144
146
145
143
R17
7A1<
7A1<
7B1<
7A4<
PHASEA1_TB0
PHASEB1_TB1
INDEX1_TB2
HOME1_TB3
4.99K
0.1W
1%
151
152
154
155
4.99K
0.1W
1%
R109
R103
4.99K
0.1W
1%
4.99K
0.1W
1%
R104
4.99K
0.1W
1%
R106
R116
3V3
4.99K
0.1W
1%
R114
R115
7A1<
C
SYM 1 OF 2
D
REV 2 01July04
DSP SECTION
GE Healthcare
Company
Block
Wed Jul
22
16:19:33
1
djin
2009
2
3
4
Path
Block
DJINN
5
ROTATION
CONTROL BOARD V3
3 of
6
Approved Document - 5133326-3SCH_r4.pdf Page 3 of 14
Figure 12-6 Rotor control board 5133326-3SCH_s2
Page 234
Sheet
Section 12.2 Main auxiliary 15kW module 5338768
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
2 of
8
13
B Size
0.1U
16V
10%
0.1U
16V
10%
C66
0.1U
16V
10%
C67
0.1U
16V
10%
C68
0.1U
16V
10%
C69
0.1U
16V
10%
C61
C51
0.1U
16V
10%
0.1U
16V
10%
C64
C58
D
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
A
5
TP10
EN_T70_MEAS
DISP1
TP11
DISCH_INHIBIT
TP21
TP18
T70_FAULT
TP34
12A1<
12A5<
12B1<
12B5<
12C1<
12C5<
PWM_UP
PWM_UN
PWM_VP
PWM_VN
PWM_WP
PWM_WN
75
77
78
79
80
81
ISA0
ISA1
ISA2
B
8B6>
FAULTA0
FAULTA1
FAULTA2
FAULTA3
123
124
125
TP16
82
83
84
85
PWMA0
PWMA1
PWMA2
PWMA3
PWMA4
PWMA5
ISA0
ISA1
ISA2
8
A
14B1<
13D2<
5B8>
14B8>
9D5>
49
50
51
52
53
54
DC_BUS_SENSE
U3
7
5A2<
GPIOD3
GPIOD0
GPIOD1
GPIOD2
GPIOD3
GPIOD4
GPIOD5
DSP56F807
FAULTA0
FAULTA1
FAULTA2
FAULTA3
PWMB0
PWMB1
PWMB2
PWMB3
PWMB4
PWMB5
57
58
59
60
61
62
PWMB0
PWMB1
PWMB2
PWMB3
PWMB4
PWMB5
ISB0
ISB1
ISB2
64
66
67
ISB0
ISB1
ISB2
FAULTB0
FAULTB1
FAULTB2
FAULTB3
71
72
73
74
FAULTB0
FAULTB1
FAULTB2
FAULTB3
B
40
41
42
43
44
45
46
47
GPIOB0
GPIOB1
GPIOB2
GPIOB3
GPIOB4
GPIOB5
GPIOB6
GPIOB7
SYM 2 OF 2
DISP5
DISP4
DISP3
DISP2
C
3V3
5B2<
5B2<
5B2<
5B2<
R15
1K
0.1W
1%
R8
1K
0.1W
1%
R11
1K
0.1W
1%
R9
0.00
0.1W
5%
R10
0.00
0.1W
5%
C
R12
1K
0.1W
1%
TP6
TP5
TP4
TP7
1
R14
0.00
0.1W
5%
R13
0.00
0.1W
5%
D
Wed Jul
THE FOLLOWING COMPONENT(S)
R10.
1
ARE NOT INCLUDED
IN
THIS
ASSEMBLY:
GE Healthcare
Company
Block
22
16:19:34
1
djin
2009
2
3
4
Path
Block
DJINN
ROTATION
CONTROL BOARD V3
5
REV 2 01July04
D
6
Sheet
4 of
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
3 of
13
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
6
8
Approved Document - 5133326-3SCH_r4.pdf Page 4 of 14
Figure 12-7 Rotor control board 5133326-3SCH_s3
Chapter 12 Generator (Djinn)
Page 235
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
3V3
1
R134
1K
0.1W
1%
R130
1K
0.1W
1%
A
2
597-5112-4XXF
R129
1K
0.1W
1%
RED
DS6
RED
1
DS5
HSMY-C190
YELLOW
597-5112-4XXF
DS8
1
1
1
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
R128
1K
0.1W
1%
R135
1K
0.1W
1%
PCB THERMAL SENSOR
3V3
3V3
3V3
DISP1
U1
DS1822
R95
1K
0.1W
1%
DISP2
3
R108
1K
0.1W
1%
VDD
DQ
4
GND
5
GPIOD3
4A5<
R60
R48
2K
0.1W
1%
ADC6
3C3<
9B7>
ADCIN1
8B2>
100
0.1W
1%
R61
R49
2K
0.1W
1%
1
GREEN
9C7>
8B3>
R62
ADCIN2.
R50
2K
0.1W
1%
ADC2
C
3V3
K2
K2
D5
BAV99
70V
D6
BAV99
70V
3
C30
C29
0.1U
16V
10%
3
3C3<
100
0.1W
1%
3V3
1 A
0.1U
16V
10%
AK
C28
3C3<
100
0.1W
1%
3V3
3
ADC1
D7
BAV99
70V
CURRENT FEEDBACK SECTION
D
REV 2 01July04
D
GE Healthcare
Company
Block
Wed Jul
22
16:19:34
1
djin
2009
2
3
4
Path
Block
DJINN
5
ROTATION
CONTROL BOARD V3
5 of
6
Approved Document - 5133326-3SCH_r4.pdf Page 5 of 14
Figure 12-8 Rotor control board 5133326-3SCH_s4
Page 236
Sheet
Section 12.2 Main auxiliary 15kW module 5338768
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
4 of
8
13
B Size
C
A
K2
8B2>
DISP5
1 A
9A7>
B
0.1U
16V
10%
DISP4
0.1U
16V
10%
4C5<
C53
1 A
4C5<
AK
B
DISP3
AK
4C5<
DS2
HSMG-C190
2
4C5<
2
DS7
HSMY-C190
YELLOW
DS4
HSMY-C190
YELLOW
4A5<
LED
2
2
A
2
STATUS
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
2
4
3
A
8
A
1K
0.1W
1%
R118
CAN_H
7C4<
R166
0
0.1W
+0.05
3V3
S
TXD
CANH
CANL
R112
8
1
7
6
C56
100P
50V
5%
68.1
VREF
C54
4
RXD
0.1U
C55
100P
50V
5%
VCC=VCC;GND=GND
R111
MSCAN_TX
5
CAN_L
7C5<
3V3
K2
BAV99
D3
B
B
AK
2
70V
1 A
100K
0.1W
1%
DS1
597-5112-4XXF
RED
3V3
C14
0.1U
16V
10%
R96
1K
0.1W
1%
2K
0.1W
1%
R43
1
R30
3
U6
TPS3823
R31
2K
C
R35
D
G
Q2
S
3
A
B
2K
4
5
VDD
4
3
W DI
MR_N
PS_RESET
1
RESET_N
C
7B4<
2
GND
2K
0.1W
1%
D2
BAV99
70V
U4
74LVC-LCX14
2N7002
C12
2K
0.1W
1%
AK
3
R34
0.1U
16V
10%
3.3V
S1
KT11B1JM
A 1
VCC=3V3;GND=GND
1
1
3
3
2
2
4
4
CAN RESET SECTION
D
Wed Jul
REV 2 01July04
D
GE Healthcare
Company
Block
22
16:19:34
1
djin
2009
2
3
4
Path
Block
DJINN
ROTATION
CONTROL BOARD V3
5
6
Sheet
6 of
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
5 of
13
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
7
U2
TJA1050
MSCAN_RX
3B7<
6
CAN TRANSCIEVER
3V3
3B3<
5
68.1
1
8
Approved Document - 5133326-3SCH_r4.pdf Page 6 of 14
Figure 12-9 Rotor control board 5133326-3SCH_s5
Chapter 12 Generator (Djinn)
Page 237
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
3V3
A
A
3B3<
TCK
3B3<
3B7<
3B3<
TMS
TDO
TDI
1
3
5
7
9
12
A
Y
13
11
TRST
3B3<
4.99K
R139
J6
4
A
5
B
Y
6
ROT_P
ROT_C
ROT_A
G
9C7>
9A7>
9D7>
9B3<
B
PS_RESET
J TAG CONNECTOR
R156
4.99K
0.1W
1%
R155
U8
4.99K
74LVC-LCX08
0.1W
1%
9
A
8
Y
10
B
U8
74LVC-LCX08
2
4
6
8
10
2
4
6
8
10
4.99K
0.1W
1%
J4
1
3
5
7
9
R131
4.99K
R132
R138
R154
4.99K
0.1W
1%
4.99K
4.99K
R137
4.99K
R136
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3V3
1
2
3
4
1
2
3
4
6C8<
DSP_RESET
R157
4.99K
0.1W
1%
3B3<
U8
R158
4.99K
0.1W
1%
U8
74LVC-LCX08
1
A
2
B
Y
MOTOR CONNECTOR
3
B
B
CONTROL CONNECTOR
48V
T70_P.
J3
TIN
9
10
11
12
13
14
15
T70__N
14B5<
B
6A6<
CAN_H
VCC
R152
1
2
3
4
5
6
7
8
1
2
3
4
5
6
7
8
100K
0.25W
1%
C
CAN_L
6B6<
ROTOR STATE
PIN
RIGHT_ANGLE
15 PIN DSUB MALE
3
PIN
STRAIGHT
TERMINAL_BLOCK_HEADER
D21
BAV99
70V
48V
ENTRY
1 A
C63
0.1U
R124
100
ADC4
3C3<
3C3<
1
2
K2
R28
2K
0.125W
1%
1
2
R26
4.99K
0.125W
1%
3V3
R29
D22
BAV99
70V
C
J1
XYZ
1 A
100
0.1W
1%
48V1
G1
G2
K2
2K
0.1W
1%
R151
0.1U
16V
10%
R125
C72
R153
AK
4.99K
9
10
11
12
13
14
15
G1
G2
4.99K
3V3
3
R33
TIN
C11
0.1U
C
TP12
TP15
100K
0.25W
1%
1
2
10K
1
2
3
4
R25
14B4<
3
4
48V1
AK
J5
ADC5
D
SECTION
GE Healthcare
Company
Block
Wed Jul
22
16:19:35
1
djin
2009
2
3
4
Path
Block
DJINN
5
ROTATION
CONTROL BOARD V3
7 of
6
Approved Document - 5133326-3SCH_r4.pdf Page 7 of 14
Figure 12-10 Rotor control board 5133326-3SCH_s6
Page 238
Sheet
Section 12.2 Main auxiliary 15kW module 5338768
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
6 of
8
13
B Size
THERMAL SENSOR/PROTECTION
REV 2 01July04
D
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
A
3V3
VCC
K2
A
B
8
VCC
2
FAULTA0
4B3<
B
BAV99
VCC
R47
4.99K
100K
R51
3
2K
2
AR1
LM393A
1
VOUT
C
10K
R58
R56
R55
10K
VCC
10K
C
U4
74LVC-LCX14
VCC=3V3;GND=GND
8
VCC
3
R52
1 A
3
D17
BAV99
ADCIN2.
4.99K
D16
1
7
VOUT
4
GND
K2
1 A
9B7>
AK
5C4<
ADCIN1
9C7>
5C6<
4
GND
D18
BAV99
R59
3
AR1
LM393A
10K
A
K2
9A7>
1 A
5C1<
6
AK
B
5
2K
R45
R123
100K
R46
10K
0.1W
1%
10K
R57
10K
R54
R53
AK
VCC
D
Wed Jul
REV 2 01July04
D
GE Healthcare
Company
Block
22
16:19:33
1
djin
2009
2
3
4
Path
Block
DJINN
ROTATION
CONTROL BOARD V3
5
6
Sheet
8 of
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
7 of
13
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
A
8
Approved Document - 5133326-3SCH_r4.pdf Page 8 of 14
Figure 12-11 Rotor control board 5133326-3SCH_s7
Chapter 12 Generator (Djinn)
Page 239
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
12C4<
11A5<>
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
A
5
12C3<
GWP
10B8>
SWP
12B3<
GVP
10A8>
SVP
6
7
MT2
LT515NP
VCC
1
2
3
IN1
IN2
IN3
P5V
+5V
6
5
4
OUT1
OUT2
OUT3
VOUT
OUT
F3
VERY FAST
DC_BUS_P.
ACTING
4
8B2>
ROT_C
7A7<
ADCIN1
8B2>
5C1<
A
2
3
1
13A2<
11C1<>
A
0V
OV
12B4<
8
IN1
IN2
IN3
P5V
+5V
6
5
4
OUT1
OUT2
OUT3
VOUT
OUT
B
5C4<
0V
10
9
E3
G3
E6
G6
E5
E4
G4
3
4
11
12
ROT_P
7A7<
ACTING
4
2
GUN
12A7<
400V
10A
C
11C5<>
12B7<
GVN
12C7>
GWN
C
MT3
LTS15NP
COMMAN
10B8>
VCC
1
2
3
IN1
IN2
IN3
P5V
+5V
6
5
4
OUT1
OUT2
OUT3
VOUT
OUT
OV
R159
100K
1W
5%
8B3>
5C6<
0V
R160
3V3
47K
1W
5%
ROT_A
R161
1K
0.1W
1%
R162
2K
0.1W
1%
1
R163
4.99K
0.1W
1%
U4
74LVC-LCX14
A
C
K
E
4
13
7A7<
3V3
R117
4.99K
0.1W
1%
U18
TLP281
D
ADCIN2.
A
B
D
DC_BUS_SENSE
12
4A5<
REV 2 01July04
12A8<
VCC=3V3;GND=GND
2
3
GE Healthcare
Company
Block
Wed Jul
22
16:20:10
1
djin
2009
2
3
4
Path
Block
DJINN
5
ROTATION
CONTROL BOARD V3
9 of
6
Approved Document - 5133326-3SCH_r4.pdf Page 9 of 14
Figure 12-12 Rotor control board 5133326-3SCH_s8
Page 240
Sheet
Section 12.2 Main auxiliary 15kW module 5338768
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
8 of
8
13
B Size
3
1
2
3
OV
2
1
VCC
N
N
G5
G
7B7<
F2
VERY FAST
DC_BUS_N.
G1
C46
10N
250V
20%
7
8
DS3
1MH
NEON_BULB
13D2<
E2
2
1
2M
1
PIN
STRAIGHT
TAB
E1
2
4
U
V
W
2
3
U
V
W
1
2
2.2U
450V
R148
PE-62917
1
A1
Q7
MT1
LTS15NP
C47
10N
250V
20%
C44
R99
220K
0.5W
5%
J7
1
FL1
1
B
BSM30GD60DLC
P
220K
PIN
STRAIGHT
TAB
SUP
10A8>
P
R100
220K
0.5W
5%
R149
A1
11A1<>
220K
1
12A4<
6
5
R101
220K
0.5W
5%
J2
GUP
12A3<
G2
400V
10A
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
2
7
P1A
1A
63V
R24
10K
1W
5%
A
8T
*
P1B
D19
MBRS1100T3
100V
1
R21
10K
1W
5%
P2A
100U
16V
C8
0.47U
50V
10%
C1
2
*
2T
P2B
R5
10K
0.125W
1%
D1
MURS120T3
R4
4.7K
0.25W
1%
R3
R6
100K
C48
0.1U
25V
5%
C2
R165
100
1W
5%
P3A
2T
1T
11A1<>
S1N
6V
SUP_NEG
11B1<
S2P
18V
SVP_POS
11C1<
SVP
S2M
*
1T
11C1<>
S2N
6V
S3P
18V
SWP_POS
S3N
6V
SWP_NEG
11B5<
S4P
18V
SUVWN_POS
11C5<
SVP_NEG
SWP
S3M
*
1T
11A5<>
S
IRF640NS
G
C9
2.2U
63V
10%
R133
300
1W
1%
1T
SUVWN_NEG
6V
S4N
11C5<>
11D5<
TP2
3
VOUT1
VOUT2
2
4
ADJ_GND
1
3.3V
C
VR2
LF50CDT
1
VIN
VCC
VOUT
3
GND
4
5V
100U
16V
20%
1N
C52
1
1W
R22
R20
C7
VIN
2
0.1U
C5
10K
3V3
VR1
LT1117-3V3
K
R164
300
1W
1%
C6
1N
50V
5%
1N
12A8<
B
COMMAN
S4M
D25
BAV99
70V
AK
1K
0.1W
1%
9C4<
3T
A
3
R2
10K
0.1W
1%
12C4<
*
C3
200
0.25W
1%
9A4<
11A5<
C10
6
Q1
12B4<
3T
MBRS1100T3
100V
C4
OUTP
D
9A4<
11D1<
*
VCC
8
R1
A
3T
100U
16V
20%
VREF
12A4<
1
C
VP
VN
RT_CT
VFB
COMP
ISENSE
9B4<
*
D20
R98
SUP
S1M
*
*
C77
2.2N
200V
5%
PS1
UC3845A
7
5
4
2
1
3
C49
11A1<
TP1
1N
50V
5%
R7
4.99K
0.125W
1%
SUP_POS
3T
*
P3B
18V
S1P
*
200V
B
100K
0.1W
0.1%
8
T1
TP23
F1
TIME_DELAY
100V
D
Wed Jul
REV 2 01July04
D
GE Healthcare
Company
Block
22
16:19:36
1
djin
2009
2
3
4
Path
Block
DJINN
ROTATION
CONTROL BOARD V3
5
6
10
Sheet
of
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
9 of
13
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
6
100U
16V
20%
48V
D24
MBRS1100T3
5
1U
25V
10%
48V1
4
3
WINDING OF THE TRANSFORMER
1
8
Approved Document - 5133326-3SCH_r4.pdf Page 10 of 14
Figure 12-13 Rotor control board 5133326-3SCH_s9
Chapter 12 Generator (Djinn)
Page 241
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
D14
MBRS1100T3
6
SWP_POS
Q1_POS
SUP_POS
10A8>
5
7
D11
MBRS1100T3
Q3_POS
10A8>
12A4<
8
100V
12C4<
100V
C20
4.7U
25V
10%
C19
4.7U
25V
10%
4.7U
25V
10%
C21
4.7U
25V
10%
4.7U
25V
10%
C25
C26
A
SW P
9B4<
9B4<
SUP
10A8>
10A8>
12C4<
SUP_NEG
10A8>
9A4<
10B8>
12C4<
9A4<
10B8>
4.7U
25V
10%
12A4<
12A4<
C27
D15
MBRS1100T3
Q1_NEG
12B4<
10B8>
SWP_NEG
100V
D10
MBRS1100T3
Q3_NEG
12D4<
100V
B
B
D12
MBRS1100T3
Q2_POS
SVP_POS
SUVWN_POS
12B4<
Q4_POS
10B8>
12C4<
C
COMMAN
SUVWN_NEG
Q2_NEG
SVP_NEG
4.7U
25V
10%
9C4<
4.7U
25V
10%
12A8<
C17
10B8>
C18
9C4<
4.7U
25V
10%
12A8<
D13
MBRS1100T3
10A8>
C16
4.7U
25V
10%
SVP
10A8>
10A8>
C22
9A4<
9A4<
C23
C24
12B4<
12B4<
12A8<
100V
4.7U
25V
10%
100V
C
D8
MBRS1100T3
10B8>
4.7U
25V
10%
10A8>
D9
MBRS1100T3
Q4_NEG
10B8>
100V
12A8<
100V
D
REV 2 01July04
D
GE Healthcare
Company
Block
Wed Jul
22
16:19:36
1
djin
2009
2
3
4
Path
Block
DJINN
5
ROTATION
CONTROL BOARD V3
11
6
Approved Document - 5133326-3SCH_r4.pdf Page 11 of 14
Figure 12-14 Rotor control board 5133326-3SCH_s10
Page 242
Section 12.2 Main auxiliary 15kW module 5338768
Sheet
of
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
10
8
of
13
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
A
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
Q4_POS
VO
3
VO
7
6
Q1
5
SUP
9A4<
4B3<
9B4<
VEE
C42
2
VO
3
VO
7
6
1U
50V
+-20%
C35
9C4<
10B8>
9C4<
DC_BUS_N
GUN
5
VEE
R79
1K
0.1W
1%
A
COMMAN
11C5<>
Q4_NEG
11D8>
R80
Q1_NEG
Q1
VCC
8
VO
7
6
PWM_VP R92
Q2
2
3
SVP
9A4<
VO
10A8>
11C1<>
4B3<
9A4<
PWM_VN
R84
8
VO
7
6
2
100
0.1W
1%
GVP
5
VEE
VCC
R71
100
1W
R89
B
5%
9C4<
GVN
5
VEE
R77
1K
0.1W
1%
1U
50V
+-20%
10K
0.125W
1%
VO
3
C33
1U
50V
+-20%
C39
10K
0.125W
1%
100
1W
5%
R72
R65
DC_BUS_N
U10
HCPL3120_300
1U
50V
+-20%
R83
1K
0.1W
1%
Q2
C40
4B3<
R66
11C4>
1U
50V
+-20%
B
Q2
100
0.1W
1%
Q2_POS
Q2
U13
HCPL3120_300
11B4>
C34
100
0.1W
1%
R78
2
R81
1K
0.1W
1%
3
VCC
8
VO
7
6
R64
10K
0.125W
1%
Q3
VO
Q3
100
0.1W
1%
PWM_WN R87
100
0.1W
1%
10B8>
11A5<>
9A4<
GWP
5
VCC
8
2
VO
7
6
3
VO
R63
10K
0.125W
1%
R69
100
1W 5%
1U
50V
+-20%
11A8>
4B3<
SW P
9A4<
DC_BUS_N
U9
HCPL3120_300
C
9C4<
GW N
5
VEE
R76
1K
0.1W
1%
R88
VEE
C38
R82
100
0.1W
1%
Q3
1U
50V
+-20%
PWM_WP R91
4B3<
Q3
R70
100
1W
5%
Q3
Q3_POS
11D4>
1U
50V
+-20%
U12
HCPL3120_300
Q2_NEG
C31
C
Q2
1U
50V
+-20%
100
0.1W
1%
100
0.1W
1%
11A1<>
100
0.1W
1%
R86
100
0.1W
1%
10A8>
GUP
R74
R73
100
1W 5%
8
R90
1U
50V
+-20%
R85
1K
0.1W
1%
2
VCC
PWM_UN
C32
100
0.1W
1%
10K
0.125W
1%
1U
50V
+-20%
4B3<
100
1W
5%
8
10K
0.125W
1%
C36
VCC
PWM_UP R93
R67
DC_BUS_N
U11
HCPL3120_300
Q1
C37
Q3_NEG
100
0.1W
1%
11B8>
D
Wed Jul
REV 2 01July04
D
GE Healthcare
Company
Block
22
16:19:32
1
djin
2009
2
3
4
Path
Block
DJINN
ROTATION
CONTROL BOARD V3
5
6
12
Sheet
of
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
11
of
13
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
A
R68
1U
50V
+-20%
Q1
11A4>
C41
U14
HCPL3120_300
11C8>
Q1_POS
Q1
8
Approved Document - 5133326-3SCH_r4.pdf Page 12 of 14
Figure 12-15 Rotor control board 5133326-3SCH_s11
Chapter 12 Generator (Djinn)
Page 243
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
A
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
A
DC_BUS_P.
9A2<
R32
470
0.5W
5%
D4
BZX84C12
12V
5%
R38
470
0.5W
5%
3V3
3
R119
1
S
G
C76
1N
630V
5%
IXTT11P50
Q26
100
B
R122
4.99K
0.1W
1%
2
D
R94
220K
0.5W
5%
U5
TLP281
R23
4
C2
B
R97
220K
0.5W
5%
Q3
FZT851
3
R107
33
1W
5%
C
10
0.1W
1%
R27
1K
0.1W
1%
2
C1
1
B
U4
74LVC-LCX14
A
C
K
E
DISCH_OK
4
5
A
B
6
3B7<
VCC=3V3;GND=GND
2
3
1
E
R16
270
0.1W
1%
C
R102
220K
5%
1W
R37
100
D27
RUR1S1560S
600V
R105
1K
100W
5%
DC_BUS_N.
J8
U7
TLP281
R18
R19
1
DISCH_INHIBIT
4A5<
100
0.1W
1%
100
0.1W
1%
A1
A
C
K
E
2
D
4
R39
100
0.1W
1%
1
PIN
STRAIGHT
TAB
3
D
REV 2 01July04
3V3
GE Healthcare
Company
Block
Wed Jul
22
16:19:32
1
djin
2009
2
3
4
Path
Block
DJINN
5
ROTATION
CONTROL BOARD V3
13
6
Approved Document - 5133326-3SCH_r4.pdf Page 13 of 14
Figure 12-16 Rotor control board 5133326-3SCH_s12
Page 244
Section 12.2 Main auxiliary 15kW module 5338768
Sheet
of
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
12
8
of
13
B Size
9C2<
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
48V
A
A
SECTION
ADC3
R150
R127
2K
0.1W
1%
3C3<
1K
R126
100
0.1W
1%
2
3V3
K D23
BAV99
70V
E
7C3<
1
0.1U
2K
R140
R144
T70_FAULT
R142
9
10K
0.1W
1%
C75
1U
50V
10%
C74
1U
50V
10%
Q4
PMBTA42
2K
0.1W
1%
10K
0.125W
C
B
U4
74LVC-LCX14
7C3<
R141
4.99K
A
A
B
8
4A5<
B
10K
0.1W
1%
VCC=3V3;GND=GND
4.99K
0.1W
1%
R44
4.99K
0.1W
1%
B
T70__N
T70_P.
R146
R145
R147
R41
10K
0.25W
1%
C71
AK
100K
0.25W
1%
EN_T70_MEAS
4A5<
3
2K
C
R40
10K
0.125W
1%
R75
Q6
PMBT2907A
R143
B
R42
2K
0.1W
1%
E
VCC
MH2
MHP4_50TB10_00
C
MH3
MHP4_50TB10_00
0.1U
16V
10%
1
MH4
MHP4_50TB10_00
C45
0.1U
16V
10%
C43
0.1U
16V
10%
0.1U
16V
C59 10%
C73
C70
0.1U
16V
10%
1
MH1
MHP4_50TB10_00
1
C
1
D
Wed Jul
REV 2 01July04
D
GE Healthcare
Company
Block
22
16:19:33
1
djin
2009
2
3
4
Path
Block
DJINN
ROTATION
CONTROL BOARD V3
5
6
14
Sheet
of
Dwg No
14
5133326-3SCH
7
Rev
Restricted
Sheet
4
13
of
13
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
TEMP SWITCH
8
Approved Document - 5133326-3SCH_r4.pdf Page 14 of 14
Figure 12-17 Rotor control board 5133326-3SCH_s13
Chapter 12 Generator (Djinn)
Page 245
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
DRAFT - WORK-IN-PROCESS. Production parts may not be defined by this document.
See the GEHC Myworkshop System to determine the status of this document.
Section 12.3 Optional auxiliary module 30kW 5338767
Figure 12-18 Optional auxiliary module 30kW 5338767ADW_s1
Page 246
Section 12.3 Optional auxiliary module 30kW 5338767
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
0$,1$8;,/,$5<
DRAFT - WORK-IN-PROCESS. Production parts may not be defined by this document.
See the GEHC Myworkshop System to determine the status of this document.
!"#$"%
%((7/('-,11$8;237%2;$':BUHY10SDJH
Figure 12-19 Optional auxiliary module 30kW 5338767ADW_s2
Chapter 12 Generator (Djinn)
Page 247
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
12.3.1 Beetle CAPA board 5395972
Approved Document - 5395972ADW_r1.pdf Page 2 of 2
Figure 12-20 Beetle CAPA board 5395972ADW
Page 248
Section 12.3 Optional auxiliary module 30kW 5338767
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
3
5
4
6
7
8
A
A
H2
H3
H4
J4
R4
J1
VP1
PIN
FASTON 6,4
90D
R2
14K
0.25W
1%
14K
0.25W
1%
VP2
PIN
FASTON 6,4
90D
P
B
B
D1
DSI30-08AS
800V
D2
DSI30-08AS
800V
D3
DSI30-08AS
800V
MH1
J3
N
J2
1
PIN
RIGHT_ANGLE
TAB
C
R3
R1
A1
VN1
14K
0.25W
1%
14K
0.25W
1%
H1
A1
1
VN2
PIN
RIGHT_ANGLE
TAB
C
H5
D
Made
By
Date
SYSTECH
Block
Tue
May 25
08:45:27
1
Title
07-MAY-2010
Path
Block
beetle_capa_v2
2010
2
3
4
BEETLE
5
1 of
6
GE Healthcare
CAPA
Sheet
Company
Dwg No
1
REV 2 01July04
D
5395972SCH
7
Rev
Restricted
Sheet
1
1 of
1
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
MH2
8
Approved Document - 5395972SCH_r1.pdf Page 2 of 2
Figure 12-21 Beetle CAPA board 5395972SCH
Chapter 12 Generator (Djinn)
Page 249
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 12.4 Power module 5396857
Figure 12-22 Power module 5329919ADW
Page 250
Section 12.4 Power module 5396857
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
12.4.1 Power board 5367800
Approved Document - 5367800ADW_r5.pdf Page 2 of 3
Figure 12-23 Power board 5367800ADW
Chapter 12 Generator (Djinn)
Page 251
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
3
5
4
6
7
8
VCC
C10
T1
1
2
3
4
5
6
7
8
A
1
2
Vcc
0.1U
50V
10%
9
3
4
11
Vout
Vref
6
GND
7
12
10
C9
10N
50V
10%
C5
0.1U
50V
10%
8
HXS_50_NP
L1
150V
100A
150V
100A
C
50A
600V
STRAP A
BB_IN_P2
B
D72_H36
50A
C2
15UF
450V
10%
22
50A
C1
15UF
450V
10%
D1
RUR1S1560S
600V
D2PAK
0V TO 440V
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
R93
B
1W
5%
22
R104
1W
5%
22
1W
1W
22
5%
D2
5%
DSEP60-06A
APT94N60L2C3
20
1W
1%
4A2<
5B2<
2D4<
1C8>
DC_BUS_N
R46
BB_BOOST_A_CMD_P
200
2
R113
2K
C
G3_P12V
C71
VCC
8
VO
7
6
5C7>
BB_BOOST_B_CMD_N
SP2
SPARE0805
1
2
U2
R12
SP1
SPARE0805
1
2
R65
2K
8
2
VO
7
6
3
VO
S
APT94N60L2C3
C12
6,8NF
630V
5%
RA01
R86
D
Q6
C19
2.2N
2KV
5%
G
10
5% 1W
R83
10K
S
R17
R64
2
0.25W
1%
NO POPULATED
2D4< 4A2< 4B2<
1C1<> 5B2<
DC_BUS_N
R84
2
0.25W
1%
C
REV.2
:
REPLACE DRIVERS
( SHEET 2 )
0.47U
50V 10%
BB_BOOST_B
REVISION
C46
5
0.47U
50V 10% G3_0V
G3_N8V
R85
2K
BB_SNUB_CMD_N
R112
2
0.25W
1%
VEE
R19
BB_SNUB_CMD_P
D
G3_P12V
C37
C36
MOSFET IXDD409YI
ECR/ECO
BY IXDD430YI
DATE
SIGN
21-DEC-2010
C59
VCC
8
2
VO
7
6
3
VO
4.7U
25V
10%
0.47U
50V 10%
G3_0V
4.7U
25V
10%
2110541
SYSTECH
4
2114074
16-MAR-2011
SYSTECH
5
2118057
04-JUL-2011
SYSTECH
G3_N8V
D
BB_SNUB
C57
5
VEE
0.47U
50V 10% G3_0V
G3_N8V
Made
By
Date
SYSTECH
Block
Title
16-MAR-2011
Path
Block
beetle_djinn_power_v2b
2011
Beetle
Djinn
Sheet
1 of
Power
V2
Dwg No
5
5367800SCH
GE Healthcare
Company
Rev
Restricted
Sheet
5
1 of
Approved Document - 5367800SCH_r5.pdf Page 2 of 6
1
2
3
4
5
Figure 12-24 Power board 5367800SCH_s1
Page 252
OFF
3
G3_P12V
200
14:18:49
R61
10K
B
1K
1W 5%
C70
VCC
R11
200
04
1K
NO POPULATED
1W 5%
Q3
R78
5%
C47
HCPL3120_300
Mon Jul
1W
G3_P12V
HCPL3120_300
U4
5C1>
22
0.47U
50V 10% G3_0V
G3_N8V
R44
0
200
5C7>
20
1W
1%
C42
6.8UF
450V
10%
5
200
5C1>
G
C32
6.8UF
450V
10%
R27
1W
5%
D
R66
5A2<
VEE
200
R47
0
0.47U
50V 10%
VO
3
R43
BB_BOOST_A_CMD_N
BB_BOOST_B_CMD_P
C33
6,8NF
630V
5%
RA01
C18
6.8UF
450V
10%
4,7UH
10%
21SP_128X0.1
DC_BUS_N
HCPL3120_300
5C1>
22
4A2<
L2
BB_IN_P3
100A
U9
5C7>
S
BB_BOOST_A
4B2<
Q9
G
R111
10K
1W
5%
APT94N60L2C3
D
R114
22
600V
R135
1W
5%
2A4<
R24
R69
22
DC_BUS_P
100A
BB_IN_P3_C
600V
R134
R127
A
D6
DSEP60-06A
600V
600V
D16
DSEP60-06A
R126
440V
D3
DSEP60-06A
BB_IN_P3_B
0V TO 440V
4C2< 4C2<
D11
DSEP60-06A
BB_IN_P3_A
A
2X200UH
4C2< 4C2<
BB_IN_P3_B
REV 2 01July04
BB_IN_P
5C6<
BB_IN_P3_A
Section 12.4 Power module 5396857
6
7
8
5
B Size
5A6>
5C1<
I_BB_MEAS_REF
R9
10K
0V TO 440V
4B2<
I_BB_MEAS
5
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5A2<
4A2<
5
6
7
8
DC_BUS_P
1A8>
G1_P12V
3C7>
C35
4.7U
25V
10%
DC_BUS_P
G1_0V
3C7>
2
R51
2K
APT94N60L2C3
G2_0V
D24
BAV99
70V
50V
3C7>
VCC
EN
7
IN
GND
5
HCPL2211
C44
4.7U
25V
10%
BH2
R119
2K
3
2 AK
VO
R121
3
A
GND
5
50V
120P
TO_CAPA_IN
G2_N8V
C7
6.8UF
450V
10%
E3435-1
U11
IXDD630YI
+ DISSIPATEUR
2
0.25W
R122
7
3
10K
6
4
C15
6.8UF
450V
10%
E3435-1
5
MEAS_1
2
FIS105
1/50
RATIO
R37
2K
G3_P12V
G3_P12V
1
R15
INV_A_L
100
G3_N8V
1K
C51
GND
HCPL2211
7
IN
120P
50V
5%
5
C50
4.7U
25V
10%
S
04
14:08:54
APT94N60L2C3
D Q8
R95
G
NPP
C27
33N
630V
5%
S
5.6
BL2
R89
DC_BUS_N
0 0.25W
R79
OUT
10K
10K
+ DISSIPATEUR
5B2<
4B2<
R92
10
8
7
IN
4A2<
1C8>
1C1<>
DC_BUS_N
8
VO
0.1U
50V
10%
7
GND
INV_OK
C62
4.7U
25V
10%
C23
4.7U
25V
10%
C
HCPL2201
D27
BAV99
70V
U6
INV_B_L_P
VCC
R99
2K
3
2 AK
VO
R103
A
GND
R32
1K
C65
HCPL2211
50V
120P
INV_B_L
5D7>
100
D
5%
GE Healthcare
Block
beetle_djinn_power_v2b
Sheet
2 of
Dwg No
5
5367800SCH
Rev
Restricted
Sheet
5
2 of
Approved Document - 5367800SCH_r5.pdf Page 3 of 6
1
2
3
4
5
6
5D7>
K
Company
Path
5D7>
5
G3_N8V
Block
2011
5A2<
3
3
5
+ DISSIPATEUR
5A2<
OUT_HT_A
G3_0V
U14
IXDD630YI
OUT
CAPA_IN
SP7
R26
2K
R100
U?13
IXDD630YI
C16
4.7U
25V
10%
1W
G3_0V
R107
0 0.25W
600V
C22
4.7U
25V
10%
0 0.25W
G3_N8V
Mon Jul
R87
47K
1W
5%
0 0.25W
VCC
EN
8
3
1
D
A
VO
AL2
R68
47K
1W
5%
G3_P12V
2
2K
G3_0V
R80
GND
PPAD
R77
VCC
3
AK 2
2K
3B7>
R14
2K
R71
10
2
U3
R73
1W
R70
SP6
K
5D7>
5.6
NPP
C17
33N
630V
5%
5.6 1W
S Q7
APT94N60L2C3
EN
VCC
2
G3_0V
D25
BAV99
70V
APT94N60L2C3
Q5 D
R76
G
C14
4.7U
25V
10%
G
R39
C29
10N
50V
10%
5D7<
2
S
D14
MURS360T3G
R91
I_INV_MEAS_N
B
C67
1
APT94N60L2C3
BL1
5D1<
2
Q4
D
PPAD
GND
1W
NPP
C21
33N
630V
5%
R16
47K
1W
5%
MID_BL1_BL2
G
R13
47K
1W
5%
1
NPP
C13
33N
630V
5%
D
I_INV_MEAS_P
VCC
U8
1
600V
MID_AL1_AL2
5.6
INV_A_L_P
3C7>
R108
150
0.25W
1%
1
3
MEAS_8
8
5
VGH_23X11_5X25
1/50
C38
6.8UF
450V
10%
E3435-1
C6
6.8UF
450V
10%
E3435-1
T3
1
D15
MURS360T3G
C
5D7>
5%
T4
G3_P12V
AL1
G3_0V
5D1>
+ DISSIPATEUR
OUT
R72
3B7>
INV_B_H
100
G1_N8V
VCC
3A7>
R50
1K
C73
HCPL2211
C39
4.7U
25V
10%
1W
R116
2
1
5
1
5.6
S
0
C8
4.7U
25V
10%
5%
120P
NPP
C41
33N
630V
5%
VCC
7
C72
4.7U
25V
10%
3
A
1K
C45
100
4
IN
0 0.25W
R123
10K
GND
PPAD
R10
INV_A_H
OUT
Q11
APT94N60L2C3
D
R120
G
0.25W
R63
R55
10
8
VO
1
5D1>
2
K
8
REV 2 01July04
2
0
VCC
3
AK 2
R60
R115
47K
1W
5%
1W
Q10
S
APT94N60L2C3
0 0.25W
R67
R8
2K
SP5
K
R57
2K
AH2
R54
U1
B
S
R53
47K
1W
5%
5.6
R117
10
7
5
B Size
INV_A_H_P
1W
5.6
NPP
C11
33N
630V
5%
R118
G
2
5D7>
C4
4.7U
25V
10%
1
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
3B7>
APT94N60L2C3
Q2 D
R59
G
G2_P12V
BH1
5D7>
2
3B7>
S
D
1
Q1
NPP
C34
33N
630V
5%
R42
47K
1W
5%
A
INV_B_H_P
U10
PPAD
GND
1W
R7
47K
1W
5%
MID_BH1_BH2
G
MID_AH1_AH2
5.6
NPP
C3
33N
630V
5%
D
R56
SP8
U15
IXDD630YI
EN
VCC
AH1
6
3
A
D26
BAV99
70V
8
Figure 12-25 Power board 5367800SCH_s2
Chapter 12 Generator (Djinn)
Page 253
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
A
7
A
DS3
HSMG-C190
2
D8
MBRS1100T3
100V
1
GREEN
C56
4.7U
25V
10%
C58
4.7U
25V
10%
R18
2.49K
0.125W
1%
ISO
G3_P12V
G3_0V
G3_P12V
1MM
ISO
D7
MBRS1100T3
100V
C55
22U
10V
10%
C54
22U
10V
10%
2C1<
1MM
G3_0V
ALIM
MOS C
+ BOOST
+ MEAS
G3
2C1<
G3_0V
ISO
0.8MM
G3_N8V
2D1<
G3_N8V
B
B
48V
C28
4.7U
100V
10%
F1
FAST_ACTION
3A
63V
C24
4.7U
100V
10%
P1
D1
C60
0.1U
100V
10%
C76
4.7U
100V
10%
ISO
T2
2T
C77
4.7U
100V
10%
4T
D5
MBRS1100T3
100V
1T
4T
ISO
1,3MM
2T
C52
4.7U
25V
10%
ISO
G2_P12V
2B1<
G2_0V
2B1<
G2_N8V
2C1<
G1_P12V
2A8<
G1_0V
2A8<
G1_N8V
2B8<
1MM
ISO
1MM
ALIM
G2
MOS A
1T
R130
SP4
1
VCC
GATE_INV_SUPPLY_CMD
VDD
7
O_N
GND
2
DISSIPATEUR
R98
5.1V
5%
SP3
1
Q12
IRF640NS
D23
BZX84C5V1
3
IN
110
0.25W
D
D9
ES2D-E3
200V
C20
2.2N
200V
5%
G
S
R29
10K
0.25W
VCC
1T
2T
D2
0
D2A
2
ISO
0.8MM
1T
ELP_32_6_20
P2A
R22
300
1W
1%
R21
300
1W
1%
6
VDD
5
O_N
GND
4
4.2MM
D13
MBRS1100T3
100V
C68
22U
10V
10%
ISO
4.2MM
C
1MM
ISO
ISO
ISO
1MM
ALIM
G1
MOS B
0.8MM
D10
BAV99
70V
K
3
IN
CH2
R129
0
C69
4.7U
25V
10%
A
AK
U5
TC4426A
D12
MBRS1100T3
100V
2
ISO
3
12V
R101
1K
CH3
1T
D4
MBRS1100T3
100V
1
12V
U5
TC4426A
6
5C7>
3T
P2
R94
4.99K
C
3T
C53
22U
10V
10%
4.2MM
2
12V
C64
D
D
REV 2 01July04
0.1U
50V
10%
GE Healthcare
Company
Block
Wed Mar
16
08:57:50
Path
Block
beetle_djinn_power_v2b
2011
Sheet
3 of
Dwg No
5
5367800SCH
Rev
Restricted
Sheet
5
3 of
Approved Document - 5367800SCH_r5.pdf Page 4 of 6
1
2
3
4
5
Figure 12-26 Power board 5367800SCH_s3
Page 254
Section 12.4 Power module 5396857
6
7
8
5
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
8
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
12V
C63
1A8>
DC_BUS_P
A
R34
R30
R31
R33
R38
100K
0.25W
0.1%
100K
0.25W
0.1%
100K
0.25W
0.1%
100K
0.25W
0.1%
100K
0.25W
0.1%
0.1U
50V
10%
C66
10N
50V
10%
5B2<
4B2<
2D4<
1C8>
1C1<>
DC_BUS_N
R109
2K
0.125W
1%
3
INP
2
INN
R110
8.66
0.125W
1%
R28
7
VP5
REFP
2A4<
R132
2K
0.125W
1%
AR1
INA117
6
VOUT
NOTE:
PIN 8 FOR INA117
IS COMP
PIN 8 FOR AD629 IS NC
BOTH PARTS ARE APPROVED
FOR PI NUMBER 2369296
C25
100K
0.25W
0.1%
100K
0.25W
0.1%
C61
10N
50V
10%
5B2<
4A2<
2D4<
1C8>
1C1<>
DC_BUS_N
5C6<
C79
4.7U
25V
10%
0.1U
50V
10%
R90
2K
0.125W
1%
3
INP
2
INN
R88
20
0.125W
1%
R35
7
VP5
REFP
R62
DC BUS
0
0.125W
+0.05
R133
2K
0.125W
1%
B
N12V
AR2
INA117
6
VOUT
NOTE:
PIN 8 FOR INA117
IS COMP
PIN 8 FOR AD629 IS NC
BOTH PARTS ARE APPROVED
FOR PI NUMBER 2369296
4
1 VN
8REFN
COMP
V_IN_MEAS_P
5C1<
V_IN_MEAS_N
5C6<
SCALE:
R96
1V => 100V
BB_IN
0
0.125W
+0.05
0
C75
N12V
0.1U
50V
10%
G3_P12V
C
1A8>
D22
MURS360T3G
BB_IN_P3_A
600V
1A8>
D20
MURS360T3G
BB_IN_P3_B
600V
C
U12
R75
2K
0.125W
1%
C48
1N
50V
10%
R74
2K
DC_BUS_N
D21
MMSZ5226BT1
VCC
VCC
2
VO
8
7
VCC
C49
0.1U
50V
10%
_BB_ZVS_OK
3
3.3V
GND
5C1<
5
HCPL2201
DC_BUS_N
D
REV 2 01July04
D
GE Healthcare
Company
Block
Wed Mar
16
08:57:50
Path
Block
beetle_djinn_power_v2b
2011
Sheet
4 of
Dwg No
5
5367800SCH
Rev
Restricted
Sheet
5
4 of
Approved Document - 5367800SCH_r5.pdf Page 5 of 6
1
2
3
4
5
6
7
5
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
B
R58
DC_BUS_MEAS_N
=> 100V
C78
4.7U
25V
10%
C74
BB_IN_P
R102
0,4V
12V
0.1U
50V
N12V 10%
12V
5A6>
A
5C1<
SCALE:
0
MEAS_OUT
1A1<
DC_BUS_MEAS_P
4
1 VN
8REFN
COMP
5A2<
8
Figure 12-27 Power board 5367800SCH_s4
Chapter 12 Generator (Djinn)
Page 255
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
C40
OUT_HT_B
160NF
5% 1000V
SP2815-3
CAPA_IN
2B8>
OUT_HT_A
2C8> 2C8>
J3
PIN
STRAIGHT
PRESSFIT POWER ELEMENT
OUT_HT_A
A
4A2<
2A4<
A
PIN
STRAIGHT
PRESSFIT POWER ELEMENT
BB_IN_P
DC_BUS_P
1A8>
J4
1A1<
4B2<
J1
4B2<
4A2<
2D4<
1C8>
R2
R1
499K
0.25W
1%
200K
0.25W
1%
DS1
1MH
1
R4
R5
200K
0.25W
1%
100K
0.25W
1%
2
1A
2A
3A
R6
DS2
1MH
1
R3
2
499K
0.25W
1%
PIN
POWER_COMBICON
RIGHT_ANGLE
DC_BUS_N
1C1<>
1
2
3
499K
0.25W
1%
DC_BUS_N
DC_BUS_N
H1
KFH-M5-15-ET
VCC
12V
48V
BB_SPARE_01_CMD_N
MH4
BB_SPARE_03_CMD_N
MH3
INV_A_H
0
R97
CH1
1
2B1<
SPARE_INV
INV_B_H
2B8<
0
R20
MH1
I_INV_MEAS_P
2B8>
C31
4.7U
25V
10%
2
VDD
402
0.25W
1%
C43
0.1U
NO POPULATED
1
3
5
7
9
11
13
15
17
19
21
23
25
27
29
31
33
35
37
39
41
43
45
47
49
2
4
6
8
10
12
14
16
18
20
22
24
26
28
30
32
34
36
38
40
42
44
46
48
50
D18
SMAJ4733A
D17
SMAJ4733A
5.1V
5%
5.1V
5%
C80
4.7U
25V
10%
NO POPULATED
DQ
2
4
6
8
10
12
14
16
18
20
22
24
26
28
30
32
34
36
38
40
42
44
46
48
50
I_BB_MEAS_REF
V_IN_MEAS_N
DC_BUS_MEAS_N
SPARE_BB2
BB_CMD_P
CH4
R49
0
R41
BB_SNUB_CMD_P
1D1<
0
R45
BB_BOOST_A_CMD_P
1C1<
FX4
KFE-4.2-6-ET
R48
BB_BOOST_B_CMD_P
1C1<
GATE_INV_SUPPLY_CMD
3C1<
INV_OK
2C8>
INV_B_L
2D8<
0
R105
INV_B_L_P
2D8<
0
R106
INV_B_H_P
2A8<
0
R81
INV_A_L_P
2D1<
0
R82
INV_A_H_P
2B1<
MH2
R23
C
1A8>
4B7>
4A7>
0
0
C30
4.7U
25V
10%
1
FX5
KFE-4.2-6-ET
1
1
FX6
KFE-4.2-6-ET
1
1
1
FX1
KFE-4.2-6-ET
GND
J2
D
FX2
KFE-4.2-6-ET
DQ
5
3
5.1V
5%
PIN
FX3
KFE-4.2-6-ET
4
INV_A_L
2D1<
I_INV_MEAS_N
2B8>
D
0
N12V
REV 2 01July04
1D1<
1C1<
1D1<
4C8>
BB_BOOST_B_CMD_N
BB_BOOST_A_CMD_N
BB_SNUB_CMD_N
_BB_ZVS_OK
48V
1
3
5
7
9
11
13
15
17
19
21
23
25
27
29
31
33
35
37
39
41
43
45
47
49
SPARE_BB1
10
1
I_BB_MEAS
V_IN_MEAS_P
DC_BUS_MEAS_P
12V
STRAIGHT
1A8>
4B7>
4A7>
1
C
CH5
R125
R124
R25
10K
0.25W
1%
R40
2.49K
RIBBON_CABLE_STANDARD
R52
0
VCC
D19
SMAJ4733A
VCC
C26
4.7U
25V
10%
U16
DS1822
1
R36
1K
48V
B
DS4
HSMG-C190
GREEN
1
DS6
HSMG-C190
GREEN
1
DS5
HSMG-C190
GREEN
GE Healthcare
Company
Block
Wed Mar
16
08:57:51
Path
Block
beetle_djinn_power_v2b
2011
Sheet
5 of
Dwg No
5
5367800SCH
Rev
Restricted
Sheet
5
5 of
Approved Document - 5367800SCH_r5.pdf Page 6 of 6
1
2
3
4
5
Figure 12-28 Power board 5367800SCH_s5
Page 256
Section 12.4 Power module 5396857
6
7
8
5
B Size
B
2
H2
2
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
STRAP B
KFH-M5-15-ET
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
12.4.2 Filament board 5394517
Approved Document - 5394517ADW_r2.pdf Page 2 of 3
Figure 12-29 Filament board 5394517ADW
Chapter 12 Generator (Djinn)
Page 257
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
5
4
ECR/ECO
REV-2
ECR-2107032
DATE
SIGN
13-SEP-10
D6
MBRS1100T3
OFF
VCC
T4
VCC
IR2110S
C51
R75
4.99K
A
HEAT_1_INV_B_H
HEAT_1_INV_B_L
4C2<
4C5<
R81
R80
R74
0
VB
VS
VCC
VDD
12
HIN
13
SD
14
LIN
HO
100V
LO
COM
GND
8
12V
INVERTER
D4
MBRS1100T3
1U
25V
10%
NOT EQUIPED
1
100V
S
1%
C46
47N
250V
10%
C49
47N
500V
10%
G
20
0.25W
7
6
Q8
IRFZ44ES
8
C26
Q10
IRFZ44ES
1
D
R20
2
15
48V
NOT EQUIPED
D
R18
12V
4.99K
4B5>
3
11
0.1U
50V
10%
4.99K
4B2>
1U
25V
10%
--C22
1U
25V
10%
7
C16
C54
1U
25V
10%
20
0.25W
1%
C53
47N
250V
10%
C56
47N
500V
10%
G
S
C18
2.2U
63V
10%
P8208
1/100
RATIO
TR1
C34
47N
250V
10%
L2
R83
20
0.25W
S
Q6
IRFZ44ES
D
C44
47N
500V
10%
R16
G
20
0.25W
1%
S
1%
0.1W
A
1%
Q4
IRFZ44ES
PLANAR_72UH
E43_10_28
C41
47N
250V
10%
C17
1U
25V
10%
R14
G
L3
PLANAR_72UH
E43_10_28
220N
630V
10%
SP2830
402
D
C37
47N
500V
10%
7
REVISION
6
C21
12V
3
3
8
2
1
1
I_INV_HEAT_1_MEAS_GROUND
I_INV_HEAT_1_MEAS
T2
VCC
IR2110S
VCC
VDD
VB
VS
7
6
12
HIN
HO
8
13
SD
14
LIN
48V
12V
LO
COM
GND
K
1
2
15
B
K1
ST2_NIL_DC48V
D8
BAV99
V
AK
C42
1U
25V
10%
6
4
A
1
1K
T3
1
VB
VS
7
6
12
HIN
HO
8
13
SD
14
12V
LO
4.99K
COM
GND
C24
1U
25V
10%
C47
1U
25V
10%
R21
VCC
20
0.25W
R77
0
1U
25V
10%
12
HEAT_2_INV_A_L
R71
D
3
11
VB
VS
VCC
VDD
HIN
13
SD
14
LIN
HO
7
6
Q9
IRFZ44ES
220N
630V
10%
SP2830
R19
8
COM
GND
Mon Sep
I_INV_HEAT_2_MEAS_GROUND
4C5<
I_INV_HEAT_2_MEAS
13
15:01:13
1
C43
47N
250V
10%
C23
2.2U
63V
10%
Q11
IRFZ44ES
D
G
1%
C48
47N
250V
10%
C45
47N
500V
10%
S
402
1
PLANAR_72UH
E43_10_28
PLANAR_72UH
E43_10_28
R82
0.1W
1%
2
C19
1U
25V
10%
Q7
IRFZ44ES
RATIO
C36
47N
250V
10%
20
0.25W
S
L4
1/100
P8208
R17
G
L5
TR2
Q5
IRFZ44ES
D
C33
47N
500V
10%
R15
G
20
0.25W
1%
S
1%
By
Date
Title
13-SEP-2010
Path
beetle_filament
2010
4
BEETLE
Block
5
6
Figure 12-30 Filament board 5394517SCH_s1
Section 12.4 Power module 5396857
FILAMENT
Sheet
1 of
Approved Document - 5394517SCH_r2.pdf Page 2 of 6
Page 258
D
C40
47N
500V
10%
INVERTER
D
Block
3
100V
C
HEATER
POWER SHEET
SYSTECH
2
1U
25V
10%
2
15
Made
4C2<
C55
47N
250V
10%
C52
47N
500V
10%
S
D5
MBRS1100T3
NOT EQUIPED
C27
20
0.25W
LO
4.99K
4B5>
HEAT_2_INV_A_H
IR2110S
C38
R70
4B2>
C35
0.1U
50V
10%
1%
NOT EQUIPED
T1
12V
VCC
D
G
C20
48V
7
R76
4.99K
1U
25V
10%
100V
1
2
15
12V
C25
D7
MBRS1100T3
12V
LIN
4C3<
S
1
VCC
VDD
4C3<
H2A
8
8
3
11
H2B
7
3
HEAT_2_INV_B_L
R78
4B5>
HEAT_2_INV_B_H
R79
4B2>
4.99K
C
R25
10K
IR2110S
0.1U
50V
10%
4C3<
7
8
C50
4C3<
H1B
Q12
2N7002
G
VCC
H1A
6
D
R24
RELAY_CMD
4C5>
5
5
4
Dwg No
5
5394517SCH
7
GE Healthcare
Company
Rev
Restricted
Sheet
2
1 of
8
5
REV 2 01July04
3
11
4.99K
_ENABLE_F
R73
4B5>
HEAT_1_INV_A_L
R72
4B5>
HEAT_1_INV_A_H
4.99K
4B2>
0.1U
50V
10%
4.99K
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
B
B Size
C39
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
4
5
6
7
8
48VA
R12
10K
0.25W
1%
R52
12VA
10K
0.1%
C32
C31
12VA
0.1U
50V
10%
12VA
4
10K
0.1%
10
AR2
8
VOUT
R67
C5
2.2N
50V
10%
1K
Q3
FDV301N
S
R35
10K
VN
5
2
1K
R40
R39
OHM
12VA
VP
10K
1
0.25W
1%
1N
50V
5%
13
B
Q1
MJD32C
C
AR1
TL084B
C30
0.1U
50V
10%
0.1U
50V
10%
B
R10
1K
0.25W
1%
K
D2
BAV99
70V
4C3<
C14
0.1U
100V
10%
R62
10K
0.25W
1%
12VA
N12VA
C29
R63
10K
0.25W
1%
E
C10
0.1U
100V
10%
14
VOUT
12
D10
100V
2
R41
4
4
N12VA
3
AK
R65
10K
A
N12VA
R13
N12VA
10K
N12VA
N12V
10
10K
CH6
12VA
1U
50V
10%
1
1
CH7
8
VOUT
AR1
TL084B
3
11
C6
1U
25V
10%
FL1
BLM11A102S
9
VN
10K
2
41.2K
R1
1
0.25W
1%
48VA
C11
POLAR_P
100
0.25W
1%
R11
VP
12VA
1N
50V
5%
1
VOUT
AR1
TL084B
VN
10K
VP
R37
R47
4
CH5
12VA
VN
C7
1U
25V
10%
U1
OPA551UA
48V
R6
1
0.25W
1%
R4
6
0.1U
50V
10%
C4
11
R38
OHM
VOUT
3
AR1
TL084B
N12VA
D11
MBRS1100T3
100V
100V
10%
E
7
2
C9
2
1K
Q2
MJD31C
48VA
R53
10K
20K
6
7
VOUT
C2
11
N12VA
POLAR_N
4C3<
0
R8
0
R66
20K
C
R69
R50
11
N12VA
NOT EQUIPED
3
11
20K
7
VOUT
AR2
TL084B
1
VOUT
AR2
R68
D3
BAV99
70V
3
BIAS_VOLTAGE_MEAS
AK
1K
A
TL084B
4B5<
C15
0.1U
50V
10%
1
A
AK
R60
R55
4
VN
5
10K
VP
2
10K
VP
6
R7
20K
K
4
20K
1
3
12VA
70V
K
2
12VA
2
D1
BAV99
R46
R51
VCC
R59
20K
20K
C
20K
VN
N12VA
MAGNITUDE DETECTOR
D
BIAS
REV 2 01July04
D
SHEET
GE Healthcare
Company
Block
Fri
Apr
30
13:23:06
1
Path
Block
beetle_filament
2010
2
3
4
5
Sheet
2 of
6
Dwg No
5
5394517SCH
7
Rev
Restricted
Sheet
2
2 of
5
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
12VA
20K
2
12VA
1
B
R42
C3
0.1U
B
1
4
5
8
G
R44
0
0.1W
+0.05
48VA
C
22P
100V
5%
R36
41.2K
FL2
BLM11A102S
0
A
48VA
C8
VP
R48
0
0.1W
+0.05
3
R43
12V
R2
20K
0.25W
0.1%
MID_48V
1
R58
10K
R5
20K
0.25W
0.1%
R45
N12VA
D
4.99K
R54
10K
0.1%
4
BIAS_PWM_16KHZ
4B2>
R49
TL084B
10K
R57
C13
0.1U
50V
10%
R9
10K
0.25W
1%
N12VA
VP
N12VA
11
C12
0.1U
50V
10%
0.1U
50V
10%
11
12
VN
10K
9
11
BIAS_CMD
4B2>
R61
VP
13
R56
AR2
14
VOUT
TL084B
VN
VP
4
A
OUTPUT AMPLIFIER
MID_48V
MBRS1100T3
MAGNITUDE SQUARE GENERATOR
VN1
VN2
VN3
FLAG
VARIABLE
8
Approved Document - 5394517SCH_r2.pdf Page 3 of 6
Figure 12-31 Filament board 5394517SCH_s2
Chapter 12 Generator (Djinn)
Page 259
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
4
5
6
7
8
A
A
12V
6
U3
TC4427
VDD
5
4
IN
F2
TIME_DELAY
48V
CH9
O
1A
63V
GND
3
R26
4.99K
6
VDD
7
2
IN
R27
4.99K
GND
D
R22
O
3
49.9
0.25W
1%
Q13
IRFR024
G
R23
4.99K
R31
10K
0.25W
1%
R32
49.9K
0.25W
1%
R28
10K
0.25W
1%
R30
4.99K
J3
FAN_N
FAN_SUPPLY_FB
S
4C2<
C
C
NOT EQUIPED
VCC
U2
DS1822
VCC
3
C57
0.1U
50V
10%
VDD
DQ
4
GND
5
THERMAL_SENSOR
4C5<
D
REV 2 01July04
D
FAN SHEET
GE Healthcare
Company
Block
Mon Sep
13
14:19:39
1
Path
Block
beetle_filament
2010
2
3
4
5
3 of
6
Approved Document - 5394517SCH_r2.pdf Page 4 of 6
Figure 12-32 Filament board 5394517SCH_s3
Page 260
Sheet
Section 12.4 Power module 5396857
Dwg No
5
5394517SCH
7
Rev
Restricted
Sheet
2
3 of
8
5
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
FAN_CMD
J5
B
1
4C2<
C1
68U
50V
20%
1
330U
20%
1.1A
U3
TC4427
R33
49.9K
0.25W
1%
1
12V
C28
68U
50V
20%
DS1
HSMY-C190
YELLOW
HIGH
2
L6
C58
0.1U
100V
10%
1
FAN FUNCTION
0.3A
LOW
2
60V
2
FAN_P
2
F1
RESETTABLE
B
D9
MBRS1100T3
100V
PIN
RIGHT_ANGLE
WIRE_TO_BOARD
PIN
RIGHT_ANGLE
WIRE_TO_BOARD
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
4
FROM AUX
J1
9
10
11
12
13
14
15
CH2
INT_CAN_H
4B5<
A
8
L1
CH3
INT_CAN_L
48V
J2
48VIN
4B2<
1
2
MH6
D10_H4_50
10U
10%
250MA
1
2
48V
R3
A
0
0.25W
PIN
RIGHT_ANGLE
TERMINAL_BLOCK_HEADER
CH4
PIN
RIGHT_ANGLE
STD_DENSITY
1
MH5
D10_H4_50
1
MH3
D10_H4_50
1
MH4
D10_H4_50
1
1
1
MH2
D10_H4_50
7
NOT EQUIPED
G1
G2
G1
G2
MH1
D10_H4_50
6
48VIN
1
2
3
4
5
6
7
8
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
5
REMPLACER PAR LE MEME AVEC FIXATION
PHOENIX 1913714
R34
0
0.1W
R64
ROTOR_STATE
CH1
CH8
0
48V
OUT
FROM CONTROL
VCC
4A5>
2B1<
2A1<
INT_CAN_L
BIAS_PWM_16KHZ
BIAS_CMD
1A1<
HEAT_1_INV_A_H
1A1<
1D1<
HEAT_1_INV_B_H
HEAT_2_INV_A_H
1D1<
HEAT_2_INV_B_H
1B1>
1D1>
3C7>
I_INV_HEAT_1_MEAS_GROUND
I_INV_HEAT_2_MEAS_GROUND
R29
FAN_SUPPLY_FB
3C2<
FAN_CMD
1
3
5
7
9
11
13
15
17
19
21
23
25
27
29
31
33
35
37
39
0
1
3
5
7
9
11
13
15
17
19
21
23
25
27
29
31
33
35
37
39
2
4
6
8
10
12
14
16
18
20
22
24
26
28
30
32
34
36
38
40
2
4
6
8
10
12
14
16
18
20
22
24
26
28
30
32
34
36
38
40
INT_CAN_H
BIAS_VOLTAGE_MEAS
_ENABLE_F
HEAT_1_INV_B_L
HEAT_1_INV_A_L
PIN
STRAIGHT
RIBBON_CABLE_LOW_PROFILE
C
POLAR_P
POLAR_N
H1A
H1B
H2A
H2B
2B8>
2C8>
1B8>
1B8>
1C8>
1C8>
1
2
3
4
5
6
1
2
3
4
5
6
4A2>
B
2C8>
1B1<
1A1<
1A1<
HEAT_2_INV_B_L
HEAT_2_INV_A_L
1D1<
1D1<
I_INV_HEAT_1_MEAS
1B1>
I_INV_HEAT_2_MEAS
THERMAL_SENSOR
RELAY_CMD
1D1>
3D5>
1C1<
N12V
C
J6
TO HV-TANK
PIN
RIGHT_ANGLE
TERMINAL_BLOCK_HEADER
REMPLACER PAR LE MEME AVEC FIXATION
PHOENIX 1913756
CONNECTOR SHEET
GE Healthcare
Company
Block
Mon Sep
13
14:20:19
1
Path
Block
beetle_filament
2010
2
3
4
5
Sheet
4 of
6
Dwg No
5
5394517SCH
7
Rev
Restricted
Sheet
2
4 of
5
REV 2 01July04
D
D
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
B
J4
12V
8
Approved Document - 5394517SCH_r2.pdf Page 5 of 6
Figure 12-33 Filament board 5394517SCH_s4
Chapter 12 Generator (Djinn)
Page 261
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
3
4
5
6
7
8
REMARKS SHEET
A
A
DEFAULT RESISTOR
GEOMETRIE : 0603
POWER : 100MW
TOLERANCE : 1%
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
B
B
C
D
D
GE Healthcare
Company
Block
Mon Sep
13
14:25:53
1
Path
Block
beetle_filament
2010
2
3
4
5
5 of
6
Approved Document - 5394517SCH_r2.pdf Page 6 of 6
Figure 12-34 Filament board 5394517SCH_s5
Page 262
Sheet
Section 12.4 Power module 5396857
Dwg No
5
5394517SCH
7
Rev
Restricted
Sheet
2
5 of
8
5
B Size
REV 2 01July04
C
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
12.4.3 Control board 5305042-2
No drawings are available for this board due to proprietary restrictions.
Chapter 12 Generator (Djinn)
Page 263
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 12.5 HV tank 5140761-2
5
PUNEETH
BENJAMIN
11/07/11
ECR2120094
TORQUE
PUNEETH
SHAJI
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
4
05/07/11
ECR2119199
LABEL ADDED
5
Approved Document - 5140761-2ADW_r5.pdf Page 3 of 5
Figure 12-35 HV tank 5140761-2ADW
Page 264
Section 12.5 HV tank 5140761-2
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
12.5.1 Int measurement board 5309420
Figure 12-36 Int measurement board 5309420ADW_s1
Chapter 12 Generator (Djinn)
Page 265
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 12-37 Int measurement board 5309420ADW_s2
Page 266
Section 12.5 HV tank 5140761-2
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
4
5
7
6
TEST_MA_CA
TP5
0
0.25W
+0.05
J5
1
2
3
4
H2B
H2A
H1B
H1A
CR2
SMBJ90CA
105.5V
PIN
RIGHT_ANGLE
TERMINAL_BLOCK_HEADER
CR4
SMBJ90CA
105.5V
CR3
SMBJ90CA
105.5V
CR1
SMBJ90CA
105.5V
10
1W
5%
NOT POPULATED
1
2
3
4
C12
0.47U
25V
10%
CR5
SMCJ15CA
15.1V
NOT POPULATED
0
TP2
C11
0.47U
25V
10%
VCC
B
CONTINUITY
J6
1
3
5
7
9
11
13
15
TEST_MA_AN
KV_CA_N
KV_AN_P
1
3
5
7
9
11
13
15
2
4
6
8
10
12
14
16
2
4
6
8
10
12
14
16
DQ
TEST_MA_CA
MA_AN_0V
MA_AN_N
MA_CA_0V
MA_CA_P
CONTINUITY
DQ
R15
10
0.25W
1%
2
4
6
8
10
1
3
5
7
9
1
3
5
7
9
0
0.25W
+0.05
TP4
R3
20K
0.1W
0.1%
C5
1N
100V
1%
R5
1K
0.0625W
0.1%
C3
47N
100V
1%
R1
KV_CA
C8
1N
100V
1%
R8
1K
0.0625W
0.1%
C7
4.7N
100V
1%
P2
MH12
D8_H4_20
MH2
D8_H4_20
MH1
D8_H4_20
MH7
D8_H4_20
MH8
D8_H4_20
MH3
D8_H4_20
MH4
D8_H4_20
MH10
D8_H4_20
C4
47N
100V
1%
R4
20K
0.1W
0.1%
R7
Made
Block
09:27:25
By
Date
1
Title
24-JUN-2009
Path
2
3
4
HV TANK INT
Block
djinn_hv_interco_v5
2009
KV_CA_N
10
0.25W
1%
D
SYSTECH
03
C2
27N
100V
1%
MH9
D8_H4_20
Approved Document - 5309420SCH_r3.pdf Page 2 of 2
Mon Aug
C1
27N
100V
1%
C
1K
0.25W
1%
MH11
D8_H4_20
KV_AN_P
R10
20K
0.1W
0.1%
CONN_POWER
MH5
D8_H4_20
B
TEST_MA_AN
R9
20K
0.1W
0.1%
E1
SC90Q
90V
MH6
D8_H4_20
MA_AN_N
TP1
10
0.25W
1%
CONN_POWER
H2
KFS2_M5
MA_AN_0V
0.25W
R20
1K
0.25W
1%
P1
H1
KFS2_M5
1%
100
0.25W
1%
R6
C6
4.7N
100V
1%
E2
SC90Q
90V
MA_CA_0V
0.25W
C9
0.47U
25V
10%
R2
KV_AN
SOCKET
STRAIGHT
DUAL_ROW_HEADER_PWR
PIN
RIGHT_ANGLE
RIBBON_CABLE_LOW_PROFILE
C
R18
MA_AN
2
4
6
8
10
10
1W
5%
0
R11
4.99
0.25W
1%
R19
J2
1%
R21
R12
4.99
0.25W
1%
CR6
SMCJ15CA
15.1V
VCC
R16
402
0.25W
1%
R22
TIN
0.635
A
C10
0.47U
25V
10%
R13
4.99
0.25W
1%
TP6
PIN
STRAIGHT
TERMINAL_BLOCK_HEADER
MA_CA_P
100
0.25W
1%
R14
4.99
0.25W
1%
5
Sheet
1 of
6
MEAS
Dwg No
1
5309420SCH
7
REV 2 01July04
1
2
3
4
R23
R24
J1
1
2
3
4
8
TP3
R17
MA_CA
A
D
3
2
GE Healthcare
Company
Rev
Restricted
Sheet
3
1 of
1
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
1
8
Figure 12-38 Int measurement board 5309420SCH_s1
Chapter 12 Generator (Djinn)
Page 267
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
12.5.2 HV BIP board 5395639
Approved Document - 5395639ADW_r2.pdf Page 2 of 2
Figure 12-39 HV BIP board 5395639ADW
Page 268
Section 12.5 HV tank 5140761-2
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
4
C101
4.7nF
4.8KV
10%
SP2813
A
C102
4.7nF
4.8KV
10%
SP2813
5
C103
4.7nF
4.8KV
10%
SP2813
C104
4.7nF
4.8KV
10%
SP2813
C105
4.7nF
4.8KV
10%
SP2813
C106
4.7nF
4.8KV
10%
SP2813
C107
4.7nF
4.8KV
10%
SP2813
7
6
C108
4.7nF
4.8KV
10%
SP2813
C109
2.4nF
4.8KV
10%
SP2814
C110
2.4nF
4.8KV
10%
SP2814
C111
2.4nF
4.8KV
10%
SP2814
C112
2.4nF
4.8KV
10%
SP2814
C113
2.4nF
4.8KV
10%
SP2814
8
C114
2.4nF
4.8KV
10%
SP2814
A
C100
4.7nF
4.8KV
10%
SP2813
CR100
CI_5252247
A1 7
6
K1
K2
5
4 K3
3 K4
1 K6
2 K5
C1
CI
mA AN
R100
INTERCO
C118
4.7nF
4.8KV
10%
SP2813
C119
4.7nF
4.8KV
10%
SP2813
C120
4.7nF
4.8KV
10%
SP2813
C121
2.4nF
4.8KV
10%
SP2814
100M
16W 0.5%
PLANAR_89X25+CAPA
S
ESS/28/21
2x4.5turn
16uH
MH1
D8_H4_20
R202
1
MH9
ETD59
12/360
C215
4.7nF
4.8KV
10%
SP2813
C
C2
C216
4.7nF
4.8KV
10%
SP2813
C217
4.7nF
4.8KV
10%
SP2813
C218
4.7nF
4.8KV
10%
SP2813
C219
4.7nF
4.8KV
10%
SP2813
C220
4.7nF
4.8KV
10%
SP2813
C125
2.4nF
4.8KV
10%
SP2814
C126
2.4nF
4.8KV
10%
SP2814
C127
2.4nF
4.8KV
10%
SP2814
C128
2.4nF
4.8KV
10%
SP2814
C129
2.4nF
4.8KV
10%
SP2814
C130
2.4nF
4.8KV
10%
SP2814
C131
2.4nF
4.8KV
10%
SP2814
ANODE
C132
2.4nF
4.8KV
10%
SP2814
1K
0.5%
16W
PLANAR
B
R101
MH11
MH13
100M
16W 0.5%
PLANAR_89X25+CAPA
MH10
MH14
R201
OUT OF BOARD
100M
0.5% 16W
PLANAR_89X25+CAPA
100M
0.5% 16W
PLANAR_89X25+CAPA
MH2
D8_H4_20
C124
2.4nF
4.8KV
10%
SP2814
MH12
1
1
R102
1
MH8
MH7
TR1
C123
2.4nF
4.8KV
10%
SP2814
C122
2.4nF
4.8KV
10%
SP2814
1
C117
4.7nF
4.8KV
10%
SP2813
1
C221
2.4nF
4.8KV
10%
SP2814
C222
2.4nF
4.8KV
10%
SP2814
C223
2.4nF
4.8KV
10%
SP2814
C224
2.4nF
4.8KV
10%
SP2814
C225
2.4nF
4.8KV
10%
SP2814
C226
2.4nF
4.8KV
10%
SP2814
C227
2.4nF
4.8KV
10%
SP2814
C228
2.4nF
4.8KV
10%
SP2814
C229
2.4nF
4.8KV
10%
SP2814
C230
2.4nF
4.8KV
10%
SP2814
C231
2.4nF
4.8KV
10%
SP2814
C232
2.4nF
4.8KV
10%
SP2814
R200
CATHODE
C
1K
0.5%
16W
PLANAR
mA CA
4.7uF
50V
10%
SP2853
CR200
CI_5252247
K6
K4
K5
K3
K2
K1
A1
C200
D1
BAT54S
30V
3
DS1822
VDD
C3
0.1U
100V
10%
DQ
4
GND
5
J1
1
D
3
C201
4.7nF
4.8KV
10%
SP2813
AK
A
U1
4.7nF
4.8KV
10%
SP2813
2
DQ
2
4
6
8
10
2
4
6
8
10
1
3
5
7
9
1
3
5
7
9
C202
4.7nF
4.8KV
10%
SP2813
C203
4.7nF
4.8KV
10%
SP2813
C204
4.7nF
4.8KV
10%
SP2813
C205
4.7nF
4.8KV
10%
SP2813
C206
4.7nF
4.8KV
10%
SP2813
C208
4.7nF
4.8KV
10%
SP2813
MH3
D8_H4_20
MH4
D8_H4_20
MH5
D8_H4_20
C211
2.4nF
4.8KV
10%
SP2814
C212
2.4nF
4.8KV
10%
SP2814
By
Date
SYSTECH
C214
2.4nF
4.8KV
10%
SP2814
Title
04-MAY-2010
Path
3
4
DJINN
Block
djinn_hv_bip_v5
2010
2
C213
2.4nF
4.8KV
10%
SP2814
MH6
D8_H4_20
Made
1
C210
2.4nF
4.8KV
10%
SP2814
D
IPS1-105-01-S-D
16:15:04
C209
2.4nF
4.8KV
10%
SP2814
MA_CA
MA_AN
KV_AN
KV_CA
Block
Wed May 05
C207
4.7nF
4.8KV
10%
SP2813
REV 2 01July04
K
5
Sheet
1 of
6
GE Healthcare
HV BIP
Company
Dwg No
1
5395639SCH
7
Rev
Restricted
Sheet
1
1 of
1
B Size
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
B
C116
4.7nF
4.8KV
10%
SP2813
1
C115
4.7nF
4.8KV
10%
SP2813
1
CI
4.7uF
50V
10%
SP2853
MEZ
8
Approved Document - 5395639SCH_r1.pdf Page 2 of 2
Figure 12-40 HV BIP board 5395639SCH_s1
Chapter 12 Generator (Djinn)
Page 269
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 12.6 Generator connector cables
Approved Document - 5557003ADW_r4.pdf Page 2 of 2
Figure 12-41 5557003, Djinn control J1 to Spyder J1
Page 270
Section 12.6 Generator connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557010ADW_r7.pdf Page 2 of 2
Figure 12-42 5557010, Djinn Filament J2 to LVLE2 J9
Chapter 12 Generator (Djinn)
Page 271
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5557032ADW_r7.pdf Page 2 of 2
Figure 12-43 5557032, Djinn to aux box
Page 272
Section 12.6 Generator connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
Figure 12-44 5557033, Cable filament board to aux box
Chapter 12 Generator (Djinn)
Page 273
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557022ADW_r6.pdf Page 2 of 2
Figure 12-45 5557022, Cricket to Djinn
Page 274
Section 12.6 Generator connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5557060ADW_r3.pdf Page 2 of 2
Figure 12-46 5557060, Djinn Aux Box to Djinn
Chapter 12 Generator (Djinn)
Page 275
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5503001ADW_r5.pdf Page 2 of 2
Figure 12-47 5503001, Aux Box to Rotor
Page 276
Section 12.6 Generator connector cables
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 12-48 5503002, Aux Box to Rotor
Chapter 12 Generator (Djinn)
Page 277
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557063ADW_r4.pdf Page 2 of 2
Figure 12-49 5557063, Shielded Cable Assy- Djinn Aux Box to Djinn Power
Page 278
Section 12.6 Generator connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557064ADW_r4.pdf Page 2 of 2
Figure 12-50 5557064, BoardCable filament Board to Auxillary
Chapter 12 Generator (Djinn)
Page 279
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5159146ADW_r5.pdf Page 2 of 2
Figure 12-51 5159146, CABLE-FILAMENT TO HV TANK
Page 280
Section 12.6 Generator connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5396123ADW_r2.pdf Page 2 of 2
Figure 12-52 5396123, DJINN HVTank to Power
Chapter 12 Generator (Djinn)
Page 281
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5144844ADW_r5.pdf Page 2 of 2
Figure 12-53 5144844, Flat Cable Control to HV Tank
Page 282
Section 12.6 Generator connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Approved Document - 5396127ADW_r2.pdf Page 2 of 2
Figure 12-54 5396127, Djinn HVtank to power-Long
Chapter 12 Generator (Djinn)
Page 283
GE HEALTHCARE
REVISION 3
Page 284
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 12.6 Generator connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 13 DPS (Detector Power Supply) assembly
Figure 13-1 DPS portion of wiring diagram
Chapter 13 DPS (Detector Power Supply) assembly
Page 285
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 13.1 DPS assembly drawing
No schematic is available for this power supply.
Figure 13-2 5419392ADW
Page 286
Section 13.1 DPS assembly drawing
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 13-3 5557069, Cable (Optima XR220amx only)
Chapter 13 DPS (Detector Power Supply) assembly
Page 287
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 13-4 5557070, Jumper cable from LVLE2 to relay and power supply (Optima XR220amx only)
Page 288
Section 13.1 DPS assembly drawing
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 13-5 5557071, relay to power supply cable (Optima XR220amx only)
Chapter 13 DPS (Detector Power Supply) assembly
Page 289
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 13-6 5557067, Cable Asm - DPS Pigtail (Optima XR220amx only)
Page 290
Section 13.1 DPS assembly drawing
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 13.2 DPS connector cables
Approved Document - 5557041ADW_r4.pdf Page 2 of 2
Figure 13-7 5557041, DPM/PC to detector tether connection (Optima XR220amx only)
Chapter 13 DPS (Detector Power Supply) assembly
Page 291
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557011ADW_r6.pdf Page 2 of 2
Figure 13-8 5557011, DPM to LVLE2
Page 292
Section 13.2 DPS connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 13-9 5557066, DPM to detector charge receptacle (Optima XR220amx only)
Chapter 13 DPS (Detector Power Supply) assembly
Page 293
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Figure 13-10 5557057, Detector charge receptacle (Optima XR220amx only)
Page 294
Section 13.2 DPS connector cables
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557022ADW_r6.pdf Page 2 of 2
Figure 13-11 5557022, Cricket to Djinn (Optima XR220amx only)
Chapter 13 DPS (Detector Power Supply) assembly
Page 295
GE HEALTHCARE
REVISION 3
Page 296
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 13.2 DPS connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 14 PC
Detector
Charge
Receptacle
Hypertronics
Backup
Tether
Hospital
Network
Hypertronics
RJ-45 P
51^
41*
802.15.4
Zigbee
UWB 802.15.3a
Adapter UWB
(Detect
or)
º
54*
USB Bulkhead
52^
52^
52^
RJ-45 P
RJ-45 P
USB A Plug
USB A Plug
USB A Plug
USB A Plug
USB A Plug
RJ-45 R
RJ-45 R
USB A REC
USB A REC
USB A REC
USB A REC
USB A REC
Positronic
P
wer Supply
S)*
Positronic
R
12 Microfit
PLG
12 Microfit
REC
802.11
WiFi
Zigbee
Adapter
(Barcode)
PC
20 MDR Plug
USB A REC
20 MDR REC
USB A Plug
12^
50^
MNL
Figure 14-1 PC portion of wiring diagram
Chapter 14 PC
Page 297
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 14.1 PC connector cables
Approved Document - 5557041ADW_r4.pdf Page 2 of 2
Figure 14-2 5557041, PC/DPM to LVLE2 (Optima XR220amx only)
Page 298
Section 14.1 PC connector cables
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 14-3 5557051, PC to hospital network (Ethernet)
Chapter 14 PC
Page 299
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557054ADW_r6.pdf Page 2 of 2
Figure 14-4 5557054, PC to UWB (detector) antenna (Optima XR220amx only)
Page 300
Section 14.1 PC connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 14-5 5557052, PC to USB bulkhead
Chapter 14 PC
Page 301
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: COMPLETE - Production parts may not be defined by this document; it is an uneditable finished draft.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Figure 14-6 5557050, PC to Spyder J20/J19
Page 302
Section 14.1 PC connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 14-7 5557012, PC to Spyder J2
Chapter 14 PC
Page 303
GE HEALTHCARE
REVISION 3
Page 304
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 14.1 PC connector cables
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Chapter 15 Other
Section 15.1 Drive login board 5378850 and Overlay board 5368325
15.1.1 Drive login board 5378850
5 AMPMODU REC
Touch
Screen
6 Micromatch
REC
6 Micromatch
Plug
6 MicroFit
Plug
6 MicroFit
REC
29
Overlay
Board
34
6 Micromatch
REC
6 Micromatch
Plug
Drive Login
Active
Board
Drive Login
Electrode
Board
HS
Figure 15-1 Drive login portion of wiring diagram
Chapter 15 Other
Page 305
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
15.1.1.1 Drive login board schematics
Figure 15-2 5378850ADW
Page 306
Section 15.1 Drive login board 5378850 and Overlay board 5368325
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
4
5
6
7
8
A
A
NOTES:
1. THE VARIATION
PWA IS 5378850
REVISION
ECR/ECO
DATE
SIGN
1
------
11-10-2009
---
2
------
6-25-2010
---
OFF
B
AND VERSION FOR THIS
B.
2.
THIS COVER SHEET CONTROLS THE REVISION
STATUS OF THE ENTIRE DOCUMENT.
THE REVISION OF ALL SHEETS OF THIS
DOCUMENT WILL BE AT THE SAME LEVEL.
THE DOCUMENT REVISION MAY BE DIFFERENT
THAN THE PHYSICAL
ITEM REVISION.
3.
THIS SCHEMATIC MEETS THE SPECIFICATIONS OF GLOBAL SCHEMATIC STANDARDS
2299773GSP.
4.
ELECTRONIC SIGNATURES FOR BOTH THE
SCHEMATIC REVIEWER(S)
AND APPROVER(S)
CAN BE FOUND WITHIN MY WORKSHOP.
5.
UNLESS OTHERWISE SPECIFIED:
RESISTORS
ARE IN OHMS.
CAPACITORS
ARE IN FARADS.
INDUCTORS ARE IN HENRIES.
6.
PARTS MARKED AS NPP ARE SELECTED FROM
THE NOT PREFERRED LIBRARY SEE DOCUMENT
5240397GSP.
B
C
D
D
GE Healthcare
Company
Block
Fri
Jun
25 10:46:37
Block
drive_login_active
2010
1
Path
2
3
4
5
Sheet
1 of
6
Dwg
3
No
5378850SCH
7
Rev
Restricted
Sheet
2
1 of
3
B Size
REV
2
01July04
C
8
Figure 15-3 5378850SCH_s1
Chapter 15 Other
Page 307
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
4
5
6
7
8
=== TO OVERLAY BOARD ===
TO IMPROVE AC PERFORMANCE, PCB SHOULD BE DESIGNED FOR SEPERATE GROUND PLANES
FOR VIN AND VOUT, WITH EACH GROUND PLANE CONNTED ONLY AT THE GND PIN OF THE DEVICE.
IN ADDITION
GROUND OF OUTPUT CAP SHOULD CONNECT DIRECTLY
TO THE PIN OF THE DEVICE.
1
=== TO ELECTRODE BOARD ===
J1
3V3
5V0
NPP
J7
A
2
4
6
I2C_SDA
U1
TPS78001
5V0
1
3
5
2
4
6
1
3
5
CHANGE_N
I2C_SCL
5V0
SOCKET
STRAIGHT
MICROMATCH_WITH_LOCKING
C17
1U
16V
10%
IN
3
EN
5
OUT
4
VSET_FB
2
GND
R26
1MEG
0.1W
1%
5V0
5V0
R14
10K
0.1W
1%
GND
1
R6
1.74MEG
0.1W
1%
GND
U3
P82B715
R15
10K
0.1W
1%
8
I2C_SDA
I2C_SCL
3
6
1
5
C4
0.1U
16V
10%
1.22V
TO 5.25V
GND_REG
GND
VCC
SX
SY
LX
LY
GND
NC1
NC2
GND_REG
BUTTON_LOCK
BUTTON_FOUR
BUTTON_THREE
BUTTON_TWO
BUTTON_ONE
C1
1U
16V
10%
GND
1
2
3
4
5
6
A
PIN
STRAIGHT
ONE_PIECE_INTERFACE
=== SPARE HEADERS ===
GND_REG
J5
2 I2C_SDA_CAP
7 I2C_SCL_CAP
1
2
3
4
5
6
4
J4
1
2
3
4
5
6
1
2
3
4
5
6
PIN
STRAIGHT
ONE_PIECE_INTERFACE
B
1
2
3
4
5
6
1
2
3
4
5
6
PIN
STRAIGHT
ONE_PIECE_INTERFACE
B
GND
3V3
3V3
3V3
J2
R5
J6
BUTTON_ONE
NPP
U2
AT42QT1060
R23
100K
0.1W
1%
6
5
4
3
2
1
0
5V0
U4
C
CHANGE_N4
3
Y
VCC
5
OE_N
1
2
A
VDD1
VDD2
VDD3
25
RST_N
LED_ONE
LED_TWO
LED_THREE
LED_FOUR
LED_LOCK_BLUE
LED_LOCK_GREEN
LED_LOCK_RED
GND
22
C3
0.1U
16V
10%
GND
C24
0.1U
16V
10%
GND_REG
GND
2
5V0
C6
1U
16V
10%
C7
1U
16V
10%
C10
1U
16V
10%
C13
1U
16V
10%
C11
1U
16V
10%
10K
0.1W
1%
1
2
3
4
5
6
C21
0.1U
16V
10%
GND_REG
C20
0.1U
16V
10%
GND_REG
IO0
IO1
IO2
IO3
IO4
IO5
IO6
CHG_N
SNS0K
SNS0
SNS1K
SNS1
SNS2K
SNS2
SNS3K
SNS3
SNS4K
SNS4
SNS5K
SNS5
28
10
1
11
2
12
7
13
8
14
9
15
SDA
SCL
23
24
VSS1
VSS2
4
18
PPAD
29
BUTTON_TWO
C19
3.3N
50V
10%
10K
0.1W
1%
1
2
3
4
5
6
1
2
3
4
5
6
PIN
STRAIGHT
ONE_PIECE_INTERFACE
R3
BUTTON_THREE
C22
3.3N
50V
10%
PIN
STRAIGHT
ONE_PIECE_INTERFACE
J3
10K
0.1W
1%
1
2
3
4
5
6
R2
BUTTON_FOUR
I2C_SDA_CAP
I2C_SCL_CAP
C23
3.3N
50V
10%
10K
0.1W
1%
1
2
3
4
5
6
C
PIN
STRAIGHT
ONE_PIECE_INTERFACE
R1
BUTTON_LOCK
C25
3.3N
50V
10%
1
2
3
4
5
6
10K
0.1W
1%
GND_REG
1.KEEP SENSE CAPS AND RESISTORS
CLOSE TO THE IC
2.PLACE
BYPASS CAPACITORS
BETWEEN VDD AND VSS NEAR THE PART
3.PLACE
QT1060 NEAR ONE PIECE HEADER
4.FOR LAYOUT - DONT USE GROUND FILL
(ADDS CAPACITIVE
LOADING)
TRY WITH RETURN TRACES INSTEAD
MH3
MH3_20
MH2
MH3_20
MH5
MH3_20
MH6
MH3_20
MH7
MH3_20
MH10
MH3_20
MH9
MH3_20
MH1
MH3_20
MH4
MH3_20
POLARIZATION
MH2_00
C2
1U
16V
10%
D
GE Healthcare
Company
Block
Tue
Jun
22 08:36:43
Block
drive_login_active
2010
1
Path
2
3
4
5
Sheet
2 of
6
Dwg
3
No
5378850SCH
7
Figure 15-4 5378850SCH_s2
Page 308
Section 15.1 Drive login board 5378850 and Overlay board 5368325
Rev
Restricted
Sheet
2
2 of
8
3
B Size
GND
REV
2
01July04
D
19
20
21
26
27
5
6
GND
R16
1K
0.1W
1%
R27
10K
0.1W
1%
R4
3
16
17
LED<6..0>
74AHC1G125
R7
10K
0.1W
1%
C18
3.3N
50V
10%
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
3
2
4
===
5
6
7
8
LED CONTROL ===
LED<6..0>
LED_ONE
LED_TWO
LED_THREE
LED_FOUR
LED_LOCK_BLUE
LED_LOCK_GREEN
LED_LOCK_RED
6
5
4
3
2
1
0
A
5V0
A
5V0
5V0
5V0
C5
C12
SP4
10K
0.1W
1%
1N
50V
10%
S
R13
DS5
LW E6SG-AABA-JKPL-1
CR7
2SJ168
G
LED_ONE
SP1
10K
0.1W
1%
2.1K
0.1W
1%
A1
B
G
49.9
0.1W
1%
A3
5V0
DS2
LW E6SG-AABA-JKPL-1
CR4
2SJ168
2.1K
0.1W
1%
K
A2
5V0
S
R10
LED_FOUR
R17
D
1N
50V
10%
R20
D
A1
K
A2
A3
WHITE
WHITE
C8
GND
SP3
10K
0.1W
1%
GND
1N
50V
10%
S
R12
2.1K
0.1W
1%
5V0
DS4
LW E6SG-AABA-JKPL-1
CR6
2SJ168
G
LED_TWO
B
49.9
0.1W
1%
C15
SP7
10K
0.1W
1%
R18
D
A1
K
A2
A3
49.9
0.1W
1%
R24
1N
50V
10%
LED_LOCK_BLUE
S
2.1K
0.1W
1%
WHITE
C
5V0
G
5V0
CR3
2SJ168
R8
C
R9
D
SP5
10K
0.1W
1%
GND
5V0
5V0
5V0
49.9
0.1W
1%
C14
LED_LOCK_RED
C9
SP2
10K
0.1W
1%
R11
LED_THREE
2.1K
0.1W
1%
2.1K
0.1W
1%
1N
50V
10%
S
G
DS3
LW E6SG-AABA-JKPL-1
CR5
2SJ168
D
K
A2
A3
G
5V0
CR2
2SJ168
49.9
0.1W
1%
CR1
2SJ168
G
2.1K
0.1W
1%
WHITE
R21
R22
A1
S
R25
LED_LOCK_GREEN
GND
DS1
Q65110A7237
D
SP6
10K
0.1W
1%
R19
A1
1N
50V
10%
S
5V0
49.9
0.1W
1%
GND
D
C2
C1
K1
C3
K3
49.9
0.1W
1%
K2
A2
GND
A3
C16
C1=RED;C2=GREEN;C3=BLUE
GND
1N
50V
10%
D
GE Healthcare
Company
Block
Tue
Jun
22 08:36:46
Block
drive_login_active
2010
1
Path
2
3
4
5
Sheet
3 of
6
Dwg
3
No
5378850SCH
7
Rev
Restricted
Sheet
2
3 of
3
B Size
REV
2
01July04
D
8
Figure 15-5 5378850SCH_s3
Chapter 15 Other
Page 309
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
15.1.1.2 Drive login board connector cables
Approved Document - 5557034ADW_r3.pdf Page 2 of 2
Figure 15-6 5557034, Drive login to overlay board
Page 310
Section 15.1 Drive login board 5378850 and Overlay board 5368325
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
15.1.1.3 Drive login electrode board 5378852
Approved Document - 5378852ADW_r2.pdf Page 3 of 3
Figure 15-7 5378852ADW
Chapter 15 Other
Page 311
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
A
A
1
------
29-10-2009
JRH
NOTES:
1. THE VARIATION
PWA IS 5378852
2
------
25-06-2010
JRH
2.
THIS COVER SHEET CONTROLS THE REVISION
STATUS OF THE ENTIRE DOCUMENT.
THE REVISION
OF ALL SHEETS OF THIS
DOCUMENT WILL BE AT THE SAME LEVEL.
3.
THIS SCHEMATIC MEETS THE SPECIFICATIONS OF THE GLOBAL SCHEMATIC STANDARD
GUIDELINES
2299773GSP.
4.
ELECTRONIC SIGNATURES FOR BOTH THE
SCHEMATIC REVIEWER(S)
AND APPROVER(S)
CAN BE FOUND WITHIN MY WORKSHOP.
5.
UNLESS OTHERWISE SPECIFIED:
RESISTORS
ARE IN OHMS.
CAPACITORS
ARE IN FARADS.
INDUCTORS ARE IN HENRIES.
REVISION
ECR/ECO
DATE
SIGN
OFF
DRAFT - WORK-IN-PROCESS. Production parts may not be defined by this document.
See the GEHC Myworkshop System to determine the status of this document.
B
AND VERSION
B.
FOR THIS
B
C
D
D
REV 2 01July04
C
GE Healthcare
Fri
Jun
25
14:08:20
Block
drive_login_electrode
2010
1
Path
2
3
4
5
1 of
6
Figure 15-8 5378852SCH_s1
Page 312
Sheet
Section 15.1 Drive login board 5378850 and Overlay board 5368325
Dwg No
2
5378852SCH
7
Rev
Restricted
Sheet
2
1 of
8
2
B Size
Company
Block
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
3
4
5
6
7
8
A
A
01
KEEP TRACES FROM ELECTRODES TO CONNECTOR AS
THIN AS POSSIBLE
TO AVOID CAPACITIVE
LOADING
02
CENTER GOLDFINGERS IN MIDDLE
SHOWN IN DIAGRAM TO THE LEFT
03
HOLES ARE PLATED,HOWEVER,
USE VIAS
SHOWN IN DIAGRAM TO THE LEFT
ONE
MH4_00
TWO
MH4_00
THREE
MH4_00
FOUR
MH4_00
OF PCB AS
OFF OF ELECTRODES
LOCK
MH4_00
I9
J1
B
1
2
3
4
5
6
B
1
2
3
4
5
6
GOLDFINGERS
NA
ONE_PIECE_INTERFACE
ISLOCALPART
DRAFT - WORK-IN-PROCESS. Production parts may not be defined by this document.
See the GEHC Myworkshop System to determine the status of this document.
04
HOLE IS FOR POLARIZATION
LABEL SILKSCREEN
ON CONNECTOR SIDE
POLARIZATION
MH3_20
MH1
MH3_20
MH2
MH3_20
POLARIZATION
MH3
MH3_20
MH4
MH3_20
C
D
D
REV 2 01July04
C
GE Healthcare
Wed Jun
30
12:36:36
Block
drive_login_electrode
2010
1
Path
2
3
4
5
Sheet
2 of
6
Dwg No
2
5378852SCH
7
Rev
Restricted
Sheet
2
2 of
2
B Size
Company
Block
8
Figure 15-9 5378852SCH_s2
Chapter 15 Other
Page 313
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
15.1.2 Overlay board 5368325
EF To be tested per Test Specification 5555005TST.
THIS DRAWING WAS MADE
BY DELTATECH CONTROLS
FOR GE HEALTHCARE.
PWA Overlay
5368325
Figure 15-10 5368325DDW
Page 314
Section 15.1 Drive login board 5378850 and Overlay board 5368325
03
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
5
REV
ECR/ECO
4
DATE
SIGN OFF
PAGE
3
2
1
DESCRIPTION OF CHANGE
1
B0109 24-JUIN-2010 MICHEL POPA
Change J2 GND connexion from pin 6 to 2, and Q6 transistor position
1
B0110 15-JUIN-2011 MICHEL POPA
Connect fixing pads to GROUND Layer
C
B
A
D
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
D
NOTES:
1. UNLESS OTHERWISE SPECIFIED
RESISTORS ARE IN OHMS.
CAPACITORS ARE IN FARADS
INDUCTORS ARE IN HENRIES
2. CORRESPONDING LAYOUT MECHANICAL
DRAWING REF: 8f1396b0108
C
B
A
This document and the information it contains are property of DeltaTech and confidential.
They shall not be reproduced or disclosed to any person except to those having a need to know them without prior written consent of C&K.
DRAW N
CHECKED
APPROVED
Approved Document - 5368325SCH_r3.pdf Page 2 of 3
5
4
3
2
M. POPA
P.MAZY
DATE W ednesday, June 15, 2011
DATE
DATE
SIZE
ARLINGTON SQUARE, Bat B
A3
2 bd MICHAEL FARADAY
SHEET
SERRIS - MARNE LA VALLEE
77716 FRANCE
1
/ 2
CUSTOMER NUMBER
5368325 SCH
DESIGNATION
REV
3
PCB Overlay
Schematic
PCB
8F1396B0110
NUMBER
8F1396B0110-SC
REV
1
1
Figure 15-11 5368325SCH_s1
Chapter 15 Other
Page 315
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
15.1.2.1 Overlay board connector cables
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
For 5557034 (Cable Assy - Drive Login to Overlay Board), see 15.1.1.1 Drive login board schematics on page 306.
Approved Document - 5557029ADW_r3.pdf Page 2 of 2
Figure 15-12 5557029, Cable Assy - Hornet to Overlay Board
Page 316
Section 15.1 Drive login board 5378850 and Overlay board 5368325
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 15.2 Cord reel
37
38
Cord
Reel
Schaffner Filter
FN2030B-16-06
Figure 15-13 Cord reel portion of wiring diagram
Chapter 15 Other
Page 317
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
15.2.1 Cord reel connector cables
Approved Document - 5557038ADW_r4.pdf Page 2 of 2
Figure 15-14 5557038, Cable Assy - Fuse to Filter
Page 318
Section 15.2 Cord reel
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 15-15 5557037, Cable Assy - Mantis to Filter
Chapter 15 Other
Page 319
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 15.3 Collimator lamp supply (CLS) 5450200
Thorax Bulkhead
4 MnL Rec
4 MnL Plug
4 MnL Plug
40
5 MnL PLG
CLS
5450200
47
5 MnL REC
J3
5 MnL PLG
J1
5 MnL Rec
3 mMnL
Rec
3 mMnL
Plug
3 mMnL
Plug
36
J5
J2
Collimator / Lock Release
switches/ Field Light
Enable / Coll. Lamp
Figure 15-16 Collimator portion of wiring diagram
Page 320
Section 15.3 Collimator lamp supply (CLS) 5450200
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
15.3.1 Collimator lamp supply schematics
Approved Document - 5450200ADW_r2.pdf Page 2 of 2
Figure 15-17 5450200ADW
Chapter 15 Other
Page 321
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
3
5
4
6
7
NOTES:
1. THE VARIATION
PWA IS 5450200
2.
A
REVISION
ECR/ECO
DATE
SIGN
OFF
1
------
25-JAN-10
---
2
------
25-MAY-10
---
3.
AND VERSION
B.
8
FOR THIS
THIS COVER SHEET CONTROLS THE REVISION
STATUS OF THE ENTIRE DOCUMENT.
THE REVISION
OF ALL SHEETS OF THIS
DOCUMENT WILL BE AT THE SAME LEVEL.
THE DOCUMENT REVISION
MAY BE DIFFERENT
THAN THE PHYSICAL
ITEM REVISION.
THIS SCHEMATIC MEETS THE SPECIFICATIONS OF GLOBAL SCHEMATIC STANDARDS
2299773GSP.
A
4.
ELECTRONIC SIGNATURES FOR BOTH THE
SCHEMATIC REVIEWER(S)
AND APPROVER(S)
CAN BE FOUND WITHIN MY WORKSHOP.
5.
UNLESS OTHERWISE SPECIFIED:
RESISTORS ARE IN OHMS.
CAPACITORS ARE IN FARADS.
INDUCTORS ARE IN HENRIES.
6.
PARTS MARKED AS NPP ARE SELECTED FROM
THE NOT PREFERRED LIBRARY SEE DOCUMENT
5240397GSP.
B
SIGNALS
ARE INDICATED
B
7.
ACTIVE-LOW
8.
DIFFERENTIAL
SIGNAL PAIRS ARE INDICATED
WITH:
THE _H SUFFIX FOR THE ACTIVE-HIGH
SIGNAL,
AND
THE _L SUFFIX FOR THE ACTIVE-LOW SIGNAL
WITH THE _N SUFFIX
9.
CURRRENT INDICATIONS
APPLY TO THE XNET
FOR ANY NET OF THIS
SCHEMATIC
C
D
D
C.
Block
Tue
Oct
19
14:44:45
Date
Jablonowski
Path
2
3
4
collimator
Block
5
Figure 15-18 5450200SCH_s1
Page 322
Title
25-MAY-2010
Section 15.3 Collimator lamp supply (CLS) 5450200
6
lamp
Sheet
1 of
collimator_lamp_supply
2010
1
By
Dwg
2
supply
No
5450200SCH
7
GE Healthcare
Company
Rev
Restricted
Sheet
2
1 of
8
2
B Size
Made
REV 2 01July04
C
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
====
2
J1
4
3
SWITCH TO FIREFLY
====
5
====
J3
6
COLLIMATOR
SW_OUT
TP5
FIELD_LIGHT_SWITCH_OUT
NC
FIELD_LIGHT_SWITCH_RETURN
1
2
3
LIGHT
FIELD_LIGHT_SWITCH_OUT
FIELD_LIGHT_SWITCH_RETURN
MINI
NC
LAMP_24V_OUT
LAMP_24V_RETURN
PIN
STRAIGHT
MATE_N_LOK
MATE N LOK
A
R5
100K
0.1W
1%
J3
SW I/F
1
2
3
====
RED
R4
FIELD
J1
INTERFACE
8
SW_RTN
TP6
RED
A
7
1
2
3
4
5
COLLIMATOR
I/F
1
2
3
4
5
PIN
STRAIGHT
MATE_N_LOK_WHITE
GND
SPACING REQUIREMENTS FOR THIS DESIGN ARE AS FOLLOWS:
2MM CREEPAGE / 1.6
MM CLEARANCE INPUT TO GND OF U1
6.1MM CREEPAGE / 5 MM CLEARANCE INPUT TO OUTPUT OF U1
ISOLATE!
B
====
J2
POWER INTO
SUPPLY
====
====
COLLIMATOR
LAMP POWER SUPPLY
B
====
ALL
4.7N
1600V
5%
P
GND_POWER
SUPPLY POWER
RED
OPEN = ON; LOW = OFF
OPEN = OFF; LOW = ON
LAMP_POWER_ON
LAMP_POWER_ON_N
1
2
3
4
BATTERIES
R1
100K
0.1W
1%
BE RATED FOR 10A
GND
U1
VE253EU
1
4
P
GND_POWER
CR1
P6KE220A
220V
C1
10U
250V
20%
LAMP_POWER_ON 2
NC3
INP
INN
GATEIN
GATEOUT
OUTP
OUTN
TRIM
SENSEP
SENSEN
C2
1U
25V
10%
24V
MIN
R2
100K
0.1W
1%
RT1
F1
SL22
RESETTABLE
OUTP
PIN
STRAIGHT
MATE_N_LOK
C
10N
500V
20%
5
9
8A
30V
5R012
LAMP_24V_OUT
12A
7
24VOUT
DS1
HSMG-C190
GREEN
2
J2
OF THE POWER SUPPLY TO
RED
6
8
R6
56.2K
0.1W
1%
R7
71.5K
0.1W
1%
2
C
1
BATTERIES
1
2
3
4
VOUT
TP4
C4
C3
BATT
TP3
TRACES AT THE OUTPUT
R8
2.1K
0.1W
1%
CW 3 R3
10K
500MW
1 10%
GND
GND
P
GND_POWER
MH2
MHP4_50TB10_00
GND_POWER
TP1
MH1
MHP4_50TB10_00
MH3
MHP4_50TB10_00
BLACK
P
GND_POWER
GND
D
GND
REV 2 01July04
D
BLACK
MH4
MHP4_50TB10_00
GE Healthcare
Company
Block
Mon
Oct
18
15:16:34
Block
2
3
4
5
Sheet
2 of
collimator_lamp_supply
2010
1
Path
6
Dwg
2
No
5450200SCH
7
Rev
Restricted
Sheet
2
2 of
2
B Size
ALL TRACES AT THE INPUT
TO THE POWER SUPPLY TO
BE RATED FOR 5A MIN
GND_LOGIC
TP2
8
Figure 15-19 5450200SCH_s2
Chapter 15 Other
Page 323
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
15.3.2 Collimator lamp supply connector cables
Approved Document - 5557036ADW_r2.pdf Page 2 of 2
Figure 15-20 5557036, Cable Assy - Firefly to CLS
Page 324
Section 15.3 Collimator lamp supply (CLS) 5450200
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 15-21 5557040, Cable Assy- Firefly to CLS
Chapter 15 Other
Page 325
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
GE HEALTHCARE
REVISION 3
Approved Document - 5557047ADW_r3.pdf Page 2 of 2
Figure 15-22 5557047, Cable Assy - CLS to Thorax Column Bulkhead -Collimator
Page 326
Section 15.3 Collimator lamp supply (CLS) 5450200
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 15.4 Power switch
2MnL PLG
2MnL REC
2 MnL PLG
35
44
On / Off Button
Figure 15-23 Power switch portion of wiring diagram
Chapter 15 Other
Page 327
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
15.4.1 Power switch connector cables
Figure 15-24 5557035, Cable Assy - Firefly to Power Switch
Page 328
Section 15.4 Power switch
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Figure 15-25 5557044, Cable Assy - Power Switch Pigtail
Chapter 15 Other
Page 329
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
Section 15.5 Wireless USB host radio board assembly 5390144-2
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
15.5.1 Wireless USB host radio board schematics
Approved Document - 5390144-2ADW_r1.pdf Page 2 of 3
Figure 15-26 5390144-2ADW
Page 330
Section 15.5 Wireless USB host radio board assembly 5390144-2
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
NOTES:
1. THE VARIATION
AND VERSION
A.
PWA IS 5390144-2
THIS COVER SHEET CONTROLS THE REVISION
STATUS OF THE ENTIRE DOCUMENT.
THE REVISION
OF ALL SHEETS OF THIS
DOCUMENT WILL BE AT THE SAME LEVEL.
3.
THIS SCHEMATIC MEETS THE SPECIFICATIONS OF THE GLOBAL SCHEMATIC STANDARD
GUIDELINES
2299773GSP.
4.
ELECTRONIC SIGNATURES FOR BOTH THE
SCHEMATIC REVIEWER(S)
AND APPROVER(S)
CAN BE FOUND WITHIN MY WORKSHOP.
5.
UNLESS OTHERWISE SPECIFIED:
RESISTORS ARE IN OHMS.
CAPACITORS ARE IN FARADS.
INDUCTORS ARE IN HENRIES
5
4
WUSB HOST RADIO
FOR THIS
2.
6
7
8
BOARD
A
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
A
3
B
REVISION
ECR/ECO
5390144
R2
2103481
15JUNE2010
JPH
5390144
R3
2114055
04MAY2011
JPH
5390144
R4
2110638
17MAY2011
JPH
2120219
15JULY2011
JPH
5390144-2
R1
DATE
SIGN
OFF
B
C
D
D
By
Date
Jeremy
Block
Tue
Jul
12
13:44:33
Title
15JULY2011
Path
2
3
4
WUSB Host
Block
5
Sheet
1 of
wusb_host_radio
2011
Approved Document - 5390144-2SCH_r1.pdf Page 2 of 6
1
Hannon
6
Radio
Board
Dwg No
5
5390144-2SCH
7
GE Healthcare
Company
Rev
Restricted
Sheet
1
1 of
5
B Size
Made
REV 2 01July04
C
8
Figure 15-27 5390144-2SCH_s1
Chapter 15 Other
Page 331
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
MAC
USB_DM
USB_DP
8
A
R32
330
0.0625W
1%
VCC33
R30
330
0.0625W
1%
R27
330
0.0625W
1%
R26
330
0.0625W
1%
1
VCC12
R33
330
0.0625W
1%
2
C87
10U
6.3V
20%
2
C47
SPARE_C0402
VCC33
2
C88
10U
6.3V
20%
PIN
RIGHT_ANGLE
USB_TYPEA
2
7
2
1
2
3
4
A
R22
1MEG
0.1W
1%
6
2
1
2
3
4
G1
G2
5
VCC5
J2
G1
G2
4
3
D1
HSMG-C190
GREEN
1
D2
HSMG-C190
GREEN
1
D3
HSMG-C190
GREEN
1
1
C77
0.1U
10V
10%
DATA6
DATA7
NC
NOT
C47
DATA_EN
DATA4
DATA5
1
SER_DIO
NC
NC
DATA0
DATA1
DATA2
DATA3
PCLK
THE FOLLOWING COMPONENT IS
INCLUDED ON THIS ASSEMBLY:
D4
HSMG-C190
GREEN
1
D5
HSMG-C190
GREEN
FUTURE:
CONNECT USB SHIELD
AND LOGIC GND WITH
1000PF
CAP
C76
0.1U
10V
10%
LED_DATA
LED_READY
LED_RESP
64
63
62
61
60
59
58
57
56
55
54
53
52
51
50
49
R18
1K
0.0625W
1%
R16
1K
0.0625W
1%
PHY_ACT
STOPC
PHY_RST_N
VCC12
LED_DATA
LED_READY
LED_RESP
I2C_SDA
I2C_SCL
VCC33
C41
0.1U
10V
10%
NC
NC
LED_BEACON
LED_PWR
NC
C43
0.1U
10V
10%
DATA9
DATA8
PHY_ACTIVE
STOPC
PHY_RESETB
GPIO7
GPIO6
GPIO5
GPIO4
SDA
SCL
VCC12_1
VCC33_1
LED0
LED1
NC1
NC6
NC5
DATA13
PHYCCA
DATA14
DATA15
RX_EN
VCC12_3
TX_EN
USB_DVCC12
XTLO
XTLI
RGL_CTRL
WAKEUP_BUT
RREF
VBUS
65PIN
U6
RTU7300
TAB
48
47
46
45
44
43
42
41
40
39
38
37
36
35
34
33
B
NC
NC
NC
CCA_STATUS
NC
NC
RXEN
VCC12S
VCC12
TXEN
XO
XI
PHYREG_EN
NC
Y1
XO
C82
0.1U
10V
10%
VCC33S
C81
0.1U
10V
10%
R17
1
22
0.0625W
1%
GND1
GND2
R31
6.19K
0.0625W
1%
R20
3
C39
22P
50V
5%
65
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
C
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
LED_PWR
MPI_SERD
DATA10
DATA11
DATA0
DATA1
DATA2
DATA3
PCLK
VCC12_4
DATA_EN
DATA4
DATA5
VCC33_2
DATA6
DATA7
DATA12
R19
1K
0.0625W
1%
B
LED_BEACON
NC2
EECS
EESK
EEDI
EEDO
UTXD
URTS
URXD
UCTS
VCC12_2
USB_AVCC12
NC3
HSDP
HSDM
USB_AVCC33
NC4
XI
22
0.0625W
1%
C42
2
4
22P
50V
5%
12MHZ
C
2
VCC33S
NC
TP8
URXD
FL6
BLM15AG601SN1
600 OHM AT 100MHZ
8
VCC
SPI_CS_N
1
3
7
CS_N
WP_N
HOLD_N
SPI_SCK
6
SPI_MOSI
5
TP11
SCK
SI
SO
2
GND
4
1
UTXD
SON8L
NPP
U12
AT25DF041A
R34
4.7K
0.0625W
1%
VCC12S
C46
0.1U
10V
10%
2
TP9
VCC33
TP10
D
VCC12
C78
0.1U
10V
10%
R29
4.7K
0.0625W
1%
C85
0.1U
10V
10%
SPI_MISO
D
C86
0.1U
10V
10%
GE Healthcare
Company
Block
Wed Jul
13
19:59:22
1
Path
Block
2
3
4
5
Figure 15-28 5390144-2SCH_s2
Page 332
Section 15.5 Wireless USB host radio board assembly 5390144-2
Sheet
2 of
wusb_host_radio
2011
Approved Document - 5390144-2SCH_r1.pdf Page 3 of 6
REV 2 01July04
1
FL3
BLM15AG601SN1
600 OHM AT 100MHZ
6
Dwg No
5
5390144-2SCH
7
Rev
Restricted
Sheet
1
2 of
8
5
B Size
USB_DP
USB_DM
NC
SPI_CS_N
SPI_SCK
SPI_MOSI
SPI_MISO
NC
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
VCC33
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
1
3
6
7
XTALN
V33P
GND1
GND2
A
C52
8.2P
50V
+/-0.25P
2
4
C61
6.8P
50V
+/-0.25P
66MHZ
8
PHY
Y2
XTALP
5
L12
OPEN
MAC SIGNAL
IS ACTIVE
RXEN
BG1_SEL_N
RF_BG3_TX
5
VCC
3
1
A<0>
A<1>
RF_BG3_RX
2
A
RFSWITCH RX_SEL_N
IS ACTIVE
LOW
2
C64
open
U8
74AUP2G14
RXEN
HIGH
C48
0.1U
10V
10%
RF_BG1_RX
RF_BG1_TX
Y<0>
Y<1>
4
6
GND
2
RX_SEL_N
BG3_SEL_N
BG1_SEL_N
V33A
THE FOLLOWING COMPONENTS ARE NOT
INCLUDED ON THIS ASSEMBLY: C47, C64
L12,
R4, R24
V33A2
RF2_TX
RF2_RX
VDDA4
RF1_RX
RF1_TX
V33A1
VDDD13
CHIP_EN
AUX
VDDD12
STOP_C
V15A
R11
22
0.0625W
1%
V33P
XTALP
XTALN
C30
0.1U
10V
10%
R12
1
2
3
4
5
6
7
8
9
10
11
12
C
C31
1U
6.3V
20%
36
35
34
33
32
31
30
29
28
27
26
25
TAB
49
C33
1U
6.3V
20%
8
VCC
BG3_SEL_N
RX_SEL_N
5
6
A<0>
B<0>
BG1_SEL_N
RX_SEL_N
1
2
A<1>
B<1>
C49
0.1U
10V
10%
CCA_STATUS
PHY_ACT
SER_DIO
NPP
R13
DATA_EN
DATA7
DATA6
3
TX_BG3_SEL_N
Y<1>
7
TX_BG1_SEL_N
4
PCLK
R24
SPARE_R0402
1
2
22
0.05W
1%
R4
SPARE_R0402
1
2
2
C
V15A
2
V33A
NPP
C34
0.1U
6.3V
10%
VCC14
D
NPP
C66
0.1U
6.3V
10%
NPP
C68
0.1U
6.3V
10%
NPP
C72
0.1U
6.3V
10%
NPP
C65
0.1U
6.3V
10%
NPP
C55
0.1U
6.3V
10%
NPP
C57
0.1U
6.3V
10%
NPP
C67
0.1U
6.3V
10%
NPP
C74
0.1U
6.3V
10%
NPP
C63
0.1U
6.3V
10%
NPP
C62
0.1U
6.3V
10%
NPP
C58
0.1U
6.3V
10%
NPP
C60
0.1U
6.3V
10%
NPP
C56
0.1U
6.3V
10%
NPP
C59
0.1U
6.3V
10%
V33A
NPP
FL5
BLM03AG601SN1
V33P
NPP
C71
0.1U
6.3V
10%
B
DATA2
DATA3
DATA4
DATA5
PHY_RST_N
RXEN
TXEN
DATA0
DATA1
Y<0>
GND
13
14
15
16
17
18
19
20
21
22
23
24
C32
0.1U
10V
10%
VDDD11
VIO4
CCA
PHY_ACT
SER_DIO
VDDD10
U4
DATA_EN
RTU7012
PCLK
DATA7
DATA6
VDDD9
VIO3
VDDD6
PHY_RSTB
RXEN
TXEN
DATA0
DATA1
VDDD7
DATA2
DATA3
DATA4
DATA5
VDDD8
22
0.0625W
1%
XTALP
XTALN
VDDA1
VDDA2
VDDA3
VDDD1
VREG
VIO1
VDDD2
ACLK
VDDD3
VIO2
U7
74AUP2G08
V33P
10K
0.05W
1%
NPP
C29
0.1U
6.3V
10%
NPP
C73
0.1U
6.3V
10%
600
1
OHM AT 100MHZ
C51
1U
6.3V
20%
D
REV 2 01July04
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
B
V33A
NPP
R25
48
47
46
45
44
43
42
41
40
39
38
37
2
GE Healthcare
Company
Block
Wed Jul
13
19:59:23
Block
2
3
4
5
Sheet
3 of
wusb_host_radio
2011
Approved Document - 5390144-2SCH_r1.pdf Page 4 of 6
1
Path
6
Dwg No
5
5390144-2SCH
7
Rev
Restricted
Sheet
1
3 of
5
B Size
V15A
STOPC
VCC14
8
Figure 15-29 5390144-2SCH_s3
Chapter 15 Other
Page 333
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
LC FILTER
2
4
3
5
6
7
8
FREQ = 1/(2*PI*SQRT(C*L))
RF FRONT END
BFU725
GAIN
V33A
A
RXEN
NPP
R5
200K
0.05W
1%
NPP
R6
100
0.05W
1%
2.7NH
AND 2.0PF
FILTERS
2.17GHZ
1.5NH
AND 0.1PF
FILTERS
5.4GHZ
V33A
RXEN
NPP
C11
0.1U
6.3V
10%
RF_435
NPP
C10
0.1P
25V
+/-0.02P
RF_436
NPP
C18
0.1P
25V
+/-0.02P
NPP
L5
1.5N
0.3N
300MA
NPP
L3
1.5N
0.3N
300MA
NPP
C13
10P
25V
5%
C
E2 E1
4
RF_441
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
RF_226
NPP
C8
2P
25V
+/-0.25P
NPP
C3
2P
25V
+/-0.25P
NPP
L2
2.7N
0.3N
300MA
NPP
L1
2.7N
0.3N
300MA
RXEN
RX_SEL_N
NPP
C1
100P
25V
5%
RF_431
1.5P
25V
+/-0.25P
NPP
C22
1.5P
25V
+/-0.25P
NPP
R1
120K
0.05W
1%
RF_225
U3
UPG2163T5N
NPP
C16
B
RF_432
NPP
C21
VCONT1
VCONT2
OUT1
3
OUT2
1
7
GND
PPAD
RF_434
B
NPP
C14
10P
25V
5%
BG3 RX
RF_433
Q2
BFU725F_N1
BG3_SEL_N
BG1_SEL_N
NPP
R2
100
0.05W
1%
IN
5
2
NPP
C12
6 RF_224
NPP
R3
RF_223
5.6
0.05W
1%
10P
25V
5%
NPP
R7
5.6
0.05W
1%
C
Q1
BFU725F_N1
B
NPP
C5
U1
UPG2163T5N
SMA ANTENNA PORT
RF_221
SHORT CENTER PIN,
1.5P
25V
+/-0.25P
E2 E1
FL212B
RF_BG3_RX
B
RX
RF_222
1.5P
25V
+/-0.25P
NPP
C2
100P
25V
5%
BG1 RX
RF_BG1_RX
VCONT1
VCONT2
RF_227
4
OUT1
RF_211
3
OUT2
1
7
GND
PPAD
IN
5
2
6RF_102
1
FL1
HFCN-3100+
3
IN OUT
2
4
G0
G1
G2
G3
TX_BG3_SEL_N
TX_BG1_SEL_N
NPP
C6
10P
25V
5%
C
NPP
C25
NPP
R8
RF_BG1_TX
RF_413
RF_414
0
0.05W
+/-0.05
L7
OPEN
3
NPP
L8
OUT
GND1
GND2
NPP
C15
1
2
3
4
2
3
4
SOCKET
STRAIGHT
ANT-SMA142_4701_801
NPP
C7
10P
25V
5%
C
TX
U2
UPG2163T5N
10P
25V
5%
G1
G2
RF_411
4
OUT1
RF_421
3
OUT2
1
7
GND
PPAD
VCONT1
VCONT2
IN
5
2
6
NPP
C4
RF_212
4P
25V
+/-0.25P
0.5-2GHZ
RF_422
0.5P
25V
+/-0.25P
C19
open
1
NPP
C9
RF_423
0.9N
0.2N
520MA
RF_101
5
6
2RF_412
NPP
C17
NPP
L6
NPP
C26
0.1P
25V
+/-0.02P
IN
FILTER
RF_424
0.9N
0.2N
520MA
D
1
10P
25V
5%
2ND HARM
FILTER
13-15GHZ
RF_BG3_TX
BG1 TX
FL2
FI212B396001
EDGE LAUNCH
J1
NPP
0.5P
L4
25V
0.6N
+/-0.25P
0.2N
600MA
3
D
THE FOLLOWING COMPONENTS ARE NOT
INCLUDED ON THIS ASSEMBLY: C19, L7
REV 2 01July04
NPP
C24
0.1U
6.3V
10%
BG3 TX
3
GE Healthcare
Company
Block
Wed Jul
13
19:59:24
Block
2
3
4
5
Figure 15-30 5390144-2SCH_s4
Page 334
Section 15.5 Wireless USB host radio board assembly 5390144-2
Sheet
4 of
wusb_host_radio
2011
Approved Document - 5390144-2SCH_r1.pdf Page 5 of 6
1
Path
6
Dwg No
5
5390144-2SCH
7
Rev
Restricted
Sheet
1
4 of
8
5
B Size
A
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
1
2
4
3
5
6
7
8
POWER
VCC5
A
VCC5
VCC15
C54
10U
6.3V
20%
C27
0.1U
10V
10%
L11
U5
NCP1529
4
SW
3
FB
5
GND
2
VIN
1
EN
C28
22P
50V
5%
C53
10U
6.3V
20%
R10
150K
0.0625W
1%
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
C45
10U
6.3V
20%
FB_VCC16
R9
100K
0.0625W
1%
VCC16 CAN BE 1.35-1.9V.
USUALLY
C89
0.1U
10V
10%
VCC5
VCC33S
L10
U13
NCP1529
2.2U
20%
1.1A
PHYREG_EN
RTU7012
VCC12S
4
VIN
SW
3
1
EN
FB
5
GND
2
L9
U11
NCP1529
2.2U
20%
1.1A
C40
10U
6.3V
20%
C44
22P
50V
5%
R21
100K
0.0625W
1%
C80
10U
6.3V
20%
FB_VCC12S
R23
100K
0.0625W
1%
C79
0.1U
10V
10%
4
VIN
1
EN
A
SW
3
FB
5
GND
2
2.2U
20%
1.1A
C36
10U
6.3V
20%
C38
22P
50V
5%
R15
453K
0.0625W
1%
FB_VCC33S
R28
100K
0.0625W
1%
SET TO 1.5-1.8V.
B
B
V15A
VCC15
FL4
BLM15AG601SN1
1
2
600
OHM AT 100MHZ
10V
C20
10U
6.3V
20%
THERE IS
RTU7012
VCC13
CAN BE 1.2V-1.5V.
BETTER
Q3
SI2302DS
S
C50
1U
6.3V
20%
SLIGHTLY
VCC12
VCC14
D6
PMEG1020EA
DIGITAL
DUE TO CURRENT
NOISE
ON VCC14
->
U9
TPS2065DBV
VCC33S
VCC33
D
G
C84
1U
6.3V
20%
C23
0.1U
10V
10%
VCC12S
C83
1U
6.3V
20%
PHYREG_EN
5
IN
4
EN
C70
1U
6.3V
20%
2.7
OUT
1
OC_N
3
GND
2
NC
TO 5.5V
C69
1U
6.3V
20%
VCC15
PHYREG_EN
SURGE THROUGH D1.
COULD TRY LDO.
PERFORMANCE ABOVE 1.3V.
C
C
U10
TPS2065DBV
VCC33
C37
1U
6.3V
20%
IN
4
EN
C35
1U
6.3V
20%
2.7
OUT
1
OC_N
3
GND
2
VCC5
VCC33
TP6
VCC33
FIDUCIALS
GFID3
GFID2
GFID1
NC
C75
1U
6.3V
20%
TO 5.5V
VCC33S
TP4
VCC33S
VCC14
TP1
VCC14
MOUNTING HOLES
RF SHIELD
D
VCC15
TP2
VCC15
VCC12S
TP5
VCC12S
VCC12
TP7
VCC12
V33P
TP3
MT1
MT3
HOLES
MT2
MH1
MHP3_10TB5_60
MH2
MHP3_10TB5_60
D
V33P
REV 2 01July04
100K
0.0625W
1%
5
VCC5
TP12
GE Healthcare
Company
Block
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13
19:59:20
Block
2
3
4
5
Sheet
5 of
wusb_host_radio
2011
Approved Document - 5390144-2SCH_r1.pdf Page 6 of 6
1
Path
6
Dwg No
5
5390144-2SCH
7
Rev
Restricted
Sheet
1
5 of
5
B Size
PHYREG_EN
R14
V33P
8
Figure 15-31 5390144-2SCH_s5
Chapter 15 Other
Page 335
GE HEALTHCARE
REVISION 3
OPTIMA XR200AMX/XR220AMX SYSTEM SCHEMATICS AND DRAWINGS
DIRECTION 5336116-1EN
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
15.5.2 Wireless USB host radio board connector cable
Approved Document - 5557054ADW_r6.pdf Page 2 of 2
Figure 15-32 5557054, Cable Assy - PC to UWB Antenna
Page 336
Section 15.5 Wireless USB host radio board assembly 5390144-2
© 2011 General Electric Company.
GE Medical Systems, a General Electric Company, going to market as GE Healthcare.
3000 N. Grandview Boulevard
Waukesha, Wisconsin 53188
USA
www.gehealthcare.com
338
GE Healthcare
Optima XR200amx
DICOM Conformance Statement
Direction 5336117-1EN
Revision 3
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR
SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X
représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement
X entraîne des dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les
personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour ellesmêmes. Avant chaque manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se
renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique,
Annales 26: Recommandations de la Commission Internationale sure la Protection Radiologique et les normes
nationales en vigueur.
WARNING
X-RAY EQUIPMENT IS DANGEROUS TO BOTH PATIENT AND OPERATOR UNLESS MEASURES OF
PROTECTION ARE STRICTLY OBSERVED.
Though this equipment is built to the highest standards of electrical and mechanical safety, the useful x-ray beam
becomes a source of danger in the hands of the unauthorized or unqualified operator. Excessive exposure to x-radiation
causes damage to human tissue.
Therefore, adequate precautions must be taken to prevent unauthorized or unqualified persons from operating this
equipment or exposing themselves or others to its radiation.
Before operation, persons qualified and authorized to operate this equipment should be familiar with the
Recommendations of the International Commission on Radiological Protection (ICRP), contained in Annals Number 26
of the ICRP, and with applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS
NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro
al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede
causar daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o
no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán
informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales
No 26: Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE
GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den
Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte
Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden
Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen
Kommission für Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für
Strahlenschutz und anderer nationaler Normenbehörden.
Warning
Page 2
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Important information
WARNING
(EN)
ПРЕДУПРЕЖДЕНИЕ
(BG)
警告
(ZH-CN)
警告
(ZH-HK)
警告
(ZH-TW)
This service manual is available in English only.
•
If a customer's service provider requires a language other than English, it is the customer's
responsibility to provide translation services.
•
Do not attempt to service the equipment unless this service manual has been consulted and is
understood.
•
Failure to heed this warning may result in injury to the service provider, operator or patient from
electric shock, mechanical or other hazards.
Tова упътване за работа е налично само на английски език.
•
Ако доставчикът на услугата на клиента изиска друг език, задължение на клиента е да
осигури превод.
•
Не използвайте оборудването, преди да сте се консултирали и разбрали упътването за
работа.
•
неспазването на това предупреждение може да доведе до нараняване на доставчика на
услугата, оператора или пациентa в резултат на токов удар, механична или друга опасност.
本维修手册仅提供英文版本。
•
•
•
如果客户的维修服务人员需要非英文版本，则客户需自行提供翻译服务。
未详细阅读和完全理解本维修手册之前，不得进行维修。
忽略本警告可能对维修服务人员、操作人员或患者造成电击、机械伤害或其他形式的伤
害。
本服務手冊僅提供英文版本。
• 倘若客戶的服務供應商需要英文以外之服務手冊，客戶有責任提供翻譯服務。
• 除非已參閱本服務手冊及明白其內容，否則切勿嘗試維修設備。
• 不遵從本警告或會令服務供應商、網絡供應商或病人受到觸電、機械性或其他的危險。
本維修手冊僅有英文版。
• 若客戶的維修廠商需要英文版以外的語言，應由客戶自行提供翻譯服務。
• 請勿試圖維修本設備，除非 您已查閱並瞭解本維修手冊。
• 若未留意本警告，可能導致維修廠商、操作員或病患因觸電、機械或其他危險而受傷。
UPOZORENJE
(HR)
Ovaj servisni priručnik dostupan je na engleskom jeziku.
•
Ako davatelj usluge klijenta treba neki drugi jezik, klijent je dužan osigurati prijevod.
•
Ne pokušavajte servisirati opremu ako niste u potpunosti pročitali i razumjeli ovaj servisni
priručnik.
•
zanemarite li ovo upozorenje, može doći do ozljede davatelja usluge, operatera ili pacijenta uslijed
strujnog udara, mehaničkih ili drugih rizika.
VÝSTRAHA
(CS)
Tento provozní návod existuje pouze v anglickém jazyce.
• V případě, že externí služba zákazníkům potřebuje návod v jiném jazyce, je zajištění překladu do
odpovídajícího jazyka úkolem zákazníka.
• Nesnažte se o údržbu tohoto zařízení, aniž byste si přečetli tento provozní návod a pochopili jeho
obsah.
• V případě nedodržování této výstrahy může dojít k poranění pracovníka prodejního servisu,
obslužného personálu nebo pacientů vlivem elektrického proudu, respektive vlivem mechanických
či jiných rizik.
Denne servicemanual findes kun på engelsk.
• Hvis en kundes tekniker har brug for et andet sprog end engelsk, er det kundens ansvar at sørge
for oversættelse.
• Forsøg ikke at servicere udstyret uden at læse og forstå denne servicemanual.
• Manglende overholdelse af denne advarsel kan medføre skade på grund af elektrisk stød,
mekanisk eller anden fare for teknikeren, operatøren eller patienten.
ADVARSEL
(DA)
Preface
Page 3
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
WAARSCHUWING
(NL)
HOIATUS
(ET)
VAROITUS
(FI)
ATTENTION
(FR)
WARNUNG
(DE)
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ
(EL)
FIGYELMEZTETÉS
(HU)
AÐVÖRUN
(IS)
Page 4
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.
• Als het onderhoudspersoneel een andere taal vereist, dan is de klant verantwoordelijk voor de
vertaling ervan.
• Probeer de apparatuur niet te onderhouden alvorens deze onderhoudshandleiding werd
geraadpleegd en begrepen is.
• Indien deze waarschuwing niet wordt opgevolgd, zou het onderhoudspersoneel, de operator of
een patiënt gewond kunnen raken als gevolg van een elektrische schok, mechanische of andere
gevaren.
See teenindusjuhend on saadaval ainult inglise keeles
• Kui klienditeeninduse osutaja nõuab juhendit inglise keelest erinevas keeles, vastutab klient
tõlketeenuse osutamise eest.
• Ärge üritage seadmeid teenindada enne eelnevalt käesoleva teenindusjuhendiga tutvumist ja
sellest aru saamist.
• Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja, operaatori või patsiendi vigastamist
elektrilöögi, mehaanilise või muu ohu tagajärjel.
Tämä huolto-ohje on saatavilla vain englanniksi.
• Jos asiakkaan huoltohenkilöstö vaatii muuta kuin englanninkielistä materiaalia, tarvittavan
käännöksen hankkiminen on asiakkaan vastuulla.
• Älä yritä korjata laitteistoa ennen kuin olet varmasti lukenut ja ymmärtänyt tämän huolto-ohjeen.
• Mikäli tätä varoitusta ei noudateta, seurauksena voi olla huoltohenkilöstön, laitteiston käyttäjän tai
potilaan vahingoittuminen sähköiskun, mekaanisen vian tai muun vaaratilanteen vuoksi.
Ce manuel d’installation et de maintenance est disponible uniquement en anglais.
• Si le technicien d'un client a besoin de ce manuel dans une langue autre que l'anglais, il incombe
au client de le faire traduire.
• Ne pas tenter d'intervenir sur les équipements tant que ce manuel d’installation et de maintenance
n'a pas été consulté et compris.
• Le non-respect de cet avertissement peut entraîner chez le technicien, l'opérateur ou le patient
des blessures dues à des dangers électriques, mécaniques ou autres.
Diese Serviceanleitung existiert nur in englischer Sprache.
• Falls ein fremder Kundendienst eine andere Sprache benötigt, ist es Aufgabe des Kunden für eine
entsprechende Übersetzung zu sorgen.
• Versuchen Sie nicht diese Anlage zu warten, ohne diese Serviceanleitung gelesen und
verstanden zu haben.
• Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des Kundendiensttechnikers, des
Bedieners oder des Patienten durch Stromschläge, mechanische oder sonstige Gefahren
kommen.
Το παρόν εγχειρίδιο σέρβις διατίθεται μόνο στα αγγλικά.
• Εάν ο τεχνικός σέρβις ενός πελάτη απαιτεί το παρόν εγχειρίδιο σε γλώσσα εκτός των αγγλικών,
αποτελεί ευθύνη του πελάτη να παρέχει τις υπηρεσίες μετάφρασης.
• Μην επιχειρήσετε την εκτέλεση εργασιών σέρβις στον εξοπλισμό αν δεν έχετε συμβουλευτεί και
κατανοήσει το παρόν εγχειρίδιο σέρβις.
• Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί τραυματισμός στον τεχνικό
σέρβις, στο χειριστή ή στον ασθενή από ηλεκτροπληξία, μηχανικούς ή άλλους κινδύνους.
Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.
• Ha a vevő szolgáltatója angoltól eltérő nyelvre tart igényt, akkor a vevő felelőssége a fordítás
elkészíttetése.
• Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási kézikönyvben leírtakat nem
értelmezték.
• Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető vagy a beteg áramütés,
mechanikai vagy egyéb veszélyhelyzet miatti sérülését eredményezheti.
Þessi þjónustuhandbók er aðeins fáanleg á ensku.
• Ef að þjónustuveitandi viðskiptamanns þarfnast annas tungumáls en ensku, er það skylda
viðskiptamanns að skaffa tungumálaþjónustu.
• Reynið ekki að afgreiða tækið nema að þessi þjónustuhandbók hefur verið skoðuð og skilin.
• Brot á sinna þessari aðvörun getur leitt til meiðsla á þjónustuveitanda, stjórnanda eða sjúklings frá
raflosti, vélrænu eða öðrum áhættum.
Preface
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
AVVERTENZA
(IT)
(JA)
경고
(KO)
BRÎDINÂJUMS
(LV)
ĮSPĖJIMAS
(LT)
ADVARSEL
(NO)
OSTRZEŻENIE
(PL)
AVISO
(PT-BR)
ATENÇÃO
(PT-PT)
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Il presente manuale di manutenzione è disponibile soltanto in lingua inglese.
• Se un addetto alla manutenzione richiede il manuale in una lingua diversa, il cliente è tenuto a
provvedere direttamente alla traduzione.
• Procedere alla manutenzione dell'apparecchiatura solo dopo aver consultato il presente manuale
ed averne compreso il contenuto.
• Il mancato rispetto della presente avvertenza potrebbe causare lesioni all'addetto alla
manutenzione, all'operatore o ai pazienti provocate da scosse elettriche, urti meccanici o altri
rischi.
このサービスマニュアルには英語版しかありません。
• サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業者の責任で行
うものとさせていただきます。
• このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでください。
• この警告に従わない場合、サービスを担当される方、操作員あるいは患者 さんが、感電や機械
的又はその他の危険により負傷する可能性があります。
본 서비스 매뉴얼은 영어로만 이용하실 수 있습니다 .
• 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우 , 번역 서비스를 제공하는 것은 고객의
책임입니다 .
• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하려고 시도하지 마십시오 .
• 본 경고 사항에 유의하지 않으면 전기 쇼크 , 기계적 위험 , 또는 기타 위험으로 인해 서비스 제공자
, 사용자 또는 환자에게 부상을 입힐 수 있습니다 .
Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.
• Ja klienta apkopes sniedzējam nepieciešama informācija citā valodā, klienta pienākums ir
nodrošināt tulkojumu.
• Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas un saprašanas.
• Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas trieciena, mehānisku vai
citu faktoru izraisītu traumu risks apkopes sniedzējam, operatoram vai pacientam.
Šis eksploatavimo vadovas yra tik anglų kalba.
• Jei kliento paslaugų tiekėjas reikalauja vadovo kita kalba – ne anglų, suteikti vertimo paslaugas
privalo klientas.
• Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar nesupratote šio
eksploatavimo vadovo.
• Jei nepaisysite šio įspėjimo, galimi paslaugų tiekėjo, operatoriaus ar paciento sužalojimai dėl
elektros šoko, mechaninių ar kitų pavojų.
Denne servicehåndboken finnes bare på engelsk.
• Hvis kundens serviceleverandør har bruk for et annet språk, er det kundens ansvar å sørge for
oversettelse.
• Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest og forstått.
• Manglende hensyn til denne advarselen kan føre til at serviceleverandøren, operatøren eller
pasienten skades på grunn av elektrisk støt, mekaniske eller andre farer.
Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.
• Jeśli serwisant klienta wymaga języka innego niż angielski, zapewnienie usługi tłumaczenia jest
obowiązkiem klienta.
• Nie próbować serwisować urządzenia bez zapoznania się z niniejszym podręcznikiem
serwisowym i zrozumienia go.
• Niezastosowanie się do tego ostrzeżenia może doprowadzić do obrażeń serwisanta, operatora
lub pacjenta w wyniku porażenia prądem elektrycznym, zagrożenia mechanicznego bądź innego.
Este manual de assistência técnica encontra-se disponível unicamente em inglês.
•
Se outro serviço de assistência técnica solicitar a tradução deste manual, caberá ao cliente
fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
A não observância deste aviso pode ocasionar ferimentos no técnico, operador ou paciente
decorrentes de choques elétricos, mecânicos ou outros.
Este manual de assistência técnica só se encontra disponível em inglês.
•
Se qualquer outro serviço de assistência técnica solicitar este manual noutro idioma, é da
responsabilidade do cliente fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
O não cumprimento deste aviso pode colocar em perigo a segurança do técnico, do operador ou
do paciente devido a choques eléctricos, mecânicos ou outros.
Preface
Page 5
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
ATENŢIE
(RO)
ОСТОРОЖНО!
(RU)
UPOZORENJE
(SR)
UPOZORNENIE
(SK)
ATENCION
(ES)
VARNING
(SV)
OPOZORILO
(SL)
DİKKAT
(TR)
Page 6
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Acest manual de service este disponibil doar în limba engleză.
•
Dacă un furnizor de servicii pentru clienţi necesită o altă limbă decât cea engleză, este de datoria
clientului să furnizeze o traducere.
•
Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi înţelegerii acestui manual de
service.
•
Ignorarea acestui avertisment ar putea duce la rănirea depanatorului, operatorului sau pacientului
în urma pericolelor de electrocutare, mecanice sau de altă natură.
Данное руководство по техническому обслуживанию представлено только на английском языке.
•
Если сервисному персоналу клиента необходимо руководство не на английском, а на
каком-то другом языке, клиенту следует самостоятельно обеспечить перевод.
•
Перед техническим обслуживанием оборудования обязательно обратитесь к данному
руководству и поймите изложенные в нем сведения.
•
Несоблюдение требований данного предупреждения может привести к тому, что
специалист по техобслуживанию, оператор или пациент получит удар электрическим током,
механическую травму или другое повреждение
Ovo servisno uputstvo je dostupno samo na engleskom jeziku.
•
Ako klijentov serviser zahteva neki drugi jezik, klijent je dužan da obezbedi prevodilačke usluge.
•
Ne pokušavajte da opravite uređaj ako niste pročitali i razumeli ovo servisno uputstvo.
•
Zanemarivanje ovog upozorenja može dovesti do povređivanja servisera, rukovaoca ili pacijenta
usled strujnog udara ili mehaničkih i drugih opasnosti.
Tento návod na obsluhu je k dispozícii len v angličtine.
•
Ak zákazníkov poskytovateľ služieb vyžaduje iný jazyk ako angličtinu, poskytnutie
prekladateľských služieb je zodpovednosťou zákazníka.
•
Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na obluhu a neporozumiete mu.
•
Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa služieb, obsluhujúcej
osoby alebo pacienta elektrickým prúdom, mechanické alebo iné ohrozenie.
Este manual de servicio sólo existe en inglés.
•
Si el encargado de mantenimiento de un cliente necesita un idioma que no sea el inglés, el cliente
deberá encargarse de la traducción del manual.
•
No se deberá dar servicio técnico al equipo, sin haber consultado y comprendido este manual de
servicio.
•
La no observancia del presente aviso puede dar lugar a que el proveedor de servicios, el
operador o el paciente sufran lesiones provocadas por causas eléctricas, mecánicas o de otra
naturaleza.
Den här servicehandboken finns bara tillgänglig på engelska. .
•
Om en kunds servicetekniker har behov av ett annat språk än engelska, ansvarar kunden för att
tillhandahålla översättningstjänster.
•
Försök inte utföra service på utrustningen om du inte har läst och förstår den här
servicehandboken.
•
Om du inte tar hänsyn till den här varningen kan det resultera i skador på serviceteknikern,
operatören eller patienten till följd av elektriska stötar, mekaniska faror eller andra faror.
Ta servisni priročnik je na voljo samo v angleškem jeziku.
•
Če ponudnik storitve stranke potrebuje priročnik v drugem jeziku, mora stranka zagotoviti prevod.
•
Ne poskušajte servisirati opreme, če tega priročnika niste v celoti prebrali in razumeli.
•
Če tega opozorila ne upoštevate, se lahko zaradi električnega udara, mehanskih ali drugih
nevarnosti poškoduje ponudnik storitev, operater ali bolnik.
Bu servis kılavuzunun sadece ingilizcesi mevcuttur.
•
Eğer müşteri teknisyeni bu kılavuzu ingilizce dışında bir başka lisandan talep ederse, bunu
tercüme ettirmek müşteriye düşer.
•
Servis kılavuzunu okuyup anlamadan ekipmanlara müdahale etmeyiniz.
•
Bu uyarıya uyulmaması, elektrik, mekanik veya diğer tehlikelerden dolayı teknisyen, operatör
veya hastanın yaralanmasına yol açabilir.
Preface
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Legal notes
TrademarkS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2
are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of
their respective holders.
Copyrights
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material
presented and contained herein may not be reproduced in any form or manner, without the written
permission of General Electric Company, Inc.
Preface
Page 7
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation
“damage in shipment” written on all copies of the freight or express bill before delivery is accepted
or “signed for” by a General Electric representative or a hospital receiving agent. Whether noted or
concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event,
within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this
14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and
MIS.” Contact your local service coordinator for more information on this process.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT
All electrical installations that are preliminary to positioning of the equipment at the site prepared for
the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds into
the Power Distribution Unit shall be performed by licensed electrical contractors. Other connections
between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE
Healthcare personnel. The products involved (and the accompanying electrical installations) are
highly sophisticated, and special engineering competence is required. In performing all electrical
work on these products, GE will use its own specially trained field engineers. All of GE’s electrical
work on these products will comply with the requirements of the applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to
perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein
contained should be thoroughly read and understood by everyone who will use the equipment
before you attempt to place this equipment in operation. GE Healthcare will be glad to assist and
cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the
useful beam, no practical design of equipment can provide complete protection. Nor can any
practical design compel the operator to take adequate precautions to prevent the possibility of any
persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully
acquainted with the recommendations of the National Council on Radiation Protection and
Measurements (NCRP) as published in NCRP Reports available from NCRP Publications, 7910
Woodmont Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission
on Radiation Protection, and take adequate steps to protect against injury.
The equipment is sold with the understanding that GE Healthcare, its agents, and representatives
have no responsibility for injury or damage which may result from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be
used.
Page 8
Preface
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Lithium Battery Cautionary Statement
DANGER - Risk of Explosion
Danger of explosion if battery is incorrectly replaced.
Replace only with the same or equivalent type recommended by the
manufacturer. Discard used batteries according to the manufacturer’s
instructions.
ATTENTION - Danger d’Explosion
Il y a danger d’explosion s’il y a replacement incorrect de la batterie.
Remplacer uniquement avec une batterie du même type ou d’un type
recommandé par le constructeur. Mettre au rébut les batteries
usagées conformément aux instructions du fabricant.
TECHNICAL MANUAL UPDATES
When operating or servicing GE Healthcare products, please contact your GE representative for
the latest revision of product documentation. Product documentation may also be available on-line
at the GE Healthcare support documentation library.
OMISSIONS AND ERRORS
Customers, please contact your GE Healthcare sales or service representatives.
GE personnel, please use the GE Healthcare complaint handling process to report all omissions,
errors, and defects in this publication.
Preface
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GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Revision history
Revision
Date
1
12OCT2011
Initial release of document
2
20FEB2012
No changes to content. Only changed the revision number to rev "2".
3
23AUG2012
Added text to front material on how to obtain most recent revisions of
technical manuals. Satisfies FDA recommendation.
Page 10
Reason for change
Preface
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Preface Publication Conventions
Standardized conventions for representing information is a uniform way of communicating
information to a reader in a consistent manner. Conventions are used so that the reader can easily
recognize the actions or decisions that must be made. There are a number of character and
paragraph styles used in this publication to accomplish this task. Please become familiar with them
before proceeding forward.
It is important that you read and understand hazard statements, and not just ignore them.
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and
style for safety communications reflected in this publication represents the harmonization of IEC/
ISO 3864 and ANSI Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential
hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify
important safety information. Text (Hazard) styles are applied to the paragraph contents that are
applicable to each specific safety statement.
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert
symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation
mark within it. It Is always used next to the signal word to indicate the severity of the hazard.
Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert
symbol and signal word are placed immediately before any paragraph they affect. Safety
information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Text Format of Signal Words
DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH, IF
NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS SIGNAL
WORD IS LIMITED TO THE MOST EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT
AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Caution - Indicates a potentially hazardous situation which, if not avoided, may result in
minor or moderate injury. It may also be used to alert against unsafe practices.
NOTICE - Indicates information or a company policy that relates directly or indirectly to the
safety of personnel or protection of property. This signal word is associated directly with a
hazard or hazardous situation and is used in place of 'DANGER,' 'WARNING,' or 'CAUTION.'
It can include:
Preface
Page 11
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
•
Destruction of a disk drive
•
Potential for internal mechanical damage, such as to a X-ray tube
Symbols and Pictorials Used
The following Symbols and Pictorials are be used in this publication. These graphical icons
(symbols) may be used to make you aware of specific types of hazards that could possibly cause
harm.
Page 12
keep_up
magnetic
biohazard
compressgas
ppe-hearing
fragile
impact
corrosive
heavyobject
ppe-2people
static_elec
heat
general
laser
ppe-respitory
keep_dry
pinch
radiation
poisongas
ppe-loto
general
explosive
electrical
flammable
ppe-eye
torque
crush/mechanical
tipping
Read Manual
ppe-gloves
ce
instuction
poisonmatl
entanglement
instuction
Preface
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such
as Purpose, Example, Comment or Note) are used to identify important but non-safety related
information. Text styles are also applied to text within each paragraph modified by the specific
prefix.
EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:
Purpose: Introduces and provides meaning as to the information contained within the chapter,
section or subsection (such as used at the beginning this chapter, for example).
Note:
Example:
Comment:
Conveys information that should be considered important to the reader.
Used to make the reader aware that the paragraph(s) that follow are examples of information
possibly stated previously.
Represents “additional” information that may or may not be relevant to your situation.
Page Layout
Publication Part Number & Revision Number
The current section and its title
are always shown in the footer of
the left (even) page.
An exclamation point in a triangle is used
to indicate important information to the user.
Paragraphs preceeded by Alphanumeric
characters (e.g. numbers) contain information that must be followed in a specific order.
Publication Title
The current chapter and its title
are always shown in the footer of
the right (odd) page.
Paragraphs preceeded by a symbol
(e.g. bullets) contain information that
has no specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location.
The document part number and revision number appears in every header on every page. Odd
numbered page footers indicate the current chapter, its title and current page number. Even page
footers show the current section and its title, as well as the current page number.
Preface
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GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text
that’s either screen input and output. Mono-spaced fonts, such courier, are used to indicated text
direction. When you type at your keyboard, you are generating computer input. Occasionally you
will see the math operator “greater-than” and “less-than” symbols used to indicate the start and
finish of variable output. When reading text generated by the computer, you are reading it as
computer generated output. In addition to direction, characters are italicized (e.g. italics) to indicate
information specific to your system or site.
Example: Fixed
Output
This paragraph’s font represents computer generated screen “fixed” output.
Its output is fixed from the sense that it does not vary from application
to application. It is the most commonly used style used to indicate
filenames, paths and text that do not change from system to system. The
character style used is a fixed width such as courier.
Example:
Variable Output
This paragraph’s font represents computer screen output that is
“variable”. It is used to represent output that varies from application
to application or system to system. Variable output is sometimes found
placed between greater-than and less-than operators for clarification. For
example: <variable_ouput> or <3.45.120.3>. In both cases, the < and >
operators are not part of the actual input.
Example: Fixed
Input
This paragraph’s font represents fixed input. It is computer input that
is typed-in via the keyboard. Typed input that does not vary from
application to application or system to system. Fixed text the user is
required to supply as input. For example: cd /usr/3p
Example:
Variable Input
This paragraph’s font represents computer input that can vary from
application to application or system to system. With variable text, the
user is required to supply system dependent input or information. Variable
input sometimes is placed between greater-than and less-than operators.
For example: <variable_input>. In these cases, the (<>) operators would
be dropped prior to input. For example: ypcat hosts | grep <3.45.120.3>
would be typed into the computer as:
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or
soft button, switch or key. Physical hardware, such as buttons and switches, are called hard keys
because they are hard wired or mechanical in nature. A keyboard or on/off switch would be a hard
key. Software or computer generated buttons are called soft keys because they are software
generated. Software driven menu buttons are an example of such keys. Soft and hard keys are
represented differently in this publication.
Example: Hard
Keys
A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style
that uses both over and under-lined bold text that is bold. This is a hard key.
Example: Soft
Keys
Whereas the computer MENU button that you would click with your mouse or touch with your hand
uses over and under-lined regular text. This is a soft key.
Page 14
Preface
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Table of contents
Chapter 1 Introduction.......................................................................................... 19
Section 1.1 Overview .............................................................................................................. 19
Section 1.2 Overall DICOM conformance statement document structure......................... 19
Section 1.3 Intended audience............................................................................................... 21
Section 1.4 Scope and field of application ........................................................................... 21
Section 1.5 Important remarks............................................................................................... 22
Section 1.6 References ........................................................................................................... 23
Section 1.7 Definitions............................................................................................................ 23
Section 1.8 Symbols and abbreviations................................................................................ 23
Chapter 2 Network conformance statement ....................................................... 25
Section 2.1 Introduction ......................................................................................................... 25
Section 2.2 Implementation model ........................................................................................ 26
2.2.1 Application data flow diagram .................................................................................................................
2.2.2 Functional AE definition ..........................................................................................................................
2.2.3 Sequencing of real-world activities..........................................................................................................
2.2.4 Worklist server AE specification..............................................................................................................
2.2.4.1 Association establishment policies ...............................................................................................
2.2.4.2 Association acceptance policy ......................................................................................................
26
26
26
27
27
30
Section 2.3 Communication profiles ..................................................................................... 30
2.3.1 Supported communication stacks (PS 3.8, PS 3.9) ................................................................................
2.3.2 OSI stack.................................................................................................................................................
2.3.2.1 Physical media support.................................................................................................................
2.3.3 TCP/IP stack ...........................................................................................................................................
2.3.3.1 API ................................................................................................................................................
2.3.3.2 Physical media support.................................................................................................................
2.3.4 Point-to-point stack .................................................................................................................................
30
30
30
30
30
30
30
Section 2.4 Extensions, specializations, privatizations ...................................................... 31
2.4.1 Standard extended, specialized, private SOPs....................................................................................... 31
2.4.2 Private transfer syntaxes......................................................................................................................... 31
Section 2.5 Configuration....................................................................................................... 31
2.5.1 AE Title/presentation address mapping .................................................................................................. 31
2.5.2 Configurable parameters......................................................................................................................... 31
Section 2.6 Support of extended character sets .................................................................. 31
Section 2.7 Security profiles .................................................................................................. 32
Table of Contents
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GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Chapter 3 Media Storage conformance statement............................................. 33
Section 3.1 Introduction ......................................................................................................... 33
Chapter 4 Digital X-ray information object implementation.............................. 35
Section 4.1 Introduction ......................................................................................................... 35
Chapter 5 Study Root Query/Retrieve information model definition ............... 37
Section 5.1 Introduction ......................................................................................................... 37
Chapter 6 Modality Worklist information model definition ............................... 39
Section 6.1 Introduction ......................................................................................................... 39
Section 6.2 Modality Worklist information model description ............................................ 39
Section 6.3 Modality Worklist information model entity-relationship model..................... 39
6.3.1 Entity descriptions ...................................................................................................................................
6.3.1.1 Scheduled Procedure Step entity description ...............................................................................
6.3.1.2 Requested Procedure entity description .......................................................................................
6.3.1.3 Imaging Service Request entity description ..................................................................................
6.3.1.4 Visit entity description ...................................................................................................................
6.3.1.5 Patient entity description ...............................................................................................................
6.3.2 Optima XR200amx system mapping of DICOM entities .........................................................................
40
40
41
41
41
41
41
Section 6.4 Information model module ................................................................................. 41
Section 6.5 Information model keys ...................................................................................... 42
6.5.1 Supported matching ................................................................................................................................
6.5.2 Scheduled Procedure Step entity............................................................................................................
6.5.2.1 SOP Common module ..................................................................................................................
6.5.2.2 Scheduled Procedure Step module ..............................................................................................
6.5.3 Requested Procedure entity....................................................................................................................
6.5.3.1 Requested Procedure module ......................................................................................................
6.5.4 Imaging Service Request entity ..............................................................................................................
6.5.4.1 Imaging Service Request module .................................................................................................
6.5.5 Visit entity ................................................................................................................................................
6.5.5.1 Visit Identification module .............................................................................................................
6.5.5.2 Visit Status module .......................................................................................................................
6.5.5.3 Visit Relationship module..............................................................................................................
6.5.5.4 Visit Admission module .................................................................................................................
6.5.6 Patient entity ...........................................................................................................................................
6.5.6.1 Patient Relationship module .........................................................................................................
6.5.6.2 Patient Identification module .........................................................................................................
6.5.6.3 Patient Demographic module........................................................................................................
6.5.6.4 Patient Medical module.................................................................................................................
42
43
43
43
44
44
45
45
45
45
45
46
46
46
46
46
47
47
Section 6.6 Private data dictionary........................................................................................ 47
Page 16
Table of Contents
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Chapter 7 Network Print SCU conformance statement ..................................... 49
Section 7.1 Introduction ......................................................................................................... 49
Chapter 8 Print Management SOP class definition............................................ 51
Section 8.1 Introduction ......................................................................................................... 51
Chapter 9 Storage Commitment Push Model SOP class definition ................. 53
Section 9.1 Introduction ......................................................................................................... 53
Chapter 10 Modality Performed Procedure Step implementation .................... 55
Section 10.1 Modality Performed Procedure Step modules ............................................... 55
Table of Contents
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GE HEALTHCARE
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Table of Contents
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Chapter 1 Introduction
Section 1.1 Overview
This DICOM Conformance Statement is divided into sections as described below:
•
Chapter 1 Introduction, which describes the overall structure, intent, and references for this
Conformance Statement.
•
Chapter 2 Network conformance statement, which specifies the GEHC equipment compliance
to the DICOM requirements for the implementation of networking features.
•
Chapter 3 Media Storage conformance statement (applicable only to Optima XR220amx
systems), which specifies the GEHC equipment compliance to the DICOM requirements for
the implementation of media storage features.
•
Chapter 4 Digital X-ray information object implementation (applicable only to Optima
XR220amx systems), which specifies the GEHC equipment compliance to DICOM
requirements for the implementation of a digital X-ray information object implementation
feature.
•
Chapter 5 Study Root Query/Retrieve information model definition (applicable only to Optima
XR220amx systems), which specifies the GEHC equipment compliance to DICOM
requirements for the implementation of the Study Root Query/Retrieve information model
feature.
•
Chapter 6 Modality Worklist information model definition, which specifies the GEHC
equipment compliance to DICOM requirements for the implementation of Basic Worklist
Management Service feature.
•
Chapter 7 Network Print SCU conformance statement (applicable only to Optima XR220amx
systems), which specifies the GEHC equipment compliance to DICOM requirements for the
implementation of the Network Print feature.
•
Chapter 8 Print Management SOP class definition (applicable only to Optima XR220amx
systems), which specifies the GEHC equipment compliance to DICOM requirements for the
implementation of the Network Print Management SOP class.
•
Chapter 9 Storage Commitment Push Model SOP class definition (applicable only to Optima
XR220amx systems), which specifies the GEHC equipment compliance to DICOM
requirements for the implementation of the Storage Commitment Push Service feature.
•
Chapter 10 Modality Performed Procedure Step implementation (applicable only to Optima
XR220amx systems), which specifies the GEHC equipment compliance to DICOM
requirements for the implementation of Performed Procedure Step (PPS) SCU features
Section 1.2 Overall DICOM conformance statement document
structure
The documentation structure of the GEHC Conformance Statements and their relationship with the
DICOM V3.0 Conformance Statements is shown in Figure 1-1.
Chapter 1 Introduction
Page 19
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Figure 1-1 Documentation structure of GEHC conformance statements
Page 20
Section 1.2 Overall DICOM conformance statement document structure
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
This document specifies the DICOM implementation. It is entitled:
Optima XR200amx
DICOM Conformance Statement
Direction 5336117-1EN
This DICOM Conformance Statement documents the DICOM Conformance Statement and
Technical Specification required to inter-operate with the GEHC network interface.
Introductory information, which is applicable to all GEHC Conformance Statements, is described in
the document:
Introduction to the Integrated DICOM/Network v3.0 (ID/Net v3.0)
Conformance Statement
Direction: 2118780
This Introduction familiarizes the reader with DICOM terminology and general concepts. It should
be read prior to reading the individual products' GEHC Conformance Statements.
The GEHC Conformance Statement, contained in this document, also specifies the Lower Layer
communications that it supports (for example, TCP/IP). However, the Technical Specifications are
defined in the DICOM Part 8 standard.
For more information including Network Architecture and basic DICOM concepts, Refer to the
Introduction.
For more information regarding DICOM, copies of the Standard may be obtained on the Internet at
http://medical.nema.org. Comments on the Standard may be addressed to:
DICOM Secretariat
NEMA
1300 North 17th Street, Suite 1847
Rosslyn, VA 22209
USA
Phone: +1.703.841.3200
Section 1.3 Intended audience
The reader of this document is concerned with software design and/or system integration issues. It
is assumed that the reader of this document is familiar with the DICOM Standards and with the
terminology and concepts which are used in that standard.
If readers are unfamiliar with DICOM terminology they should first refer to the document listed
below, then read the DICOM Standard itself, prior to reading this DICOM Conformance Statement
document.
Introduction to the Integrated DICOM/Network v3.0 (ID/Net v3.0)
Conformance Statement
Direction: 2118780
Section 1.4 Scope and field of application
It is the intent of this document, in conjunction with the Introduction to the Integrated DICOM/
Network v3.0 (ID/Net v3.0) Conformance Statement, Direction: 2118780, to provide an
unambiguous specification for GEHC implementations. This specification, called a Conformance
Statement, includes a DICOM V3.0 Conformance Statement and is necessary to ensure proper
processing and interpretation of GEHC medical data exchanged using DICOM V3.0. The GEHC
Conformance Statements are available to the public.
The reader of this DICOM Conformance Statement should be aware that different GEHC devices
are capable of using different Information object definitions. For example, a GEHC CT Scanner may
Chapter 1 Introduction
Page 21
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
send images using the CT Information Object, MR Information Object, Secondary Capture Object,
etc.
Included in this DICOM Conformance Statement are the module definitions which define all data
elements used by this GEHC implementation. If the user encounters unspecified private data
elements while parsing a GEHC Data Set, the user is well advised to ignore those data elements
(per the DICOM standard). Unspecified private data element information is subject to change
without notice. If, however, the device is acting as a “full fidelity storage device”, it should retain and
re-transmit all of the private data elements that are sent by GEHC devices.
Section 1.5 Important remarks
The use of these DICOM Conformance Statements, in conjunction with the DICOM Standards, is
intended to facilitate communication with GE imaging equipment. However, by itself, it is not
sufficient to ensure that inter-operation will be successful. The user (or user's agent) needs
to proceed with caution and address at least four issues:
•
Integration - The integration of any device into an overall system of interconnected devices
goes beyond the scope of standards (DICOM V3.0), and of this introduction and associated
DICOM Conformance Statements when interoperability with non-GE equipment is desired.
The responsibility to analyze the applications requirements and to design a solution that
integrates GE imaging equipment with non-GE systems is the user's responsibility and should
not be underestimated. The user is strongly advised to ensure that such an integration analysis
is correctly performed.
•
Validation - Testing the complete range of possible interactions between any GE device and
non-GE devices, before the connection is declared operational, should not be overlooked.
Therefore, the user should ensure that any non-GE provider accepts full responsibility for all
validation required for their connection with GE devices. This includes the accuracy of the
image data once it has crossed the interface between the GE imaging equipment and the nonGE device and the stability of the image data for the intended applications.
Such a validation is required before any clinical use (diagnosis and/or treatment) is performed.
It applies when images acquired on GE imaging equipment are processed/displayed on a nonGE device, as well as when images acquired on non-GE equipment are processed/displayed
on a GE console or workstation.
Page 22
•
Future Evolution - GE understands that the DICOM Standard will evolve to meet the user's
growing requirements. GE is actively involved in the development of the DICOM Standard.
DICOM will incorporate new features and technologies and GE may follow the evolution of the
Standard. The GEHC protocol is based on DICOM as specified in each DICOM Conformance
Statement. Evolution of the Standard may require changes to devices that have implemented
DICOM. In addition, GE reserves the right to discontinue or make changes to the support of
communications features (on its products) reflected on by these DICOM Conformance
Statements. The user should ensure that any non-GE provider, which connects with GE
devices, also plans for the future evolution of the DICOM Standard. Failure to do so will likely
result in the loss of function and/or connectivity as the DICOM Standard changes and GE
Products are enhanced to support these changes.
•
Interaction - It is the sole responsibility of the non-GE provider to ensure that communication
with the interfaced equipment does not cause degradation of GE imaging equipment
performance and/or function.
Section 1.5 Important remarks
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Section 1.6 References
A list of references that is applicable to all GEHC Conformance Statements is included in the
Introduction to the Integrated DICOM/Network v3.0 (ID/Net v3.0) Conformance Statement,
Direction: 2118780.
The information object implementation refers to DICOM PS 3.3 (Information object definition).
Section 1.7 Definitions
A set of definitions which is applicable to all GEHC Conformance Statements is included in the
Introduction to the Integrated DICOM/Network v3.0 (ID/Net v3.0) Conformance Statement,
Direction: 2118780.
Section 1.8 Symbols and abbreviations
A list of symbols and abbreviations which is applicable to all GEHC Conformance Statements is
included in the Introduction to the Integrated DICOM/Network v3.0 (ID/Net v3.0) Conformance
Statement, Direction: 2118780.
Chapter 1 Introduction
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GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
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DICOM CONFORMANCE STATEMENT
Section 1.8 Symbols and abbreviations
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Chapter 2 Network conformance statement
Section 2.1 Introduction
This section of the DICOM Conformance Statement specifies the compliance to DICOM
conformance requirements for the relevant Networking features on this GEHC product. Note that
the format of this section strictly follows the format defined in DICOM Standard PS 3.2
(Conformance). Refer to that part of the standard while reading this section.
The details of the DICOM conformance related to other information objects and information models
supported by this product are included in subsequent sections of this DICOM Conformance
Statement.
The Optima XR200amx system is an Integrated Digital X-ray System:
•
It allows a user to query for and display DICOM modality worklist information from a remote
hospital or radiology department information system computer. For example, a user may wish
to query for all procedures scheduled to be performed on the system. In this situation, the
Optima XR200amx system is providing the DICOM Modality Worklist SOP class service as a
service class user (SCU).
Chapter 2 Network conformance statement
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GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Section 2.2 Implementation model
2.2.1 Application data flow diagram
The Basic and Specific Application models for this device are shown in Figure 2-1:
Figure 2-1 Basic and specific application models for this device
Note:
Refer also to Chapter 3 Media Storage conformance statement and Chapter 7 Network Print SCU
conformance statement of the current document for Media Storage and Network Print Management
SCU Conformance Statement.
2.2.2 Functional AE definition
WORKLIST SERVER AE:
The WORKLIST SERVER AE is automatically brought up when the Optima XR200amx system is
powered on.
The remote Worklist SCP must be manually configured on the Optima XR200amx system. The
configuration of remote Worklist SCP is done through the UTILITIES > NETWORK
CONNECTIONS.
The WORKLIST SERVER AE is invoked by the real-world activity Refresh Worklist.
For this operation, the user selects the REFRESH WORKLIST button of the Worklist screen in order
to obtain latest modality worklist from the RIS. The WORKLIST SERVER sends a query defined by
the user to remote AEs and returns the results to the user interface.
The WORKLIST SERVER AE initiates the following functions:
•
Build the Worklist query according to the criteria defined by the user in the Query Definition
Window.
•
Send the query to Worklist Provider: Initiates a DICOM association with the Worklist Provider.
If the remote Worklist Provider accepts a presentation context applicable to modality worklist,
the WORKLIST SERVER AE issues a modality worklist query request via the C-FIND service.
2.2.3 Sequencing of real-world activities
WORKLIST SERVER AE:
The user will usually refresh the Worklist before the image acquisition in order to get the very latest
information from the RIS.
1.
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Upon user request, the system initiates a modality worklist query (as a modality worklist SCU)
Section 2.2 Implementation model
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to the modality worklist SCP with a given set of query parameters.
2.
The modality worklist SCP returns responses that match the query parameters.
3.
Items from the returned worklist responses are filtered according to the query parameters
4.
Only the items matching the query parameters are presented to the user.
5.
Each item of the returned worklist responses selected for image acquisition is included in
acquired DICOM images related to the responses.
2.2.4 Worklist server AE specification
This Application Entity provides Standard Conformance to the following DICOM V3.0 SOP classes
as an SCU:
SOP class name
SOP class UID
Modality Worklist Information Model – FIND
1.2.840.10008.5.1.4.31
2.2.4.1 Association establishment policies
2.2.4.1.1 General
The DICOM Application Context Name (ACN), which is always proposed, is:
Application Context Name
1.2.840.10008.3.1.1.1
The Maximum Length PDU negotiation is included in all association establishment requests. The
maximum length PDU for an association initiated by the WORKLIST SERVER AE is:
Maximum Length PDU
28Kbytes
The SOP class Extended negotiation is not supported.
The maximum number of Presentation Context Items that will be proposed is 1.
The user information Items sent by this product are:
•
Maximum PDU Length
•
Implementation UID
2.2.4.1.2 Number of associations
The WORKLIST SERVER AE (SCU) will initiate only one DICOM association at a time to perform
a modality worklist query of a single remote AE.
2.2.4.1.3 Asynchronous nature
Asynchronous mode is not supported. All operations will be performed synchronously.
2.2.4.1.4 Implementation identifying information
The implementation UID for this DICOM implementation is:
Optima XR200amx system implementation UID
1.2.840.113619.6.308
Optima XR200amx system implementation version name
Optima XR200amx
Chapter 2 Network conformance statement
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2.2.4.1.5 Association initiation by real-world activity
2.2.4.1.5.1 Real-world activity: Worklist query
2.2.4.1.5.1.1 Associated real-world activity
The operator of the system initiates a query for a modality worklist by pressing the REFRESH
WORKLIST button of the Worklist screen. The Worklist Server will then initiate an association with
the remote AE in order to query for the worklist A user can configure a number of parameters that
directly control the worklist query request. The user can request worklist items that are intended for
the system the user is working at, all items that apply to the modality of the system the user is
working at or all worklist items available. These selections and their affects on worklist query
parameters are given below:
This system:
•
Modality, (0008,0060) - set to DX
•
Scheduled Station AE Title, (0040,0001) - set to Query AE title
This modality:
•
Modality, (0008,0060) - set to DX
•
Scheduled Station AE Title, (0040,0001) - zero-length (universal matching)
All systems:
•
Modality, (0008,0060) - zero-length (universal matching)
•
Scheduled Station AE Title, (0040,0001) - zero-length (universal matching)
The scheduled dates of procedures of interest can be specified for query by selecting a specific date
range. The date ranges available are Today, Tomorrow or between two given dates. These
selections and their affects on worklist query parameters are given below:
Today:
Scheduled Procedure Step Start Date, (0040,0002) - set to YYYYMMDDYYYYMMDD, where
YYYYMMDD is the current date.
Tomorrow:
Scheduled Procedure Step Start Date, (0040,0002) - set to YYYYMMDDYYYYMMDD, where
YYYYMMDD is tomorrow date.
Between 2 dates:
Scheduled Procedure Step Start Date, (0040,0002) - set to YYYYMMDDYYYYMMDD’, where
YYYYMMDD is set to given From date and YYYYMMDD’ is set to given To date.
Patient name:
Patient Name, (0010,0010) - set to given Patient Name
Patient ID:
Patient ID, (0010,0020) - set to given Patient ID
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Section 2.2 Implementation model
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2.2.4.1.5.1.2 Proposed presentation context table
The following table shows the proposed presentation contexts for the Worklist Server AE after realworld activity “Worklist Query” has been initiated:
Presentation context table - proposed
Abstract syntax
Transfer syntax
Name
UID
Name list
UID list
Modality Worklist
Information Model - FIND
1.2.840.10008.5.1.4.31
Implicit VR
Little Endian
1.2.840.10008.1.2
Role
Extended
negotiation
SCU
None
2.2.4.1.5.1.2.1 SOP Specific DICOM conformance statement for the Worklist SOP class
Following are the Status codes that are more specifically processed when receiving messages from
a Modality Worklist SCP:
If the remote AE does not support the proposed Presentation Context, an appropriate error is
logged and the operator is notified.
This implementation can receive multiple C-FIND results over a single association. Only one
association is opened at a time.
Each C-FIND response received from the remote AE is parsed to verify the length/type of the items
in the response. Upon detecting any error in the response data, the Worklist Server AE will ignore
the bad data and carry on to the next C-FIND response.
On receipt of any error from the remote AE, the Worklist Server will issue a CFIND-CANCEL and,
upon receipt of a C-FIND-RSP (or if an applicable timer expires), will close the association.
Warnings received from the remote AE are ignored.
Each C-FIND operation supports an “Association Timer.” This timer starts when the association
request is sent or received and stops when the association is established. The default time-out
value is 15 seconds.
If the above timer expires, the association is aborted (A-ABORT) and the operation in progress is
considered to have failed. Any previously received worklist items are kept.
2.2.4.1.5.1.2.2 Record acceptance policy
All worklist items coming from the remote AE are accepted. Nevertheless, the system filters each
received worklist item checking that it matches the query parameters. If the received worklist item
matches the query parameter, then it is stored in the local Worklist database and displayed to the
user, else it is ignored.
The filter checks the following fields:
Tag value
Worklist attribute
Acceptance
0008,0005
Specific Character Set
Check that value is empty or equal to ISO_IR 100
0008,0060
Modality
Check that value is empty or equal to DX
0010,0010
Patient Name
If value defined in Query Definition Window, check
that value matches the defined value
0010,0020
Patient ID
If value defined in Query Definition Window, check
that value matches the defined value
0040,0001
Scheduled Station AE
Title
If matching is defined in the query parameters, then
check that value is empty or equal to the defined
value in query parameters setting.
Chapter 2 Network conformance statement
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Tag value
Worklist attribute
Acceptance
0040,0002
Scheduled Procedure
Step Start Date
If matching is defined in the query parameters, then
check that value is empty or equal to the defined
value in query parameters setting.
2.2.4.2 Association acceptance policy
The Worklist Server AE does not respond to attempts by a remote AE to open an association.
Section 2.3 Communication profiles
2.3.1 Supported communication stacks (PS 3.8, PS 3.9)
DICOM Upper Layer Protocol is supported using TCP/IP as specified in DICOM PS 3.8.
2.3.2 OSI stack
OSI stack not supported.
2.3.2.1 Physical media support
Not applicable.
2.3.3 TCP/IP stack
The TCP/IP stack is inherited from a LINUX operating system.
2.3.3.1 API
Not applicable to this product.
2.3.3.2 Physical media support
DICOM is indifferent to the Physical medium over which TCP/IP executes (e.g. Ethernet V2.0, IEEE
802.3, ATM, FDDI)
Note:
For more information about the Physical Media available on Optima XR200amx system, Refer to
the Product Data Sheet.
2.3.4 Point-to-point stack
A 50-pin ACR-NEMA connection is not applicable to this product.
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Section 2.3 Communication profiles
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Section 2.4 Extensions, specializations, privatizations
2.4.1 Standard extended, specialized, private SOPs
None supported.
2.4.2 Private transfer syntaxes
None supported.
Section 2.5 Configuration
2.5.1 AE Title/presentation address mapping
The Optima XR200amx system allows the user to Add, Remove, and Update the mapping of
remote AE titles to IP addresses and ports. These options can be selected from the Network
Connections displayed when the Utilities Button is selected on the Worklist.
The system allows the configuration of the following
Worklist Server AE
AE Title, IP Address, Port Number
2.5.2 Configurable parameters
The following fields are configurable:
•
Local IP Address
•
Local IP Netmask
•
Default Router IP Address for local network. Only one default router IP Address can be
configured for all remote nodes.
The Local Listening Port Number for C-STORE SCP DICOM service is not configurable and set to
4010.
The Local Listening Port Number for STORAGE COMMITMENT DICOM service is not configurable
and set to 4010.
The following fields are configurable for every remote DICOM AE including Worklist provider:
•
Remote AE Title
•
Remote IP Address
•
Listening TCP/IP Port Number
Section 2.6 Support of extended character sets
The Optima XR200amx system will support only the ISO_IR 100 (ISO 8859-1:1987 Latin alphabet
N 1. supplementary set) as extended character sets.
Chapter 2 Network conformance statement
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Section 2.7 Security profiles
The product does not conform to any defined DICOM Security Profiles.
It is assumed that the product is used within a secured environment. It is assumed that a secured
environment includes at a minimum:
Page 32
1.
Firewall or router protections to ensure that only approved external hosts have network access
to the product.
2.
Firewall or router protections to ensure that the product only has network access to approved
external hosts and services.
3.
Any communications with external hosts and services outside the locally secured environment
use appropriate secure network channels (such as a Virtual Private Network (VPN)) The
Optima XR200amx system will support only the ISO_IR 100 (ISO 8859-1:1987 Latin alphabet
N 1. supplementary set) as extended character sets.
Section 2.7 Security profiles
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Chapter 3 Media Storage conformance
statement
Section 3.1 Introduction
Not applicable to Optima XR200amx system.
Chapter 3 Media Storage conformance statement
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DICOM CONFORMANCE STATEMENT
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DICOM CONFORMANCE STATEMENT
Chapter 4 Digital X-ray information object
implementation
Section 4.1 Introduction
Not applicable to Optima XR200amx system.
Chapter 4 Digital X-ray information object implementation
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OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
GE HEALTHCARE
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DICOM CONFORMANCE STATEMENT
Chapter 5 Study Root Query/Retrieve
information model definition
Section 5.1 Introduction
Not applicable to Optima XR200amx system.
Chapter 5 Study Root Query/Retrieve information model definition
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DICOM CONFORMANCE STATEMENT
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DICOM CONFORMANCE STATEMENT
Chapter 6 Modality Worklist information
model definition
Section 6.1 Introduction
This section specifies the use of the DICOM Modality Worklist information model used to organize
data and against which a Modality Worklist Query will be performed. The contents of this section
are:
Section 6.2 Modality Worklist information model description
Section 6.3 Modality Worklist information model entity-relationship model
Section 6.4 Information model module
Section 6.6 Private data dictionary
Section 6.2 Modality Worklist information model description
In order to serve as a Service Class Provider (SCP) of the Modality Worklist Service Class, a
DICOM Application Entity (AE) possesses information about the attributes of a number of managed
worklist items. These items are organized into Modality Worklist information modules. In this
Service Class, the information model plays a role similar to an information object definition of most
other DICOM Service Classes.
Section 6.3 Modality Worklist information model entityrelationship model
The Entity-Relationship diagram for the Modality Worklist information model schema is shown in
Figure 6-1. It represents the information that composes a Worklist Item. In this figure, the following
diagrammatic convention is established to represent the information organization:
•
each entity is represented by a rectangular box
•
each relationship is represented by a diamond shaped box.
•
the fact that a relationship exists between two entities is depicted by lines connecting the
corresponding entity boxes to the relationship boxes.
Chapter 6 Modality Worklist information model definition
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Figure 6-1 Modality Worklist information model E/R diagram
6.3.1 Entity descriptions
Refer to DICOM Standard PS 3.3 (Information object definitions) and PS 3.4 (Service Class
Specifications) for a description of each of the Entities contained within the Modality Worklist
information model.
6.3.1.1 Scheduled Procedure Step entity description
A Scheduled Procedure Step is an arbitrarily defined scheduled unit of service that is specified by
the Procedure Plan for a Requested Procedure. It specifies one or more Action Items (events)
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Section 6.3 Modality Worklist information model entity-relationship model
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DICOM CONFORMANCE STATEMENT
involving equipment (i.e. imaging modality equipment), human resources, location and time (i.e.
start time, stop time, duration).
6.3.1.2 Requested Procedure entity description
A Requested Procedure is an instance of a Procedure of a given Procedure Type. An instance of a
Requested Procedure includes all of the items of information that are specified by an instance of a
Procedure Plan that is selected for the Requested Procedure by the imaging service provider.
6.3.1.3 Imaging Service Request entity description
An Imaging Service Request is a set of one or more Requested Procedures selected from a list of
Procedure Types. An Imaging Service Request is submitted by one authorized imaging service
requester to one authorized imaging service provider in the context of one Service Episode.
6.3.1.4 Visit entity description
A Visit is the context in which the treatment or management of an arbitrary subset of a Patient’s
medical conditions occurs. A Visit is limited to the description of a Patient’s activities at a single
facility.
6.3.1.5 Patient entity description
A Patient is a person receiving, or registered to receive, healthcare services.
6.3.2 Optima XR200amx system mapping of DICOM entities
Table 6-1 Mapping of DICOM entities to Optima XR200amx system entities
DICOM entity
Optima XR200amx system entity
Scheduled Procedure Step
Series
Requested Procedure
Study/Exam
Imaging Service Request
Study/Exam
Visit
Study/Exam
Patient
Patient
Section 6.4 Information model module
Within an entity of the DICOM V3.0 Modality Worklist information model, attributes are grouped into
related set of attributes. A set of related attributes is termed a module. A module facilitates the
understanding of the semantics concerning the attributes and how the attributes are related with
each other. A module grouping does not infer any encoding of information into data sets.
Table 6-2 identifies the defined modules within the entities that comprise the DICOM V3.0 Modality
Worklist information model. Modules are identified by module name. See DICOM V3.0 PS 3.3 and
PS 3.4 for a complete definition of the entities, modules, and attributes.
Table 6-2 Modality Worklist information model modules
Entity name
Module name
Section reference
Scheduled Procedure Step
SOP Common
6.5.2.1 SOP Common module
Chapter 6 Modality Worklist information model definition
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Entity name
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Module name
Section reference
Scheduled Procedure Step
6.5.2.2 Scheduled Procedure Step module
Requested Procedure
Requested Procedure
6.5.3.1 Requested Procedure module
Imaging Service Request
Imaging Service Request
6.5.4.1 Imaging Service Request module
Visit
Visit Identification
6.5.5.1 Visit Identification module
Visit Status
6.5.5.2 Visit Status module
Visit Relationship
6.5.5.3 Visit Relationship module
Visit Admission
6.5.5.4 Visit Admission module
Patient Relationship
6.5.6.1 Patient Relationship module
Patient Identification
6.5.6.2 Patient Identification module
Patient Demographic
6.5.6.3 Patient Demographic module
Patient Medical
6.5.6.4 Patient Medical module
Patient
Section 6.5 Information model keys
Refer to DICOM Standard PS 3.3 (Information object definitions) and PS 3.4 (Service Class
Specifications) for a description of each of the Entities contained within the Modality Worklist
information model.
The following module descriptions are included to specify what data elements are supported and
what type of matching can be applied. It should be noted that they are the same ones as defined in
the DICOM V3.0 Standard PS 3.4 (Service Class Specifications) and include:
•
Name
•
Tag group and element numbers
•
Expected matching key type: R-required, O-optional
•
Expected Return Key Type:
-
1 - non-zero value required
-
1C - conditionally of type 1
-
2 - required to be present, possibly with zero-length value
-
2C - conditionally of type 2
-
3 - optional
•
Mapped into The Image - whether this data is mapped into subsequently acquired images
•
Notes - clarification of this implementation’s use/treatment of this attribute
All data elements in the following module descriptions are requested by default by the Worklist
Server AE.
Data elements for which values can be sent for matching purposes are described as such. Data
elements for which values are Not sent are sent with zero length and universal matching will apply.
This is the default case if no other description to the contrary is provided.
6.5.1 Supported matching
Following are the types of matching that can be request by the implementation:
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•
Single Value matching
•
Universal Matching
Section 6.5 Information model keys
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•
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DICOM CONFORMANCE STATEMENT
Range of date, Range of Time
6.5.2 Scheduled Procedure Step entity
6.5.2.1 SOP Common module
Table 6-3 SOP Common module attributes
Attribute
name
Tag
Expected Expected Mapped
matching returned into
key type key type image
Specific
Character
Set
(0008,0005) O
1C
No
Displayed Updatabl
to user
e by user
Note
No
Matching is supported,
matching value is
“ISO_IR100” and it is not
dynamically configurable.
No
6.5.2.2 Scheduled Procedure Step module
Table 6-4 Scheduled Procedure Step module attributes
Attribute name Tag
Expected Expected Mapped
matching returned into
key type key type image
Displayed Updatabl
to user
e by user
Note
Scheduled
(0040,0100) R
Procedure Step
Sequence
1
No
N/A
N/A
>Scheduled
(0040,0001) R
Station AE Title
1
No
No
No
Matching is supported as
follows: either no AE title
is supplied (universal
matching), or the Query
AE title (See Note) is
supplied for matching;
this is user selectable.
>Scheduled
(0040,0002) R
Procedure Step
Start Date
1
No
Yes
No
Matching is supported as
one of the following; this
is user selectable:
• today only,
• tomorrow only,
• from date1 to date2,
date1 and date2 being
defined by user
Returned values must be
exactly 8 numeric
characters, in
YYYYMMDD or
YYYY.MM.DD format
Chapter 6 Modality Worklist information model definition
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Attribute name Tag
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Expected Expected Mapped
matching returned into
key type key type image
Displayed Updatabl
to user
e by user
Note
Matching is supported as
follows: either no
Modality is supplied
(universal matching), or
the system’s Modality is
supplied (i.e. DX) for
matching: this is user
selectable.
>Modality
(0008,0060) R
1
Yes
Yes
No
>Scheduled
Performing
Physician's
Name
(0040,0006) R
2
Yes
Yes
Yes
(0040,0007) O
>Scheduled
Procedure Step
Description
1C
Yes
Yes
Yes
>Scheduled
Action Item
Code
Sequence
(0040,0008) O
1C
No
No
No
>>Code Value
(0008,0100) O
1C
No
No
No
>>Coding
Scheme
Designator
(0008,0102) O
1C
No
No
No
>>Code
Meaning
(0008,0104) O
3
No
No
No
>Scheduled
(0040,0009) O
Procedure Step
ID
1
No
No
No
If not provided by HIS
6.5.3 Requested Procedure entity
6.5.3.1 Requested Procedure module
Table 6-5 Requested Procedure module attributes
Attribute name
Tag
Expected Expected Mapped
matching returned into
key type key type image
Displayed Updatabl
to user
e by user
Requested
Procedure ID
(0040,1001)
O
1
Yes
Yes
No
Requested
Procedure
Description
(0032,1060)
O
1C
Yes
Yes
Yes
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Section 6.5 Information model keys
Note
If not provided by
HIS
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Attribute name
Tag
Expected Expected Mapped
matching returned into
key type key type image
Displayed Updatabl
to user
e by user
Requested
Procedure Code
Sequence
(0032,1064)
O
1C
Yes
No
No
>Code Value
(0008,0100)
O
1C
Yes
No
No
>Coding Scheme
Designator
(0008,0102)
O
1C
Yes
No
No
>Code Meaning
(0008,0104)
O
3
Yes
No
No
Study Instance UID (0020,000D)
O
1
Yes
No
No
Referenced Study
Sequence
(0008,1110)
O
2
Yes
No
No
>Referenced SOP
Class UID
(0008,1150)
O
1C
Yes
No
No
>Referenced SOP
Instance UID
(0008,1155)
O
1C
Yes
No
No
Note
6.5.4 Imaging Service Request entity
6.5.4.1 Imaging Service Request module
Table 6-6 Imaging Service Request module attributes
Attribute name
Tag
Expected Expected Mapped
matching returned into
key type key type image
Displayed Updatabl
to user
e by user
Accession Number
(0008,0050) O
2
Yes
Yes
Yes if not
provided
by HIS
Referring Physician
Name
(0008,0090) O
2
Yes
Yes
Yes
Note
6.5.5 Visit entity
6.5.5.1 Visit Identification module
None of the data element from Visit Identification module are requested.
6.5.5.2 Visit Status module
None of the data element from Visit Status module are requested.
Chapter 6 Modality Worklist information model definition
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6.5.5.3 Visit Relationship module
Table 6-7 Visit Relationship module attributes
Expected Expected Mapped
matching returned into
key type key type image
Displayed Updatabl
to user
e by user
Attribute name
Tag
Referenced Patient
Sequence
(0008,1120) O
2
Yes
No
No
>Referenced SOP Class (0008,1150) O
UID
2
Yes
No
No
>Referenced SOP
Instance UID
2
Yes
No
No
(0008,1155) O
Note
6.5.5.4 Visit Admission module
None of the data elements from Visit Admission module are requested.
6.5.6 Patient entity
6.5.6.1 Patient Relationship module
None of the data elements from Patient Relationship module are requested.
6.5.6.2 Patient Identification module
Table 6-8 Patient Identification module attributes
Attribute
name
Tag
Patient's
Name
(0010,0010) R
1
Patient ID
(0010,0020) R
1
Page 46
Expected Expected Mapped
matching returned into
key type key type image
Displayed Updatabl
to user
e by user
Note
Yes
Yes
Yes if not
provided
by HIS
Matching is supported as
follows: either no patient
name is supplied
(universal matching), or
the patient name entered
by the user in the Query
Definition screen is
supplied for matching
Yes
Yes
Yes if not
provided
by HIS
Matching is supported as
follows: either no patient
ID is supplied (universal
matching), or the patient
ID entered by the user in
the Query Definition
screen is supplied for
matching
Section 6.5 Information model keys
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6.5.6.3 Patient Demographic module
Table 6-9 Patient Demographic module attributes
Attribute name
Tag
Expected Expected Mapped
matching returned into
key type key type image
Displayed Updatabl
to user
e by user
Patient Birth Date (0010,0030) O
2
Yes
Yes
Yes
Patient's Sex
2
Yes
Yes
Yes
(0010,0040) O
Note
6.5.6.4 Patient Medical module
None of the data elements from Patient Medical module are requested.
Section 6.6 Private data dictionary
The Optima XR200amx system implementation does not define any private attributes within the
Modality Worklist information model.
Chapter 6 Modality Worklist information model definition
Page 47
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
Page 48
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Section 6.6 Private data dictionary
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Chapter 7 Network Print SCU conformance
statement
Section 7.1 Introduction
Not applicable to Optima XR200amx system.
Chapter 7 Network Print SCU conformance statement
Page 49
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
Page 50
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Chapter 8 Print Management SOP class
definition
Section 8.1 Introduction
Not applicable to Optima XR200amx system.
Chapter 8 Print Management SOP class definition
Page 51
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
Page 52
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Chapter 9 Storage Commitment Push Model
SOP class definition
Section 9.1 Introduction
Not applicable to Optima XR200amx system.
Chapter 9 Storage Commitment Push Model SOP class definition
Page 53
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
Page 54
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
Chapter 10 Modality Performed Procedure
Step implementation
Section 10.1 Modality Performed Procedure Step modules
Not applicable to Optima XR200amx system.
Chapter 10 Modality Performed Procedure Step implementation
Page 55
GE HEALTHCARE
DIRECTION 5336117-1EN, REVISION 3
Page 56
OPTIMA XR200AMX
DICOM CONFORMANCE STATEMENT
© 2011 General Electric.
GE Medical Systems, a General Electric Company, going to market as GE Healthcare.
3000 N. Grandview Boulevard
Waukesha, Wisconsin 53188
USA
www.gehealthcare.com
58
To view this Operator Manual,
please refer to
Operator Manual DVD 5336121-399,
provided with the system.
Front cover
GE Healthcare
Optima XR200amx/XR220amx
System Manual
Direction 5336122-1EN, Rev 15
GE HEALTHCARE
REVISION 15
Warning
OPTIMA XR200AMX/XR220AMX SYSTEM MANUAL
DIRECTION 5336122-1EN
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR
SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X
représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement
X entraîne des dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les
personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour ellesmêmes. Avant chaque manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se
renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique,
Annales 26: Recommandations de la Commission Internationale sure la Protection Radiologique et les normes
nationales en vigueur.
WARNING
X-RAY EQUIPMENT IS DANGEROUS TO BOTH PATIENT AND OPERATOR UNLESS MEASURES OF
PROTECTION ARE STRICTLY OBSERVED.
Though this equipment is built to the highest standards of electrical and mechanical safety, the useful x-ray beam
becomes a source of danger in the hands of the unauthorized or unqualified operator. Excessive exposure to x-radiation
causes damage to human tissue.
Therefore, adequate precautions must be taken to prevent unauthorized or unqualified persons from operating this
equipment or exposing themselves or others to its radiation.
Before operation, persons qualified and authorized to operate this equipment should be familiar with the
Recommendations of the International Commission on Radiological Protection (ICRP), contained in Annals Number 26
of the ICRP, and with applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS
NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro
al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede
causar daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o
no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán
informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales
No 26: Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE
GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den
Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte
Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden
Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen
Kommission für Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für
Strahlenschutz und anderer nationaler Normenbehörden.
Page 2
GE HEALTHCARE
SYSTEM MANUAL
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Important information
WARNING
(EN)
ПРЕДУПРЕЖДЕНИЕ
(BG)
警告
(ZH-CN)
警告
(ZH-HK)
警告
(ZH-TW)
This service manual is available in English only.
•
If a customer's service provider requires a language other than English, it is the customer's
responsibility to provide translation services.
•
Do not attempt to service the equipment unless this service manual has been consulted and is
understood.
•
Failure to heed this warning may result in injury to the service provider, operator or patient from
electric shock, mechanical or other hazards.
Tова упътване за работа е налично само на английски език.
•
Ако доставчикът на услугата на клиента изиска друг език, задължение на клиента е да
осигури превод.
•
Не използвайте оборудването, преди да сте се консултирали и разбрали упътването за
работа.
•
неспазването на това предупреждение може да доведе до нараняване на доставчика на
услугата, оператора или пациентa в резултат на токов удар, механична или друга опасност.
本维修手册仅提供英文版本。
•
•
•
如果客户的维修服务人员需要非英文版本，则客户需自行提供翻译服务。
未详细阅读和完全理解本维修手册之前，不得进行维修。
忽略本警告可能对维修服务人员、操作人员或患者造成电击、机械伤害或其他形式的伤
害。
本服務手冊僅提供英文版本。
• 倘若客戶的服務供應商需要英文以外之服務手冊，客戶有責任提供翻譯服務。
• 除非已參閱本服務手冊及明白其內容，否則切勿嘗試維修設備。
• 不遵從本警告或會令服務供應商、網絡供應商或病人受到觸電、機械性或其他的危險。
本維修手冊僅有英文版。
• 若客戶的維修廠商需要英文版以外的語言，應由客戶自行提供翻譯服務。
• 請勿試圖維修本設備，除非 您已查閱並瞭解本維修手冊。
• 若未留意本警告，可能導致維修廠商、操作員或病患因觸電、機械或其他危險而受傷。
UPOZORENJE
(HR)
Ovaj servisni priručnik dostupan je na engleskom jeziku.
•
Ako davatelj usluge klijenta treba neki drugi jezik, klijent je dužan osigurati prijevod.
•
Ne pokušavajte servisirati opremu ako niste u potpunosti pročitali i razumjeli ovaj servisni
priručnik.
•
zanemarite li ovo upozorenje, može doći do ozljede davatelja usluge, operatera ili pacijenta uslijed
strujnog udara, mehaničkih ili drugih rizika.
VÝSTRAHA
(CS)
Tento provozní návod existuje pouze v anglickém jazyce.
• V případě, že externí služba zákazníkům potřebuje návod v jiném jazyce, je zajištění překladu do
odpovídajícího jazyka úkolem zákazníka.
• Nesnažte se o údržbu tohoto zařízení, aniž byste si přečetli tento provozní návod a pochopili jeho
obsah.
• V případě nedodržování této výstrahy může dojít k poranění pracovníka prodejního servisu,
obslužného personálu nebo pacientů vlivem elektrického proudu, respektive vlivem mechanických
či jiných rizik.
Denne servicemanual findes kun på engelsk.
• Hvis en kundes tekniker har brug for et andet sprog end engelsk, er det kundens ansvar at sørge
for oversættelse.
• Forsøg ikke at servicere udstyret uden at læse og forstå denne servicemanual.
• Manglende overholdelse af denne advarsel kan medføre skade på grund af elektrisk stød,
mekanisk eller anden fare for teknikeren, operatøren eller patienten.
ADVARSEL
(DA)
Page 3
GE HEALTHCARE
SYSTEM MANUAL
WAARSCHUWING
(NL)
HOIATUS
(ET)
VAROITUS
(FI)
ATTENTION
(FR)
WARNUNG
(DE)
ΠΡΟΕΙ∆ΟΠΟΙΗΣΗ
(EL)
FIGYELMEZTETÉS
(HU)
AÐVÖRUN
(IS)
Page 4
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.
• Als het onderhoudspersoneel een andere taal vereist, dan is de klant verantwoordelijk voor de
vertaling ervan.
• Probeer de apparatuur niet te onderhouden alvorens deze onderhoudshandleiding werd
geraadpleegd en begrepen is.
• Indien deze waarschuwing niet wordt opgevolgd, zou het onderhoudspersoneel, de operator of
een patiënt gewond kunnen raken als gevolg van een elektrische schok, mechanische of andere
gevaren.
See teenindusjuhend on saadaval ainult inglise keeles
• Kui klienditeeninduse osutaja nõuab juhendit inglise keelest erinevas keeles, vastutab klient
tõlketeenuse osutamise eest.
• Ärge üritage seadmeid teenindada enne eelnevalt käesoleva teenindusjuhendiga tutvumist ja
sellest aru saamist.
• Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja, operaatori või patsiendi vigastamist
elektrilöögi, mehaanilise või muu ohu tagajärjel.
Tämä huolto-ohje on saatavilla vain englanniksi.
• Jos asiakkaan huoltohenkilöstö vaatii muuta kuin englanninkielistä materiaalia, tarvittavan
käännöksen hankkiminen on asiakkaan vastuulla.
• Älä yritä korjata laitteistoa ennen kuin olet varmasti lukenut ja ymmärtänyt tämän huolto-ohjeen.
• Mikäli tätä varoitusta ei noudateta, seurauksena voi olla huoltohenkilöstön, laitteiston käyttäjän tai
potilaan vahingoittuminen sähköiskun, mekaanisen vian tai muun vaaratilanteen vuoksi.
Ce manuel d’installation et de maintenance est disponible uniquement en anglais.
• Si le technicien d'un client a besoin de ce manuel dans une langue autre que l'anglais, il incombe
au client de le faire traduire.
• Ne pas tenter d'intervenir sur les équipements tant que ce manuel d’installation et de maintenance
n'a pas été consulté et compris.
• Le non-respect de cet avertissement peut entraîner chez le technicien, l'opérateur ou le patient
des blessures dues à des dangers électriques, mécaniques ou autres.
Diese Serviceanleitung existiert nur in englischer Sprache.
• Falls ein fremder Kundendienst eine andere Sprache benötigt, ist es Aufgabe des Kunden für eine
entsprechende Übersetzung zu sorgen.
• Versuchen Sie nicht diese Anlage zu warten, ohne diese Serviceanleitung gelesen und
verstanden zu haben.
• Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des Kundendiensttechnikers, des
Bedieners oder des Patienten durch Stromschläge, mechanische oder sonstige Gefahren
kommen.
Το παρόν εγχειρίδιο σέρβις διατίθεται μόνο στα αγγλικά.
• Εάν ο τεχνικός σέρβις ενός πελάτη απαιτεί το παρόν εγχειρίδιο σε γλώσσα εκτός των αγγλικών,
αποτελεί ευθύνη του πελάτη να παρέχει τις υπηρεσίες μετάφρασης.
• Μην επιχειρήσετε την εκτέλεση εργασιών σέρβις στον εξοπλισμό αν δεν έχετε συμβουλευτεί και
κατανοήσει το παρόν εγχειρίδιο σέρβις.
• Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί τραυματισμός στον τεχνικό
σέρβις, στο χειριστή ή στον ασθενή από ηλεκτροπληξία, μηχανικούς ή άλλους κινδύνους.
Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.
• Ha a vevő szolgáltatója angoltól eltérő nyelvre tart igényt, akkor a vevő felelőssége a fordítás
elkészíttetése.
• Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási kézikönyvben leírtakat nem
értelmezték.
• Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető vagy a beteg áramütés,
mechanikai vagy egyéb veszélyhelyzet miatti sérülését eredményezheti.
Þessi þjónustuhandbók er aðeins fáanleg á ensku.
• Ef að þjónustuveitandi viðskiptamanns þarfnast annas tungumáls en ensku, er það skylda
viðskiptamanns að skaffa tungumálaþjónustu.
• Reynið ekki að afgreiða tækið nema að þessi þjónustuhandbók hefur verið skoðuð og skilin.
• Brot á sinna þessari aðvörun getur leitt til meiðsla á þjónustuveitanda, stjórnanda eða sjúklings frá
raflosti, vélrænu eða öðrum áhættum.
GE HEALTHCARE
SYSTEM MANUAL
AVVERTENZA
(IT)
(JA)
경고
(KO)
BRÎDINÂJUMS
(LV)
ĮSPĖJIMAS
(LT)
ADVARSEL
(NO)
OSTRZEŻENIE
(PL)
AVISO
(PT-BR)
ATENÇÃO
(PT-PT)
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Il presente manuale di manutenzione è disponibile soltanto in lingua inglese.
• Se un addetto alla manutenzione richiede il manuale in una lingua diversa, il cliente è tenuto a
provvedere direttamente alla traduzione.
• Procedere alla manutenzione dell'apparecchiatura solo dopo aver consultato il presente manuale
ed averne compreso il contenuto.
• Il mancato rispetto della presente avvertenza potrebbe causare lesioni all'addetto alla
manutenzione, all'operatore o ai pazienti provocate da scosse elettriche, urti meccanici o altri
rischi.
このサービスマニュアルには英語版しかありません。
 サービスを担当される業者が英語以外の言語を要求される場合、翻訳作業はその業者の責任で行
うものとさせていただきます。
 このサービスマニュアルを熟読し理解せずに、装置のサービスを行わないでください。
この警告に従わない場合、サービスを担当される方、操作員あるいは患者さんが、感電や機械
的又はその他の危険により負傷する可能性があります。
본 서비스 매뉴얼은 영어로만 이용하실 수 있습니다 .
• 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우 , 번역 서비스를 제공하는 것은 고객의
책임입니다 .
• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하려고 시도하지 마십시오 .
• 본 경고 사항에 유의하지 않으면 전기 쇼크 , 기계적 위험 , 또는 기타 위험으로 인해 서비스 제공자
, 사용자 또는 환자에게 부상을 입힐 수 있습니다 .
Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.
• Ja klienta apkopes sniedzējam nepieciešama informācija citā valodā, klienta pienākums ir
nodrošināt tulkojumu.
• Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas un saprašanas.
• Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas trieciena, mehānisku vai
citu faktoru izraisītu traumu risks apkopes sniedzējam, operatoram vai pacientam.
Šis eksploatavimo vadovas yra tik anglų kalba.
• Jei kliento paslaugų tiekėjas reikalauja vadovo kita kalba – ne anglų, suteikti vertimo paslaugas
privalo klientas.
• Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar nesupratote šio
eksploatavimo vadovo.
• Jei nepaisysite šio įspėjimo, galimi paslaugų tiekėjo, operatoriaus ar paciento sužalojimai dėl
elektros šoko, mechaninių ar kitų pavojų.
Denne servicehåndboken finnes bare på engelsk.
• Hvis kundens serviceleverandør har bruk for et annet språk, er det kundens ansvar å sørge for
oversettelse.
• Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest og forstått.
• Manglende hensyn til denne advarselen kan føre til at serviceleverandøren, operatøren eller
pasienten skades på grunn av elektrisk støt, mekaniske eller andre farer.
Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.
• Jeśli serwisant klienta wymaga języka innego niż angielski, zapewnienie usługi tłumaczenia jest
obowiązkiem klienta.
• Nie próbować serwisować urządzenia bez zapoznania się z niniejszym podręcznikiem
serwisowym i zrozumienia go.
• Niezastosowanie się do tego ostrzeżenia może doprowadzić do obrażeń serwisanta, operatora
lub pacjenta w wyniku porażenia prądem elektrycznym, zagrożenia mechanicznego bądź innego.
Este manual de assistência técnica encontra-se disponível unicamente em inglês.
•
Se outro serviço de assistência técnica solicitar a tradução deste manual, caberá ao cliente
fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
A não observância deste aviso pode ocasionar ferimentos no técnico, operador ou paciente
decorrentes de choques elétricos, mecânicos ou outros.
Este manual de assistência técnica só se encontra disponível em inglês.
•
Se qualquer outro serviço de assistência técnica solicitar este manual noutro idioma, é da
responsabilidade do cliente fornecer os serviços de tradução.
•
Não tente reparar o equipamento sem ter consultado e compreendido este manual de assistência
técnica.
•
O não cumprimento deste aviso pode colocar em perigo a segurança do técnico, do operador ou
do paciente devido a choques eléctricos, mecânicos ou outros.
Page 5
GE HEALTHCARE
SYSTEM MANUAL
ATENŢIE
(RO)
ОСТОРОЖНО!
(RU)
UPOZORENJE
(SR)
UPOZORNENIE
(SK)
ATENCION
(ES)
VARNING
(SV)
OPOZORILO
(SL)
DİKKAT
(TR)
Page 6
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Acest manual de service este disponibil doar în limba engleză.
•
Dacă un furnizor de servicii pentru clienţi necesită o altă limbă decât cea engleză, este de datoria
clientului să furnizeze o traducere.
•
Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi înţelegerii acestui manual de
service.
•
Ignorarea acestui avertisment ar putea duce la rănirea depanatorului, operatorului sau pacientului
în urma pericolelor de electrocutare, mecanice sau de altă natură.
Данное руководство по техническому обслуживанию представлено только на английском языке.
•
Если сервисному персоналу клиента необходимо руководство не на английском, а на
каком-то другом языке, клиенту следует самостоятельно обеспечить перевод.
•
Перед техническим обслуживанием оборудования обязательно обратитесь к данному
руководству и поймите изложенные в нем сведения.
•
Несоблюдение требований данного предупреждения может привести к тому, что
специалист по техобслуживанию, оператор или пациент получит удар электрическим током,
механическую травму или другое повреждение
Ovo servisno uputstvo je dostupno samo na engleskom jeziku.
•
Ako klijentov serviser zahteva neki drugi jezik, klijent je dužan da obezbedi prevodilačke usluge.
•
Ne pokušavajte da opravite uređaj ako niste pročitali i razumeli ovo servisno uputstvo.
•
Zanemarivanje ovog upozorenja može dovesti do povređivanja servisera, rukovaoca ili pacijenta
usled strujnog udara ili mehaničkih i drugih opasnosti.
Tento návod na obsluhu je k dispozícii len v angličtine.
•
Ak zákazníkov poskytovateľ služieb vyžaduje iný jazyk ako angličtinu, poskytnutie
prekladateľských služieb je zodpovednosťou zákazníka.
•
Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na obluhu a neporozumiete mu.
•
Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa služieb, obsluhujúcej
osoby alebo pacienta elektrickým prúdom, mechanické alebo iné ohrozenie.
Este manual de servicio sólo existe en inglés.
•
Si el encargado de mantenimiento de un cliente necesita un idioma que no sea el inglés, el cliente
deberá encargarse de la traducción del manual.
•
No se deberá dar servicio técnico al equipo, sin haber consultado y comprendido este manual de
servicio.
•
La no observancia del presente aviso puede dar lugar a que el proveedor de servicios, el
operador o el paciente sufran lesiones provocadas por causas eléctricas, mecánicas o de otra
naturaleza.
Den här servicehandboken finns bara tillgänglig på engelska. .
•
Om en kunds servicetekniker har behov av ett annat språk än engelska, ansvarar kunden för att
tillhandahålla översättningstjänster.
•
Försök inte utföra service på utrustningen om du inte har läst och förstår den här
servicehandboken.
•
Om du inte tar hänsyn till den här varningen kan det resultera i skador på serviceteknikern,
operatören eller patienten till följd av elektriska stötar, mekaniska faror eller andra faror.
Ta servisni priročnik je na voljo samo v angleškem jeziku.
•
Če ponudnik storitve stranke potrebuje priročnik v drugem jeziku, mora stranka zagotoviti prevod.
•
Ne poskušajte servisirati opreme, če tega priročnika niste v celoti prebrali in razumeli.
•
Če tega opozorila ne upoštevate, se lahko zaradi električnega udara, mehanskih ali drugih
nevarnosti poškoduje ponudnik storitev, operater ali bolnik.
Bu servis kılavuzunun sadece ingilizcesi mevcuttur.
•
Eğer müşteri teknisyeni bu kılavuzu ingilizce dışında bir başka lisandan talep ederse, bunu
tercüme ettirmek müşteriye düşer.
•
Servis kılavuzunu okuyup anlamadan ekipmanlara müdahale etmeyiniz.
•
Bu uyarıya uyulmaması, elektrik, mekanik veya diğer tehlikelerden dolayı teknisyen, operatör
veya hastanın yaralanmasına yol açabilir.
GE HEALTHCARE
SYSTEM MANUAL
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Legal notes
TRADEMARKS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2
are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of
their respective holders.
COPYRIGHTS
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material
presented and contained herein may not be reproduced in any form or manner, without the written
permission of General Electric Company, Inc.
Page 7
GE HEALTHCARE
SYSTEM MANUAL
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation
“damage in shipment” written on all copies of the freight or express bill before delivery is accepted
or “signed for” by a General Electric representative or a hospital receiving agent. Whether noted or
concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event,
within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this
14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and
MIS.” Contact your local service coordinator for more information on this process.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT
All electrical installations that are preliminary to positioning of the equipment at the site prepared for
the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds into
the Power Distribution Unit shall be performed by licensed electrical contractors. Other connections
between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE
Healthcare personnel. The products involved (and the accompanying electrical installations) are
highly sophisticated, and special engineering competence is required. In performing all electrical
work on these products, GE will use its own specially trained field engineers. All of GE’s electrical
work on these products will comply with the requirements of the applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to
perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein
contained should be thoroughly read and understood by everyone who will use the equipment
before you attempt to place this equipment in operation. GE Healthcare will be glad to assist and
cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the
useful beam, no practical design of equipment can provide complete protection. Nor can any
practical design compel the operator to take adequate precautions to prevent the possibility of any
persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully
acquainted with the recommendations of the National Council on Radiation Protection and
Measurements (NCRP) as published in NCRP Reports available from NCRP Publications, 7910
Woodmont Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission
on Radiation Protection, and take adequate steps to protect against injury.
The equipment is sold with the understanding that GE Healthcare, its agents, and representatives
have no responsibility for injury or damage which may result from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be
used.
Page 8
GE HEALTHCARE
SYSTEM MANUAL
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
LITHIUM BATTERY CAUTIONARY STATEMENT
DANGER - Risk of Explosion
Danger of explosion if battery is incorrectly replaced.
Replace only with the same or equivalent type recommended by the
manufacturer. Discard used batteries according to the manufacturer’s
instructions.
ATTENTION - Danger d’Explosion
Il y a danger d’explosion s’il y a replacement incorrect de la batterie.
Remplacer uniquement avec une batterie du même type ou d’un type
recommandé par le constructeur. Mettre au rébut les batteries
usagées conformément aux instructions du fabricant.
TECHNICAL MANUAL UPDATES
When operating or servicing GE Healthcare products, please contact your GE representative for
the latest revision of product documentation. Product documentation may also be available on-line
at the GE Healthcare support documentation library.
OMISSIONS AND ERRORS
Customers, please contact your GE Healthcare sales or service representatives.
GE personnel, please use the GE Healthcare complaint handling process to report all omissions,
errors, and defects in this publication.
Page 9
GE HEALTHCARE
SYSTEM MANUAL
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Revision history
Optima Class A
Revision
Date
1
28SEP2011
Reason for change
Initial release of document.
Updated Regulatory Testing chapter. Refer to SPR HCSDM00103500.
Validation updates Refer to SPRs: HCSDM00103500, HCSDM00104175,
HCSDM00104185, HCSDM00104239, HCSDM00104254, HCSDM00104548,
HCSDM00104550, HCSDM00104554, HCSDM00105012, HCSDM00105013,
HCSDM00105014, HCSDM00105016, HCSDM00105017, HCSDM00105018,
HCSDM00105019, HCSDM00105021, HCSDM00105022, HCSDM00105023,
HCSDM00105027, HCSDM00105246, HCSDM00105247, HCSDM00105248,
HCSDM00105249, HCSDM00105252, HCSDM00105253, HCSDM00105257,
HCSDM00105259, HCSDM00105262, HCSDM00105479, HCSDM00105537
2
28OCT2011
3
09NOV2011
Updated Load From Cold sections. Refer to SPR HCSDM0010749.
4
14NOV2011
Validation updates. Refer to SPRs: HCSDM00108056, HCSDM00108058,
HCSDM00108059, HCSDM00108068, HCSDM00108075, HCSDM00108076,
HCSDM00108095, HCSDM00108096, HCSDM00108097, HCSDM00108098
5
17NOV2011
Validation updates. Refer to SPRs: HCSDM00109056, HCSDM00109082
6
05DEC2011
Validation updates. Refer to SPR HCSDM00111281
Added Chapter 4, Section 4.13 - IP Address Change Procedure.
7
05FEB2012
Added Note to Chapter 3, Sections 3.2.1.2.1 (after step 14) and 3.2.1.2.2 (after step
15) on changing the Internal IP Address.
Updated Chapter 8, Section 8.5.16.3 (step 15) to correct wiring connection from NO
to NC.
Refer to SPR HCSDM00120703.
8
12JUL2012
9
18JUL2012
Page 10
Added "Perform QAP" step to Finalization Sections 8.6.2.4, 8.6.3.4, 8.6.5.4, 8.6.6.4,
8.6.7.4, 8.6.8.4, 8.6.8.4, 8.6.15.4. Refer to SPR HCSDM00140842.
Updated Chapter 8, Sections 8.4.1 - Drive Wheel and 8.4.4 - Front Caster to show
proper lifting/supporting of unit. Refer to TrackWise 8111422.
Updated Chapter 8, Sections 8.4.1 - Drive Wheel and 8.4.4 - Front Caster to show
proper lifting/supporting of unit. Refer to SPR HCSDM00147300.
GE HEALTHCARE
SYSTEM MANUAL
Revision
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Date
Reason for change
Updated Chapter 8, Section 8.6.5 - Tube mount - detent side (cathode side) and
Section 8.6.6 - Tube mount - friction side (anode side) to show new version of tube
mounts. Refer to ECO 2122380.
Added text to front material on how to obtain most recent revisions of technical
manuals. Satisfies FDA recommendation.
10
29SEP2012
Updated PM Checklist and PM Procedures to add hand switch visual inspection,
functional checks, cleaning and 3-year replacement. Refer to CAPA 5970812.
Added ’Detector firmware download’ procedure to the System Data & Software
chapter. Refer to SPR HCSDM00157822.
Updated Chapter 7, Section 7.1.6.1 Step 4 to "Verify that the selected kVp and mAs
are displayed in the protocol modification frames and the left side of the status bar.
Both displays should match." Refer to TrackWise 8987140.
Chapter 8, added new Section 8.4.6 - Column replacement. Refer to ECO 2147940.
Chapter 7, Section 7.2.2, added Note about potential test equipment damage. Refer
to HCSDM00188252.
Chapter 4, Section 4.13, updated text in Steps 3 and 6. Refer to HCSDM00185329.
Chapter 7, Section 7.1.1, corrected spelling error 'equipmentte'. Refer to
HCSDM00188263.
Chapter 2, Section 2.4, deleted Section 2.4.3 - PM Checklist. Refer to
HCSDM00188249.
Chapter 8, added new Section 8.2.4 - Spyder to Board Data Module Cable
Replacement. Refer to ECR 2144543.
Chapter 8, Section 8.5.11, updated procedure to support new BDM cable. Refer to
ECR 2144543.
11
19SEP2013
Chapter 4, Sections 4.10.3.1 and 4.10.3.2, added Notes about need to reset system
after DAP reconnection. Refer to HCSDM00188256.
Chapter 8, Section 8.6.10.3, added Note about need to reset system after DAP
reconnection. Refer to HCSDM00188256.
Chapter 8, added new Section 8.4.2.3.1 - Battery Pack Integration. Refer to
HCSDM00188260.
Chapter 8, Section 8.4.1.2.2, added Loctite 242 (2 places). Refer to
HCSDM00191982.
Chapter 8, Section 8.6.2.3, updated text in Steps 2 and 4 to save existing hardware
for reuse. Refer to HCSDM00202552.
Chapter 7, added new Section 7.3 - Tube Radiation Leakage Test. Refer to
HCSDM00192198.
Chapter 8, Section 8.6.2.3 - Column replacement, added note before Step 1
regarding carriage safety lock. Refer to HCSDM00202552.
Chapter 3, Section 3.4, updated steps 3-5 with correct navigation links. Refer to
HCSDM00188263.
Chapter 5, added new Section 5.6.3 - DAP Calibration.
12
14NOV2013
Chapter 2, Table 2-4, added DAP Calibration reference.
Chapter 8, Section 8.6.10.4, added step for DAP Calibration. Refer to
HCSDM00159583.
Page 11
GE HEALTHCARE
SYSTEM MANUAL
Revision
OPTIMA XR200AMX/XR220AMX SYSTEM MANUALADVANCED
Date
Reason for change
Chapter 4, Section 4.10.3, changed Figures 4-9 and 4-10 to show DAP meter in lower
set of collimator rails. Refer to HCSDM00264083.
Chapter 4, Section 4.10.3.2, added steps to remove cable cover and then put back
on at end of procedure. Refer to ECO 2160317.
Chapter 4, Section 4.10.4, added Wireless Handswitch Installation section. Refer to
ECO 2162103.
13
01MAY2014
Chapter 3, Section 3.2.1.2.1, step 4, added to check and record existing system IP
address prior to SW download. Refer to HCSDM00264080.
Chapter 3, Section 3.2.1.2.1 and Section 3.2.1.2.2, added step 16 instruction to load
operator manual. Reference link to Section 4.8 Installing the operator manual. Refer
to HCSDM00264101.
Chapter 7, Section 7.2.1, changed bin measurement point in Table 7-20 to "Screw
used for mounting strain relief of wired handswitch cable". Changed Fig 7-16 to show
new measurement point. Refer to ECO 2148874.
Chapter 8, Section 8.3, added cable cover installation procedure. Refer to ECO
2160317.
Chapter 4, Section 4.2.6, added “FIPS ON” column in table 4-7 and table 4-8 for
wireless Authentication requirement.
Chapter 4, Section 4.8, Section 4.9, Section 4.13, added notes regarding consulting
your administrator for Account and Password information.
14
03DEC2014
Chapter 4, Section 4.10.4, added tablet holder assembly installation procedure.
Chapter 8, Section 8.7.16, added tablet support arm assembly replacement
procedure.
Chapter 8, Section 8.7.16, added Tablet clamp assembly replacement procedure.
Chapter 8, added torque requirement in some parts replacement procedure. Refer to
DOC1633766.
15
Page 12
06FEB2015
Chapter 4, Section 4.10.4 revised tablet holder assembly installation procedure refer
to ECR/O 2186522
Chapter 8 Section 8.7.16 revised tablet holder assembly replacement procedure refer
to ECR/O 2186522
Preface publication conventions
GE HEALTHCARE
REVISION 15
OPTIMA XR200AMX/XR220AMX SYSTEM MANUAL
DIRECTION 5336122-1EN
Preface Publication Conventions
Standardized conventions for representing information is a uniform way of communicating
information to a reader in a consistent manner. Conventions are used so that the reader can easily
recognize the actions or decisions that must be made. There are a number of character and
paragraph styles used in this publication to accomplish this task. Please become familiar with them
before proceeding forward.
It is important that you read and understand hazard statements, and not just ignore them.
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and
style for safety communications reflected in this publication represents the harmonization of IEC/
ISO 3864 and ANSI Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential
hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify
important safety information. Text (Hazard) styles are applied to the paragraph contents that are
applicable to each specific safety statement.
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert
symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation
mark within it. It Is always used next to the signal word to indicate the severity of the hazard.
Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert
symbol and signal word are placed immediately before any paragraph they affect. Safety
information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Text Format of Signal Words
DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH, IF
NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS SIGNAL
WORD IS LIMITED TO THE MOST EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT
AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Caution - Indicates a potentially hazardous situation which, if not avoided, may result in
minor or moderate injury. It may also be used to alert against unsafe practices.
NOTICE - Indicates information or a company policy that relates directly or indirectly to the
safety of personnel or protection of property. This signal word is associated directly with a
hazard or hazardous situation and is used in place of 'DANGER,' 'WARNING,' or 'CAUTION.'
It can include:
Page 13
GE HEALTHCARE
REVISION 15
OPTIMA XR200AMX/XR220AMX SYSTEM MANUAL
DIRECTION 5336122-1EN
•
Destruction of a disk drive
•
Potential for internal mechanical damage, such as to a X-ray tube
Symbols and Pictorials Used
The following Symbols and Pictorials are be used in this publication. These graphical icons
(symbols) may be used to make you aware of specific types of hazards that could possibly cause
harm.
Page 14
keep_up
magnetic
biohazard
compressgas
ppe-hearing
fragile
impact
corrosive
heavyobject
ppe-2people
static_elec
heat
general
laser
ppe-respitory
keep_dry
pinch
radiation
poisongas
ppe-loto
general
explosive
electrical
flammable
ppe-eye
torque
crush/mechanical
tipping
Read Manual
ppe-gloves
ce
instuction
poisonmatl
entanglement
instuction
GE HEALTHCARE
REVISION 15
OPTIMA XR200AMX/XR220AMX SYSTEM MANUAL
DIRECTION 5336122-1EN
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such
as Purpose, Example, Comment or Note) are used to identify important but non-safety related
information. Text styles are also applied to text within each paragraph modified by the specific
prefix.
EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:
Purpose: Introduces and provides meaning as to the information contained within the chapter,
section or subsection (such as used at the beginning this chapter, for example).
Note:
Example:
Comment:
Conveys information that should be considered important to the reader.
Used to make the reader aware that the paragraph(s) that follow are examples of information
possibly stated previously.
Represents “additional” information that may or may not be relevant to your situation.
Page Layout
Publication Part Number & Revision Number
The current section and its title
are always shown in the footer of
the left (even) page.
An exclamation point in a triangle is used
to indicate important information to the user.
Paragraphs preceeded by Alphanumeric
characters (e.g. numbers) contain information that must be followed in a specific order.
Publication Title
The current chapter and its title
are always shown in the footer of
the right (odd) page.
Paragraphs preceeded by a symbol
(e.g. bullets) contain information that
has no specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location.
The document part number and revision number appears in every header on every page. Odd
numbered page footers indicate the current chapter, its title and current page number. Even page
footers show the current section and its title, as well as the current page number.
Page 15
GE HEALTHCARE
REVISION 15
OPTIMA XR200AMX/XR220AMX SYSTEM MANUAL
DIRECTION 5336122-1EN
Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text
that’s either screen input and output. Mono-spaced fonts, such courier, are used to indicated text
direction. When you type at your keyboard, you are generating computer input. Occasionally you
will see the math operator “greater-than” and “less-than” symbols used to indicate the start and
finish of variable output. When reading text generated by the computer, you are reading it as
computer generated output. In addition to direction, characters are italicized (e.g. italics) to indicate
information specific to your system or site.
Example: Fixed
Output
This paragraph’s font represents computer generated screen “fixed” output.
Its output is fixed from the sense that it does not vary from application
to application. It is the most commonly used style used to indicate
filenames, paths and text that do not change from system to system. The
character style used is a fixed width such as courier.
Example:
Variable Output
This paragraph’s font represents computer screen output that is
“variable”. It is used to represent output that varies from application
to application or system to system. Variable output is sometimes found
placed between greater-than and less-than operators for clarification. For
example: <variable_ouput> or <3.45.120.3>. In both cases, the < and >
operators are not part of the actual input.
Example: Fixed
Input
This paragraph’s font represents fixed input. It is computer input that
is typed-in via the keyboard. Typed input that does not vary from
application to application or system to system. Fixed text the user is
required to supply as input. For example: cd /usr/3p
Example:
Variable Input
This paragraph’s font represents computer input that can vary from
application to application or system to system. With variable text, the
user is required to supply system dependent input or information. Variable
input sometimes is placed between greater-than and less-than operators.
For example: <variable_input>. In these cases, the (<>) operators would
be dropped prior to input. For example: ypcat hosts | grep <3.45.120.3>
would be typed into the computer as:
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or
soft button, switch or key. Physical hardware, such as buttons and switches, are called hard keys
because they are hard wired or mechanical in nature. A keyboard or on/off switch would be a hard
key. Software or computer generated buttons are called soft keys because they are software
generated. Software driven menu buttons are an example of such keys. Soft and hard keys are
represented differently in this publication.
Example: Hard
Keys
A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style
that uses both over and under-lined bold text that is bold. This is a hard key.
Example: Soft
Keys
Whereas the computer MENU button that you would click with your mouse or touch with your hand
uses over and under-lined regular text. This is a soft key.
Page 16
GE HEALTHCARE
REVISION 15
OPTIMA XR200AMX/XR220AMX SYSTEM MANUAL
DIRECTION 5336122-1EN
Table of contents
Chapter 1
Safety / Before You Begin ............................................................ 23
Section 1.1 Energy sources........................................................................... 23
Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power...... 24
1.2.1 Preparing for LOTO...................................................................................................... 24
1.2.2 Performing LOTO......................................................................................................... 26
1.2.3 Returning system to service......................................................................................... 29
Section 1.3 Electrostatic discharge (ESD) ................................................... 30
1.3.1
1.3.2
1.3.3
1.3.4
1.3.5
Chapter 2
Important ESD considerations when working on a mobile system ..............................
Generating static ..........................................................................................................
Personal grounding methods and equipment ..............................................................
Grounding the work area..............................................................................................
Recommended materials and equipment ....................................................................
30
30
31
31
32
Planned Maintenance.................................................................... 33
Section 2.1 Before you begin ........................................................................ 33
Section 2.2 Planned maintenance schedule ................................................ 33
Section 2.3 System performance .................................................................. 33
Section 2.4 Planned maintenance procedures ............................................ 33
2.4.1 Before you begin - safety precautions.......................................................................... 33
2.4.2 Tools required .............................................................................................................. 33
2.4.3 PM Procedures ............................................................................................................ 34
Chapter 3
System data and software ............................................................ 43
Section 3.1 Backing up system data ............................................................ 43
3.1.1 What is included in a system backup? ......................................................................... 43
3.1.2 Performing a system backup........................................................................................ 43
Section 3.2 Performing Load From Cold (LFC)............................................ 44
3.2.1 Loading or upgrading system software ........................................................................ 44
Section 3.3 Performing a FW Load From Cold (LFC) .................................. 47
Section 3.4 Restoring generator firmware only ........................................... 47
Section 3.5 Detector firmware download ..................................................... 48
Section 3.6 Restoring system data ............................................................... 48
3.6.1 Before you begin .......................................................................................................... 48
3.6.2 Restoring system data ................................................................................................. 48
Section 3.7 System self recovery.................................................................. 49
Chapter 4
Configuration ................................................................................. 51
Section 4.1 When should I configure the system?...................................... 51
Page 17
GE HEALTHCARE
REVISION 15
OPTIMA XR200AMX/XR220AMX SYSTEM MANUAL
DIRECTION 5336122-1EN
Section 4.2 Using the System Configuration Tool (SUIF) ........................... 51
4.2.1 Site configuration .........................................................................................................
4.2.2 Networking configuration .............................................................................................
4.2.3 General configuration ..................................................................................................
4.2.4 Hardware configuration................................................................................................
4.2.5 Generator configuration ...............................................................................................
4.2.6 Wireless configuration .................................................................................................
4.2.7 Options configuration...................................................................................................
4.2.8 InSite configuration ......................................................................................................
4.2.9 PNF configuration ........................................................................................................
4.2.10 Time Server configuration..........................................................................................
4.2.11 Secure Login configuration ........................................................................................
52
53
53
54
54
55
58
58
58
60
60
Section 4.3 Changing Auto Protocol Assist settings .................................. 61
Section 4.4 DICOM connectivity configuration ............................................ 61
4.4.1 Network host configuration .......................................................................................... 61
4.4.2 Printer configuration..................................................................................................... 64
Section 4.5 Image management..................................................................... 66
Section 4.6 Image processing........................................................................ 66
4.6.1 Enabling EMI reduction................................................................................................ 66
Section 4.7 Loading demo images ................................................................ 67
4.7.1 Loading images from CD ............................................................................................. 67
Section 4.8 Installing the Operator Manual .................................................. 67
Section 4.9 Login and user management ..................................................... 68
Section 4.10 Installing hardware options ....................................................... 68
4.10.1
4.10.2
4.10.3
4.10.4
4.10.5
Installing the barcode reader .....................................................................................
Configuring the barcode reader .................................................................................
Installing the Dose Area Product (DAP) meter ..........................................................
Installing the tablet holder assembly..........................................................................
Installing the wireless exposure handswitch..............................................................
68
71
74
79
82
Section 4.11 Importing custom IP looks from Definium AMX 700................ 92
Section 4.12 Enabling Advanced Service mode ............................................ 93
Section 4.13 IP Address Change Procedure .................................................. 93
4.13.1 Snapshot Tool Configuration ..................................................................................... 94
Chapter 5
Calibration .................................................................................... 103
Section 5.1 Preparing for calibrations ........................................................ 103
5.1.1 Saving changes ......................................................................................................... 103
Section 5.2 Touchscreen calibration........................................................... 103
5.2.1 Calibrating the touchscreen ....................................................................................... 103
Section 5.3 Generator calibration................................................................ 104
5.3.1 Setting filament drive level......................................................................................... 104
5.3.2 Viewing and resetting tube and generator usage data .............................................. 104
Section 5.4 Detector calibration .................................................................. 105
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5.4.1 Executing bad pixel and gain calibrations .................................................................. 105
Section 5.5 Image quality calibration ......................................................... 107
5.5.1 Calibrating the printer................................................................................................. 107
Section 5.6 Hardware calibration ................................................................ 108
5.6.1 Drive handle calibration.............................................................................................. 108
5.6.2 Touch screen calibration ............................................................................................ 108
5.6.3 DAP calibration .......................................................................................................... 108
Section 5.7 PACS image tests ..................................................................... 110
5.7.1
5.7.2
5.7.3
5.7.4
Chapter 6
Comparing PACS test images ...................................................................................
Determining PACS burn/no-burn configuration..........................................................
Optional PACS tests ..................................................................................................
PACS image comparison results ...............................................................................
111
111
114
117
Mechanical adjustment procedures .......................................... 119
Section 6.1 Column related assemblies ..................................................... 119
6.1.1 Column balance procedure ........................................................................................ 119
6.1.2 Tube latch to arm pin adjustment procedure.............................................................. 122
6.1.3 Column rotational detent procedure........................................................................... 125
Chapter 7
Regulatory testing....................................................................... 129
Section 7.1 U.S. federally required tests .................................................... 129
7.1.1
7.1.2
7.1.3
7.1.4
7.1.5
7.1.6
Required test equipment ............................................................................................
Preparing for testing...................................................................................................
Collimator testing .......................................................................................................
Generator tests ..........................................................................................................
Beam Quality Test......................................................................................................
Testing generator operator indicators ........................................................................
129
129
130
136
143
144
Section 7.2 Testing electrical safety ........................................................... 144
7.2.1 Performing ground resistance testing ........................................................................ 145
7.2.2 Performing leakage current testing ............................................................................ 154
Section 7.3 Tube Radiation Leakage Test - Optional ................................ 157
7.3.1
7.3.2
7.3.3
7.3.4
7.3.5
Chapter 8
Personnel Requirements............................................................................................
Preliminary requirements ...........................................................................................
Purpose......................................................................................................................
Common Errors:.........................................................................................................
X-Ray Tube Leakage Radiation Requirement: ..........................................................
157
157
158
158
158
Replacement procedures .......................................................... 163
Section 8.1 Cover management .................................................................. 163
8.1.1
8.1.2
8.1.3
8.1.4
8.1.5
8.1.6
Side cover removal ....................................................................................................
Top cover removal .....................................................................................................
Front cover removal ...................................................................................................
Front bin removal .......................................................................................................
Rear bin removal........................................................................................................
Column skirt cover removal........................................................................................
164
164
166
170
171
174
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DIRECTION 5336122-1EN
8.1.7 Tube head cover removal .......................................................................................... 175
Section 8.2 Cable replacement .................................................................... 176
8.2.1
8.2.2
8.2.3
8.2.4
General cable replacement........................................................................................
High voltage cable replacement ................................................................................
"Super cable" 5557068 cable replacement................................................................
Spyder to Board Data Module Cable Replacement...................................................
176
181
190
192
Section 8.3 Cable cover installation............................................................ 195
Section 8.4 Software Load From Cold ........................................................ 196
Section 8.5 Base assembly .......................................................................... 197
8.5.1 Drive wheel ................................................................................................................
8.5.2 Battery packs .............................................................................................................
8.5.3 Front bumper assembly or bumper switch.................................................................
8.5.4 Front caster................................................................................................................
8.5.5 Spring applied brake (column rotational brake) .........................................................
8.5.6 Column support assembly .........................................................................................
8.5.7 Rear bin kickplate ......................................................................................................
8.5.8 Rear bin mounting bracket - Optima XR200amx only ...............................................
8.5.9 Motor brake and motor reducer assembly .................................................................
8.5.10 Caterpillar base transition board..............................................................................
197
201
207
210
215
218
229
232
234
237
Section 8.6 Thorax assembly....................................................................... 239
8.6.1 Spyder system controller ...........................................................................................
8.6.2 Locust drive board .....................................................................................................
8.6.3 Locust drive board fuses............................................................................................
8.6.4 Firefly charger board..................................................................................................
8.6.5 Firefly board fuses .....................................................................................................
8.6.6 Cricket battery board .................................................................................................
8.6.7 Cricket board fuses....................................................................................................
8.6.8 Hornet UIF board .......................................................................................................
8.6.9 Drive login active board collector...............................................................................
8.6.10 Top cover or display & inverter collector..................................................................
8.6.11 Board data module ..................................................................................................
8.6.12 System PC...............................................................................................................
8.6.13 Wireless USB host radio board................................................................................
8.6.14 Whip antenna...........................................................................................................
8.6.15 Digital detector.........................................................................................................
8.6.16 Detector bin park switch ..........................................................................................
8.6.17 Detector charge cable assembly .............................................................................
8.6.18 Detector bin shock absorber....................................................................................
8.6.19 Docking connector: detector side ............................................................................
8.6.20 Beetle Djinn set of cables ........................................................................................
8.6.21 Djinn 15kW Auxiliary module ...................................................................................
8.6.22 Djinn power module .................................................................................................
8.6.23 Djinn HV tank...........................................................................................................
8.6.24 Djinn 30kW auxiliary module ...................................................................................
8.6.25 Drive handle assembly ............................................................................................
8.6.26 Mantis power supply ................................................................................................
8.6.27 EMI filter..................................................