MN1-5099 Rev.0
ULTRASOUND DIAGNOSTIC
EQUIPMENT
SSD-3500
Manual number: MN1-5099
Rev.0
0123
ALOKA CO., LTD.
MN1-5099 Rev.0
VS-FlexGrid Pro
Copyright(C)1999 Videosoft Corporation
MN1-5099 Rev.0
Safety alert symbols
The four indications [Danger], [Warning], [Caution] and [Note] used on this equipment and in this instruction
manual have the following meaning.
Danger
・ Indicates an imminently hazardous situation which, if not avoided, will result in death or serious injury.
・ A warning message is inserted here.
Warning
・Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
・ A warning message is inserted here.
Caution
・Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury.
・A caution message is inserted here.
Note
・Indicates a strong request concerning an item that must be observed in order to prevent damage or
deterioration of the equipment and also to ensure that it is used efficiently.
・An explanatory text is inserted here.
1
MN1-5099 Rev.0
CONTENTS
1.
Precautions for Use
1-1. Purpose of Use ................................................................................................................ 1-1
1-1-1. Precautions concerning acoustic power........................................................... 1-2
1-1-2. Use of ultrasound gel ....................................................................................... 1-2
1-1-3. Use of general agents....................................................................................... 1-2
1-2. Classification................................................................................................................... 1-3
1-3. Safety .............................................................................................................................. 1-4
1-4. Environmental Conditions .............................................................................................. 1-5
1-4-1. Working environment ...................................................................................... 1-5
1-4-2. Storage environmental ..................................................................................... 1-5
1-5. Power Requirements ...................................................................................................... 1-6
1-6. Electromagnetic environment ........................................................................................ 1-7
1-7. Safety Instructions for Connecting Network Devices ..................................................... 1-8
1-7-1. Electrical safety Instructions for Connecting Network Devices ...................... 1-8
1-7-2. Other precautions ............................................................................................. 1-8
2.
Meaning of Symbols, Indications and Terms
2-1. Symbols and Indications ................................................................................................. 2-1
1）Safety alert symbols ................................................................................................ 2-1
2）Other symbols and indications ................................................................................ 2-2
2-2. Meaning of Terms........................................................................................................... 2-4
2-3. Position of Labels ........................................................................................................... 2-5
3.
Installation Method
3-1. Environmental Conditions of Installation Location........................................................ 3-1
（1）Working environment .......................................................................................... 3-1
（2）Installation location.............................................................................................. 3-2
（3）Power source ........................................................................................................ 3-2
3-2. Installing the Equipment ................................................................................................ 3-3
3-3. Connecting a Probe to the Equipment ............................................................................ 3-4
3-4. Connecting Options to the Equipment ............................................................................ 3-6
3-4-1. Connecting the equipment to the physiological signal terminal ..................... 3-6
4.
Specifications and Name of Each Part
4-1. Specifications ................................................................................................................. 4-1
4-2. Name and Function of Each Part ................................................................................... 4-4
4-2-1. Exterior drawing and name of each part ......................................................... 4-4
4-2-2. Front panel ....................................................................................................... 4-6
4-2-3. Left side panel .................................................................................................. 4-7
4-2-4. Rear panel ........................................................................................................ 4-8
2
MN1-5099 Rev.0
4-2-5.
4-2-6.
5.
Caster................................................................................................................ 4-8
Viewing monitor .............................................................................................. 4-9
COMPOSITION
5-1. Standard composition...................................................................................................... 5-1
5-2. Options ........................................................................................................................... 5-2
6.
Principle of Operation
6-1. Principle of Operation..................................................................................................... 6-1
7.
Cleaning and Sterilizing
7-1. Method of Cleaning and Sterilizing the Equipment ...................................................... 7-1
7-2. Cleaning and Sterilizing Conditions .............................................................................. 7-2
8.
Preparations for Use
8-1. Starting Inspection ......................................................................................................... 8-1
8-1-1. External Inspection........................................................................................... 8-1
8-1-2. Checking and Replacing Consumables ............................................................ 8-1
8-1-3. Washing and Sterilizing Probes ....................................................................... 8-1
8-1-4. Operation check................................................................................................ 8-2
8-2. Preparations for Use........................................................................................................ 8-2
9.
Screen Display
9-1. Character Display............................................................................................................ 9-1
9-1-1. Automatic display area .................................................................................... 9-2
9-1-2. Character display in the comment area ............................................................ 9-2
9-2. Graphic Display ............................................................................................................. 9-3
10. After Using the Equipment
10-1. Switching OFF the Equipment .....................................................................................10-1
10-2. Cleaning the Equipment................................................................................................10-1
10-3. State of the Equipment and Accessories ......................................................................10-2
11. Storing the Equipment
11-1. Preparations for Storing the Equipment........................................................................ 11-1
11-2. Storage Location and Environmental Conditions ........................................................ 11-2
12. Moving the Equipment
12-1. State of the Equipment and Accessories Before Moving the Equipment ..................... 12-1
12-2. Inspection Before Re-use ............................................................................................. 12-2
3
MN1-5099 Rev.0
13. Safety Inspection
13-1. Maintenance and Inspection ........................................................................................ 13-1
13-2. Safety Inspection........................................................................................................... 13-3
13-3. Checking the Measurement Accuracy .......................................................................... 13-6
14. TROUBLESHOOTING
14-1. Messages ....................................................................................................................... 14-2
1）Messages ................................................................................................................. 14-3
2）Assistant Messages.................................................................................................. 14-8
15. DISPOSAL the Equipment ..................................................................................... 15-1
16. APPENDIX
16-1
16-2
16-3
Probe use and care
16-1-1. Indications and Applications For Use
16-1-2. Contraindication
16-1-3. Warnings
16-1-4. Cautions
16-1-5. Probe Connection
16-1-6. Cleaning
16-1-7. Disinfection
16-1-8. Sterilization
16-1-9. Probe Covers
16-1-10. Storage
16-1-11. Specifications
16-1-12. Clinical Measurement Accuracy
16-1-13. Clinical Measurement Range
Acoustic Output Safety Information
16-2-1. Acoustic Exposure Safety
16-2-2. Interaction Between Ultrasound and Matter
16-2-3. Possible Biological effects
16-2-4. Derivation and Meaning of Indices
16-2-5. ALARA recommendations
16-2-6. References
Acoustic Output Tables
16-3-1. Acoustic Output Measurements
16-3-2. Definitions
16-3-3. Default Setting
4
16-1
16-1
16-4
16-4
16-4
16-4
16-5
16-6
16-7
16-8
16-8
16-9
16-11
16-12
16-13
16-13
16-13
16-13
16-15
16-17
16-18
16-19
16-19
16-19
16-20
MN1-5099 Rev.0
1-1. Purpose of Use
1-1. Purpose of Use
This equipment is intended to be used by doctors and other qualified persons for performing slice diagnoses and
blood circulation diagnoses in the following parts of the human body. Do not use it for any other applications.
・
・
・
・
・
・
・
・
・
・
Thorax
Abdomen
Perineum and pelvis
Lower limbs
Back
Upper limbs
Head
Cranial nerves
Neck
Child
Caution
・ The intended use of probe differs depending upon the type of probe.
Select a probe that meets your purpose of use.
・ Do not use it for any application that is not covered in the instruction manual of the probe.
The probe can harm the human body.
This section consists of 8 pages.
1-1
1. PRECAUTIONS FOR USE
1. PRECAUTIONS FOR USE
MN1-5099 Rev.0
1-1. Purpose of Use
1. PRECAUTIONS FOR USE
1-1-1. Precautions concerning acoustic power
The tissues of the human body consist of soft tissues, water, bone, and other tissues. Ultrasound energy is
progressively absorbed and attenuated by the body as it penetrates it, hence tissues located behind water, which
causes only a small degree of attenuation, receive a relatively large amount of ultrasound energy.
Also, it is necessary to be careful of bioeffects due to heat in the vicinity of tissues, such as bone, that readily
convert ultrasound energy into heat.
Particularly, a fetus at the bone formation stage is exposed to a high risk of damage due to heating because almost
all of the ultrasound energy passes through the amniotic fluid without being attenuated. Even in the case of a
fetus prior to bone development, the cells are active, hence there is a possibility of growth being affected, even
when the temperature rise is low.
Pro-sound SSD-3500 shows the dynamics of blood flow using the Ultrasound Doppler Method.
Mechanical bioeffects such as heating and cavitation occur when the body is exposed to ultrasound energy for a
long period. You can reduce the risk of damage to the tissues by interrupting the ultrasound energy before it
reaches the level at which tissue damage occurs. To this end, it is necessary to obtain a grasp of the functions of
the equipment, acquire familiarity with the method of operating it, and understand the parameters that affect the
acoustic power. Also, get into the habit of always freezing the image as soon as you have obtained the necessary
diagnostic information.
Caution
・ Use as low an output as possible within reason.
・ Scan the body for only as long as is necessary to make a diagnosis. Prolonged use can harm the human body.
・ Hold a probe tightly not to slip, especially when using ultrasound gel or others; otherwise, the probe may
slip out of your hands and hit a patient.
1-1-2. Use with an ultrasound enhancing agent
If you wish to use an ultrasound enhancing agent, be sure to use only a substance that has been approved for use
as an ultrasound enhancing agent.
Before using an enhancing agent, carefully read the instructions for using the enhancing agent and also any
cautionary notes.
1-1-3. Use with a general pharmaceutical
If you perform an ultrasound examination after having the patient ingest a general pharmaceutical, the ultrasound
may affect the pharmacological effect of the pharmaceutical.
Before using a general pharmaceutical, carefully read the instructions for using the pharmaceutical and also any
cautionary notes.
1-2
MN1-5099 Rev.0
1-2. Classification
According to the type of protection against electric shock:
・ Class I equipment
According to the degree of protection against electric shock:
・ Type BF equipment
Classification
Probe
Physiological signal
Type BF equipment
All probes
ECG lead
Table Classification according to degree of protection
[Remark]
Type BF equipment refers to a component of the ultrasound diagnostic equipment, which is consisting of the
ultrasound probe and ECG lead only and not used directly for a heart but applied indirectly from outside.
According to the degree of protection against harmful ingress of water:
・ Ordinary equipment
Warning
The equipment is not protected in any way against water ingress, so do not use it in a place where there is a
possibility of water getting into it.
Take care not to spill liquid onto or into the equipment. This is because of the danger of electric shock. If
you do happen to spill liquid on the equipment, contact one of Aloka's sales offices or agents listed on the
back cover of this instruction manual.
According to the degree of safety of application in the presence of a flammable anaesthetic
mixture with air or with oxygen or nitrous oxide:
・ Equipment is not suitable for use in the presence of a flammable anaesthetic mixture with air or with oxygen
or nitrous oxide.
Danger
Do not use this equipment in a flammable atmosphere.
It may cause an explosion if used in such an atmosphere
According to the mode of operation:
・ Continuous operation
1-3
1. PRECAUTIONS FOR USE
1-2. Classification
MN1-5099 Rev.0
1-3. Safety / 1-4. Environmental Conditions
1. PRECAUTIONS FOR USE
1-3. Safety
Warning
Do not remodel or modify equipment.
Unexpected accident can take place.
Warning
Clean and disinfect a probe every time it is used.
Using contaminated probes may result in infection.
Warning
Wear medical gloves during inspection, and wash your hands after inspection; otherwise you may become
infected from patients.
Avoid rapid temperature change which may cause condensation.
Avoid using where condensation exist.
Caution
Always use this in dried state. Condensation may appear when using from cold to warm places.
Use without proper care, then, can cause short-circuiting.
Caution
Use of an ultrasonic beam into the air without coating the probe with an ultrasound medium, may cause
surface temperature to rise.
Before using, coat probe adequately with ultrasound gel.(*)
When probe is not in use even during an examination, freeze image.
In the event that the surface temperature feels abnormal, immediately stop using the probe, and contact our
office.
(*) When performing a puncture or a surgical operation, use ultrasound medium as described in the
instruction manual for the probe.
1-4
MN1-5099 Rev.0
1-4. Environmental Conditions
1-4-1. Working environment
This equipment is intended to be used under the following environmental conditions. Be sure to install it in an
environment that satisfies these conditions.
Working environment
Ambient temperature:
Relative humidity:
Atmospheric pressure:
10 - 40°C
30 - 75%
700 - 1060 hPa
Caution
Always use this in dried state. Condensation may appear when moving from cold to warm places.
Use without proper care, then, can cause short-circuiting.
1-4-2. Storage environment
Store the equipment in an environment that satisfies the following conditions.
Storage environment
Ambient temperature:
-10 - 50°C
Relative humidity:
10 - 90 %
Atmospheric pressure:
700 - 1060 hPa
Avoid rapid temperature change which may cause condensation.
Avoid using where condensation exist.
Caution
The presence of electromagnetic waves may result in a mis-diagnosis or a breakdown of the equipment. If the
equipment is to be used near a motor (elevator, pump room, etc.), power transmission line or wireless
equipment, it is necessary to electrostatically shield it.
1-5
1. PRECAUTIONS FOR USE
1-4. Environmental Conditions
MN1-5099 Rev.0
1-5. Power Requirements
1. PRECAUTIONS FOR USE
1-5. Power Requirements
The power requirements for this equipment are as follows.
Power requirements
Unit
Rated supply voltages or voltage ranges
(100 V specifications)
(115 V specifications)
(200 - 240 V specifications)
100 V
115 V
200 - 240 V
Rated frequency or rated frequency range
50/60 Hz
Power input
1000 VA
Auxiliary mains socket outlets
300 VA
Table Power requirements
1-6
MN1-5099 Rev.0
1-6. Electromagnetic environment
This equipment complies with International Standard IEC 60601-1-2.
Caution
・Install this equipment where the electromagnetic radiation does not affect.
・Note that the electromagnetic radiation may cause the following phenomena on this equipment.
・Distortion in viewing monitor
・Noise on physiological signals
・Noise from loudspeaker
・Noise on image
・Position this equipment and its cables (e.g. probe cables, ECG cables, I/O cables, etc.) as far away as
possible from other medical electrical equipment.
・Note that electromagnetic radiation from this equipment may cause the abnormal operation on the other
medical electrical equipment nearby. In this case, stop using such equipment immediately.
・This equipment intended to use in hospitals and/or institutions in order to prevent the electromagnetic
interference.
Use this equipment in facilities equivalent to the hospital or institution.
・Note that electromagnetic radiation from this equipment may cause the disturbance to the radio receiver,
TV set, etc.
Position this equipment as far away as possible from the radio receiver, TV set, and its cables and antenna.
・Do not use the portable radio communication devices (e.g. cellular phone, cordless phone, radio
transceiver, etc.) near this equipment.
1-7
1. PRECAUTIONS FOR USE
1-6. Electromagnetic environment
MN1-5099 Rev.0
1-7. Safety Instructions for Connecting Network Devices
1. PRECAUTIONS FOR USE
1-7. Safety Instructions for Connecting Network Devices
1-7-1.
Electrical safety Instructions for Connecting Network Devices
The following instructions are applicable, when connecting network devices to the Ultrasound system.
The instructions are provided in order for the entire system with network devices to meet
IEC60601-1-1 Electrical Safety Standard.
[Remark]
Connecting to network equipment requires the optional DICOM library (SOP-3500-10)
1.
Network Devices
All non-medical network devices connected to the Ultrasound system, including Hubs, Work Stations and
Personal
Computers, must comply with IEC60950 standard and must be Class I device.
2.
Installation and Network Connections
2.1
Non-medical devices must be kept at least 1.5 meters away from a patient.
2.2
When connecting the Ultrasound system with Computer Devices located out side of the Ultrasound
examination room, a separation device (Network Hub) must be used in-between.
1-7-2.
Other precautions
Once you switch ON the ultrasound diagnostic equipment, do not switch it OFF again for 2〜3 minutes. If you
switch OFF the equipment while it is starting up, the hard disk may break down.
A primary battery is used to maintain the unit in an operable condition. If the battery runs down, the clock on the
system is shown a wrong time.. (In this case, the operation of the ultrasound diagnostic equipment is unaffected.)
If the above phenomenon occurs, the battery must be replaced, so contact your nearest Aloka branch to do this.
The equipment contains a primary battery (lithium battery), so when disposing of it conform to the "Laws
Relating to the Disposal and Cleaning of Waste".
1-8
MN1-5099 Rev.0
2-1. Symbols and Indications
2-1. Symbols and Indications
1) Safety alert symbols
The four indications [Danger], [Warning], [Caution] and [Note] used on this equipment and in this instruction
manual have the following meaning.
Danger
・ Indicates an imminently hazardous situation which, if not avoided, will result in death or serious injury.
・ A warning message is inserted here.
Warning
・ Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
・ A warning message is inserted here.
Caution
・ Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury.
・ A caution message is inserted here.
Note
・ Indicates a strong request concerning an item that must be observed in order to prevent damage or
deterioration of the equipment and also to ensure that it is used efficiently.
・ An explanatory text is inserted here.
This section consists of 6 pages.
2-1
2. MEANING OF SYMBOLS, INDICATIONS AND TERMS
2. MEANING OF SYMBOLS, INDICATIONS
AND TERMS
MN1-5099 Rev.0
2-1. Symbols and Indications
2）Other symbols and indications
The following marks are used in this equipment and this instruction manual.
2. MEANING OF SYMBOLS, INDICATIONS AND TERMS
Symbol
Position
Position
Danger
Various places
Carefully read the pertinent items in this manual, and handle
the equipment with great care.
ANSI standard Z535.3
IEC60601-1, Attached table D
BS 5378 PART1, Appendix A
Biohazard
On the side of
ANSI standard Z535.3
probe connector
ISO7000 No.0659
BS 5378 PART1, Appendix A
Various places
Be careful of explosion
Be careful of electric shock
Various places
ANSI standard Z535.3
BS 5378 PART1, Appendix A
Be careful of fire
Various places
BS 5378 PART1, Appendix A
Various places
Be careful of acoustic power
Table Symbols and indications
2-2
MN1-5099 Rev.0
2-1. Symbols and Indications
Symbol
Position
Meaning
Type BF applied part;
cable connector
IEC60601-1, Attached table D
Power switch
Indicates the ON position of the switch.
IEC60417-5007
Power switch
Indicates the OFF position of the switch.
IEC60417-5008
〜
Rear panel
Alternating current
IEC60417-5032
Rear panel
Equi-potential terminals
IEC60417-5021
IPX8
Foot switch
Protected against the effects of continuos immersion in water
MP-2345B
MP-2614B
IEC60529
Table Symbols and indications
2-3
2. MEANING OF SYMBOLS, INDICATIONS AND TERMS
Probe connector 1
MN1-5099 Rev.0
2-2. Meaning of Terms
2-2. Meaning of Terms
2. MEANING OF SYMBOLS, INDICATIONS AND TERMS
The following terms used in this instruction manual have the meaning described below.
[Remark]:
An item that must be known in order to use the equipment.
Assembly:
Installing and connecting the standard component parts and options in the main equipment using
tools.
Caution
This equipment must be assembled by a person recognized by Aloka when it is delivered to the customer's
premises. It must not be assembled by the customer.
Installation:
Placing the assembled equipment in an environment where it can be used by the customer, then
installing and connecting the peripheral equipment.
Moving:
Moving the equipment in its assembled form manually.
Caution
Transport not conforming to instructed state can cause failure.
For transport of Device, be sure to contact us.
2-4
MN1-5099 Rev.0
2-3. Position of Labels
2-3. Position of Labels
2
3
4
P-4309
This product is protected by one or more of the patents listed below
US Pat. : 4,573,477 4,641,668 4,622,977 5,152,294
5,313,948 5,515,849 5,568,812 5,706,816
5,911,691 6,135,959
: 0,092,841 0,100,094 0,144,968 0,228,069
Eu Pat.
0,432,771 0,754,957 0,809,119
ALOKA CO.,LTD.
2-5
P-3259D
2. MEANING OF SYMBOLS, INDICATIONS AND TERMS
1
MN1-5099 Rev.0
2-1. Symbols and Indications
Labels
Warning • Caution message
2. MEANING OF SYMBOLS, INDICATIONS AND TERMS
1
To ensure proper grounding and reduce the risk of electric shock, connect only to a
hospital grade outlet.
2
Caution to reduce the risk of electric shock, do not remove cover. Refer servicing to
qualified personnel.
3
Risk of explosion if used in the presence of flammable anesthetics.
4
Use acoustic exposure levels As Low As Reasonable Achievable (the ALARA
principle) to obtain diagnostic information. Minimize exposure time.
CONTROL
PROBE 1
PROBE 2
2-6
MN1-5099 Rev.0
3-1. Environmental Conditions of Installation Location
3. INSTALLATION METHOD
3-1. Environmental Conditions of Installation Location
Caution
This equipment must be assembled by a person recognized by Aloka when it is delivered to the user's
premises.
It must not be assembled by the user.
Install this equipment in a stable place where there is no possibility of causing the equipment to fall or topple
over.
(1) Working environment
This equipment is intended to be used under the following environmental conditions.
Working environment
Ambient temperature: 10 - 40°C
Relative humidity:
30 - 75%
Atmospheric pressure: 700 - 1060 hPa
Avoid rapid temperature change which may cause dew condensation.
Avoid using where dew condensation or waterdrops exist.
Caution
Always use this in dried state. Condensation may appear when moving from cold to warm places.
Use without proper care, then, can cause short-circuiting.
This section consists of 6 pages.
3-1
3. INSTALLATION METHOD
［Remark］
In this instruction manual, installation refers to the placing of assembled equipment in an environment where it
can be used by the customer, and installing and connecting the peripheral equipment.
MN1-5099 Rev.0
3-1. Environmental Conditions of Installation Location
（2）Installation location
Install the equipment in a location where sufficient clearance can be obtained on both sides of it.
3. INSTALLATION METHOD
Rear
後
前
Front
30 mm以上
min
30mm
30
mm 以上
min
30mm
Fig. Installation location
Caution
Be sure to leave sufficient space on both sides of the equipment otherwise the temperature inside the
equipment will rise, resulting in a possible breakdown.
（3）Power source
Install the equipment no more than 3.0 meters away from a power outlet in the wall. Ensure that the power outlet
satisfies the following conditions.
Power outlet
Plug
100 V ― 120 V
specifications
200 V ― 240 V
specifications
Table Plugs and power outlets
3-2
MN1-5099 Rev.0
3-2. Installing the Equipment
3-2. Installing the Equipment
Installation procedure
q
Move the equipment to the place where it is to be installed.
If the temperature and humidity of the place where the equipment was stored are different from the
temperature and humidity of the room to which the equipment is newly moved, condensation may occur.
Leave the equipment to stand for a while in the newly installed location to allow it to become acclimated to
the environment before switching it ON. If you switch ON the equipment while there is condensation inside
it, a breakdown may occur.
w
Set the lock levers of the front casters in the ON position.
Fig. Lock levers of front casters
e
Install and connect the peripheral equipment.
[Remark]
For details of this procedure, refer to sub-section 3-4.
r
If you moved and re-installed equipment that was used in a different location, ensure that there are no
loose parts, damage, or signs of wear on the equipment. Check to see if any of the cables of the peripheral
equipment are protruding from the equipment.
t
Insert the power plug into the power outlet.
Warning
・ Insert the power plug directly into a power outlet in the wall.
・ Do not connect the equipment to an extension cable, or to a branched circuit. This may cause you to
receive an electric shock.
y
Connect a probe to the equipment.
[Remark]
For details of this procedure, refer to sub-section 3-3.
3-3
3. INSTALLATION METHOD
Caution
MN1-5099 Rev.0
3-3. Connecting a Probe to the Equipment
3-3. Connecting a Probe to the Equipment
On the front panel of the equipment are probe connectors. Connect probes to these connectors.
Ensure that the pins on the probe connector are not bent. If you attempt to insert a connector with bent pins,
you are liable to damage the probe connector on the equipment.
<Method of connecting an electronic type probe>
RELEASE
3. INSTALLATION METHOD
Note
The lock lever of the connector moves over the range shown right.
Lock lever
Movable
range
LOCK
[Remark]
When connecting a probe to the connector on the equipment, ensure that
the lock lever (marked with a circle) is in the RELEASE position.
Mark
Fig. Lock lever
q
Insert the connector of the electronic type probe firmly into the
connector on the front panel of the equipment.
w
RELEASE
Once you have inserted the connector completely, turn the lock
lever 1/4 of a turn clockwise to the LOCK position.
Fig. Connector
3-4
LOCK
Movable
range
MN1-5099 Rev.0
3-3. Connecting a Probe to the Equipment
Note
If the lock lever is difficult to turn, check to see if the connector is inserted completely.
If you attempt to turn the lock lever without firmly inserting the probe connector, you are liable to damage
both the probe connector and the connector on the equipment.
3. INSTALLATION METHOD
e
Finally, confirm that the probe connector is fixed securely to the
connector on the equipment.
Fig. Connector
3-5
MN1-5099 Rev.0
3-3. Connecting a Probe to the Equipment
3-4. Connecting Options to the Equipment
3-4-1. Connecting the equipment to the physiological signal terminal
3. INSTALLATION METHOD
Note
This option must be assembled by a person recognized by Aloka when it is delivered to the user's premises.
It must not be assembled by the user.
Connect only options specified by Aloka to this equipment.
（1）Connecting the ECG lead cord
On the front panel are connector sockets for connecting an ECG lead cord.
ECG
ECG lead cord
Fig. Connecting the ECG lead cord
q
Insert the connector of the ECG lead cord firmly into the connector on the panel with the groove on the
connector faces upward.
w
Before connecting the ECG lead cord to the patient, insert the three jacks of the ECG lead cord into the
corresponding ECG electrodes.
[Remark]
The ECG lead method is second limb lead.
3-6
MN1-5099 Rev.0
4-1. Specifications
4. SPECIFICATIONS AND NAME OF EACH
PART
Scanning method:
Electronic sector scan
Electronic convex scanning
Electronic linear scanning
Modes:
B
B/B
B/M
M
B/D (PW modes)
D (PW modes)
Flow
Power flow
Tissue Doppler Imaging
VOL
Direction of slice image display:
Longitudinal inversion
Lateral inversion
90 degrees rotation
Image depth:
13 steps between 2 to 24 cm
[Remark]
Image depth varies with the probes.
This section consists of 10 pages.
4-1
4. SPECIFICATIONS AND NAME OF EACH PART
4-1. Specifications
MN1-5099 Rev.0
4-1. Specifications
Image adjustment
4. SPECIFICATIONS AND NAME OF EACH PART
Gain:
STC:
Contrast:
AGC:
Acoustic Power:
Image processing:
30 to 90 dB
8 slide controls
16 steps
16 steps
100% to 0%
GAMMA; RERIEF; POST PROCESS; FTC;
FRAME CORRELATION
Character display
ID (number of patient being examined):
NAME (name of patient being examined):
Date, time:
Probe frequency:
Heartrate value:
EGC sync delay time value:
Display in comment area:
Display of hospital name:
14 characters
24 characters
Automatic display
Automatic display
Automatic display
Automatic display
Max 60 characters × 33 lines
20 characters × 2 lines
Measurement function:
Basic measurements
Cardiac measurements
(Option)
Obstetric measurements
Gynecological measurements
Peripheral vascular measurements
Urological measurements
Other measurements
Accuracy of display:
±5%
Preset function:
15 settings can be made.
Physiological signals:
ECG
4-2
MN1-5099 Rev.0
4-1. Specifications
M mode display
Display method:
Scrolling / Moving Bar
Sweep speed:
Can be set to one of 7 values
D mode display:
(PW)
Pulse modulation
High speed Fourier conversion (FFT) method
Power spectrum display
Approx. ±6.22 cm/s to ±318.8 cm/s
Switchable through 12 steps (for Auto operation)
Flow
Processing method:
Self-correlating method
Speed range :
Approx. ±6.22 cm/s to ±199.2 cm/s
Low frequency rejection filter: MTI filter Switchable through 6 steps
Cine memory function:
Search
Scroll
Store, review
Loop playback
Dimensions
Width:
Depth:
Height:
490mm
790mm
1350-1490mm
Weight:
100kg
[Remark]
The actual dimensions and weight of the equipment are within ±10% of the above values.
4-3
4. SPECIFICATIONS AND NAME OF EACH PART
Modulation method:
Signal analysis:
Display pattern:
Speed range :
Low frequency rejection filter:
MN1-5099 Rev.0
4-2. Name and Function of Each Part
4-2. Name and Function of Each Part
4-2-1.
Exterior drawing and name of each part
（1）Viewing monitor
4. SPECIFICATIONS AND NAME OF EACH PART
（2）Handle
（7）Operation panel
（3）Probe holder
（4）Rear panel
（6）Left side panel
（5）Front panel
（8）Caster
Fig. Exterior drawing
4-4
MN1-5099 Rev.0
4-2. Name and Function of Each Part
（1）Viewing monitor:
Displays diagnostic images. Can also display external video signals.
（2）Handle:
Used to carry the equipment about.
（4）Rear panel:
On the rear panel are power cable.
（5）Front panel:
This panel has connectors for connecting probes, a foot switch connector,
a floppy drive, and a power switch, etc.
（6）Left side panel:
This panel has a circuit breaker.
（7）Operation panel:
Has various switches for setting the operation of the equipment.
→ For details, refer to Section 1 of the How to Use Instruction.
Note
Do not lift the equipment by the panel or apply an unreasonable force to it because this may cause the
equipment to break down.
（8） Caster:
Used to move the equipment.
→ For details, refer to Section 12.
4-5
4. SPECIFICATIONS AND NAME OF EACH PART
（3）Probe holder:
Place the probes and ultrasound gel on the probe holder.
[Remark]
During an operation, do not put the Intraoperative probe in use on the probe holder.
MN1-5099 Rev.0
4-2. Name and Function of Each Part
4-2-2. Front panel
（1）Power switch
（2）Floppy drive
4. SPECIFICATIONS AND NAME OF EACH PART
（3）Volume knob
（7）Electronic probe connectors
（4） ECG connector
（5）VOL control
（6）Foot switch connector
Cable connector
Fig. Front panel
（1）Power switch
This switch supplies power to the equipment.
Setting the switch to the I side turns ON the equipment and causes the lamp
at top left of the operation panel to light green, indicating that power is
being supplied to the equipment.
When the switch is set to the ○ side, power to the equipment is cut off.
（2）Floppy drive
The floppy drive enables you to transfer data inside the system to a 3.5
floppy disk, or to transfer data from another piece of equipment to the
system via a floppy disk.
（3）Volume knob
Adjusts the volume of the Doppler sound.
（4）ECG connector
Used for connecting the ECG signal cable.
（5）VOL control Cable connector
This connector is for a connecting VOL control cable when connecting an
optional electronic convex scanner.
[Remark]
This connector is not attached if the optional VOL mode unit (EU-9084B) is not to be connected.
（6）Foot switch connector
Used for connecting to the optional foot switch.
4-6
MN1-5099 Rev.0
4-2. Name and Function of Each Part
（7）Electronic probe connector
These connectors are for connecting the electronic convex, linear
and sector probes. When two probes are connected, press the
PROBE switch on the operation panel.
[Remark]
Do not connect probes other than electronic probes to these connectors.
（1）Circuit breaker
Fig. Left side panel
（1） Circuit breaker
This is a switch that is used to supply power to the equipment.
Normally, leave it ON.
4-7
4. SPECIFICATIONS AND NAME OF EACH PART
4-2-3. Left side panel
MN1-5099 Rev.0
4-2. Name and Function of Each Part
4-2-4. Rear panel
(1) Potential equalizing terminal
4. SPECIFICATIONS AND NAME OF EACH PART
AC INPUT
（2）Protective earth terminal
Fig. Rear panel
（1）Potential equalizing terminal
This terminal is intended to equalize the potential between this equipment and other
equipment.
（2）Protective earth terminal
This terminal is for connecting the equipment to a protective earth via the power
cable.
4-2-5. Caster
（1）Lock lever
Fig. Front and rear casters
（1）Lock lever
Set to ON to fix each front caster.
4-8
MN1-5099 Rev.0
4-2. Name and Function of Each Part
4-2-6. Viewing monitor
Fig. Viewing monitor
（1）Rotary knob
Adjusts the brightness or the contrast of the observation monitor screen.
For details, refer to 8-2. Preparations for Use.
4-9
4. SPECIFICATIONS AND NAME OF EACH PART
（1）Rotary knob
MN1-5099 Rev.0
4-2. Name and Function of Each Part
4. SPECIFICATIONS AND NAME OF EACH PART
4-10
MN1-5099 Rev.0
5-1. Standard composition
5. COMPOSITION
5-1. Standard composition
Type number
USI - 152
1
Viewing monitor
IPC-1550
1
Power cord (100V〜120V)
CP-116
1
Power cord (200V〜240V)
CP-117
1
Videoprinter control cable
AUW1-150
1
Colorprinter control cable
L-CABLE-342
1
Videoprinter installation metal fittings
MP-FX3500-1
1
Customized Switch Label
P32-SSD4000-1
1
Function Switch Label
P32-SSD3500-1
1
Instruction manual
MN1-5099
1
MN1-5100
1
MN1-5101
1
This section consists of 6 pages.
5-1
5. COMPOSITION
Diagnostic equipment proper
MN1-5099 Rev.0
5-2. Options
5-2. Options
(1) Peripheral equipment
Recording
equipment
5. COMPOSITION
Functional
expansion
Color Printer
Color Printer
Color Printer
Color Printer
B/W Printer
B/W Printer
B/W Printer
B/W Printer
B/W Printer
VCR
VCR
MO unit
EU nations
UP-21MD(UC) (100V〜120V)
─
UP-21MD(CED) (200V〜240V)
○
CP900UM (100V〜120V)
─
CP900E (200V〜240V)
○
UP-895MD (100V〜120V)
─
UP-895CE (200V〜240V)
○
UP-895MD/SYN
○
P91W (100V〜120V)
─
P91E (200V〜240V)
○
SVO-9500MD (NTSC)
─
SVO-9500MDP(PAL)
○
MOU-3500
○
Outside EU
○
○
○
○
○
○
○
○
○
○
○
○
Physiological signal unit
VOL mode unit
PEU-3500
EU-9084B
○
○
○
○
CARDIO APPLICATION
SOFTWARE
TDI FUNCTION SOFTWARE
DICOM LIBRARY SOFTWARE
SOP-3500-3
SOP-3500-9
SOP-3500-10
○
○
○
○
○
○
MP-2345B
MP-2614B
○
○
○
○
MP-FX3500-2
○
○
MP-FX3500-3
○
○
MP-FX3500-4
LKi-630
○
○
○
○
equipment
SOFTWARE
Other equipment
Foot switch
Triple foot switch
Colorprinter installation
metal fittings for UP-21MD
Colorprinter installation
metal fittings for CP-900
VCR installation metal fittings
for SVO-9500
Cable hanger
5-2
MN1-5099 Rev.0
5-2. Options
（2）Table of optional probes (EU nations)
Caution
Use probes only for their intended purpose. Do not use them incorrectly.
[Remark]
For details of using a probe or scanner, refer to the instruction manual for the probe or scanner.
Name
Type No.
Main
Application
UST-5293-5
5MHz,90゜,
Remarks
part of body
Cardiac
Intracorporeal
Rotary plane
Transesophageal
electronic sector
probe
Neurosurgey
Electronic sector
UST-5298
90゜
Cardiac, General
Surface of body
probe
UST-5299
90゜
Cardiac
Surface of body
Puncture electronic
UST-5268P-5
5MHz,90゜,
Intraoperative
UST-979-3.5
3.5MHz,60R,60゜
UST-990-5
5MHz,60R,60゜
UST-9121
14R,120゜
UST-9123
60R,60゜
UST-9101-7.5
7.5MHz,40R,60゜
UST-9124
9R,180゜
OB/GYN
Intracorporeal
Transvagina
UST-984-5
5MHz,14R,118゜
OB/GYN
Intracorporeal
Transvagina
UST-9112-5
5MHz,14R,118゜
OB/GYN
Intracorporeal
Transvagina
UST-670P-5
5MHz,9R,120゜
Urinary organ
Intracorporeal
Transrectal
UST-676P
9R,120゜
Urinary organ
Intracorporeal
Transrectal
Intraoperative
sector probe
Electronic convex
probe
Abdominal,
Surface of body
General
Abdominal,
Surface of body
General
Abdominal,
Surface of body
General
Abdominal,
Surface of body
General
Abdominal,
Surface of body
General
Transvaginal
electronic convex
probe
Transrectal
electronic convex
probe電子
5-3
5. COMPOSITION
specifications
Transesophageal
Applicable
MN1-5099 Rev.0
5-2. Options
Name
Type No.
Main
Application
Remarks
part of body
specifications
Intraoperative
Applicable
UST-987-7.5
7.5MHz,20R,65゜
Intraoperative
Intraoperative
UST-995-7.5
7.5MHz,20R,65゜
Intraoperative
Intraoperative
UST-9104-5
5MHz,20R,65゜
Intraoperative
Intraoperative
UST-9113P-3.5
3.5MHz,60R,60゜
Abdominal
Surface of body
UST-5045P-3.5
3.5MHz,80mm
Abdominal
Surface of body
UST-5540P-7.5
7.5MHz,25mm
Abdominal
Surface of body
UST-5524-7.5
7.5MHz,42mm
Peripheral vessels
Surface of body
electronic convex
probe
5. COMPOSITION
Puncture electronic
convex probe
Puncture electronic
linear probe
Electronic linear
Beam steering
probe
UST-5710-7.5
7.5MHz,60mm
Thyroid
Surface of body
UST-5524-5
5MHz,42mm
Thyroid
Surface of body
Peripheral vessels
Surface of body
Intraoperative
Intraoperative
Beam steering
UST-5546
38mm,
Beam steering
Intraoperative
UST-5542
Beam steering
electronic
linear probe
29mm
UST-5526L-7.5
7.5MHz,33mm
Intraoperative
Intraoperative
UST-5536-7.5
7.5MHz,33mm
Intraoperative
Intraoperative
UST-579T-7.5
7.5MHz,60mm
Intraoperative
Intraoperative
UST-5531
10mm
Intraoperative
Intraoperative
Urinary organ
Intracorporeal
Transrectal
OB/GYN
Surface of body
EU-9084B is
Beam steering
Transrectal
UST-672-5/7.5
7.5MHz,60mm
composite probe
Electronic convex
5MHz,9R,120゜
ASU-1001
14R,90°
necessary
sector scanner
Transvaginal
ASU-1003
OB/GYN
9R, 163゜
Intracorporeal
Transvaginal
electronic convex
EU-9084B is
sector scanner
necessary
5-4
MN1-5099 Rev.0
5-2. Options
(3) Table of optional probes (Outside EU )
Caution
Use probes only for their intended purpose. Do not use them incorrectly.
[Remark]
For details of using a probe or scanner, refer to the instruction manual for the probe or scanner.
Name
Type No.
Main
Application
UST-5293-5
5MHz,90゜,
Remarks
part of body
Cardiac
Intracorporeal
Rotary plane
Transesophageal
electronic sector
probe
Neurosurgey
Electronic sector
UST-5298
90゜
Cardiac, General
Surface of body
probe
UST-5299
90゜
Cardiac
Surface of body
Puncture electronic
UST-5268P-5
5MHz,90゜,
Intraoperative
UST-979-3.5
3.5MHz,60R,60゜
UST-990-5
5MHz,60R,60゜
UST-9121
14R,120゜
UST-9123
60R,60゜
UST-9101-7.5
7.5MHz,40R,60゜
UST-9124
9R,180゜
OB/GYN
Intracorporeal
Transvagina
UST-984-5
5MHz,14R,118゜
OB/GYN
Intracorporeal
Transvagina
UST-9112-5
5MHz,14R,118゜
OB/GYN
Intracorporeal
Transvagina
UST-670P-5
5MHz,9R,120゜
Intraoperative
sector probe
Electronic convex
probe
Abdominal,
Surface of body
General
Abdominal,
Surface of body
General
Abdominal,
Surface of body
General
Abdominal,
Surface of body
General
Abdominal,
Surface of body
General
Transvaginal
electronic convex
probe
Transrectal
Urinary organ
Intracorporeal
Transrectal
electronic convex
probe電子
Transrectal
UST-676P
9R,120゜
Urinary organ
5-5
Intracorporeal
5. COMPOSITION
specifications
Transesophageal
Applicable
MN1-5099 Rev.0
5-2. Options
Name
Type No.
Main
Application
Remarks
part of body
specifications
Intraoperative
Applicable
UST-987-7.5
7.5MHz,20R,65゜
Intraoperative
Intraoperative
UST-995-7.5
7.5MHz,20R,65゜
Intraoperative
Intraoperative
UST-9104-5
5MHz,20R,65゜
Intraoperative
Intraoperative
UST-9113P-3.5
3.5MHz,60R,60゜
Abdominal
Surface of body
UST-5045P-3.5
3.5MHz,80mm
Abdominal
Surface of body
UST-5540P-7.5
7.5MHz,25mm
Abdominal
Surface of body
UST-5524-7.5
7.5MHz,42mm
Peripheral vessels
Surface of body
electronic convex
probe
5. COMPOSITION
Puncture electronic
convex probe
Puncture electronic
linear probe
Electronic linear
Beam steering
probe
UST-5710-7.5
7.5MHz,60mm
Thyroid
Surface of body
UST-5524-5
5MHz,42mm
Thyroid
Surface of body
Peripheral vessels
Surface of body
Intraoperative
Intraoperative
Beam steering
UST-5546
38mm,
Beam steering
Intraoperative
UST-5542
Beam steering
electronic
linear probe
29mm
UST-5526L-7.5
7.5MHz,33mm
Intraoperative
Intraoperative
UST-5536-7.5
7.5MHz,33mm
Intraoperative
Intraoperative
UST-579T-7.5
7.5MHz,60mm
Intraoperative
Intraoperative
UST-5531
10mm
Intraoperative
Intraoperative
Urinary organ
Intracorporeal
Transrectal
OB/GYN
Surface of body
EU-9084B is
Beam steering
Transrectal
UST-672-5/7.5
7.5MHz,60mm
composite probe
Electronic convex
5MHz,9R,120゜
ASU-1001
14R,90°
necessary
sector scanner
Transvaginal
ASU-1003
OB/GYN
9R, 163゜
Intracorporeal
Transvaginal
electronic convex
EU-9084B is
sector scanner
necessary
5-6
MN1-5099 Rev.0
6-1. Principle of Operation
6. PRINCIPLE OF OPERATION
6-1. Principle of Operation
This ultrasound diagnostic equipment uses electric sector probes, electric convex probes, and electric linear
probes.
The method of transmitting and receiving varies depending on the sector, convex and linear probes. The electric
sector scan uses the phase control system to obtain several ultrasound waves that form the slice image of a fan.
This system is explained below.
To swing the ultrasound wave leftward on the slice image, the oscillators' transmitting timing of the ultrasound
waves should be made delayed gradually from the right oscillator to the left. Since the left oscillators receive the
echo earlier than the right oscillators, the left oscillators should transmit the ultrasound waves late by prolonging
the delay timing with the delay line. This makes the reception timing of each oscillator be synchronized, which
forms one ultrasound wave. To swing the wave rightward on the slice image, the transmitting and receiving
timing of the rightmost oscillator should be made delayed the most. The operations above are repeated to form
the scanning plane of the fan.
For electric convex scan and electric linear scan, multiple oscillators constitute a block which transmits and
receives ultrasound waves. So, the ultrasound transmitted from each oscillator forms one ultrasound wave,
showing the same effect as that of the ultrasound wave oscillated from the center of the multiple oscillators.
After the first oscillator transmits and receives the ultrasound, other oscillators of the first block transmit and
receives successively to form the second ultrasound wave. The center of the second ultrasound is shifted from the
center of the first ultrasound by one oscillator. The operations shown above are repeated to form several
ultrasound waves, which constitutes a scanning plane.
The obtained ultrasound as shown above are converted to video signals with the digital scanning converter, and
are displayed on the display monitor.
This section consists of 2 pages.
6-1
6. PRINCIPLE OF OPERATION
The probe that has an array of the rectangular oscillators receives the electrical pulses from the transmission
circuit, and oscillates ultrasound waves. Then, the probe receives the reflective echo from the body of a subject,
and outputs the signals for sliced images.
MN1-5099 Rev.0
6-1. Principle of Operation
This equipment also transmits and receives the ultrasound in the same direction several times, and detects the
difference of the ultrasound waves of each time, which makes it possible to detect the data of the liquid, such as
blood flow (the direction, the speed and the variation). It is also possible to color the data and superimpose them
on the B mode image.
Optional VOL mode supporting unit EU-9084B can make pseudo three-dimensional images to show the surface
of the body.
6. PRINCIPLE OF OPERATION
6-2
MN1-5099 Rev.0
7-1. Method of Cleaning and Sterilizing the Equipment
7. CLEANING AND STERILIZING
7-1. Method of Cleaning and Sterilizing the Equipment
Cleaning consists of cleaning that is carried out at the end of each day, cleaning that must be carried out once a
week, and cleaning that is carried out as necessary after use.
（1）Cleaning that is carried out at the end of each day
（2）Cleaning that must be carried out once a week
・Cleaning the operation panel
・Cleaning the externals and the probe holder
・Cleaning the monitor
Clean the equipment with a soft, dry cloth. If the equipment is very dirty, remove the dirt with a soft cloth that
has been immersed in a weak solution of a neutral detergent, then wipe off the detergent.
Note
Do not clean the equipment in such a way that liquid gets inside it because of the risk of damaging the
internal circuits.
（3）Cleaning that is carried out as necessary after use
・Cleaning the head of the printer
・Cleaning the head of the VCR
[Remark]
For the method of cleaning the peripheral equipment, refer to each instruction manual.
・Cleaning the foot switch
Clean the photo switch with a soft, dry cloth. If the photo switch is very dirty, remove the dirt with a soft cloth
that has been immersed in a weak solution of a neutral detergent, then wipe off the detergent.
This section consists of 2 pages.
7-1
7. CLEANING AND STERILIZING
・Cleaning the surface of the probe
[Remark]
The method of cleaning the probe differs depending upon the kind of probe. For details, refer to the instruction
manual for the probe.
・Cleaning the floor and removing moisture where the equipment is installed
If you use the equipment in a dusty location, the ventilation may deteriorate or the temperature inside
the equipment may become abnormally high.
MN1-5099 Rev.0
7-2. Cleaning and Sterilizing Conditions
7-2. Cleaning and Sterilizing Conditions
Caution
Do not sterilize the equipment with chemical liquids or gases because of the risk of damaging the internal
circuits.
Note
The method of cleaning and sterilizing the probes differs depending upon the type of probe. For details,
refer to the instruction manual for the probe.
7. CLEANING AND STERILIZING
7-2
MN1-5099 Rev.0
8-1. Starting Inspection
8. PREPARATIONS FOR USE
8-1. Starting Inspection
8-1-1. External Inspection
Warning
If you continue to use equipment that is defective as a result of an inspection, you risk causing injury to the
patient. If you discover a defect, switch off the equipment immediately, then contact one of Aloka's sales
offices or agents listed on the back cover of the instruction manual.
8-1-2. Checking and Replacing Consumables
Confirm that there is an adequate supply of consumables including ultrasound gel and printing paper. For details
of the method of replacing the printing paper, refer to the instruction manual.
8-1-3. Cleaning , disinfecting and Sterilizing Probes
Confirm that the probes to be used have been cleaned, disinfected and sterilized according to the purpose of use.
Warning
If you use a contaminated probe, you run the risk of infecting a patient. Before using a probe, clean, disinfect
and sterilize it according to the instruction manual for the probe.
Use the needle guide adapter and needle after sterilizing them.
Warning
Using contaminated devices may result in infection. Before using a probe, clean, disinfect and sterilize it
according to the instruction manual for the probe.
This section consists of 2 pages.
8-1
8. PREPARATIONS FOR USE
Perform the following external inspection before using the equipment.
1)
Check to ensure that there are no scratches or cracks on the enclosure or panel.
2)
Check to ensure that there are no scratches, cracks or discoloration on the power cable and the plug.
3)
Check to ensure that there are no scratches or cracks on the connecting parts of probes.
MN1-5099 Rev.0
8-1. Starting Inspection / 8-2. Preparations for Use
8-1-4. Operation check
q
Turn ON the power switch on the equipment.
→ The equipment is set up in 90 seconds, then a B mode image appears.
w
Confirm that the connected probe, the image display and the frequency match each other.
→ For details of the image display, refer to 9. SCREEN DISPLAY.
e
Check to see if the date and time displayed at top right of the screen are correct.
→ If the date and time are incorrect, be sure to adjust them to the correct values.
For details of setting the date and time, refer to Section 5 of the How to Use Instruction.
Caution
8. PREPARATIONS FOR USE
If the date and time display is incorrect, the equipment may be broken. Stop using the equipment, then
contact one of Aloka's sales offices or agents listed on the back cover of the instruction manual.
8-2. Preparations for Use
q
Adjust the contrast or the brightness of monitor.
w
Press the rotary knob of monitor.
→An adjusting screen is displayed.
e
Turn the rotary knob and select a contrast （
）or a brightness（
）, then press the rotary knob
again.
→Turing the rotary knob, you can adjust either a contrast or a brightness.
r
Press the rotary knob again.
→The adjustment is complete.
t
Turn the rotary knob and select EXIT（ EXIT ）and press the rotary knob once again.
→The adjusting screen is disappeared.
Note
Do not change any setting other than Contrast or Brightness.
There are some cases of image displayed distortedly.
8-2
MN1-5099 Rev.0
9-1. Character Display
9. SCREEN DISPLAY
9-1. Character Display
The various character information displayed on the screen is called a character display. There are three kinds
of displayed information.
1）Information that is entered using the menu and always displayed by the backup function:
Contents of the 'Hospital Name' area
Contents of the 'Date and Time' area
2）Information concerning condition settings for the probe used and ultrasound image:
Contents of automatic display area 1
Contents of automatic display area 2
3）Information for patient identification and comments concerning the ultrasound image
Display area for ID, NAME, etc.
Text area
ALOKA ALOKA
HOPSPITAL
:No ID
:
:
Y
'02/09/18
:M 11:23:36
407/408 1
54Hz
Text Area
60 charactersx 33 lines
Automatic display area 1
3.5M 6.0 R15 G69 C8 A4
1:Abdomen
DVA: 89%
Automatic display area 2
Fig.Character display on screen
This section consists of 4 pages.
9-1
Display area for
Hospital name, ID,
NAME
9. SCREEN DISPLAY
［Remark］
Refer to 9-1-1 "Automatic display area" regarding the displayed contents of these display areas.
MN1-5099 Rev.0
9-1. Character Display
9-1-1. Automatic display area
（１）Automatic display area 1
In this area are displayed information concerning B mode image.
3.5M
6.0
R15
G69
C8
A4
Fig. Example of a display in automatic display area 1
3.5M ： Frequency of probe
The frequency of probe used now is displayed.
6.0
： Transmissin frequency of the selected probe
R15
： Information concerning the display depth
Indicates the display depth as a centimeter.
G69 ： Information concerning the gain
The image gain is indicated within the range 30 〜 90.
9. SCREEN DISPLAY
C8
： Information concerning contrast
The contrast is indicated within the range 1 〜 8.
A4
： Information concerning AGC
AGC is indicated within the range 0 (off) 〜 7.
（２）Automatic display area 2
1.Abdomen
DVA: 89%
Fig. Example of a display in automatic display area 2
1.Abdomen :
In this area are displayed the preset name that is starting.
DVA: 89%
Information concerning the setting of the acoustic power
:
9-1-2. Character display in the text area
You can set the display to ON or OFF using the menu.
ALOKA ALOKA
HOPSPITAL
:No ID
:
:
Y
'02/09/18
:M 11:23:36
407/408 1
54Hz
3.5M 6.0 R15 G69 C8 A4
1:Abdomen
DVA: 89%
511/512
：Indicates the number of images taken into the cine memory.
54Hz
：Indicates the frame rate in B mode.
9-2
MN1-5099 Rev.0
9-2. Graphic Display
9-2. Graphic Display
（3）
ALOKA ALOKA
HOPSPITAL
（1）
:No ID
:
:
Y
'02/09/18
:M 11:23:36
407/408 1
54Hz
（4）
1:Abdomen
DVA: 89%
Fig. B mode image
(1)
Gray scale bar
The gray scale bar is displayed on a B mode image as a 64-step gray scale.
(2)
(3)
Scale mark
Range
One graduation
R2〜R6
0.5cm
R8〜R24
1.0cm
Active mark
A [●] mark indicates an active state (An active
image is the image on which operations can be
performed when two or more images are
displayed.)
A [○] mark indicates a non-active state.
Front direction mark
[Remark]
An active mark on viewing monitor screen coincides with the
Fig. Probe
front direction mark on the probe.
(4)
Focus mark
Indicates the set focal points.
Fig. Focus mark
9-3
9. SCREEN DISPLAY
3.5M 6.0 R15 G69 C8 A4
（2）
MN1-5099 Rev.0
9-2. Graphic Display
ALOKA ALOKA
HOPSPITAL
:No ID
:
:
Y
66
'02/09/18
:M 11:23:36
511/512 1
54Hz
66
F24
（1）
（2）
3.5M 6.0 R15 G69 C8 A4
9. SCREEN DISPLAY
1:Abdomen
DVA: 89%
Fig. B mode + flow image
(1)
This image is a color representation of the set flow velocity and dispersion set by color coding.
(2)
Flow area
The flow display is limited to this area.
You can change the position and size of the area.
［Remark］
The power flow is also displayed in the flow area.
9-4
MN1-5099 Rev.0
10-1. Switching OFF the Equipment / 10-2. Cleaning the Equipment
10. AFTER USING THE EQUIPMENT
10-1. Switching OFF the Equipment
Upon completion of the operation, be sure to switch OFF the equipment using the following procedure. If you
neglect to carry out this procedure after you have finished using the equipment, a breakdown may occur or the
equipment may fail to function correctly the next time you carry out an examination.
Procedure for switching OFF the equipment
q
Freeze the displayed image.
w
Remove the VCR tape or other recording medium from the peripheral equipment.
e
Put the power switch in the（○）position.
[Remark]
The power switch is located on the front panel of the equipment.
Clean the equipment after switching it OFF. Cleaning should be carried out at the end of each day, once a week,
and after use.
（1）Cleaning that is carried out at the end of each day
Carry out the following cleaning.
・ Cleaning the surface of the probe
Wipe off ultrasound gel remaining on the probe.
Note
The method of cleaning the probe differs depending upon the type of probe. For details, refer to the
instruction manual for the probe.
・ Cleaning the ECG electrodes
Wipe the cream off the electrodes.
・ Cleaning the installation location
If you use the equipment in a dusty location, the ventilation may deteriorate or the temperature inside the
equipment may become abnormally high. Be sure, to clean the area where the equipment is installed.
This section consists of 2 pages.
10-1
10. AFTER USING THE EQUIPMENT
10-2. Cleaning the Equipment
MN1-5099 Rev.0
10-2. Cleaning the Equipment / 10-3. State of the Equipment and Accessories
（2）Cleaning that must be carried out once a week
・ Cleaning the operation panel
・ Cleaning the external equipment and probe holder
・ Cleaning the monitor
[Remark]
For details of the cleaning procedure, refer to 7. "Cleaning and Sterilizing".
（3）Cleaning that is carried out as necessary after use
・ Cleaning the head of the peripheral equipment (printer)
・ Cleaning the head of the VCR
[Remark]
For details of the above procedure, refer to the instruction manual provided with each item of peripheral
equipment.
10. AFTER USING THE EQUIPMENT
10-3. State of the Equipment and Accessories
After cleaning the equipment, return the equipment and accessories to their original state.
・ Place the probe in the probe holder or case.
・ Disconnect the ECG lead cord.
Note
Take care that the ECG lead cord do not get entangled.
・ Cover the equipment with a cloth.
10-2
MN1-5099 Rev.0
11-1. Preparations for Storing the Equipment
11. STORING THE EQUIPMENT
11-1. Preparations for Storing the Equipment
When not using the equipment for a long period, carry out the work described in 10. "AFTER USING THE
EQUIPMENT", then carry out the following preparations for storing the equipment. If the storage condition of
the equipment is unsatisfactory, the equipment may break down or fail to function satisfactorily.
Storage preparation procedure
q
Disconnect and remove all peripheral equipment. Place the peripheral equipment in its case or wrap it in a
soft cloth or a sponge and store it separately. Bunch the cables of the peripheral equipment together when
storing them.
w
Disconnect all of the probes. Place each probe in its case or wrap it in a soft cloth or a sponge and store it
separately.
Once you have moved the equipment to the storage location, set the lock levers of the front casters in the
ON position to fix the front casters.
r
Cover the equipment with a cloth.
This section consists of 2 pages.
11-1
11. STORING THE EQUIPMENT
e
MN1-5099 Rev.0
11-2. Storage Location and Environmental Conditions
11-2. Storage Location and Environmental Conditions
When storing the equipment, store it in a long term storage environment. Particularly, be careful of condensation
when storing the equipment in place, such as a warehouse, where the temperature and/or humidity varies
markedly.
Storage environment
Ambient temperature:
– 10 - 50℃
Relative humidity:
10 - 90%
Atmospheric pressure:
700 - 1060 hPa
Avoid rapid temperature change which may cause condensation.
Avoid using where condensation exist.
Caution
Always use this in dried state. Condensation may appear by moving from cold to warm places.
Use without proper care, then, can cause short-circuiting.
11. STORING THE EQUIPMENT
11-2
MN1-5099 Rev.0
12-1. State of the Equipment and Accessories Before Moving the Equipment
12. MOVING THE EQUIPMENT
Caution
Transport not conforming to instructed state can cause failure.
For transport of Device, be sure to contact us.
12-1. State of the Equipment and Accessories Before Moving the
Equipment
Moving preparation procedure
First, carry out the work described in 10. "AFTER USING THE EQUIPMENT", then move the equipment using
the following procedure.
q
Unplug the power cable from the power outlet.
Caution
・Be sure to grasp the plug when unplugging the power cable.
・Do not pull on the power cable because this may cause damage or short circuit.
Wind the power cable around the power cable hanger at the back of the equipment.
Note
・Do not wind or twist the power cable so hard that it gets crushed.
e
Disconnect the peripheral equipment that is not fixed, place it in its case or wrap it in a soft cloth or a
sponge. Bunch the cables of the peripheral equipment so that they do not protrude from the ultrasound
equipment or get caught beneath the casters.
r
Remove probes that are not fixed to the probe holder, and place them separately in a case or wrap them in
a soft cloth or sponge. Bunch the cables of the probes so that they do not protrude from the ultrasound
equipment or get caught beneath the casters.
t
Additionally, when moving the equipment, set the lock levers of the front casters in the OFF position.
y
Grasp the handle firmly when moving the equipment.
This section consists of 2 pages.
12-1
12. MOVING THE EQUIPMENT
w
MN1-5099 Rev.0
12-1. State of the Equipment and Accessories Before Moving the Equipment / 12-2. Inspection Before Re-use
Caution
・ The equipment is heavy and does not stop easily once it starts moving. When it is necessary to move the
equipment over a long distance, tilt it, or move it along a passageway that has stairs, have least two
persons move it.
・ When moving the equipment along a passageway that has stairs, take great care to ensure that you do not
apply strong vibration.
・ If you apply an unreasonably large force to the equipment in the horizontal direction, it may topple over.
Do not tilt the equipment by more than 10 degrees.
・ Do not grasp the equipment at a point other than the handle when moving or lifting it, because this may
result in breakage.
・ Do not strike the equipment against other equipment or materials in the passageway, walls, or columns.
Also, take care not to strike the CRT filter of the monitor.
・ Do not move the equipment along damp passageways.
12-2. Inspection Before Re-use
Before re-using the equipment after moving it for a long period, carry out the following checks and ensure that
the equipment is normal.
・ Inspect the equipment for scratches, dents or other external damage.
12. MOVING THE EQUIPMENT
・ Be careful of condensation, and be sure to leave the equipment to stand for a while in the room to which it
has been moved to allow it to become acclimated to the new environment.
[Remark]
When installing the equipment, refer to Section 3 "INSTALLATION METHOD".
12-2
MN1-5099 Rev.0
13-1. Maintenance and Inspection
13. SAFETY INSPECTION
13-1. Maintenance and Inspection
If you use the equipment for a long period without maintaining it, it may fail to function correctly or may become
damaged as a result of deterioration of parts and consumables that undergo discharge over a period of time. In
order to prevent this, you must maintain and inspect the equipment.
There are three kinds of inspection, daily inspection, weekly inspection, and monthly inspection.
For details of the daily inspection, refer to Section 8. "PREPARATIONS FOR USE".
Weekly inspection
Carry out the following inspection items once a week.
・ Check to ensure that neither the monitor nor the monitor arm is loose.
・ Check to ensure that the Brightness and Contrast settings on the monitor are correct.
・ Check to ensure that the Brightness and Contrast settings on the peripheral equipment (printer) are correct.
Carry out the following inspection items once a month.
・ Check to ensure that the casters are locked securely (the front caster locks fix the mounting trolley in place,
and the rear casters are fixed in the direction of advance).
・ Check to ensure that none of the screws fixing the operation panel and handles are loose.
・ Check to ensure that there are no cracks, dents or other enclosure signs of damage on the equipment.
This section consists of 16 pages.
13-1
13. SAFETY INSPECTION
Monthly inspection
MN1-5099 Rev.0
13-1. Maintenance and Inspection
Caution
If you find any loose parts, cracks, dents or other signs of damage on the equipment, make a suitable
indication on the equipment, such as attaching a "BROKEN" tag to it, then contact one of Aloka's sales
offices or agents listed on the back cover of this instruction manual.
Note
The inspection items for each probe differ depending upon the kind of probe. For details, refer to the
instruction manual for the probe.
13. SAFETY INSPECTION
13-2
MN1-5099 Rev.0
13-2. Safety Inspection
13-2. Safety Inspection
Perform a safety inspection at least once a year in respect of the following items.
Keep a record of inspection results.
1. Earth leakage current
2. Enclosure leakage current
3. Patient leakage current from the applied part to earth
4. Patient leakage current via an type F applied part to earth caused by an external voltage on the applied part.
5. Impedance for protective contact to earth
[Remark]
Make a copy of the form shown on Page 13-15, enter the inspection results in the copy and keep it as a record of
the inspection.
Periodic Safety Inspection Procedure, and Measurement
Have the following inspection performed by a qualified (*1) engineer, and confirm that the measured values are
no greater than the values in the table.
Normal condition
0.5 mA max
0.1 mA max
Single fault condition
1 mA max
0.5 mA max
0.1 mA max
0.5 mA max
0.1Ω max
5 mA max
-
Table: Standard values for periodic safety inspection (Extracted from IEC 60601-1.)
Warning
If you continue to use equipment that has been found to be defective as a result of an inspection, you risk
causing injury to the patient. If you discover a defect, switch off the equipment immediately, then contact
one of Aloka's sales offices or agents listed on the back cover of this instruction manual.
Place a suitable indication, such as "DO NOT USE", on the equipment to prevent it from being used
inadvertently.
*1 This refers to qualifications to carry out safety inspections on electrical medical equipment.
If there is no suitably qualified person at the customer's place, Aloka's serviceman will carry out this
inspection at charge.
If you require a serviceman, contact one of Aloka's sales offices or agents listed on the back cover of this
instruction manual.
13-3
13. SAFETY INSPECTION
Item
Earth leakage current
Enclosure leakage current
Patient leakage current from the
applied part to earth
Patient leakage current via an type F applied
part to earth caused by an external voltage on
the applied part.
Impedance for protective contact to earth
MN1-5099 Rev.0
13-2. Safety Inspection
（1）Earth leakage current
Perform a leakage current test according to Fig.16 of IEC 60601-1 by using the measurement power supply
circuit shown in Fig.10 of IEC 60601-1.
This equipment does not have FE (Functional earth terminal).
（2）Enclosure leakage current
Perform a leakage current test according to Fig.18 of IEC 60601-1 by using the measuring supply circuit shown
in Fig.10 of IEC 60601-1.
Check the leakage at any part of the enclosure apart from connectors. To do this, apply two sheets of metal foil of
maximum dimensions 20 × 10 cm to arbitrary parts of the enclosure, then measure the leakage current between
one metal foil and earth, and also between the two metal foils.
（3）Patient leakage current from the applied part to earth
Perform a leakage current test according to Fig.20 of IEC 60601-1 by using the measuring supply circuit shown
in Fig.10 of IEC 60601-1.
If you are using several probes simultaneously, immerse them all in a salt water solution, then measure the
leakage current from the salt water solution to earth. Do not immerse the probes past the "maximum immersion
point" indicated in the instruction manual for each probe.
Short all three of the ECG lead jacks, and measure the leakage current between the shorted part and ground.
13. SAFETY INSPECTION
13-4
MN1-5099 Rev.0
13-2. Safety Inspection
（4）Patient leakage current via an type F applied part to earth caused by an external voltage
on the applied part
Perform a leakage current test according to Fig.21 of IEC 60601-1 by using the measuring supply circuit shown
in Fig.10 of IEC 60601-1.
If you are using several probes simultaneously, immerse them all in a salt water solution, then measure the
leakage current from the salt water solution to the external voltage. Do not immerse the probes past the
"maximum immersion point" indicated in the instruction manual for each probe.
Short all three of the ECG lead jacks, and measure the leakage current between the shorted part and the part to
which the external voltage is applied.
（5）Impedance for protective contact to earth
Measure the impedance between the protective earth contact in the appliance inlet and accessible metal part
which is protectively earthed of the equipment according to clause 18.(f) of IEC 60601-1.
Caution
When measuring the impedance for, do not bring the probe of the tester into contact with the signal line pins
of the connector. This is because the measuring current may cause damage to the signal line circuit.
Note
13-5
13. SAFETY INSPECTION
Check the power circuits (including power outlets) in the hospital (e.g. measure the protective earth
impedance) at least once a year.
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
13-3. Checking the Measurement Accuracy
At least once a year, carry out the following measurements using an ultrasound phantom (*2) in order to check
the measurement accuracy and calculation accuracy, and keep a record of the results.
・ Distance measurement accuracy (horizontal and vertical directions)
・ Resolution and sensitivity (horizontal direction and vertical direction)
・ Doppler measurement accuracy
Note
For details of checking resolution and sensitivity, refer to the instruction manual for the probe.
*2 An ultrasound phantom is made of a substance the ultrasound properties of which resemble those of human
body tissues. It contains part of different densities and targets separated by known distances. Some phantoms
contain a mechanism for performing Doppler measurement. A phantom is used for checking the performance
of probes and the ultrasound diagnostic equipment, and also for adjusting the image settings.
Inspection method
・Distance measurement accuracy
Perform an inspection concerning distance measurement accuracy. Using the ultrasound phantom, determine the
horizontal direction and vertical direction distances. Record the measurement results for each measurement.
13. SAFETY INSPECTION
・Doppler measurement accuracy
Perform an inspection of the flow velocity measurement accuracy. Next, using an ultrasound phantom that has a
Doppler measurement mechanism, determine the flow velocity by Doppler measurement. Record the
measurement results for each measurement.
13-6
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
Evaluation of results
・Distance measurement accuracy
For details of the allowable range of distance measurement, refer to the instruction manual.
If the measurement accuracy (%) exceeds the value indicated in the instruction manual, judge the equipment to be
abnormal.
・Doppler measurement accuracy
For details of the allowable range of flow velocity accuracy, refer to the instruction manual.
If the measurement accuracy (%) exceeds the value indicated in the instruction manual, judge the equipment to be
abnormal.
Caution
If you discover an abnormality, it is conceivable that the connected probe or ultrasound diagnostic
equipment has broken down. If you use the equipment in such a condition, an incorrect diagnosis is likely
to result, so stop using the equipment and contact one of Aloka's sales offices or agents listed on the back
cover of this instruction manual.
13. SAFETY INSPECTION
13-7
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
Inspection Procedure
<Before carrying out an inspection>
q
Copy the measurement accuracy inspection data sheet on pages 13-13 to 13-15, and write the necessary
items.
w
Connect the probe to be used for inspecting the equipment, then switch on the equipment.
e
Call the optimum preset for the probe connected to the equipment.
If there is a record of the previous inspection, change the settings of the preset so that they are the same as
those used for the previous inspection.
r
Select the Image 1 to 3 of the preset setup, and record the displayed screen using a printer or recorder.
t
Select the Doppler of the preset setup, and record the displayed screen using a printer or recorder.
y
Select the Flow of the preset setup, and record the displayed screen using a printer or recorder.
[Remark]
Select "Color" for Display Priority when "Flow" is selected for the preset. In any setting other than that, the
Doppler sensitivity can not compared accurately.
Note
13. SAFETY INSPECTION
Be sure to record the preset screen in order to leave details of the current set status.
Do not change a setting with the menu after recording the preset screen.
Refer to 6 Preset of How to Use for details of performing a preset operation.
u
Paste the record of the preset screen to the data sheet. If you recorded the preset screen to a VCR, indicate
details identifying the VCR at the place on the data sheet where the record is to be pasted.
i
Start the set preset.
<Distance measurement accuracy>
q
Activate the B mode.
w
Set all of the STC knobs to the center position.
e
Adjust the DEPTH/RANGE switch so as to obtain the optimum display depth for the inspection.
[Remark]
Refer to the instruction manual of the probe for the optimum display depth.
r
Apply the probe to an ultrasound phantom.
t
If there is a record of the previous inspection, adjust the various switches so that the values conform to R
(display depth), G (gain), C (contrast) and DVA (acoustic power) of the previous record.
13-8
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
y
If there is no record of the previous inspection, adjust the GAIN, CONT, and ACOUSTIC POWER
switches so as to obtain the optimum image.
u
Press the FREEZE switch to freeze the image.
i
Using the caliper marks, measure the distance between targets separated by a known distance in the
horizontal direction.
[Remark]
For the method of measuring distance using the caliper marks, refer to 1-9-1-1 of the MEASUREMENT
Instruction.
Record the displayed image using a camera or a recorder.
!0
Taking the known distance between targets of an ultrasound phantom as 'a', and the distance measured
using the caliper marks as 'b', calculate the distance measurement accuracy in the horizontal direction
using the following equation.
Distance measurement accuracy =｜b - a｜/a × 100 (%)
!1
Calculate the distance measurement accuracy in the vertical direction using steps i - !0.
!2
Record the distance measurement accuracy in the horizontal and vertical directions in the data sheet.
!3
Paste the recorded image onto the data sheet.
If you record the recorded image to a VCR, indicate the particulars of the VCR at the pasting position on
the data sheet.
<Resolutions>
q
Display a B mode image.
w
Move all of the STC knobs to the center position.
e
Adjust the DEPTH/RANGE switch so as to obtain the optimum display depth for carrying out the
inspection.
[Remark]
For details of the optimum display depth, refer to the instruction manual of the probe.
r
Place the probe against the phantom.
t
If you have a record of the previous inspection, adjust each switch so that the settings match the recorded
R (display depth), G (gain) and C (contrast), and DVA (acoustic output) values.
y
If you do not have a record of the previous inspection, adjust the GAIN, CONT, ACOUSTIC POWER
knob until the optimum image is obtained.
13-9
13. SAFETY INSPECTION
o
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
u
Press the FREEZE switch to freeze the image.
i
Record the image using a printer or recorder.
o
Paste the record of the image to the data sheet. If you recorded the image to a VCR, indicate details
identifying the VCR at the place on the data sheet where the record is to be pasted.
<Doppler measurements>
q
Display a B/D mode image.
w
Place the probe against the phantom that has a mechanism of Doppler measurements. (Hereafter called
Doppler phantom.)
e
Set the velocity of the flow of the Doppler phantom.
If you have a record of the previous inspection, set to the recorded velocity.
r
Adjust the M/D gain knob.
If you have a record of the previous inspection, adjust to the recorded position of the M/D gain knob.
13. SAFETY INSPECTION
t
Record the position of the M/D gain knob on the data sheet.
y
Move the Doppler cursor to the area where the blood flows, and display the Doppler signal.
u
Press the FREEZE switch to freeze the image.
i
Move the cursor to the Doppler wave, and measure the velocity of the flow.
o
Record the image using a printer or recorder.
!0
Paste the record of the image to the data sheet. If you recorded the image to a VCR, indicate details
identifying the VCR at the place on the data sheet where the record is to be pasted.
<Doppler sensitivity>
q
Display a B+ flow mode image.
w
Place the probe against the Doppler phantom.
e
Set the velocity of the flow of the Doppler phantom.
If you have a record of the previous inspection, set to the recorded velocity.
13-10
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
r
Adjust the flow gain knob.
If you have a record of the previous inspection, adjust to the recorded position of the flow gain knob.
t
Record the position of the flow gain knob on the data sheet.
y
Press the FREEZE switch to freeze the image.
u
Record the image using a printer or recorder.
i
Paste the record of the image to the data sheet. If you recorded the image to a VCR, indicate details
identifying the VCR at the place on the data sheet where the record is to be pasted.
13. SAFETY INSPECTION
13-11
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
Measurement Accuracy Inspection Data Sheet
Ultrasound examination
equipment
Model No.
Manufacturing No.
Probe
Model No.
Manufacturing No.
Camera
Model No.
Settings
Manufacturing No.
Inspection date
Position and name of inspector
Image Control preset screen Pasting position
Particulars of ultrasound phantom
(control No., date of purchase, S/N, etc.)
Distance measurement accuracy
13. SAFETY INSPECTION
Horizontal direction Image pasting position
Known distance between targets: a
Measured distance: b
Distance measurement accuracy
｜b - a｜
× 100 =
a
Vertical direction Image pasting position
cm
cm
%
Known distance between targets: a
Measured distance: b
Distance measurement accuracy
｜b - a｜
× 100 =
a
13-12
cm
cm
%
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
Resolution
Image pasting position
Details identifying the Doppler phantom
(control No., date of purchase, S/N, etc.)
Position for pasting Doppler control preset image
13. SAFETY INSPECTION
Position for pasting Flow Control preset image
Velocity of flow of phantom
Velocity of flow:
13-13
m/s
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
Position for pasting B/D mode image
Image pasting position
Position for pasting B+ flow mode image
M/D gain knob
FLOW gain knob
13. SAFETY INSPECTION
13-14
MN1-5099 Rev.0
13-3. Checking the Measurement Accuracy
ULTRASOUND DIAGNOSTIC EQUIPMENT Safety Inspection Data Sheet
Ultrasound
diagnostic
equipment
Probes
MODEL:
S/N:
MODEL:
S/N:
Impedance for protective contact to earth
Allowable value: 0.1Ω
13-15
S12:close/open
S12:close/open
Between two points of
enclosure
S13:close/open
ECG lead cord
S5:
normal/reverse
PCG microphone
S13:close/open
ECG lead cord
13. SAFETY INSPECTION
Other
MODEL:
S/N:
Peripheral
Equipments
Inspected
Inspector Dep./Signature
Data
All possible combinations
S5:normal/reverse
Earth
of positions of switches
leakage
current
Normal condition
Allowable value: 0.5mA S1 CLOSE
Single fault condition
S1 OPEN
Allowable value: 1mA
All possible combinations
S5:normal/reverse
Enclosure
of positions of switches
leakage
current
Measuring points
Between enclosure
and earth
Normal condition
S1 CLOSE
Allowable value: 0.1mA S7 CLOSE
Single fault condition
S1 OPEN
Allowable value: 0.5mA S7 CLOSE
S1 CLOSE
S7 OPEN
All possible combinations
S5:normal/reverse
Patient
of positions of switches
leakage
current
Measuring points
Probe(s)
form
applied
Normal condition
S1 CLOSE
part
Allowable value: 0.1mA S7 CLOSE
Single fault condition
S1 OPEN
Allowable value: 0.5mA S7 CLOSE
S1 CLOSE
S7 OPEN
All possible combinations
S5:
Patient
of positions of switches
normal/reverse
leakage
current via Measuring points
Probe(s)
a type F
applied
Single fault condition
S1 CLOSE
part to
Allowable value: 0.5mA
earth
caused by
an external
voltage on
the applied
part
MN1-5099 Rev.0
13. SAFETY INSPECTION
13-16
MN1-5099 Rev.0
14. TROUBLESHOOTING
14. TROUBLESHOOTING
No.
Trouble
Cause
Action
1
No image is displayed and the
POWER lamp is off even
though the power switch is
ON.
Check to ensure that the power
cable is connected.
Confirm rear panel cable
connection is secure.
2
No image is displayed (gray
scale bar and characters
present.) with the POWER
lamp lit.
Check if GAIN is set at
minimum.
Is probe connected correctly?
Adjust the GAIN knob.
Check if ACOUSTIC
POWER is set to minimum.
Increase the ACOUSTIC
POWER setting.
Is FREEZE switch ON?
Press the FREEZE switch.
Secure probe connector.
Turn main power off. Turn back
on after 50 sec.
3
Overall image quality is
deteriorated.
Check the monitor's
CONTRAST and
BRIGHTNESS levels.
Adjust monitor CONTRAST and
BRIGHTNESS.
Is EXT switch set to EXT?
Set to INT, for normal operation.
Are all power and video cables
connected?
Secure all cable connections.
Check that the settings for the
POST PROCESS
(ENHANCE) and AGC are
correct.
* If trouble still cannot be solved, contact us.
This section consists of 10 pages.
14-1
Set the control to the normal
setting or to OFF.
14. TROUBLESHOOTING
4
POWER lamp is on but no
image or characters appear.
MN1-5099 Rev.0
14-1. Messages
14-1. Messages
In the event of an abnormality, this equipment outputs a warning message indicating the correct method of
operation, and an alarm tone.
These are as follows.
1）
Message
This appears at the center of the screen.
2）
Assistance messages
When you use the keyboard to operate a function in a menu, assistance messages appear in the message
area at the bottom of the screen.
Message area
14. TROUBLESHOOTING
Assistance messages area
14-2
MN1-5099 Rev.0
14-1. Messages
1) Message
Operation
Action
q
When you press the CTRL+R to
delete the data that is preset or
saved, the right message appears.
Continue and Cancel to be
selected also appear.
Back up file Reset will destroy any
data on this system.
Do you still wish to continue?
Select Continue or Cancel.
w
When the data cannot be written to
the hard disk in the Preset
Control, the right message
appears. OK to be selected also
appears.
Hard disk Access error. Hard disk
requires being diagnosed.
Select OK.
When the data cannot be read from
the FD (the disk crashed) in the
e Preset Control, the right
message appears. OK to be
selected also appears.
Disk crashed.
Select OK.
The data has started to be written in
the Preset Control even when no
FD is inserted or the Disk is not
r
formatted. The right message
appears, and Retry and Cancel to
be selected also appear.
Error: No disk, or disk unformatted.
Select Retry or Cancel.*1
The data has started to be written in
the Preset Control even when the
t FD is write-protected. The right
message appears, and Retry and
Cancel to be selected also appear.
Error: Disk write protected.
Select Retry or Cancel.*2
Disk space is insufficient when you
attempt to write the data on the FD
y in the Preset Control. The right
message appears and Continue and
Cancel to be selected also appear.
Error: Insufficient disk space.
Please insert new disk.
Space of HD is insufficient when
you attempt to transfer the data of
u FD or MO to the HD. The right
message appears, and OK to be
selected also appears.
Error: Disk full.
Please delete data
The data of HD is crashed and is
Disk access error: System parameter
i initialized. The right message
has been initialized.
appears, and OK to be selected also
Please contact service for assistance.
appears.
14-3
Select Continue or Cancel.
*3
Select OK.
Select OK.
14. TROUBLESHOOTING
Message
MN1-5099 Rev.0
14-1. Messages
Operation
When the image is transmitted to
the network from the Image
o Browser, the right message
appears. The transmission status is
displayed on the dialogue.
When the image is saved to the
external media from the Image
!0 Browser, the right message
appears. The saving status is
displayed on the dialogue.
Message
Sending images to storage.
Action
Complete the data
transmission.
14. TROUBLESHOOTING
Store images to Removable disk.
Complete the data saving.
Cannot find study information
Select Retry or Cancel.
Cannot find series information
Select Retry or Cancel.
DICOM image file not found.
Select Retry or Cancel.
Searching...Please wait.
Complete the search of the
information.
The image that is searched in the
Image Browser cannot be
!5 opened. The right message appears,
and Retry and Cancel to be
selected also appear.
Unable to open list file ******** (File
name).
Select Retry or Cancel.
The image that is searched in the
Image Browser cannot be
!6 displayed. The right message
appears, and Retry and Cancel to
be selected also appear.
Unable to load image information.
Select Retry or Cancel.
The information of the image that
is searched in the Image Browser
!7 cannot be read. The right message
appears, and Retry and Cancel to
be selected also appear.
Unable to read image information.
Select Retry or Cancel.
The data cannot be found when you
attempt to search the study
information in the Image
!1
Browser. The right message
appears, and Retry and Cancel to
be selected also appear.
The data cannot be found when you
attempt to search the series
information in the Image
!2
Browser. The right message
appears, and Retry and Cancel to
be selected also appear.
The data cannot be found when you
attempt to search the DICOM
information in the Image
!3
Browser. The right message
appears, and Retry and Cancel to
be selected also appear.
!4
The right message appears during
searching the information.
14-4
MN1-5099 Rev.0
14-1. Messages
Operation
The image data that is loaded in the
Image Browser cannot be built.
!8 The right message appears, and
Retry and Cancel to be selected
also appear.
Message
Action
Select Retry or Cancel.
In progress. Please wait.
Complete the conversion.
After DICOM file is converted to
@00 BMP or TIFF, the right message
appears.
Process completed.
Wait for 2 sec or switch to
another function.
When the communications in the
network have a problem, the right
@1
message appears. Retry and
Cancel to be selected also appear.
Network configuration error.
Select Retry or Cancel.
When the DICOM printer in the
network has a problem, the right
@2
message appears. Retry and
Cancel to be selected also appear.
Printer configuration error.
Select Retry or Cancel.
When the removable disk is
@3 crashed, the right message appears.
OK to be selected also appears.
Disk crashed.
Select OK.
Removable disk is not ready.
Select OK.
When DICOM file is being
!9 converted to BMP or TIFF, the
right message appears.
When the removable disk cannot
@4 be recognized, the right message
appears. OK to be selected also
appears.
The data has started to be written
even when no Disk is inserted into
the disk drive or the Disk is not
@5
formatted. The right message
appears, and Retry and Cancel to
be selected also appear.
Error: No disk, or disk unformatted.
Select Retry or Cancel.*1
The data has started to be written
even when the Disk is write@6 protected. The right message
appears, and Retry and Cancel to
be selected also appear.
Error: Disk write protected.
Select Retry or Cancel.*2
14-5
14. TROUBLESHOOTING
Unable to build image information.
MN1-5099 Rev.0
14-1. Messages
Operation
Message
Action
Disk space is insufficient when
you attempt to write the data on the
@7 Disk. The right message appears
and Continue and Cancel to be
selected also appear.
Error: Insufficient disk space.
Please insert new disk.
When the image is transmitted to
the SCP that does not have a server
@8 function, the right message appears.
Retry and Cancel to be selected
also appear.
Verification SCP not supported.
Select Retry or Cancel.
When a communications error
@9 occurs in the printer, the right
message appears. Retry and
Cancel to be selected also appear.
Printer communication error.
Select Retry or Cancel.
When a communications error
#0 occurs in the network, the right
message appears. Retry and
Cancel to be selected also appear.
Network communication error.
Select Retry or Cancel.
Remote *******. "*******" does not
support Worklist.
Select Retry or Cancel.
No worklist records found.
Showing old records.
Select Retry or Cancel.
Select Continue or Cancel.
*3
#1
#2
14. TROUBLESHOOTING
#3
#4
When the worklist servers (HIS,
RIS) in the hospital cannot
#5 transmit the data, the right message
appears. Retry and Cancel to be
selected also appear.
When a new worklist cannot be
#6 found, the right message appears.
Retry and Cancel to be selected
also appear.
14-6
MN1-5099 Rev.0
14-1. Messages
Operation
Message
Action
The patient ID is not entered when
#7 the search starts. The right message
appears, and OK to be selected also
appears.
Please enter 'PATIENT ID'.
#8 While the ID research screen
appears, the right message appears.
Loading Patient.
Complete the search.
While the patient data is retrieved
#9 from the search list, the right
message appears.
Copying Patient.
Complete the retrieving of the
patient data.
$0 While the patient data is written to
the HD, the right message appears.
Writing Patient.
When the patient data is selected
$1 from the HIS and RIS, the right
message appears.
Receiving Patient.
When the patient data cannot be
$2 found, the right message appears,
and Retry and Cancel to be
selected also appear.
Cannot find patient information.
Select OK.
Complete the writing of the
patient data.
Complete the receiving of the
patient data.
Select Retry or Cancel.
The "NEW PATIENT" is pressed
while the data is stored in the
$3 equipment. The right message
appears, and OK and Cancel to be
selected also appear.
Store Memory Clear.
Image data will be deleted.
When C echo check starts, the
right message appears.
Echo Check to *******: *******
started.
Wait for 2 sec or until check is
finished.
Echo Check to *******: *******
successful.
Wait for 2 sec or switch to
another function.
$4
$6
The connected probe is not suitable
for this equipment.
Invalid probe connected.
14-7
Disconnect the connected probe
from the equipment.
14. TROUBLESHOOTING
$5 When C echo check ends, the
right message appears.
Select OK or Cancel.
MN1-5099 Rev.0
14-1. Messages
2) Assistant Messages
Operation
Message
Action
When the software for operating the
q menu or switches is not ready to
operate, the right message appears.
Invalid Function:
This function is inoperable.
Wait for 5 sec or select another
software that can be operated.
When the computation time of the
w software is 2 sec or more, the right
message appears.
In progress. Please wait.
Wait until the waiting status of
the computation time ends.
Process completed.
Wait for 5 sec until the display
disappears. Or switch to
another function.
When the computation of the
e software completes in 2 sec or
more, the right message appears.
r The right message appears during
the use of Menu Move.
When some options in the submenu of the step setting of the
t MANUAL FOCUS are
highlighted, the right message
appears.
When the step is set to "n steps
or more" in the MANUAL
y
FOCUS, the right message
appears.
14. TROUBLESHOOTING
After the fetus mark to be rotated is
u displayed, the right message is
displayed for 5 sec.
i The right message appears during
the use of Body Mark Move.
Use <TRACK BALL> to move the
menu. Then press <SET> key.
Press the SET key.
Use <Menu ROTARY ENCODER
KNOB> to highlight the focal point.
Then press <- -> key.
Press the "sw" on the right and
left sides of the menu. Or
switch to another function.
Note: Selected FOCUS is not
recommended.
Wait for 5 sec or set the same
step as that of the auto focus.
Or switch to another function.
Press <MARK REF> key to rotate
fetus mark.
Wait for 5 sec or clear the body
mark. Or display any body
mark other than the fetus mark.
Or switch to another function.
Conform press <SET> key.
Quit <Cancel> key and Reset
<MARK REF> key.
Press the SET key.
When the recorder is powered OFF,
or when the BUSY signal does not
o
return in the specified time, the
right message appears.
Printer Error: Check printer power.
Wait for 5 sec or until the
BUSY signal changes to the
waiting status.
When the EMPTY ERROR is
!0 transmitted from the external
printer, the right message appears.
Printer Empty: Check printer paper.
Wait for 5 sec or until the
EMPTY ERROR signal is
transmitted.
Image stored successfully. #**/99.
Wait for 5 sec until the
message disappears.
!1
When the data is saved in the
memory, the right message appears.
14-8
MN1-5099 Rev.0
14-1. Messages
Operation
The STORE SW (including the
Print SW) is pressed when the
!2
Freeze is not selected. The right
message appears.
The data has started to be written
while "Store Media" is Disk
!3 even when no Disk is inserted or
the Disk is not formatted. The
right message appears.
The data has started to be written
while "Store Media" is Disk
!4 even when the Disk is writeprotected. The right message
appears.
Disk space is insufficient while
"Store Media" is Disk when
!5
you attempt to write the data on the
Disk. The right message appears.
Message
Action
<FREEZE> the image.
Then try again.
Wait for 5 sec or select the
FREEZE. Or switch to another
function.
Wait for 5 sec, or switch to
another function.
Error: Disk write protected.
Wait for 5 sec, or switch to
another function.
Error: Insufficient disk space.
Please insert new disk.
Wait for 5 sec, or switch to
another function.
An error of communicating with
the server in the network occurs
!6
while "Store Media" is Net.
The right message appears.
Error: Network communication error.
Wait for 5 sec, or switch to
another function.
Too many images are stored while
"Store Media" is Cine
!7
(Insufficient HD space).
The right message appears.
Error: Disk full; Please delete images.
Wait for 5 sec, or switch to
another function.
System in AUTO-FREEZE.
Press <FREEZE> key to resume.
Press the FREEZE SW to
reset the FREEZE.
!8
When the FREEZE is activated
automatically after the equipment
!9 has not operated for 20 minutes
with the FREEZE being OFF,
the right message appears.
@00
@1
When the image is transmitted to
the PC printer, the right message
appears.
Sending images to printer.
Complete the transmission.
@2
When the backup file cannot be
loaded during maintenance, the right
message appears.
Backup data file not found.
Switch to another function.
14-9
14. TROUBLESHOOTING
Error: No disk, or disk unformatted.
MN1-5099 Rev.0
14-1. Messages
Operation
Message
Action
14. TROUBLESHOOTING
@3
When the network library fails to
be initialized, the right message
appears.
Network library initialization error.
@4
When the ZOOM SW full-lights
up, the message is displayed for 5
sec.
Use <ROTARY ENCODER KNOB>
to activate zoom.
Wait for 5 sec, or end the
ZOOM. Or Switch to another
function.
@5
When the R wave can not be
detected in 5 sec or more while
SYNC is set to ON, or when the
R wave of the body cannot be
detected in 5 sec or more, the right
message appears.
Detection Error: R-wave of ECG is
not detected.
Enter the R-wave signal that
can be synchronized.
@6
When you attempt to set the
continuous or step real time
settings using the trackball or the
rotary SW so that the values go
beyond the setting limit, the right
message appears.
Function example: AGC, CONT,
POWER, ZOOM, M-WINDOW,
FLOW, SCAN, AREA, PUNC
(MEASURE), VIEW, DOP
Contrast, SWEEP SPEED,
DEPTH, VEL RANGE,
ACOUSTIC POWER, STEERED
BEAM, M GAIN.
(In exclusive of letters, an image
cursor, BASE LINE and others)
Range Limit: Selection is not
available.
Wait for 2 sec, or switch to
another function.
@7
When you move the Flow Area to
the area in which the image cannot
Reduce <VEL RANGE> to lower the
be displayed in the currently set
area or extend the area downward.
VEL RANGE with the trackball,
the right message appears.
14-10
Switch to another function.
Wait for 5 sec, set the FLOW
to off or press the lower switch
of VEL RANGE.
MN1-5099 Rev.0
15. DISPOSAL the Equipment
15. DISPOSAL THE EQUIPMENT
Caution
You should recycle or dispose of this equipment properly according to your organization rules and your local
laws.
15. DISPOSAL THE EQUIPMENT
This section consists of 2 pages.
15-1
MN1-5099 Rev.0
15. DISPOSAL THE EQUIPMENT
15-2
MN1-5099 Rev.0
16-1. Probe use and care
16. APPENDIX
16-1. Probe use and care
16-1-1. Indications and Applications For Use
Aloka's probes are divided into three families : External , Endocavity and Intraoperative .
For each probe , the chart on the next page gives the family and primary and secondary applications for each
probe .
All of electronic probes ( UST - series ) are capable of the following modes of operation , depending on the
upgrades included with the system :
B
M
B/M
B / PWD
PWD
M/CD
CD
B/CD/PWD
The use of Doppler modes in fetal applications should be limited to high risk patients .
The use of Doppler modes is contraindicated for routine fetal examinations .
All examinations should be done following the ALARA principle to limit acoustic exposure .
Please refer to the ultrasound safely information later this appendix .
16. APPENDIX
This section consists of 54 pages.
16-1
MN1-5099 Rev.0
16-1. Probe use and care
16. APPENDIX
Transducer
UST-5293(S)-5
Type
Transesophageal
electronic sector
probe
Family
Endocavity
Primary Intended Uses
Cardiac
UST-5298
Electronic sector
probe
External
Cardiac
UST-5299
electronic sector
probe
External
Cardiac
UST-5268P-5
electronic sector
probe
Intraoperative
Burr-hole
UST-979-3.5
Electronic
convex probe
External
Abdominal, General
UST-990-5
Electronic
convex probe
External
Abdominal, General
UST-9121
Electronic
convex probe
External
Abdominal, General
UST-9123
Electronic
convex probe
External
Abdominal, General
UST-9101-7.5
Electronic
convex probe
External
Abdominal, General
UST-9124
Transvaginal
electronic
convex probe
Endocavity
Endvaginal Gynecological
UST-984-5
Transvaginal
electronic
convex probe
Endocavity
Endvaginal Gynecological
UST-9112-5
Transvaginal
electronic
convex probe
Endocavity
Endvaginal Gynecological
UST-670P-5
Transrectal
electronic
convex probe
Endocavity
Endorectal
UST-987-7.5
Electronic
convex probe
Intraoperative
Intraoperative
UST-995-7.5
Electronic
convex probe
Intraoperative
Intraoperative
UST-9104-5
Electronic
convex probe
Intraoperative
Intraoperative
UST-5045P-3.5
Puncture electronic External
linear probe
Abdominal, Puncture
UST-5540P-7.5
Puncture electronic External
linear probe
Abdominal, Puncture
UST-5524-7.5
Electronic
linear probe
External
Peripheral Vessel
UST-5524-5
Electronic
linear probe
External
Peripheral Vessel
UST-5710-7.5
Electronic
linear probe
External
Mammary gland and the
thyroid gland
UST-5546
Electronic
linear probe
External
Peripheral Vessel
UST-5542
Intraoperative liner Intraoperative
probe
Intraoperative
16-2
Secondary Uses
MN1-5099 Rev.0
16-1. Probe use and care
Transducer
UST-5526L-7.5
Type
Family
Intraoperative liner Intraoperative
probe
Primary Intended Uses
Intraoperative
UST-5536-7.5
Intraoperative liner Intraoperative
probe
Intraoperative
UST-579T-7.5
Intraoperative liner Intraoperative
probe
Intraoperative
UST-5531
Intraoperative liner Intraoperative
probe
Intraoperative
UST-672-5/7.5
Combined convex
and Linear probe
Endocavity
Endorectal,Biplane
ASU-1001
Electronic convex
sector probe
External
Gynecological,Fetal
ASU-1003
Transvaginal
electronic convex
sector probe
Endocavity
Endvaginal Gynecological
UST-676P-5
Transrectal
electronic
convex probe
Endocavity
Endorectal
UST-9113P-3.5
Puncture electronic External
convex probe
Secondary Uses
Abdominal, Puncture
16. APPENDIX
16-3
MN1-5099 Rev.0
16-1. Probe use and care
16-1-2. Contraindication
1. Doppler modes are not intended for routine fetal examinations . Doppler modes in fetal examinations are
only to be used where clinically indicated, such as in known or suspected high risk pregnancies .
16-1-3. Warnings
1. Federal law restricts this device to use by or on order of a physician .
2. Only authorized, trained personnel should use probes .
3. These probes cannot be autoclaved . Disposable sterile probe covers are required for applications in sterile
fields . Refer to the Cleaning, Sterilization and Disinfection sections of this manual for further instructions .
4. At present, there are no known methods available to properly clean and sterilize probes exposed to
Creutzfeld-Jacob disease. Therefore, neurosurgical probes used on patients with Creutzfeld-Jacob
disease must be destroyed in order to prevent inadvertent transmission of this disease.
16-1-4. Cautions
1. These probes are precision instruments . Avoid dropping or other sudden impacts .
2. Be careful not to scratch the probe lens .
3. Avoid stretching or bending the cable .
4. Do not immerse the probe connector or adjacent cable in any liquid .
5. If a probe is not operating properly , or is otherwise suspected of being faulty , stop using it and contact
Customer Service for assistance .
6. Keep the probes clean and dry .
Do not allow ultrasound gel , water or any other foreign matter to dry on the probes .
16. APPENDIX
7. Before connecting or disconnecting a probe , either turn the system power off , freeze the image or inactivate
the probe port .
8. Do not store or operate the probes in temperatures above 120°F .
16-1-5. Probe Connection
CAUTION：
Before connecting or disconnecting a probe , either turn the system power off , freeze the
image or inactivate the probe port.
1. Turn the connector dial counterclockwise until the index mark on the dial is in line with the " Release " mark
on the connector .
2. With the cable pointing upwards, plug the connector into the probe located on the right side of the system
console . Be sure to push the connector in until it fully seated
16-4
MN1-5099 Rev.0
16-1. Probe use and care
3. Turn the connector dial clockwise until the index mark on the dial in line with the " Lock " mark on the
connector .
To disconnect the probe , turn the connector dial counterclockwise until the index mark on the dial is in line with
the " Release " mark on the connector . Pull the straight out of the probe port . Do not pull the connector by the
cable .
16-1-6. Cleaning
This procedure is applicable to probes in all three probe families . All of the probes should be cleaned following
this procedure after every use . For Endocavity or Intraoperative family probes, follow with either disinfection or
sterilization , depending on the application .
Biopsy guides should be removed and cleaned separately following this procedure .
Biopsy guides may be autoclave for sterilization after cleaning .
1. Use running water to remove any residual gel or debris from the probe .
Do not expose the junction between the cable and the probe to water or other liquids .
2. Use a dampened gauze pad or other soft cloth and a small amount of liquid soap to thoroughly wipe the
probe . Do not use an abrasive cleanser .
3. Rinse the probe and guide thoroughly in running water, and wipe with a gauze pad moistened with 70%
isopropyl alcohol . Visually inspect both devices to ensure that foreign matter and residue are removed .
4. Dry the probe with a gauze pad .
CAUTION：
16-5
16. APPENDIX
For External family probes, do not immerse the probe more than 1" beyond the transducer
elements . For Endocavity family probes, do not immerse the probe beyond the insertion
area . For Intraoperative probes, do not immerse the connector or adjacent length of cable.
Never immerse the connector in any liquid.
MN1-5099 Rev.0
16-1. Probe use and care
16-1-7. Disinfection
This procedure is applicable to probes in the Endocavity family . If any of these probes are to be used
intraoperatively, the sterilization procedure as described in the next section must be used.
For invasive applications,sterile probe covers must be used . In addition, Aloka strongly recommends that the
probe be disinfected via chemical disinfection between uses. Use a 2% glutaraldehyde solution according to the
following procedure. The use of other disinfection methods has not been evaluated by Aloka for material
compatibility or effectiveness, and may violate any applicable warranties. Use a fresh batch of solution and
prepare it according to the manufacturer's instructions.
The procedure described below is only effective for the insertion area. If sterilization is required, use sterile
probe covers. The biopsy guide may be autoclave according to standard practice.
CAUTION：
Do not immerse the connector in any liquid. Do not immerse Endocavity family probes
beyond the insertion area.
1. Clean the probe thoroughly following the procedure in the previous section of this manual.
2. Prepare a 2% glutaraldehyde solution according to the manufacturer's instructions.
If required, be sure to activate the solution as directed, and do not use any solution that has been active past
its indicated shelf life.
3. Immerse the insertion area of the probe in a chemical disinfecting solution. Do not inunerse the probe
beyond the insertion area. Do not expose the junction between the probe housing and cable to any liquid.
4. Soak the probe for 3 hours.
16. APPENDIX
5. Upon removal, rinse the probe thoroughly with sterile water or sterile saline. To ensure that no residue
remains, follow the manufacturer's instructions for proper rinse procedures, including adequate rinse water
volumes and times.
6. Apply a sterile, disposable probe cover prior to invasive applications or uses in sterile fields.
NOTE：
Do not allow the probe to soak for more than 12 hours.
NOTE：
Use only disinfecting solutions that have been registered with the Environmental Protection
Agency.
16-6
MN1-5099 Rev.0
16-1. Probe use and care
16-1-8. Sterilization
This procedure is applicable to all the probes in the Intraoperative family.
For applications in sterile fields, a disposable sterile probe cover must be used. In addition, Aloka strongly
recommends that the probe be sterilized via chemical sterilization between uses. Use a 2% glutaraldehyde
solution according to the following procedure.
The use of other sterilization methods has not been evaluated by Aloka for material compatibility or effectiveness
and may violate any applicable warrantee. Use a fresh batch of solution and prepare it according to the
manufacturer's instruction. Be sure the probe is clean before proceeding.
1. Clean and rinse the probe thoroughly following the cleaning procedure as explained in previous sections.
2. Prepare a 2% glutaraldehyde solution according to the manufacturer's directions. If required, be sure to
activate the solution as directed, and do not use any solution that has been active past its indicated effective
shelf life.
3. Immerse the probe and adjacent section of cable in the glutaraldehyde solution. Do not immerse the
connector as the connector and connector-cable junction are not water-tight.
4. Soak the probe in the 2% glutaraldehyde solution for 12 hours.
5. Upon removal. rinse the probe thoroughly with sterile water or sterile saline. To ensure that no residue
remains, follow the manufacturer's instructions for proper rinse procedures, including adequate rinse water
volumes and times.
6. Use a sterile disposable probe cover for applications in sterile fields.
Do not allow the probe to soak for periods longer than 12 hours.
NOTE：
Use only sterilizing solutions that have been registered with the Environmental Protection
Agency.
16-7
16. APPENDIX
NOTE：
MN1-5099 Rev.0
16-1. Probe use and care
16-1-9. Probe Covers
For applications where the probe must be sterile. ALOKA recommends the use of disposable sterile probe
covers. Disposable sterile probe covers are available from various manufacturers for use with this probe.
To apply a probe cover, follow these steps：
1. Remove the probe cover from its pouch. Use sterile technique if indicated.
2. Turn the cover partially inside out and squeeze sterile, water-based coupling gel into the end of the cover.
For optimal imaging, use a small amount of gel.
3. Insert probe fully into the cover and roll or slide the cover down over the entire probe.
4. Press out any air bubbles that may have formed around the probe tip.
5. Apply sterile. water-based coupling gel to the outside of the probe as required by the application.
For intraoperative applications, the moisture of the organ(s) or structure(s) of interest are usually sufficient
If desired, a small amount of sterile saline may be used to wet the surface.
NOTE：
To ensure safety and effectiveness of a probe cover, it is recommended that they be
purchased form a manufacturer who registered with FDA.
NOTE：
Users of latex probe covers should be aware of recommendations made in the FDA's 1991
Medical Alert regarding "Allergic Reactions to Medical Device Containing Latex ".
Copies of this document are available from FDA.
16-1-10. Storage
16. APPENDIX
Keep the probe away from excessive humidity and direct sunlight. Store between 14° and 104°F. Do not expose
to excessive pressure or vacuum ( as may be found in autoclave or ethylene oxide sterilization units).
Handle carefully to avoid damage. It is recommended that the probe be stored in its case during transport and
when not in use.
16-8
16-9
Electronic
Phased Array
Electronic
90°
Phased Array
Electronic
90°
Phased Array
Electronic
90°
Phased Array
Electronic
60°
Convex array
Electronic
60°
Convex array
Electronic
120°
Convex array
Electronic
60°
Convex array
Electronic
60°
Convex array
Electronic
180°
Convex array
Electronic
118°
Convex array
Electronic
118°
Convex array
Electronic
120°
Convex array
Electronic
65°
Convex array
Electronic
65°
Convex array
Electronic
65°
Convex array
UST-5293(S)-5
UST-5298
UST-5299
UST-5268P-5
UST-979-3.5
UST-990-5
UST-9121
UST-9123
UST-9101-7.5
UST-9124
UST-984-5
UST-9112-5
UST-670P-5
UST-987-7.5
UST-995-7.5
UST-9104-5
Scan
Angle or
Width
90°
Scanning
Method
16. APPENDIX
Transducer
Imaging
Frequency
B,M,B/M,B/PWD,PWD, 3.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 6.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5.0MHz
M/CD,CD,B/CD/PWD
40mm
9mm
14mm
14mm
9mm
20mm
20mm
20mm
B,M,B/M,B/PWD,PWD, 3.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 3.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 3.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5.0MHz
M/CD,CD,B/CD/PWD
Modes of Operation
60mm
14mm
60mm
60mm
N/A
N/A
N/A
N/A
Curvature
Radius
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
Operating
Temp.
None
None
Puncture
guide tube
MP-2452
None
None
None
None
None
None
None
None
Puncture
adapter
MP-2450
None
None
None
None
Standard
Accessories
Puncture
adapter
MP-2458
Puncture
adapter
MP-2458
None
Puncture
adapter
MP-2473
Puncture
adapter
MP-2473
Puncture
adapter
MP-2474
Puncture
adapter
MP-2473
Puncture
adapter
MP-2482
Puncture
guide tube
MP-2748SET
Puncture
guide tube
MP-2445SET
Puncture
guide tube
MP-2445SET
None
None
None
None
None
Options
MN1-5099 Rev.0
16-1. Probe use and care
16-1-11. Specifications
The chart on following page gives the specifications for all of the probes for the SSD-3500.
16-10
Electronic
90°
convex sector
array
Transvaginal 163°
electronic
convex
sector array
Electronic
180°
Convex array
ASU-1001
UST-9113P-3.5
UST-676P
ASU-1003
Combined
Convex and
Linear array
Electronic
60°
Convex array
120°and
60mm
60mm
33mm
33mm
UST-672-5/7.5
26mm
10mm
Electronic
Linear array
Electronic
Linear array
UST-5531
38mm
UST-579T-7.5
Electronic
Linear array
UST-5546
60mm
Electronic
Linear array
Electronic
Linear array
UST-5710-7.5
42mm
UST-5536-7.5
Electronic
Linear array
UST-5524-5
42mm
Electronic
Linear array
Electronic
Linear array
UST-5524-7.5
25mm
UST-5526L-7.5
Electronic
Linear array
UST-5540P-7.5
Electronic
Linear array
Electronic
Linear array
UST-5045P-3.5
Scan
Angle or
Width
80mm
UST-5542
Scanning
Method
16. APPENDIX
Transducer
60mm
9mm
9mm
14mm
9mm
N/A
N/A
N/A
N/A
N/A
N/A
N/A
N/A
N/A
N/A
N/A
Curvature
Radius
Imaging
Frequency
B,M,B/M,B/PWD,PWD, 3.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 6.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 6.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 3.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5/7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 10.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 8.0MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 7.5MHz
M/CD,CD,B/CD/PWD
B,M,B/M,B/PWD,PWD, 3.5MHz
M/CD,CD,B/CD/PWD
Modes of Operation
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
50-104°
Operating
Temp.
Puncture
guide tube
MP-2452
Puncture
adapter
MP-2458
None
None
None
None
None
None
None
None
None
None
None
Puncture
guide tube
MP-2416
Puncture
guide tube
MP-2483
None
Standard
Accessories
None
None
None
None
Puncture
adapter
MP-2448
Puncture
guide tube
MP-2451
None
None
None
None
Echo coupler
ECM12,ECM-13
Echo coupler
ECM12,ECM-13
Puncture
adapter
MP-2456
Echo coupler
MP-2463
None
Echo coupler
ECM-14
None
Options
MN1-5099 Rev.0
16-1. Probe use and care
MN1-5099 Rev.0
16-1. Probe use and care
16-1-12. Clinical Measurement Accuracy
The following is the accuracy to each measurement feature which can be expected with the SSD-3500.
Measurement Feature
General Tolerance
Round-off Tolerance
Distance in B-mode
± 3%
±0.01cm ＜10cm distance
±0.1cm ＞10cm distance
Area by trace in B-mode
± 6%
±0.01cm2 ＜100cm2 area
±0.1cm2 ＞100cm 2 area
Circumference by trace
in B-mode
± 6%
±0.01cm ＜10cm distance
±0.1cm ＞10cm distance
Area by ellipses in B-mode
± 5%
±0.01cm2 ＜100cm2 area
±0.1cm2 ＞100cm 2 area
Volume in B-mode
± 7%
±0.01cm3 ＜100cm3 volume
Excursion in M-mode
± 3%
±0.01cm ＜10cm distance
±0.1cm ＞10cm distance
Time interval in M-mode
± 3%
±1ms
±0.01s
Velocity in Doppler mode
± 10%
±0.1cm/sec
Heart rate
±1BPM or ±5 %
＜1000ms time
＞1000ms time
±1beat per minute
16. APPENDIX
16-11
MN1-5099 Rev.0
16-1. Probe use and care
16-1-13. Clinical Measurement Range
The following is the maximum measurement range per each measurement feature which can be expected with the
SSD-3500.
Transducer
Distance
(max)
Area
(Trace)
Area
(Ellipse)
Circumfere
nce
(Trace)
Volume
Excursion
Velocity
Doppler
Time
Interval
Heart
Rate
16. APPENDIX
UST-5293-5
44.2cm
889.6 cm2
999.9 cm2
99.9 cm
999.9cm3
24.0 cm
796.9 cm/s
7.96s
15 - 992
BPM
UST-5298
44.2
889.6
999.9
99.9
999.9
24.0
796.9 cm/s
7.96
15 - 992
UST-5299
44.2
889.6
999.9
99.9
999.9
24.0
999.9
7.96
15 - 992
UST-5268P-5
23.1
347.5
999.9
76.3
999.9
15.0
455.4
7.96
15 - 992
UST-979-3.5
44.2
889.6
999.9
99.9
999.9
24.0
531.2
7.96
15 - 992
UST-990-5
44.2
889.6
999.9
99.9
999.9
24.0
455.4
7.96
15 - 992
UST-9121
35.0
557.6
999.9
96.7
999.9
19.0
531.2
7.96
15 - 992
UST-9123
44.2
889.6
999.9
99.9
999.9
24.0
531.2
7.96
15 - 992
UST-9101-7.5
23.1
347.5
999.9
76.3
999.9
15.0
265.6
7.96
15 - 992
UST-9124
31.3
446.4
999.9
86.6
999.9
17.0
455.4
7.96
15 - 992
UST-984-5
31.3
446.4
999.9
86.6
999.9
17.0
455.4
7.96
15 - 992
UST-9112-5
31.3
446.4
999.9
86.6
999.9
17.0
455.4
7.96
15 - 992
UST-670P-5
31.3
446.4
999.9
86.6
999.9
17.0
455.4
7.96
15 - 992
UST-987-7.5
22.1
222.4
999.9
61.1
999.9
12.0
265.6
7.96
15 - 992
UST-995-7.5
22.1
222.4
999.9
61.1
999.9
12.0
265.6
7.96
15 - 992
UST-9104-5
31.3
446.4
999.9
86.6
999.9
17.0
455.4
7.96
15 - 992
UST-5045P-3.5
35.0
557.6
999.9
96.7
999.9
19.0
531.2
7.96
15 - 992
UST-5540P-7.5
18.4
154.5
999.9
50.9
999.9
10.0
265.6
7.96
15 - 992
UST-5524-7.5
18.4
154.5
999.9
50.9
999.9
10.0
265.6
7.96
15 - 992
UST-5524-5
22.1
222.4
999.9
61.1
999.9
12.0
455.4
7.96
15 - 992
UST-5710-7.5
22.1
222.4
999.9
61.1
999.9
12.0
265.6
7.96
15 - 992
UST-5546
18.4
154.5
999.9
50.9
999.9
10.0
265.6
7.96
15 - 992
UST-5542
18.4
154.5
999.9
50.9
999.9
10.0
265.6
7.96
15 - 992
UST-5526L-7.5
22.1
222.4
999.9
61.1
999.9
12.0
265.6
7.96
15 - 992
UST-5536-7.5
22.1
222.4
999.9
61.1
999.9
12.0
265.6
7.96
15 - 992
UST-579T-7.5
22.1
222.4
999.9
61.1
999.9
12.0
265.6
7.96
15 - 992
UST-5531
9.2
38.6
999.9
25.5
999.9
5.0
265.6
7.96
15 - 992
UST-672-5
23.1
347.5
999.9
76.3
999.9
15.0
455.4
7.96
15 - 992
UST-672-7.5
23.1
347.5
999.9
76.3
999.9
15.0
265.6
7.96
15 - 992
ASU-1001
35.0
557.6
999.9
96.7
999.9
19.0
531.2
7.96
15 - 992
ASU-1003
31.3
446.4
999.9
86.6
999.9
17.0
455.4
7.96
15 - 992
UST-676P
31.3
446.4
999.9
86.6
999.9
17.0
455.4
7.96
15 - 992
UST-9113P-3.5
44.2
889.6
999.9
99.9
999.9
24.0
531.2
7.96
15 - 992
UST-5534T-7.5
18.4
154.5
999.9
50.9
999.9
10.0
265.6
7.96
15 - 992
16-12
MN1-5099 Rev.0
16-2. Acoustic Output Safety Information
16-2. Acoustic Output Safety Information
16-2-1. Acoustic Exposure Safety
16-2-2. Interaction Between Ultrasound and Matter
Ultrasound introduces energy into the body. This energy , like all other sound , is in the form of mechanical
pressure waves. Typical frequencies range from 3 Mhz ( megahertz ,or millions of cycles per second ) to 10 Mhz.
The ultrasound image created by the SSD-3500 is possible because some of the energy in the original sound wave
is reflected back to be " heard " by the transducer. Only a very small portion of the original wave is reflected.
Almost all of the energy is absorbed by the tissue.
The energy introduced into and absorbed by the body during ultrasound exposure causes reactions in tissue.
These reaction are divided into two categories : Mechanical and Thermal .
Mechanical effects are due to the pressure waves causing mechanical or physical movement of the tissues and
tissue components . These components such as cells , fluids , etc. , oscillate . If conditions are favorable , it is
possible that these oscillations may affect the structure or function of living tissue . At present , mechanical
effects are though to be instantaneous in nature , and depend roughly on the intensity of the ultrasound pulse.
An extreme example of the mechanical effects of ultrasound is shock - wave lithotripsy , where focused
ultrasound waves are used to break apart kidney stones .
The second type of effect , the thermal effect , is due to the tissues absorbing the energy of the ultrasound berm .
As the sound wave passes through the body , its energy is scattered and absorbed by tissue . Unlike mechanical
effects , thermal effects are thought to be temporal in nature , and related to the tissue volume , perfusion rate ,
exposure time and duty factor ( the fraction of time the transducer is actually transmitting ) . Among the
physiological effects known to occur due to tissue heating are cell death and increased chance for fetal anomalies
16-2-3. Possible Biological effects
Mechanical effects are due to oscillating pressure waves that occur as the ultrasound passes through.
This pressure wave acts on microscopic gas bubbles and other nucleation sites in tissue.
These nucleation sites, although presently poorly understood, are believed to serve as starting points for the
development of gas bubbles. Because gas is much more compressible than fluid, the microscopic gas bubbles can
expand and contract greatly in comparison to the immediately surrounding tissue and fluid. The large change in
size may damage tissue.
16-13
16. APPENDIX
Mechanical Effects
MN1-5099 Rev.0
16-2. Acoustic Output Safety Information
There are two categories mechanical effects: Steady-state and Transient.
Steady - state effects arise from the repeated expansion and contraction of the microbubble in response to the
varying pressure in the ultrasonic pulse . This oscillation can lead to a phenomenon known as " microstreaming ",
where the oscillation of gas bubbles in tissue leads to motion in the fluid around the gas bubble . It has been
shown that microstreaming can lead to disruption of cell membranes .
Transient mechanical effects occur when the pressure change due the oscillating ultrasonic wave causes a gas
bubble to expand and then implode violently in a process called " cavitation " . Although this phenomenon occurs
on the microscopic level , it has been demonstrated to produce extremely high temperatures and pressures in the
immediate vicinity, which can lead to cell death .
The potential for mechanical effects is related to the peak negative ( rarefactional ) pressure of the ultrasound
wave and its frequency . Higher values of negative pressure ( a stronger or higher amplitude wave ) increase the
potential for mechanical effects . Higher frequencies decrease the potential for mechanical effects .
At this time , there is no solid evidence that cavitation occurs in human tissue with the output intensities available
on current diagnostic ultrasound equipment . However , mechanical effects are theoretically possible .
Thermal
Thermal effects occur over longer periods of time , where absorption of the ultrasound energy results is heating of
tissues . Excessive heating can lead disruptions in cellular processes and structures . especially in developing fetal
tissue . As stated previously , only a small fraction of the energy introduced into the body is reflected back at the
transducer to form an image . The rest of the energy must be absorbed by the tissues . The resultant heating is
localized primarily in two areas : Where the beam enters the body and where the beam is focused.
16. APPENDIX
Because of differences in their physical properties, different tissues absorb ultrasound energy at different rates.
Absorption is affected by the ultrasonic power (energy per unit of time), the volume of tissue involved and its
perfusion rate, or the amount of blood flow through the target tissue. Bone tissue, with its higher density and
lower perfusion than soft tissue, absorbs more ultrasound energy. Bone tissue at the surface will absorb the largest
portion, and has the highest susceptibility to heating from ultrasound exposure.
Bone tissue not at the surface, but at the focus point of the beam, will also absorb a higher portion of energy. Soft
tissue absorbs the least.
16-14
MN1-5099 Rev.0
16-2. Acoustic Output Safety Information
Because tissue absorbs ultrasound energy at different rates, a single model to describe all of the different
properties of different tissues is not available.
Currently, there are three different models to describe thermal effects in tissue . The three models are 1)Soft
Tissue 2 ) Bone at focus and 3 ) Bone at the surface .
The type of ultrasound beam also influences the potential for thermal effects . In uncanned modes ( ex : M - mode
) , the ultrasound energy is repeatedly directed down a single beam , resulting in a higher concentration of
ultrasound energy in a smaller tissue volume . This tends to increase the thermal effects in the tissue . In Scanned
models ( B ) . the ultrasonic energy is spread over a large volume of tissue , with greater perfusion , so thermal
effects are not as great . At this time , there is no solid evidence that the temperature increases possible with
currently available diagnostic ultrasound equipment are harmful .
16-2-4. Derivation and Meaning of Indices
Introduction
Older systems had no convenient way of displaying acoustic output information in a format readily
understandable by the operator . Without a real - time display of output . it was difficult to judge the patient's
acoustic exposure during an examination . As a means of controlling output to recognized safe levels , application
- specific exposure limits were established the Foot and Drug Administration .
In 1992 , the AIUM , along with NEMA (National Electrical Manufacturer's Association ) and the FDA .
established a means of displaying in real - time the potential for thermal and mechanical effects . The Standard for
Real - Time Display of Thermal and Mechanical
Acoustic Output Indices on Diagnostic Ultrasound Equipment (the Output Display Standard) establishes the
methods for calculating and displaying the relative potential for acoustic effects . The indices displayed as
described in standard allow the user to address the exposure risks against clinical benefits and determine
appropriate output levels for the particular exam . Acoustic exposure can now be monitored and controlled in real
- time during any diagnostic ultrasound examination.
16-15
16. APPENDIX
Systems like the SSD-3500 that have implemented the Output Display Standard calculate the relative potential for
either mechanical or thermal effects through the display of indices. These indices are based on current tissue
exposure models. In each index. a value of 1.0 or higher indicates an elevated risk for bioeffects. However, the
index values are not absolute measurements of the potential for bioeffects. They are relative measures of potential
based upon current theory.
MN1-5099 Rev.0
16-2. Acoustic Output Safety Information
Introduction
Current research indicates that the potential for mechanical bioeffects is dependent upon the rarefactional
( negative ) pressure of the sound wave and its frequency . The Mechanical Index (MI ) displayed on the
SSD-3500 is based on these two parameters .
The formula used for the MI uses the peak rarefactional pressure , derated according to a homogeneous tissue
model to depth were the value is maximized , divided by the square root of the center frequency . It is required to
be displayed if the probe - system combination is able to exceed a mechanical index value of 1.0 . If this is the
case , it is required to be displayed in B - mode , because this is the mode where mechanical effects are thought to
be the most significant .
The MI is not intended to be absolute measure of the potential for mechanical bioeffects . It cannot be used
determine if mechanical bioeffects are actually occurring . The index is provided to aid the user reducing acoustic
exposure by providing a relative measure of exposure in real - time . Ultrasound examinations should use
techniques that keep the index values as low as possible while still gathering diagnostic quality images in a
efficient manner .
Thermal
There are 3 thermal indices : TIS (soft tissue ) . TIB (Bone focus ) and TIC ( Bone at surface ) . Each of these
indices applies to a different tissue model . The three different model were developed because of the differences
in thermal effects of bone and soft tissue .
Bone absorbs ultrasound more readily than soft tissue , and can be lower in perfusion . Temperature increases are
higher for bone than for soft tissue for the same level of energy exposure . Heating qualities of bone are also
dependent on location . For bone at the surface ( as in neonatal cephalic applications ) , all of the ultrasound
energy passes through the bone , with no attenuation from intervening tissue . Expect temperature rises to be
highest with this model . For bone at the focus point ( as may be present during 3rd trimester fetal examinations )
, the bone only absorbs part of the total energy , but will be the area with the highest suspected temperature rise.
Soft tissues also absorb ultrasound energy and the potential exists for significant heating.
16. APPENDIX
A Thermal Index is requited to be displayed if the system is able to exceed either a Soft Tissue Index (TIS) or a
Bone at Focus (TIB) Index of 1.0 or higher.
16-16
MN1-5099 Rev.0
16-2. Acoustic Output Safety Information
16-2-5. ALARA recommendations
The ALARA principle stands for " As low as reasonably achievable " . It is widely used in imaging techniques
that use ionizing radiation , where any exposure is considered to be harmful . Implementation of ALARA requires
the collection of quality diagnostic information while minimizing exposure to the patient .
The real - time display of mechanical and thermal allows the user to implement ALARA by constantly displaying
the for mechanical and thermal effects . This way , the user can judge any added diagnostic benefit increased
exposure may have . Also the indices allow the user to set machine parameters that lower the potential for thermal
and mechanical effects .
The second way to reduce exposure is to reduce examination time . The mechanical and thermal indices are real time displays of the potential for bioeffects at that time . They are not cumulative . It is dependent upon the skill
and experience of operator to ensure that each examination is done as efficiently as possible to gather diagnostic
quality images without excess exposure time .
Controls
Mechanical
The mechanical index is primarily dependent upon the frequency of the probe and the acoustic power . Other
parameters of the SSD-3500 that can affect the MI include the focus and Image Select functions . To reduce the
mechanical index , first choose a probe with the appropriate center frequency for the study being performed .
Then , reduce the acoustic power to the lowest level that delivers quality diagnostic information . Finally , be
aware that changes to the focus and Image Select settings may affect the MI . This is especially important in 2nd
and 3rd trimester fetal exam .
The MI is only displayed during B -mode scans . In other modes , thermal effects are more important , so the TI is
displayed .
Thermal
16-17
16. APPENDIX
Because the thermal indices are time-dependent phenomena, control of thermal indices is more complicated. The
first step to implementing ALARA is to display the appropriate index. The Soft Tissue index (TIS) should be
displayed when there is no bone tissue either at the surface or at the focus point. For Transcranial or neonatal
cephalic applications, where there is bone at or near the transducer surface, the TIC index will give the best
estimate of the potential for thermal bioeffects. When there is bone at the focus point, such as in second and third
trimester fetal exam, the TIB index will give the best estimation.
Once the proper index is displayed, steps can be taken to monitor and reduce the thermal index value. As with
the Ml, the choice of the correct probe is important for penetration depth and image resolution. Scanned versus
uncanned modes are also important. Uncanned modes such as M - mode and Pulsed - wave Doppler concentrate
the ultrasound energy on a single beam, Ieading to increased energy in a smaller tissue volume, which increases
the potential for heating in that volume.
MN1-5099 Rev.0
16-2. Acoustic Output Safety Information
The focus can increase the aperture (number of active elements in the transducer), increasing the total energy.
The aperture tends to be larger for deeper focus distances. However, the overall thermal index can be affected by
other factors such as focus depth. Be aware that changes to the focus can affect the TI.
16-2-6. References
The above explanation of acoustic exposure and the ALARA principle is only intended to augment, not replace,
an accredited education program in ultrasound. In addition to professional training, the following references are
excellent sources for additional information on bioeffects and the Mechanical and Thermal indices.
Bioeffects and Safety of Diagnostic Ultrasound -American Institute of Ultrasound in Medicine 1993
Medical ultrasound Safety -American institute of Ultrasound in Medicine 1994
Standard for Real - Time Display of Thermal and Mechanical Acoustic Output lndices on
Diagnostic Ultrasound Equipment AIUMlNEMA 1992
16. APPENDIX
16-18
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-3. Acoustic Output Tables
16-3-1. Acoustic Output Measurements
The acoustic measurements contained in this manual were made with the SSD-3500 ultrasound system set to the
maximum output in each mode. Measurements were obtained in water following procedures outlined by the
FDA, AIUM and NEMA.
The derated intensities provided are estimated from 3 factors.
1. The intensity as measured water.
2. The depth at which the intensity is obtained.
3. The acoustic frequency of the probe.
Derated intensities are estimated from these factors using the following formula :
I (derated) = I (water) exp (- 0.069fz)
where I (derated) is the estimated intensity in tissue, I (water) is the intensity measured in water at a distance z
and f is the acoustic frequency. This equation assumes the acoustic attenuation in tissue is uniform, and generally
overestimates the in situs exposure. However, there are instances where this model may underestimate the in
situs exposure, such as when the beam passes through significant fluid - filled structures.
16-3-2. Definitions
MI
TISscan
TISnon - scan
TIB
TIC
Aarpt
Pr0.3
W0
Zbp
dep (Z )
Fe
Derated peak rarefactional pressure(megapascals)
Ultrasonic power except for TISscan, in which case it is the ultrasonic power passing
through a one centimeter window.(mW)
Derated ultrasonic power at axial distance z1.
Derated spatial peak, temporal average intensity at axial distance z1.
Axial distance corresponding to the location of max [min ( W0.3 ( Z ) , I ta0.3 ( .1 )
Xlcm2 )] where Z≧Zbp. ( centimeters )
1.69 ( Aarpt ) . For MI , zsp is the axial distance at which Pr0.3 is measured ; for TIB
, zsp is the axial distance at which TIB is maximum (zsp = zp0.3) ( centimeters )
Equivalent beam diameter as a function of axial distance z , and equal to
[ (4 / π)(Wo / Ita(z) ) ], where Ita (z) is the temporal - average intensity as a
function of z ( centimeters )
The center frequency of the ultrasonic pulse.
16-19
16. APPENDIX
W0.3
Ita0.3(z1)
Z1
Mechanical Index .
Soft Tissue Thermal Index in an auto -scanning mode.
Soft Tissue Thermal Index in a non - autoscanning mode.
Bone Thermal Index
Cranial Thermal Index
Area of the active aperture(cm2)
MN1-5099 Rev.0
16-3. Acoustic Output Tables
Dim . of Aarpt
PD
PRF
Prat Pllmax
FL
ROC
dep at Pllmax
Active aperture dimensions for azimuthal and elevational planes ( centimeters )
Pulse Duration.
Pulse Repetition Frequency.
Peak rarefactional pressure at the point where the free -field , spatial - peak pulse
intensily integral is a maximum. (Megapascals)
Focal length , or azimuthal and elevational lengths,.
Radius of curvature.
Equivalent beam diameter at the point where the free-field , spatial - peak pulse
integral ia maximum.
16-3-3. Default Setting
The default acoustic output settings for the SSD-3500 are as follows.
{ Default values are set at the Track I Iimits for the primary application of the probe.
Charts of the default settings will be included in the final 510 ( K ) submission. }
16. APPENDIX
16-20
16-21
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
100
3.75MHz
F5
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
35
3.3
2.5
n/a
71
10
13
3.3
n/a
n/a
n/a
n/a
Yes
4.0
contact
100
3.75MHz
F5
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
35
3.3
2.5
n/a
87
10
13
3.3
n/a
n/a
n/a
n/a
Yes
4.0
contact
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
18
2.1
14
78
B
20
2.1
15
55
Mode
16. APPENDIX
parameter
Maximum power
(B+M)p
100
3MHz
F4
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
38
3.0
2.5
n/a
71
10
13
3.0
n/a
n/a
n/a
n/a
Yes
4.0
contact
19
1.9
14
81
(B+M)Ispta
Mp
3.3
2.1
2.5
68
100
3.75MHz
F5
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
35
3.3
2.5
1000
n/a
10
13
3.3
n/a
n/a
n/a
n/a
Yes
4.0
contact
Convex / Gynecological, Fetal, Abdominal
Acoustic power is controllable by the user.
ASU-1001
100
3.75MHz
F4
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
38
2.8
2.4
1000
n/a
10
13
3.3
n/a
n/a
n/a
n/a
Yes
4.0
contact
3.2
2.0
2.4
78
MIspta
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F4
10.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
39
2.7
2.1
983
n/a
10
13
3.7
n/a
n/a
n/a
n/a
Yes
4.0
contact
(B+D)
21
2.7
16
641
Dp
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3MHz
F4
33.2
n/a
n/a
n/a
n/a
n/a
n/a
n/a
34
2.8
2.4
2604
n/a
10
13
3.0
n/a
n/a
n/a
n/a
Yes
4.0
contact
(B+D)
41
1.8
31
953
DIspta
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
F4
16.6
n/a
n/a
n/a
n/a
n/a
39
2.7
2.1
1628
n/a
10
13
3.7
n/a
n/a
n/a
n/a
Yes
4.0
contact
18
2.4
14
555
Mflowp
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3MHz
n/a
n/a
F4
33.2
n/a
n/a
n/a
n/a
n/a
34
2.8
2.4
2604
n/a
10
13
3.0
n/a
n/a
n/a
n/a
Yes
4.0
contact
42
2.2
32
985
MflowIspta
100
3.75MHz
F5
15
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
F4
33.2
MID
HIGH
#5
5
n/a
39
2.7
2.1
n/a
15
10
13
3.7
n/a
n/a
n/a
n/a
Yes
4.0
contact
25
2.2
18
328
100
3.75MHz
F5
4
HIGH
25
PENET
n/a
3MHz
n/a
n/a
F4
6.2
MID
HIGH
#5
5
n/a
34
2.8
2.4
n/a
18
10
13
3.0
n/a
n/a
n/a
n/a
Yes
4.0
contact
39
1.9
29
491
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
100
3.75MHz
F5
4
HIGH
25
PENET
PENET
3.75MHz
F4
12.4
F5
6.2
MID
HIGH
#5
5
HIGH
39
2.7
2.1
n/a
6.9
10
13
3.7
n/a
n/a
n/a
n/a
Yes
4.0
contact
43
2.7
33
1039
100
3.75MHz
F5
4
HIGH
25
PENET
PENET
3MHz
F4
24.9
F4
12.4
MID
HIGH
#5
5
HIGH
34
2.8
2.4
n/a
8.7
10
13
3.0
n/a
n/a
n/a
n/a
Yes
4.0
contact
61
2.1
46
1216
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-22
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
18
1.6
2.4
n/a
145
6.2
5.7
4.8
n/a
n/a
n/a
n/a
Yes
3.0
contact
24
3.0
2.3
n/a
145
7.0
5.7
4.7
n/a
n/a
n/a
n/a
Yes
3.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
5.5
1.3
14
13
100
5MHz
F6
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW)
(MPa)
BIspta
Bp
4.2
1.6
12
11
100
6MHz
F4
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
Mode
Acoustic power is controllable by the user.
18
1.6
2.4
1002
n/a
6.2
5.7
4.8
n/a
n/a
n/a
n/a
Yes
3.0
contact
(B+M)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
0.49
1.6
1.4
22
100
6MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
Mp
MIspta
18
1.7
2.4
1002
n/a
6.2
5.7
4.7
n/a
n/a
n/a
n/a
Yes
3.0
contact
(B+M)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
0.54
1.6
1.5
23
100
5MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
Convex / Endovaginal Gynecological, Fetal
16. APPENDIX
ASU-1003
19
1.5
2.1
1572
n/a
6.2
5.7
5.9
n/a
n/a
n/a
n/a
Yes
3.0
contact
(B+D)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.9
1.9
8.4
145
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
6MHz
F4
10.0
Dp
19
1.6
2.3
2170
n/a
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
3.0
contact
(B+D)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
5.6
1.8
16
255
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
16.6
DIspta
19
1.6
2.3
2170
n/a
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
3.0
contact
F4
16.6
n/a
n/a
n/a
n/a
n/a
6.0
1.9
17
278
100
n/a
n/a
3
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
Mflowp
19
1.6
2.3
4340
n/a
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
3.0
contact
F4
33.2
n/a
n/a
n/a
n/a
n/a
6.4
1.4
18
292
100
n/a
n/a
3
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
MflowIspta
19
1.5
2.1
n/a
30
6.2
5.7
5.9
n/a
n/a
n/a
n/a
Yes
3.0
contact
F4
19.9
MID
HIGH
#5
5
n/a
3.7
1.8
10
43
100
5MHz
F6
17
HIGH
25
PENET
n/a
6MHz
n/a
n/a
19
1.6
2.3
n/a
26
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
3.0
contact
F4
33.2
MID
HIGH
#5
5
n/a
6.1
1.5
17
78
100
5MHz
F6
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
19
1.5
2.1
n/a
12
6.2
5.7
5.9
n/a
n/a
n/a
n/a
Yes
3.0
contact
F5
6.2
MID
HIGH
#5
5
HIGH
7.3
1.9
20
222
100
5MHz
F6
3
HIGH
25
PENET
PENET
6MHz
F4
12.4
19
1.6
2.3
n/a
14
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
3.0
contact
F4
10.0
MID
HIGH
#5
5
HIGH
9.7
1.7
27
308
100
5MHz
F6
3
HIGH
25
PENET
PENET
5MHz
F4
19.9
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
Linear / Abdominal
16-23
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
100
3.75MHz
F4
6
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
70
2.1
3.5
1000
n/a
24
13
3.2
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+M)
100
3.75MHz
F4
6
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
70
2.1
3.5
n/a
74
24
13
3.2
n/a
n/a
n/a
n/a
Yes
1.3
contact
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
(mW)
(MPa)
Mp
9.4
2.6
3.0
130
B
57
2.6
18
72
Mode
16. APPENDIX
parameter
Maximum power
Acoustic power is controllable by the user.
UST-5045P-3.5
100
3MHz
F4
6
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
76
1.9
3.7
1000
n/a
24
13
3.2
n/a
n/a
n/a
n/a
Yes
1.3
contact
8.7
2.2
2.8
137
MIspta
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F4
16.6
n/a
n/a
n/a
n/a
n/a
n/a
n/a
74
1.8
3.2
1628
n/a
24
13
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+D)
(B+Bflow+D)
72
2.6
23
1476
Dp
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3MHz
F4
79.7
n/a
n/a
n/a
n/a
n/a
n/a
n/a
72
2.0
3.7
6250
n/a
24
13
3.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+D)
(B+Bflow+D)
142
1.7
46
2790
DIspta
100
n/a
n/a
6
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
F4
16.6
n/a
n/a
n/a
n/a
n/a
74
1.8
3.2
1628
n/a
24
13
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
60
2.9
19
1237
Mflowp
100
n/a
n/a
6
n/a
n/a
n/a
PENET
3MHz
n/a
n/a
F4
39.8
n/a
n/a
n/a
n/a
n/a
72
2.0
3.7
3125
n/a
24
13
3.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
136
2.5
43
2634
MflowIspta
100
3.75MHz
F4
15
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
F4
33.2
MID
HIGH
#5
5
n/a
74
1.8
3.2
n/a
26
24
13
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
92
2.9
30
654
100
3.75MHz
F4
6
HIGH
25
PENET
n/a
3MHz
n/a
n/a
F4
6.2
MID
HIGH
#5
5
n/a
72
2.0
3.7
n/a
17
24
13
3.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
139
2.5
44
1088
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-24
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
11
1.3
1.9
n/a
72
4.3
5.5
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
5.5
1.1
2.6
n/a
72
3.6
5.5
4.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
4.7
1.7
24
135
100
3.75MHz
F1
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW)
(MPa)
BIspta
Bp
6.1
2.3
26
114
100
6MHz
F2
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
Mode
Acoustic power is controllable by the user.
11
1.3
1.9
n/a
56
4.3
5.5
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
5.4
2.3
23
136
100
6MHz
F2
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
(B+M)p
5.5
1.1
2.6
n/a
56
3.6
5.5
4.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
4.2
1.7
21
141
100
3.75MHz
F1
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
(B+M)Ispta
11
1.3
1.9
1002
n/a
4.3
5.5
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.4
2.3
5.7
97
100
6MHz
F2
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
Mp
12
1.3
1.8
1002
n/a
4.3
5.5
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.5
2.1
6.3
97
100
5MHz
F2
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
MIspta
Phased Array / Intraoperative, Burr-hole, Small parts, Peripheral Vascular
16. APPENDIX
UST-5268P-5
10
1.3
1.6
2170
n/a
4.3
5.5
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
(Mflow)
(B+D)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
9.2
2.9
39
704
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F2
16.6
Dp
10
1.3
1.6
7440
n/a
4.3
5.5
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
(Mflow)
(B+D)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
13
2.0
57
1010
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F2
56.9
DIspta
11
1.2
1.7
n/a
20
4.3
5.5
5.8
n/a
n/a
n/a
n/a
Yes
1.0
contact
F2
24.9
MID
HIGH
#5
5
n/a
8.8
2.8
38
763
100
3.75MHz
F1
4
HIGH
25
PENET
n/a
6MHz
n/a
n/a
15
1.6
1.9
n/a
22
5.4
5.5
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
F3
16.6
MID
HIGH
#5
5
n/a
16
2.7
56
985
100
3.75MHz
F1
15
HIGH
25
PENET
n/a
5MHz
n/a
n/a
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
10
1.3
1.6
n/a
4.7
4.3
5.5
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
F2
12.4
MID
HIGH
#5
5
HIGH
17
2.9
59
1042
100
3.75MHz
F1
4
HIGH
25
PENET
PENET
5MHz
F3
24.9
15
1.6
1.9
n/a
4.7
5.4
5.5
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
F1
12.4
MID
HIGH
#5
5
HIGH
16
2.9
58
1046
100
3.75MHz
F1
4
HIGH
25
PENET
PENET
5MHz
F3
24.9
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-25
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
100
3.75MHz
F2
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
14
1.4
1.9
n/a
72
5.7
5.5
4.2
n/a
n/a
n/a
n/a
Yes
1.0
contact
100
5MHz
F2
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
14
1.3
1.8
n/a
72
5.7
5.5
4.5
n/a
n/a
n/a
n/a
Yes
1.0
contact
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm )
(mW/cm 2)
(%)
(MHz)
11
2.8
35
150
(mW)
(MPa)
2
12
2.4
37
154
Bp
Mode
16. APPENDIX
parameter
Maximum power
BIspta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
14
1.3
1.8
n/a
56
5.7
5.5
4.5
n/a
n/a
n/a
n/a
Yes
1.0
contact
100
5MHz
F2
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
9.8
2.8
31
206
(B+M)
Phased Array / Cardiac, Dome TEE
Acoustic power is controllable by the user.
UST-5293-5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
14
1.3
1.8
1002
n/a
5.7
5.5
4.5
n/a
n/a
n/a
n/a
Yes
1.0
contact
100
5MHz
F2
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.5
2.8
7.9
181
M
n/a
n/a
n/a
n/a
n/a
n/a
n/a
14
1.2
1.7
2170
n/a
5.7
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
(Mflow)
(B+D)
(B+Bflow+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F2
16.6
13
3.4
41
1039
Dp
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
1.8
1.8
4340
n/a
7.2
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
(Mflow)
(B+D)
(B+Bflow+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
33.2
27
2.8
68
1368
DIspta
F2
24.9
MID
HIGH
#5
5
n/a
14
1.2
1.7
n/a
17
5.7
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
100
3.75MHz
F2
15
HIGH
25
PENET
n/a
5MHz
n/a
n/a
16
3.4
50
960
F2
6.2
MID
HIGH
#5
5
n/a
14
1.2
1.7
n/a
16
5.7
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
100
5MHz
F4
21
HIGH
25
PENET
n/a
5MHz
n/a
n/a
18
3.3
56
1093
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-26
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
(̲)
(⊥)
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(Hz)
(Hz)
(mm)
(mm)
prr(PRF)
srr(SRF)
Output beam dimensions
(mm)
(̲)
(⊥)
wpb6
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
4.1
n/a
n/a
n/a
n/a
Yes
1.1
contact
2.0
3.4
n/a
72
9.6
8.0
3.9
n/a
n/a
n/a
n/a
Yes
1.1
contact
2.0
3.5
n/a
72
9.6
8.0
100
3.75MHz
F5
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
33
100
5MHz
F5
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
37
(mW/cm )
(mW/cm 2)
(%)
(MHz)
2
31
1.9
40
94
30
2.0
39
70
(mW)
(MPa)
BIspta
Bp
Mode
lP
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
Acoustic power is controllable by the user.
3.9
n/a
n/a
n/a
n/a
Yes
1.1
contact
(B+M)
(B+M)
2.0
3.5
1002
n/a
9.6
8.0
100
3.75MHz
F5
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
33
6.9
1.9
9.0
158
MIspta
4.1
n/a
n/a
n/a
n/a
Yes
1.1
contact
2.0
3.4
1002
n/a
9.6
8.0
100
5MHz
F5
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
37
6.7
2.0
8.8
129
Mp
Phased Array / Cardiac, Pediatric
16. APPENDIX
UST-5298
(B+D)
4.7
n/a
n/a
n/a
n/a
Yes
1.1
contact
1.8
4.1
2170
n/a
9.6
8.0
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F5
16.6
n/a
n/a
n/a
n/a
n/a
n/a
n/a
34
24
2.5
31
527
Dp
(B+D)
3.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
1.8
3.9
4340
n/a
8.8
8.0
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F4
44.3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
29
41
2.1
58
1166
DIspta
4.7
n/a
n/a
n/a
n/a
Yes
1.1
contact
1.8
4.1
2170
n/a
9.6
8.0
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
F5
16.6
n/a
n/a
n/a
n/a
n/a
34
34
3.0
44
739
Mflowp
3.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
1.8
3.9
2441
n/a
8.8
8.0
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
F4
24.9
n/a
n/a
n/a
n/a
n/a
29
47
2.7
67
1375
MflowIspta
4.7
n/a
n/a
n/a
n/a
Yes
1.1
contact
1.8
4.1
n/a
14
9.6
8.0
100
3.75MHz
F5
19
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F5
19.9
MID
HIGH
#5
5
n/a
34
35
3.0
45
405
3.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
2.0
2.8
n/a
17
9.6
8.0
100
3.75MHz
F5
15
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
F5
33.2
MID
HIGH
#5
5
n/a
33
48
2.5
62
741
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
4.7
n/a
n/a
n/a
n/a
Yes
1.1
contact
1.8
4.1
n/a
3.8
9.6
8.0
100
3.75MHz
F5
4
HIGH
25
PENET
PENET
5MHz
F4
19.9
F5
10.0
MID
HIGH
#5
5
HIGH
34
27
2.5
37
621
3.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
1.8
3.9
n/a
10
8.8
8.0
100
3.75MHz
F5
4
HIGH
25
PENET
PENET
3.75MHz
F4
19.9
F5
10.0
MID
HIGH
#5
5
HIGH
29
54
2.5
74
1224
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-27
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
100
2.5MHz
F2
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
38
3.0
3.3
n/a
73
11
12
2.5
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
1.88MHz
F3
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
42
3.4
3.6
n/a
72
12
12
2.1
n/a
n/a
n/a
n/a
Yes
1.3
contact
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm )
(mW/cm 2)
(%)
(MHz)
94
2.0
66
204
(mW)
(MPa)
2
87
1.8
72
206
Bp
Mode
16. APPENDIX
parameter
Maximum power
BIspta
Phased Array / Cardiac
Acoustic power is controllable by the user.
UST-5299
n/a
n/a
n/a
n/a
n/a
n/a
n/a
42
3.4
3.6
n/a
55
12
12
2.1
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
1.88MHz
F3
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
83
2.0
58
285
(B+M)p
n/a
n/a
n/a
n/a
n/a
n/a
n/a
44
3.1
3.1
n/a
63
12
12
2.6
n/a
n/a
n/a
n/a
Yes
1.3
contact
98
3MHz
F3
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
94
1.9
66
315
(B+M)Ispta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
42
3.4
3.6
1006
n/a
12
12
2.1
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
1.88MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
2.0
15
258
Mp
n/a
n/a
n/a
n/a
n/a
n/a
n/a
45
3.3
3.2
1002
n/a
12
12
2.5
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
2.5MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
1.8
16
294
MIspta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
46
2.8
2.8
1563
n/a
12
12
2.9
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+D)
(B+Bflow+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3MHz
F3
19.9
59
2.2
42
1025
Dp
n/a
n/a
n/a
n/a
n/a
n/a
n/a
46
2.8
2.8
5208
n/a
12
12
2.9
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+D)
(B+Bflow+D)
89
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3MHz
F3
66.4
97
1.6
68
1666
DIspta
F3
19.9
n/a
n/a
n/a
n/a
n/a
46
2.8
2.8
1563
n/a
12
12
2.9
n/a
n/a
n/a
n/a
Yes
1.3
contact
98
n/a
n/a
4
n/a
n/a
n/a
PENET
3MHz
n/a
n/a
96
2.7
67
1653
Mflowp
F3
66.4
n/a
n/a
n/a
n/a
n/a
46
2.8
2.8
5208
n/a
12
12
2.9
n/a
n/a
n/a
n/a
Yes
1.3
contact
69
n/a
n/a
4
n/a
n/a
n/a
PENET
3MHz
n/a
n/a
97
1.6
68
1666
MflowIspta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
F3
33.2
MID
HIGH
#5
5
n/a
46
2.8
2.8
n/a
13
12
12
2.9
n/a
n/a
n/a
n/a
Yes
1.3
contact
89
2.5MHz
F2
24
HIGH
25
PENET
n/a
3MHz
n/a
n/a
96
2.5
68
1048
F3
6.2
MID
HIGH
#5
5
n/a
46
2.8
2.8
n/a
16
12
12
2.9
n/a
n/a
n/a
n/a
Yes
1.3
contact
70
1.88MHz
F2
17
HIGH
25
PENET
n/a
3MHz
n/a
n/a
96
2.0
68
1075
(B+Bflow)p (B+Bflow)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-28
(mm)
(mm)
(mm)
(mm)
l ts
Inclusive modes
(%)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(⊥)
(̲)
(%)
contact
contact
2.2
n/a
51
12
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
29
8.4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.3
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
2.3
n/a
51
8.6
6.0
4.7
n/a
n/a
n/a
n/a
Yes
1.0
100
6MHz
F8
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
100
5MHz
F5
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
19
1.7
27
105
13
3.0
25
70
(mW)
(MPa)
BIspta
Bp
Mode
l tt
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
Acoustic power is controllable by the user.
contact
2.3
n/a
45
8.6
6.0
4.7
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.3
100
5MHz
F5
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
12
3.0
24
117
(B+M)
Linear / Peripheral Vascular, Small parts
16. APPENDIX
UST-5524-5
contact
2.3
1002
n/a
8.6
6.0
4.7
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.3
100
5MHz
F5
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.1
3.0
4.1
111
M
contact
(B+D)
2.5
1628
n/a
8.6
6.0
3.8
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.6
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F5
16.6
26
2.8
50
1107
Dp
contact
(B+D)
3.2
3906
n/a
12
6.0
3.8
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
37
1.9
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F6
39.8
61
2.0
88
1510
DIspta
contact
2.5
1628
n/a
8.6
6.0
3.8
n/a
n/a
n/a
n/a
Yes
1.0
F5
16.6
n/a
n/a
n/a
n/a
n/a
24
1.6
95
n/a
n/a
3
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
30
3.0
57
1274
Mflowp
contact
3.2
4340
n/a
12
6.0
3.8
n/a
n/a
n/a
n/a
Yes
1.0
F6
44.3
n/a
n/a
n/a
n/a
n/a
37
1.9
92
n/a
n/a
3
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
67
2.0
97
1677
MflowIspta
contact
2.5
n/a
30
8.6
6.0
3.8
n/a
n/a
n/a
n/a
Yes
1.0
F5
39.8
MID
HIGH
#5
5
n/a
24
1.6
100
6MHz
F6
6
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
50
2.9
95
1223
contact
3.2
n/a
22
12
6.0
3.8
n/a
n/a
n/a
n/a
Yes
1.0
F6
6.2
MID
HIGH
#5
5
n/a
37
1.9
100
7.5MHz
F4
3
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
73
2.2
108
1444
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
contact
2.5
n/a
18
8.6
6.0
3.8
n/a
n/a
n/a
n/a
Yes
1.0
F5
10.0
MID
HIGH
#5
5
HIGH
24
1.6
100
6MHz
F8
8
HIGH
25
PENET
PENET
3.75MHz
F6
19.9
63
2.8
100
1552
contact
3.2
n/a
25
12
6.0
3.8
n/a
n/a
n/a
n/a
Yes
1.0
F6
12.4
MID
HIGH
#5
5
HIGH
37
1.9
89
6MHz
F2
10
HIGH
25
PENET
PENET
3.75MHz
F6
24.9
70
2.0
102
1587
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-29
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
100
7.5MHz
F8
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
7.2
1.3
n/a
145
12
6.0
6.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
100
10MHz
F5
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.1
1.4
n/a
145
8.6
6.0
6.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
18
2.7
25
158
Bp
7.7
3.8
15
62
Mode
16. APPENDIX
parameter
Maximum power
BIspta
100
10MHz
F5
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.1
1.4
1002
n/a
8.6
6.0
6.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
0.89
3.8
1.7
83
Mp
Linear / Peripheral Vascular, Small parts
Acoustic power is controllable by the user.
UST-5524-7.5
100
6MHz
F5
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
1.2
1.5
1002
n/a
8.6
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.3
3.3
2.5
93
MIspta
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F5
19.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.2
1.6
2604
n/a
8.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
15
3.2
29
1071
Dp
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F5
24.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.2
1.6
3255
n/a
8.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
18
3.1
35
1290
DIspta
100
n/a
n/a
3
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
F5
16.6
n/a
n/a
n/a
n/a
n/a
24
1.2
1.6
2170
n/a
8.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
16
3.6
31
1135
Mflowp
100
n/a
n/a
3
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
F5
24.9
n/a
n/a
n/a
n/a
n/a
24
1.2
1.6
3255
n/a
8.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
18
3.1
35
1290
MflowIspta
100
10MHz
F5
3
HIGH
25
n/a
PENET
5MHz
F5
19.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.1
1.4
n/a
16
8.6
6.0
6.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
13
3.5
25
863
(B+D)p
100
7.5MHz
F8
3
HIGH
25
n/a
PENET
5MHz
F5
24.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
1.2
1.6
n/a
20
8.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
17
3.1
31
1049
(B+D)Ispta
100
10MHz
F5
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F8
33.2
MID
HIGH
#5
5
n/a
24
1.1
1.4
n/a
26
8.6
6.0
6.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
23
3.2
34
849
100
7.5MHz
F8
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F8
33.2
MID
HIGH
#5
5
n/a
24
7.4
1.6
n/a
26
12
6.0
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
24
2.2
35
859
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
100
10MHz
F5
8
HIGH
25
PENET
PENET
5MHz
F5
19.9
F8
10.0
MID
HIGH
#5
5
HIGH
24
1.1
1.4
n/a
25
8.6
6.0
6.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
30
3.5
51
1604
100
7.5MHz
F8
8
HIGH
25
PENET
PENET
5MHz
F5
19.9
F8
10.0
MID
HIGH
#5
5
HIGH
24
1.2
1.6
n/a
25
8.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
31
3.2
52
1613
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-30
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
100
6MHz
F8
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
22
12
2.0
n/a
152
19
4.2
6.3
n/a
n/a
n/a
n/a
Yes
0.80
contact
(B+M)
100
7.5MHz
F2
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
13
1.1
1.6
n/a
152
4.8
4.2
6.4
n/a
n/a
n/a
n/a
Yes
0.80
contact
(B+M)
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm )
(mW/cm 2)
(%)
(MHz)
2
18
1.6
23
133
Bp
3.9
2.4
19
38
Mode
BIspta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
13
1.1
1.6
1002
n/a
4.8
4.2
6.4
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
7.5MHz
F2
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
0.45
2.4
2.2
38
Mp
Linear / Laparoscopic Intraoperative
Acoustic power is controllable by the user.
UST-5526L-7.5
16. APPENDIX
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
1.2
1.9
1002
n/a
7.2
4.2
6.4
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
7.5MHz
F3
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
0.64
2.4
2.1
40
MIspta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
11
1.3
1.9
2604
n/a
4.8
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
(Mflow)
(B+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F2
19.9
8.9
2.5
44
536
Dp
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
1.4
2.8
3255
n/a
9.6
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
(Mflow)
(B+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
24.9
19
2.3
48
695
DIspta
F2
33.2
MID
HIGH
#5
5
n/a
11
1.3
1.9
n/a
28
4.8
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
6MHz
F8
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
10
2.1
42
326
F4
33.2
MID
HIGH
#5
5
n/a
26
1.4
2.8
n/a
28
9.6
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
6MHz
F8
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
17
2.0
40
418
(B+Bflow)p (B+Bflow)Ispta
F2
10.0
MID
HIGH
#5
5
HIGH
11
1.3
1.9
n/a
14
4.8
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
6MHz
F8
3
HIGH
25
PENET
PENET
5MHz
F4
19.9
25
2.5
75
873
F4
10.0
MID
HIGH
#5
5
HIGH
26
1.4
2.8
n/a
14
9.6
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
6MHz
F8
3
HIGH
25
PENET
PENET
5MHz
F4
19.9
31
2.4
74
946
(B+Bflow+D)p (B+Bflow+D)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
MN1-5099 Rev.0
16-3. Acoustic Output Tables
0.75
1.3
1002
n/a
2.9
2.0
7.7
n/a
n/a
n/a
n/a
Yes
0
contact
4.8
2.3
n/a
299
7.2
2.0
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
(̲)
(⊥)
8.5
n/a
n/a
n/a
n/a
Yes
0
contact
(B+M)
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(Hz)
(Hz)
(mm)
(mm)
7.7
n/a
n/a
n/a
n/a
Yes
0
contact
(B+M)
16. APPENDIX
16-31
prr(PRF)
srr(SRF)
Output beam dimensions
(mm)
(̲)
(⊥)
wpb6
(%)
0.75
1.3
n/a
299
2.9
2.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
8.1
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm )
(mW/cm 2)
(%)
(MHz)
2
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.3
M
(mW)
(MPa)
0.17
2.3
3.0
24
100
7.5MHz
F2
2
n/a
n/a
n/a
n/a
n/a
n/a
n/a
4.1
1.5
28
120
100
7.5MHz
F8
2
HIGH
25
n/a
n/a
n/a
n/a
n/a
Bp
1.5
2.3
26
57
100
7.5MHz
F2
2
HIGH
25
n/a
n/a
n/a
n/a
n/a
Mode
lP
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
BIspta
Linear / Intraoperative, Small parts
Acoustic power is controllable by the user.
UST-5531
7.5
n/a
n/a
n/a
n/a
Yes
0
contact
(B+D)
0.73
1.4
3255
n/a
2.9
2.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
3.1
3.8
2.9
67
508
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
7.5MHz
F2
16.6
Dp
7.5
n/a
n/a
n/a
n/a
Yes
0
contact
(B+D)
0.73
1.4
3906
n/a
2.9
2.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
3.1
4.4
2.9
77
587
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
7.5MHz
F2
19.9
DIspta
7.5
n/a
n/a
n/a
n/a
Yes
0
contact
0.73
1.4
1965
n/a
2.9
2.0
F2
10.0
n/a
n/a
n/a
n/a
n/a
3.1
3.0
3.3
51
392
100
n/a
n/a
2
n/a
n/a
n/a
PENET
7.5MHz
n/a
n/a
Mflowp
7.5
n/a
n/a
n/a
n/a
Yes
0
contact
0.73
1.4
3906
n/a
2.9
2.0
F2
19.9
n/a
n/a
n/a
n/a
n/a
3.1
4.4
2.9
77
587
100
n/a
n/a
2
n/a
n/a
n/a
PENET
7.5MHz
n/a
n/a
MflowIspta
7.5
n/a
n/a
n/a
n/a
Yes
0
contact
(B+Bflow+D)
0.73
1.4
n/a
48
2.9
2.0
F2
19.9
MID
HIGH
#5
5
n/a
3.1
5.4
3.3
87
785
100
7.5MHz
F8
2
HIGH
25
PENET
n/a
7.5MHz
n/a
n/a
(B+Bflow)p
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
7.6
n/a
n/a
n/a
n/a
Yes
0
contact
(B+Bflow+D)
4.7
2.3
n/a
59
7.2
2.0
F8
8.3
MID
HIGH
#5
5
n/a
8.0
8.5
1.4
60
1115
78
10MHz
F5
2
HIGH
25
PENET
n/a
7.5MHz
n/a
n/a
(B+Bflow)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-32
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
pIob
parameter
Maximum power
100
6MHz
F8
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
22
12
2.0
n/a
152
19
4.2
6.3
n/a
n/a
n/a
n/a
Yes
0.80
contact
(B+M)
100
7.5MHz
F2
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
13
1.1
1.6
n/a
152
4.8
4.2
6.4
n/a
n/a
n/a
n/a
Yes
0.80
contact
(B+M)
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
18
1.6
23
133
Bp
3.9
2.4
19
38
Mode
BIspta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
13
1.1
1.6
1002
n/a
4.8
4.2
6.4
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
7.5MHz
F2
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
0.45
2.4
2.2
38
Mp
Linear / Laparoscopic Intraoperative
Acoustic power is controllable by the user.
UST-5536-7.5
16. APPENDIX
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
1.2
1.9
1002
n/a
7.2
4.2
6.4
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
7.5MHz
F3
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
0.64
2.4
2.1
40
MIspta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
11
1.3
1.9
2604
n/a
4.8
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
(Mflow)
(B+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F2
19.9
8.9
2.5
44
536
Dp
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
1.4
2.8
3255
n/a
9.6
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
(Mflow)
(B+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
24.9
19
2.3
48
695
DIspta
F2
33.2
MID
HIGH
#5
5
n/a
11
1.3
1.9
n/a
28
4.8
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
6MHz
F8
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
10
2.1
42
326
F4
33.2
MID
HIGH
#5
5
n/a
26
1.4
2.8
n/a
28
9.6
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
6MHz
F8
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
17
2.0
40
418
(B+Bflow)p (B+Bflow)Ispta
F2
10.0
MID
HIGH
#5
5
HIGH
11
1.3
1.9
n/a
14
4.8
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
6MHz
F8
3
HIGH
25
PENET
PENET
5MHz
F4
19.9
25
2.5
75
873
F4
10.0
MID
HIGH
#5
5
HIGH
26
1.4
2.8
n/a
14
9.6
4.2
5.0
n/a
n/a
n/a
n/a
Yes
0.80
contact
100
6MHz
F8
3
HIGH
25
PENET
PENET
5MHz
F4
19.9
31
2.4
74
946
(B+Bflow+D)p (B+Bflow+D)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
MN1-5099 Rev.0
16-3. Acoustic Output Tables
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
(̲)
(⊥)
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(Hz)
(Hz)
(mm)
(mm)
6.6
n/a
n/a
n/a
n/a
Yes
0.85
contact
6.2
n/a
n/a
n/a
n/a
Yes
0.85
contact
(B+M)
6.6
n/a
n/a
n/a
n/a
Yes
0.85
contact
(B+M)
6.3
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.1
2.3
1002
n/a
8.6
7.0
1.0
2.4
1002
n/a
8.6
7.0
100
6MHz
F5
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.6
1.9
n/a
241
12
7.0
1.0
2.4
n/a
241
8.6
7.0
16. APPENDIX
16-33
prr(PRF)
srr(SRF)
Output beam dimensions
(mm)
(̲)
(⊥)
wpb6
(%)
100
7.5MHz
F5
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.2
2.9
1.9
73
MIspta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
n/a
n/a
n/a
n/a
n/a
n/a
n/a
40
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
Mp
1.1
3.0
1.8
70
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
100
6MHz
F6
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
100
7.5MHz
F5
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW)
(MPa)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
15
2.6
19
107
Bp
9.2
3.0
15
87
Mode
lP
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
BIspta
Linear / Intraoperative, Small parts
Acoustic power is controllable by the user.
UST-5540P-7.5
5.1
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.3
1.9
1310
n/a
8.6
7.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
27
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F5
10.0
6.2
2.7
10
363
Dp
5.1
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.5
2.1
2170
n/a
12
7.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
41
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F6
16.6
13
2.3
16
561
DIspta
5.1
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.3
1.9
1310
n/a
8.6
7.0
F5
10.0
n/a
n/a
n/a
n/a
n/a
27
100
n/a
n/a
3
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
7.9
3.0
13
461
Mflowp
5.1
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.5
2.1
3255
n/a
12
7.0
F6
24.9
n/a
n/a
n/a
n/a
n/a
41
100
n/a
n/a
3
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
15
2.1
19
662
MflowIspta
6.6
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.0
2.4
n/a
8.2
8.6
7.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
100
7.5MHz
F5
3
HIGH
25
n/a
PENET
5MHz
F6
10.0
7.0
2.7
8.8
294
(B+D)p
5.1
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.5
2.1
n/a
14
12
7.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
41
100
6MHz
F6
3
HIGH
25
n/a
PENET
5MHz
F6
16.6
11
2.3
14
453
(B+D)Ispta
6.6
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.0
2.4
n/a
44
8.6
7.0
F6
33.2
MID
HIGH
#5
5
n/a
26
100
7.5MHz
F5
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
16
2.3
20
652
5.1
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.5
2.1
n/a
41
12
7.0
F6
8.3
MID
HIGH
#5
5
n/a
41
100
6MHz
F6
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
16
1.7
20
693
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
6.6
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.0
2.4
n/a
16
8.6
7.0
F6
6.2
MID
HIGH
#5
5
HIGH
26
100
7.5MHz
F5
3
HIGH
25
PENET
PENET
5MHz
F6
12.4
20
2.7
25
863
5.1
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.5
2.1
n/a
21
12
7.0
F6
10.0
MID
HIGH
#5
5
HIGH
41
100
6MHz
F6
3
HIGH
25
PENET
PENET
5MHz
F6
19.9
23
2.1
28
956
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-34
l tt
l ts
Inclusive modes
Initialization mode
Acoustic output freeze
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(̲)
(⊥)
prr(PRF)
srr(SRF)
Output beam dimensions
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(⊥)
wpb6
8.1
n/a
n/a
n/a
n/a
Yes
0.85
contact
n/a
n/a
n/a
Yes
0.85
contact
7.7
3.5
5.4
0.90
n/a
138
8.5
n/a
5.8
3.5
0.78
0.86
n/a
138
n/a
n/a
n/a
n/a
n/a
n/a
13
n/a
n/a
n/a
n/a
n/a
n/a
12
(cm/sec)
(%)
n/a
n/a
n/a
n/a
n/a
n/a
(cm/sec)
HIGH
25
n/a
HIGH
25
n/a
n/a
n/a
F8
2
n/a
n/a
(MHz)
(%)
(cm)
F4
2
100
10MHz
100
13MHz
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
5.6
2.0
21
109
(mW)
(MPa)
BIspta
Bp
3.2
3.8
16
60
Mode
lP
Triplex Velocity Range
Flow Filter
Flow Scan Area
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Doppler Velocity Range
Doppler Image Select
Doppler Frequency Select
Doppler Focus
B/W Scan Area
Color Image Select
B/W Focus
B/W-Range
B/W Line Density
pIob
Ispta
DVA%
B/W Frequency Select
parameter
Maximum power
Acoustic power is controllable by the user.
n/a
n/a
n/a
Yes
0.85
contact
8.5
n/a
5.8
3.5
0.78
0.86
n/a
125
n/a
n/a
n/a
n/a
n/a
12
n/a
n/a
n/a
n/a
n/a
n/a
HIGH
25
n/a
F4
2
100
13MHz
3.1
3.8
15
93
(B+M)p
Linear / Peripheral Vascular, Small parts
16. APPENDIX
UST-5542
n/a
n/a
n/a
Yes
0.85
contact
8.1
n/a
7.7
3.5
5.4
0.90
n/a
125
n/a
n/a
n/a
n/a
n/a
13
n/a
n/a
n/a
n/a
n/a
n/a
HIGH
25
n/a
F8
2
100
10MHz
5.4
2.0
20
111
(B+M)Ispta
n/a
n/a
n/a
Yes
0.85
contact
8.5
n/a
5.8
3.5
0.78
0.86
1002
n/a
n/a
n/a
n/a
n/a
n/a
12
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
F4
2
100
13MHz
0.37
3.8
1.8
77
M
n/a
n/a
n/a
Yes
0.85
contact
6.1
n/a
5.8
3.5
0.89
1.1
1572
n/a
n/a
n/a
n/a
n/a
n/a
12
n/a
F4
10.0
n/a
PENET
6MHz
n/a
n/a
n/a
n/a
n/a
100
n/a
3.2
2.7
16
385
Dp
n/a
n/a
n/a
Yes
0.85
contact
6.1
n/a
5.8
3.5
0.89
1.1
3906
n/a
n/a
n/a
n/a
n/a
n/a
12
n/a
F4
24.9
n/a
PENET
6MHz
n/a
n/a
n/a
n/a
n/a
100
n/a
3.8
1.8
19
459
DIspta
n/a
n/a
n/a
Yes
0.85
contact
6.1
n/a
5.8
3.5
0.89
1.1
1572
n/a
n/a
n/a
n/a
n/a
n/a
12
10.0
n/a
n/a
F4
PENET
6MHz
n/a
n/a
n/a
n/a
2
100
n/a
2.7
3.0
13
324
Mflowp
n/a
n/a
n/a
Yes
0.85
contact
6.1
n/a
5.8
3.5
0.89
1.1
3125
n/a
n/a
n/a
n/a
n/a
n/a
12
19.9
n/a
n/a
F4
PENET
6MHz
n/a
n/a
n/a
n/a
2
100
n/a
4.0
2.6
20
471
MflowIspta
n/a
n/a
n/a
Yes
0.85
contact
8.5
n/a
5.8
3.5
0.78
0.86
n/a
9.8
n/a
n/a
n/a
n/a
n/a
12
n/a
F4
10.0
n/a
PENET
6MHz
HIGH
25
n/a
F4
2
100
13MHz
2.8
3.4
14
311
(B+D)p
n/a
n/a
n/a
Yes
0.85
contact
6.1
n/a
5.8
3.5
0.89
1.1
n/a
24
n/a
n/a
n/a
n/a
n/a
12
n/a
F4
24.9
n/a
PENET
6MHz
HIGH
25
n/a
F8
2
100
10MHz
3.5
1.8
17
374
(B+D)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
n/a
n/a
n/a
Yes
0.85
contact
8.5
n/a
5.8
3.5
0.78
0.86
n/a
38
MID
HIGH
#5
5
n/a
12
24.9
n/a
n/a
F8
n/a
6MHz
HIGH
25
PENET
F4
8
100
13MHz
4.0
3.1
15
266
n/a
n/a
n/a
Yes
0.85
contact
6.2
n/a
7.7
3.5
5.6
1.1
n/a
38
MID
HIGH
#5
5
n/a
13
24.9
n/a
n/a
F8
n/a
6MHz
HIGH
25
PENET
F8
8
100
10MHz
4.3
1.6
16
271
(B+Bflow)p (B+Bflow)Ispta
n/a
n/a
n/a
Yes
0.85
contact
8.5
n/a
5.8
3.5
0.78
0.86
n/a
16
MID
HIGH
#5
5
HIGH
12
6.2
F4
12.4
F5
PENET
5MHz
HIGH
25
PENET
F4
8
100
13MHz
3.8
3.4
17
297
n/a
n/a
n/a
Yes
0.85
contact
6.1
n/a
5.8
3.5
0.89
1.1
n/a
18
MID
HIGH
#5
5
HIGH
12
6.2
F4
12.4
F8
PENET
6MHz
HIGH
25
PENET
F8
8
100
10MHz
6.6
2.6
29
638
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-35
(mm)
l ts
Inclusive modes
(%)
(mm)
(MHz)
(%)
(Hz)
(mm)
(mm)
(Hz)
(mm)
(mm)
(mm)
(⊥)
(̲)
(⊥)
(̲)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
contact
contact
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
Yes
1.0
4.0
6.6
n/a
136
9.6
1.2
n/a
12
5.8
4.0
6.8
n/a
136
6.0
1.2
n/a
14
0.95
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.8
29
143
100
7.5MHz
F7
2
HIGH
25
n/a
n/a
n/a
11
4.1
20
58
100
10MHz
F4
2
HIGH
25
n/a
n/a
n/a
(mW)
(MPa)
Bp
4.8
Mode
l tt
Acoustic output freeze
Acoustic Initialization fraction
Initialization mode
fawf
Acoustic Power-up fraction
Power-up mode
srr(SRF)
Output beam dimensions
prr(PRF)
lP
wpb6
Triplex Velocity Range
Flow Filter
Flow Scan Area
Color Velocity Range
Color Line Density
Color Average
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
parameter
Maximum power
BIspta
n/a
n/a
12
5.8
1.2
n/a
125
9.6
4.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
14
0.95
1.2
n/a
125
6.0
4.0
6.8
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.8
28
148
100
7.5MHz
F7
2
HIGH
25
n/a
n/a
n/a
11
(B+M)Ispta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
4.1
20
92
100
10MHz
F4
2
HIGH
25
n/a
n/a
n/a
4.7
(B+M)p
Linear / Peripheral Vascular, Small parts
Acoustic power is controllable by the user.
16. APPENDIX
UST-5546
contact
Yes
1.0
n/a
n/a
n/a
4.0
6.8
n/a
n/a
6.0
1.2
1002
14
0.95
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
4.1
2.3
77
100
10MHz
F4
2
n/a
n/a
n/a
n/a
n/a
0.55
Mp
contact
Yes
1.0
n/a
n/a
n/a
4.0
6.2
n/a
n/a
6.0
1.3
1002
14
0.96
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
3.7
3.0
79
100
7.5MHz
F4
2
n/a
n/a
n/a
n/a
n/a
0.73
MIspta
contact
Yes
1.0
n/a
n/a
n/a
4.0
5.1
n/a
n/a
6.0
1.4
3255
13
1.1
n/a
n/a
n/a
n/a
n/a
n/a
n/a
F4
24.9
3.5
52
1086
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
12
Dp
contact
Yes
1.0
n/a
n/a
n/a
4.0
5.1
n/a
n/a
6.0
1.4
5208
13
1.1
n/a
n/a
n/a
n/a
n/a
n/a
n/a
F4
39.8
2.8
53
1107
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
13
DIspta
contact
Yes
1.0
n/a
n/a
n/a
4.0
5.1
n/a
n/a
4.8
1.3
2170
9.9
1.0
n/a
n/a
n/a
n/a
F3
16.6
n/a
n/a
n/a
3.9
45
857
100
n/a
n/a
2
n/a
n/a
n/a
PENET
5MHz
8.6
Mflowp
contact
Yes
1.0
n/a
n/a
n/a
4.0
5.1
n/a
n/a
6.0
1.4
5208
13
1.1
n/a
n/a
n/a
n/a
F4
39.8
n/a
n/a
n/a
2.8
53
1107
100
n/a
n/a
2
n/a
n/a
n/a
PENET
5MHz
13
MflowIspta
contact
Yes
1.0
n/a
n/a
n/a
4.0
6.8
n/a
20
6.0
1.2
n/a
14
0.95
n/a
n/a
n/a
n/a
n/a
n/a
n/a
F4
24.9
3.7
44
876
100
10MHz
F4
2
HIGH
25
n/a
PENET
5MHz
10
(B+D)p
contact
Yes
1.0
n/a
n/a
n/a
4.0
5.1
n/a
18
6.0
1.4
n/a
13
1.1
n/a
n/a
n/a
n/a
n/a
n/a
n/a
F4
44.3
2.7
44
904
100
7.5MHz
F7
2
HIGH
25
n/a
PENET
5MHz
11
(B+D)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
contact
Yes
1.0
n/a
n/a
n/a
4.0
6.8
n/a
24
6.0
1.2
n/a
14
0.95
5
n/a
HIGH
#5
F8
33.2
MID
n/a
n/a
3.6
56
834
100
10MHz
F4
2
HIGH
25
PENET
n/a
5MHz
21
contact
Yes
1.0
n/a
n/a
n/a
4.0
5.1
n/a
26
9.6
1.6
n/a
17
6.5
5
n/a
HIGH
#5
F8
19.9
MID
n/a
n/a
2.2
58
859
100
7.5MHz
F7
2
HIGH
25
PENET
n/a
5MHz
22
(B+Bflow)p (B+Bflow)Ispta
contact
Yes
1.0
n/a
n/a
n/a
4.0
6.8
n/a
12
6.0
1.2
n/a
14
0.95
5
HIGH
HIGH
#5
F8
10.0
MID
F5
19.9
3.7
73
1235
100
10MHz
F4
2
HIGH
25
PENET
PENET
5MHz
24
contact
Yes
1.0
n/a
n/a
n/a
4.0
5.1
n/a
12
7.2
1.8
n/a
18
1.2
5
HIGH
HIGH
#5
F8
10.0
MID
F5
19.9
3.1
74
1241
100
7.5MHz
F7
2
HIGH
25
PENET
PENET
5MHz
24
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-36
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
parameter
Maximum power
100
7.5MHz
F8
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
22
13
1.2
n/a
85
19
6.0
6.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
100
10MHz
F3
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
1.4
1.1
n/a
85
7.2
6.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
29
2.5
25
169
(mW)
(MPa)
BIspta
Bp
7.0
3.5
16
46
Mode
Acoustic power is controllable by the user.
Linear / Small parts
16. APPENDIX
UST-5710-7.5
100
10MHz
F3
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
1.4
1.1
1002
n/a
7.2
6.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
0.81
3.5
1.9
66
Mp
100
6MHz
F3
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
19
1.7
1.2
1002
n/a
7.2
6.0
5.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.2
3.4
2.8
79
MIspta
(Mflow)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F3
19.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
1.4
1.4
2604
n/a
7.2
6.0
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
18
3.4
42
1195
Dp
(Mflow)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F3
39.8
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
1.4
1.4
5208
n/a
7.2
6.0
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
20
2.5
46
1310
DIspta
100
10MHz
F3
3
HIGH
25
n/a
PENET
5MHz
F3
19.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
1.4
1.1
n/a
8.1
7.2
6.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
15
3.5
35
961
(B+D)p
100
7.5MHz
F8
3
HIGH
25
n/a
PENET
5MHz
F3
24.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
1.4
1.4
n/a
10
7.2
6.0
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
19
3.2
40
1063
(B+D)Ispta
100
10MHz
F3
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F8
33.2
MID
HIGH
#5
5
n/a
20
1.4
1.1
n/a
15
7.2
6.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
45
3.0
41
1210
100
7.5MHz
F8
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F8
33.2
MID
HIGH
#5
5
n/a
22
13
1.4
n/a
15
19
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
48
2.1
42
1226
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
100
10MHz
F3
3
HIGH
25
PENET
PENET
5MHz
F6
19.9
F8
10.0
MID
HIGH
#5
5
HIGH
20
1.4
1.1
n/a
8.1
7.2
6.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
72
3.5
74
1629
98
7.5MHz
F8
3
HIGH
25
PENET
PENET
5MHz
F5
19.9
F8
10.0
MID
HIGH
#5
5
HIGH
22
13
1.4
n/a
8.1
19
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
65
2.7
72
1806
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
1.4
1.1
1002
n/a
7.2
6.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
22
13
1.2
n/a
85
19
6.0
6.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
(̲)
(⊥)
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(Hz)
(Hz)
(mm)
(mm)
prr(PRF)
srr(SRF)
Output beam dimensions
(mm)
(̲)
(⊥)
wpb6
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
1.4
1.1
n/a
85
7.2
6.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
100
7.5MHz
F8
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
100
10MHz
F3
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
Mp
(mW)
(MPa)
100
10MHz
F3
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
0.81
3.5
1.9
66
29
2.5
25
169
Bp
7.0
3.5
16
46
Mode
16. APPENDIX
16-37
lP
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
parameter
Maximum power
BIspta
5.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.7
1.2
1002
n/a
7.2
6.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
19
100
6MHz
F3
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.2
3.4
2.8
79
MIspta
Dp
18
3.4
42
1195
(Mflow)
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
1.4
2604
n/a
7.2
6.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F3
19.9
Linear / Intraoperative, Small parts, Peripheral Vascular
Acoustic power is controllable by the user.
UST-579T-7.5
(Mflow)
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
1.4
5208
n/a
7.2
6.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F3
39.8
20
2.5
46
1310
DIspta
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
1.1
n/a
8.1
7.2
6.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
100
10MHz
F3
3
HIGH
25
n/a
PENET
5MHz
F3
19.9
15
3.5
35
961
(B+D)p
5.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
1.4
n/a
10
7.2
6.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
100
7.5MHz
F8
3
HIGH
25
n/a
PENET
5MHz
F3
24.9
19
3.2
40
1063
(B+D)Ispta
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
1.1
n/a
15
7.2
6.0
F8
33.2
MID
HIGH
#5
5
n/a
20
100
10MHz
F3
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
45
3.0
41
1210
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
13
1.4
n/a
15
19
6.0
F8
33.2
MID
HIGH
#5
5
n/a
22
100
7.5MHz
F8
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
48
2.1
42
1226
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
1.1
n/a
8.1
7.2
6.0
F8
10.0
MID
HIGH
#5
5
HIGH
20
100
10MHz
F3
3
HIGH
25
PENET
PENET
5MHz
F6
19.9
72
3.5
74
1629
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
13
1.4
n/a
8.1
19
6.0
F8
10.0
MID
HIGH
#5
5
HIGH
22
98
7.5MHz
F8
3
HIGH
25
PENET
PENET
5MHz
F5
19.9
65
2.7
72
1806
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-38
(mm)
(mm)
(mm)
(mm)
l ts
Inclusive modes
(%)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(⊥)
(̲)
(%)
contact
contact
2.5
n/a
71
7.0
5.5
4.6
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
28
6.3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
2.6
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
2.3
n/a
71
5.7
5.5
4.8
n/a
n/a
n/a
n/a
Yes
1.0
100
5MHz
F7
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
100
6MHz
F4
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
8.9
1.3
23
23
(mW)
(MPa)
BIspta
Bp
6.3
1.6
20
21
Mode
l tt
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
Acoustic power is controllable by the user.
contact
2.3
n/a
63
5.7
5.5
4.8
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
2.6
100
6MHz
F4
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
6.1
1.6
20
32
(B+M)p
Convex / Endorectal, Endovaginal
16. APPENDIX
UST-670P-5
contact
2.3
n/a
63
4.8
5.5
4.7
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
2.4
100
5MHz
F3
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
6.2
1.6
23
34
(B+M)Ispta
contact
2.3
1002
n/a
5.7
5.5
4.8
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
2.6
100
6MHz
F4
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.1
1.6
3.4
28
Mp
contact
2.3
1002
n/a
4.8
5.5
4.7
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
2.4
100
5MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.1
1.6
4.0
29
MIspta
contact
(Mflow)
(B+D)
3.9
2170
n/a
3.1
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
8.6
1.4
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F1
16.6
9.7
2.5
57
338
Dp
contact
(Mflow)
(B+D)
2.3
3255
n/a
5.7
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
2.6
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
24.9
19
2.0
59
483
DIspta
contact
3.9
n/a
12
3.1
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
F1
24.9
MID
HIGH
#5
5
n/a
8.6
1.4
100
5MHz
F7
15
HIGH
25
PENET
n/a
5MHz
n/a
n/a
12
2.5
65
216
contact
2.5
n/a
15
7.0
5.5
5.7
n/a
n/a
n/a
n/a
Yes
1.0
F6
24.9
MID
HIGH
#5
5
n/a
15
5.4
100
5MHz
F7
4
HIGH
25
PENET
n/a
6MHz
n/a
n/a
16
1.9
41
382
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
contact
3.9
n/a
6.8
3.1
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
F1
6.2
MID
HIGH
#5
5
HIGH
8.6
1.4
100
5MHz
F7
4
HIGH
25
PENET
PENET
5MHz
F4
12.4
19
2.5
76
443
contact
2.3
n/a
9.2
5.7
5.5
4.9
n/a
n/a
n/a
n/a
Yes
1.0
F4
10.0
MID
HIGH
#5
5
HIGH
26
2.6
100
5MHz
F7
4
HIGH
25
PENET
PENET
5MHz
F4
19.9
32
2.2
102
673
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
2.6
2.3
n/a
63
5.7
5.5
4.8
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
28
6.3
2.5
n/a
71
7.0
5.5
4.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
(̲)
(⊥)
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(Hz)
(Hz)
(mm)
(mm)
prr(PRF)
srr(SRF)
Output beam dimensions
(mm)
(̲)
(⊥)
wpb6
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
4.8
n/a
n/a
n/a
n/a
Yes
1.0
contact
2.6
2.3
n/a
71
5.7
5.5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
100
5MHz
F7
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
100
6MHz
F4
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
100
6MHz
F4
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
6.1
1.6
20
32
(mW)
(MPa)
(B+M)p
8.9
1.3
23
23
Bp
6.3
1.6
20
21
Mode
16. APPENDIX
16-39
lP
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
parameter
Maximum power
BIspta
4.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
2.4
2.3
n/a
63
4.8
5.5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
100
5MHz
F3
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
6.2
1.6
23
34
(B+M)Ispta
Convex / Endorectal, Bi-plane, Intraoperative
Acoustic power is controllable by the user.
UST-672-5/7.5 (C)
4.8
n/a
n/a
n/a
n/a
Yes
1.0
contact
2.6
2.3
1002
n/a
5.7
5.5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
23
100
6MHz
F4
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.1
1.6
3.4
28
Mp
4.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
2.4
2.3
1002
n/a
4.8
5.5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
100
5MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.1
1.6
4.0
29
MIspta
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
(Mflow)
(B+D)
(Mflow)
(B+D)
2.6
2.3
3255
n/a
5.7
5.5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
24.9
19
2.0
59
483
DIspta
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
3.9
2170
n/a
3.1
5.5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
8.6
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F1
16.6
9.7
2.5
57
338
Dp
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
3.9
n/a
12
3.1
5.5
F1
24.9
MID
HIGH
#5
5
n/a
8.6
100
5MHz
F7
15
HIGH
25
PENET
n/a
5MHz
n/a
n/a
12
2.5
65
216
5.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
5.4
2.5
n/a
15
7.0
5.5
F6
24.9
MID
HIGH
#5
5
n/a
15
100
5MHz
F7
4
HIGH
25
PENET
n/a
6MHz
n/a
n/a
16
1.9
41
382
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.4
3.9
n/a
6.8
3.1
5.5
F1
6.2
MID
HIGH
#5
5
HIGH
8.6
100
5MHz
F7
4
HIGH
25
PENET
PENET
5MHz
F4
12.4
19
2.5
76
443
4.9
n/a
n/a
n/a
n/a
Yes
1.0
contact
2.6
2.3
n/a
9.2
5.7
5.5
F4
10.0
MID
HIGH
#5
5
HIGH
26
100
5MHz
F7
4
HIGH
25
PENET
PENET
5MHz
F4
19.9
32
2.2
102
673
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-40
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
parameter
Maximum power
100
5MHz
F6
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
42
1.8
2.8
n/a
85
14
6.0
5.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
100
6MHz
F4
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
28
1.2
2.0
n/a
85
9.6
6.0
5.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
14
2.0
17
32
Bp
8.8
2.5
15
30
Mode
BIspta
100
6MHz
F4
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
28
1.2
2.0
n/a
71
9.6
6.0
5.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
7.9
2.5
14
49
(B+M)
100
6MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
28
1.2
2.0
1002
n/a
9.6
6.0
5.7
n/a
n/a
n/a
n/a
Yes
1.0
contact
1.0
2.5
1.8
48
M
Convex / Endorectal, Bi-plane, Intraoperative
Acoustic power is controllable by the user.
UST-672-5/7.5 (L)
16. APPENDIX
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F5
33.2
n/a
n/a
n/a
n/a
n/a
n/a
n/a
36
1.3
2.4
4340
n/a
12
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
(Mflow)
(B+D)
(Mflow)
(B+D)
40
2.3
55
1575
DIspta
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
19.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
28
1.3
2.0
2604
n/a
9.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
26
2.8
45
1264
Dp
100
5MHz
F6
15
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F4
24.9
MID
HIGH
#5
5
n/a
28
1.3
2.0
n/a
30
9.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
22
2.7
38
377
100
5MHz
F6
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F5
33.2
MID
HIGH
#5
5
n/a
36
1.3
2.4
n/a
15
12
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
31
2.2
42
443
(B+Bflow)p (B+Bflow)Ispta
100
5MHz
F6
3
HIGH
25
PENET
PENET
5MHz
F5
19.9
F4
10.0
MID
HIGH
#5
5
HIGH
28
1.3
2.0
n/a
8.1
9.6
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
52
2.8
78
1614
100
5MHz
F6
3
HIGH
25
PENET
PENET
5MHz
F5
19.9
F5
10.0
MID
HIGH
#5
5
HIGH
36
1.3
2.4
n/a
8.1
12
6.0
5.1
n/a
n/a
n/a
n/a
Yes
1.0
contact
56
2.6
78
1636
(B+Bflow+D)p (B+Bflow+D)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
MN1-5099 Rev.0
16-3. Acoustic Output Tables
4.7
n/a
n/a
n/a
n/a
Yes
0.97
contact
(B+M)
1.6
2.6
1002
n/a
6.2
5.7
5.5
n/a
n/a
n/a
n/a
Yes
0.97
contact
(B+M)
3.0
2.2
n/a
134
7.0
5.7
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
(̲)
(⊥)
4.6
n/a
n/a
n/a
n/a
Yes
0.97
contact
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(Hz)
(Hz)
(mm)
(mm)
prr(PRF)
srr(SRF)
Output beam dimensions
(mm)
(̲)
(⊥)
wpb6
(%)
5.5
n/a
n/a
n/a
n/a
Yes
0.97
contact
1.6
2.6
n/a
134
6.2
5.7
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
100
6MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.7
2.5
1002
n/a
6.2
5.7
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
100
5MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.4
2.4
4.0
58
100
5MHz
F5
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
MIspta
100
6MHz
F4
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
Mp
11
2.5
31
27
(mW)
(MPa)
1.3
2.5
3.6
54
14
2.2
35
33
Bp
Mode
16. APPENDIX
16-41
lP
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
parameter
Maximum power
BIspta
Convex / Endorectal, Endovaginal
Acoustic power is controllable by the user.
UST-676P
(B+D)
5.9
n/a
n/a
n/a
n/a
Yes
0.97
contact
1.6
2.4
977
n/a
6.2
5.7
n/a
n/a
n/a
n/a
n/a
n/a
n/a
22
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
6MHz
F4
6.2
6.9
3.2
20
318
Dp
(B+D)
4.9
n/a
n/a
n/a
n/a
Yes
0.97
contact
1.8
2.0
1310
n/a
6.2
5.7
n/a
n/a
n/a
n/a
n/a
n/a
n/a
25
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
10.0
11
2.6
31
420
DIspta
4.9
n/a
n/a
n/a
n/a
Yes
0.97
contact
1.8
2.0
1310
n/a
6.2
5.7
F4
10.0
n/a
n/a
n/a
n/a
n/a
25
100
n/a
n/a
3
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
12
2.7
33
449
Mflow
5.9
n/a
n/a
n/a
n/a
Yes
0.97
contact
1.6
2.4
n/a
27
6.2
5.7
F4
19.9
MID
HIGH
#5
5
n/a
22
100
5MHz
F5
17
HIGH
25
PENET
n/a
6MHz
n/a
n/a
7.3
2.2
20
77
4.9
n/a
n/a
n/a
n/a
Yes
0.97
contact
1.8
2.0
n/a
24
6.2
5.7
F4
33.2
MID
HIGH
#5
5
n/a
25
100
5MHz
F5
3
HIGH
25
PENET
n/a
5MHz
n/a
n/a
10
1.6
28
98
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
5.9
n/a
n/a
n/a
n/a
Yes
0.97
contact
1.6
2.4
n/a
10
6.2
5.7
F4
6.2
MID
HIGH
#5
5
HIGH
22
100
5MHz
F5
3
HIGH
25
PENET
PENET
6MHz
F4
12.4
16
2.6
45
464
4.9
n/a
n/a
n/a
n/a
Yes
0.97
contact
1.8
2.0
n/a
9.3
6.2
5.7
F4
6.2
MID
HIGH
#5
5
HIGH
25
100
5MHz
F5
3
HIGH
25
PENET
PENET
5MHz
F4
12.4
21
2.3
59
521
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-42
(mm)
(mm)
(mm)
(mm)
l ts
Inclusive modes
(%)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(⊥)
(̲)
(%)
contact
contact
2.6
n/a
82
13
8.0
6.0
n/a
n/a
n/a
n/a
Yes
0.90
n/a
n/a
n/a
n/a
n/a
n/a
n/a
25
8.4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
1.1
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
2.5
n/a
82
9.6
8.0
5.4
n/a
n/a
n/a
n/a
Yes
0.90
100
6MHz
F7
2
HIGH
25
n/a
n/a
n/a
n/a
n/a
100
6MHz
F2
2
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
26
1.9
25
75
16
3.1
21
43
(mW)
(MPa)
BIspta
Bp
Mode
l tt
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
Acoustic power is controllable by the user.
Convex / Abdominal, Pediatric
16. APPENDIX
UST-9101-7.5
contact
(B+M)
2.5
1002
n/a
9.6
8.0
5.4
n/a
n/a
n/a
n/a
Yes
0.90
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
1.1
100
6MHz
F2
2
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.9
3.1
2.4
93
Mp
contact
(B+M)
2.5
1002
n/a
9.6
8.0
5.2
n/a
n/a
n/a
n/a
Yes
0.90
n/a
n/a
n/a
n/a
n/a
n/a
n/a
27
1.2
100
5MHz
F2
2
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.9
3.0
2.5
96
MIspta
contact
(B+D)
2.2
2170
n/a
9.6
8.0
5.0
n/a
n/a
n/a
n/a
Yes
0.90
n/a
n/a
n/a
n/a
n/a
n/a
n/a
27
1.2
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F2
16.6
17
3.0
23
867
Dp
contact
(B+D)
2.3
4340
n/a
13
8.0
5.0
n/a
n/a
n/a
n/a
Yes
0.90
n/a
n/a
n/a
n/a
n/a
n/a
n/a
39
1.4
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F3
33.2
24
2.1
24
939
DIspta
contact
2.2
2170
n/a
9.6
8.0
5.0
n/a
n/a
n/a
n/a
Yes
0.90
F2
16.6
n/a
n/a
n/a
n/a
n/a
27
1.2
100
n/a
n/a
2
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
22
3.3
28
1094
Mflowp
contact
2.2
3255
n/a
9.6
8.0
5.0
n/a
n/a
n/a
n/a
Yes
0.90
F2
24.9
n/a
n/a
n/a
n/a
n/a
27
1.2
100
n/a
n/a
2
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
24
2.8
31
1195
MflowIspta
contact
2.2
n/a
30
9.6
8.0
5.0
n/a
n/a
n/a
n/a
Yes
0.90
F2
24.9
MID
HIGH
#5
5
n/a
27
1.2
100
6MHz
F8
15
HIGH
25
PENET
n/a
5MHz
n/a
n/a
22
3.1
28
276
contact
2.2
n/a
15
13
8.0
5.0
n/a
n/a
n/a
n/a
Yes
0.90
F8
33.2
MID
HIGH
#5
5
n/a
34
8.6
100
6MHz
F8
2
HIGH
25
PENET
n/a
5MHz
n/a
n/a
35
1.6
34
480
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
contact
2.2
n/a
11
9.6
8.0
5.0
n/a
n/a
n/a
n/a
Yes
0.90
F8
6.2
MID
HIGH
#5
5
HIGH
27
1.2
100
6MHz
F8
8
HIGH
25
PENET
PENET
5MHz
F2
12.4
31
3.0
34
901
contact
2.3
n/a
14
13
8.0
5.0
n/a
n/a
n/a
n/a
Yes
0.90
F8
10.0
MID
HIGH
#5
5
HIGH
39
1.4
100
6MHz
F8
8
HIGH
25
PENET
PENET
5MHz
F3
19.9
44
2.6
43
1201
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-43
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
100
6MHz
F6
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
27
10
2.0
n/a
104
13
8.0
5.0
n/a
n/a
n/a
n/a
Yes
1.1
contact
(B+M)
14
2.1
20
45
100
5MHz
F3
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
36
2.9
2.2
n/a
104
8.8
8.0
4.4
n/a
n/a
n/a
n/a
Yes
1.1
contact
(B+M)
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
17
1.6
16
77
Bp
Mode
16. APPENDIX
parameter
Maximum power
BIspta
100
5MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
36
2.9
2.2
1002
n/a
8.8
8.0
4.4
n/a
n/a
n/a
n/a
Yes
1.1
contact
2.3
2.1
3.3
52
Mp
1.5
2.0
3.4
54
MIspta
100
5MHz
F2
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
2.1
2.0
1002
n/a
5.6
8.0
4.6
n/a
n/a
n/a
n/a
Yes
1.1
contact
Convex / Intraoperative, Neonatal Cephalic
Acoustic power is controllable by the user.
UST-9104-5
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
6MHz
F3
16.6
n/a
n/a
n/a
n/a
n/a
n/a
n/a
35
2.7
1.8
2604
n/a
8.8
8.0
5.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
(B+D)
12
2.1
18
392
Dp
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F3
39.8
n/a
n/a
n/a
n/a
n/a
n/a
n/a
38
2.6
2.1
5208
n/a
8.8
8.0
4.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
(B+D)
25
1.7
35
635
DIspta
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
F3
16.6
n/a
n/a
n/a
n/a
n/a
38
2.6
2.1
2170
n/a
8.8
8.0
4.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
22
2.3
31
546
Mflowp
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
F3
39.8
n/a
n/a
n/a
n/a
n/a
38
2.6
2.1
5208
n/a
8.8
8.0
4.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
25
1.7
35
635
MflowIspta
100
6MHz
F6
17
HIGH
25
PENET
n/a
6MHz
n/a
n/a
F3
19.9
MID
HIGH
#5
5
n/a
35
2.7
1.8
n/a
17
8.8
8.0
5.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
15
2.4
21
299
100
6MHz
F6
4
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
F8
6.2
MID
HIGH
#5
5
n/a
32
10
2.3
n/a
22
13
8.0
3.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
38
1.3
37
693
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
100
6MHz
F6
4
HIGH
25
PENET
PENET
6MHz
F3
12.4
F6
6.2
MID
HIGH
#5
5
HIGH
35
2.7
1.8
n/a
12
8.8
8.0
5.8
n/a
n/a
n/a
n/a
Yes
1.1
contact
20
2.1
24
567
100
6MHz
F6
4
HIGH
25
PENET
PENET
5MHz
F2
19.9
F6
10.0
MID
HIGH
#5
5
HIGH
29
2.1
1.9
n/a
14
5.6
8.0
4.9
n/a
n/a
n/a
n/a
Yes
1.1
contact
34
2.1
51
906
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-44
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
(mm)
(mm)
(%)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(%)
(MHz)
(mW/cm )
2
n/a
n/a
n/a
n/a
n/a
n/a
n/a
30
2.5
2.0
1002
n/a
7.7
8.0
4.5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
30
2.5
2.0
n/a
71
7.7
8.0
4.5
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
57
100
5MHz
F6
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
30
100
5MHz
F6
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
Yes
1.0
contact
2.2
2.7
1.7
2.2
16
(mW)
(MPa)
B
10
Mode
Mp
n/a
n/a
n/a
n/a
Yes
1.0
contact
n/a
n/a
n/a
n/a
n/a
n/a
n/a
25
2.1
2.0
1002
n/a
6.3
8.0
4.6
58
100
5MHz
F5
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.2
2.8
1.4
MIspta
Dp
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
2.0
1.9
3255
n/a
6.3
8.0
4.9
705
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F5
24.9
2.4
36
18
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+D)
(B+Bflow+D)
Convex / Endovaginal Gynecological, Fetal
Acoustic power is controllable by the user.
UST-9112-5
16. APPENDIX
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+D)
(B+Bflow+D)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
33
2.3
1.9
7440
n/a
7.7
8.0
4.9
784
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F6
56.9
1.6
37
23
DIspta
n/a
n/a
n/a
n/a
Yes
1.0
contact
F5
16.6
n/a
n/a
n/a
n/a
n/a
26
2.0
1.9
2170
n/a
6.3
8.0
4.9
593
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
2.6
30
15
Mflowp
n/a
n/a
n/a
n/a
Yes
1.0
contact
F6
24.9
n/a
n/a
n/a
n/a
n/a
33
2.3
1.9
3255
n/a
7.7
8.0
4.9
749
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
2.3
35
22
MflowIspta
n/a
n/a
n/a
n/a
Yes
1.0
contact
F5
24.9
MID
HIGH
#5
5
n/a
26
2.0
1.9
n/a
12
6.3
8.0
4.9
248
100
5MHz
F6
17
HIGH
25
PENET
n/a
5MHz
n/a
n/a
2.6
33
17
n/a
n/a
n/a
n/a
Yes
1.0
contact
F5
33.2
MID
HIGH
#5
5
n/a
26
2.0
1.9
n/a
17
6.3
8.0
4.9
297
100
5MHz
F6
4
HIGH
25
PENET
n/a
5MHz
n/a
n/a
2.5
40
20
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-45
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
pIob
100
3.75MHz
F8
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
45
13
3.5
n/a
113
19
10
3.9
n/a
n/a
n/a
n/a
Yes
1.3
contact
26
2.0
17
28
100
5MHz
F3
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
53
2.3
3.6
n/a
113
16
10
4.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
39
1.3
20
55
Bp
Mode
16. APPENDIX
parameter
Maximum power
BIspta
Convex / Puncture, Abdominal
Acoustic power is controllable by the user.
UST-9113P-3.5
n/a
n/a
n/a
n/a
n/a
n/a
n/a
53
2.3
3.6
1000
n/a
16
10
4.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+M)
100
5MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
4.3
2.0
2.8
71
Mp
n/a
n/a
n/a
n/a
n/a
n/a
n/a
53
2.4
3.8
1000
n/a
16
10
3.4
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+M)
100
3MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
4.5
1.7
2.9
73
MIspta
n/a
n/a
n/a
n/a
n/a
n/a
n/a
36
2.1
3.9
1628
n/a
9.6
10
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+D)
(B+Bflow+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F2
16.6
30
2.2
32
723
Dp
n/a
n/a
n/a
n/a
n/a
n/a
n/a
55
2.2
3.6
3255
n/a
16
10
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+D)
(B+Bflow+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F3
33.2
86
2.1
55
1549
DIspta
F2
33.2
n/a
n/a
n/a
n/a
n/a
36
2.1
3.9
3255
n/a
9.6
10
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
51
2.4
53
1204
Mflowp
F3
39.8
n/a
n/a
n/a
n/a
n/a
55
2.2
3.6
3906
n/a
16
10
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
81
2.2
52
1450
MflowIspta
F2
44.3
MID
HIGH
#5
5
n/a
36
2.1
3.9
n/a
26
9.6
10
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
3.75MHz
F8
4
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
56
2.4
54
385
F8
6.2
MID
HIGH
#5
5
n/a
53
12
3.6
n/a
22
19
10
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
3.75MHz
F8
4
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
114
1.4
59
740
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-46
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
(mm)
(mm)
(%)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(%)
(MHz)
(mW/cm 2)
n/a
n/a
n/a
n/a
Yes
0.85
contact
31
100
3.75MHz
F5
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
41
3.2
3.0
n/a
66
10
8.5
3.5
30
100
3.75MHz
F4
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
40
2.6
3.1
n/a
66
10
8.5
3.5
n/a
n/a
n/a
n/a
Yes
0.85
contact
1.8
25
22
BIspta
1.9
25
22
(mW)
(MPa)
Bp
Mode
Acoustic power is controllable by the user.
Convex / Abdominal
16. APPENDIX
UST-9121
n/a
n/a
n/a
n/a
Yes
0.85
contact
(B+M)
67
100
3.75MHz
F4
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
40
2.6
3.1
1000
n/a
10
8.5
3.5
1.9
4.1
3.5
M
n/a
n/a
n/a
n/a
Yes
0.85
contact
(B+D)
544
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F3
10.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
34
2.3
3.3
983
n/a
8.3
8.5
3.7
2.6
33
23
Dp
n/a
n/a
n/a
n/a
Yes
0.85
contact
(B+D)
790
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F4
16.6
n/a
n/a
n/a
n/a
n/a
n/a
n/a
42
2.6
2.8
1628
n/a
10
8.5
3.7
2.3
42
36
DIspta
n/a
n/a
n/a
n/a
Yes
0.85
contact
470
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
F3
16.6
n/a
n/a
n/a
n/a
n/a
34
2.3
3.3
1628
n/a
8.3
8.5
3.7
2.4
29
20
Mflowp
n/a
n/a
n/a
n/a
Yes
0.85
contact
811
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
F4
39.8
n/a
n/a
n/a
n/a
n/a
42
2.6
2.8
3906
n/a
10
8.5
3.7
1.9
43
38
MflowIspta
n/a
n/a
n/a
n/a
Yes
0.85
contact
205
100
3.75MHz
F5
17
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
F3
33.2
MID
HIGH
#5
5
n/a
34
2.3
3.3
n/a
11
8.3
8.5
3.7
2.2
37
27
n/a
n/a
n/a
n/a
Yes
0.85
contact
252
100
3.75MHz
F5
4
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
F5
6.2
MID
HIGH
#5
5
n/a
42
3.1
2.8
n/a
14
10
8.5
3.7
1.7
40
35
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
n/a
n/a
n/a
n/a
Yes
0.85
contact
870
100
3.75MHz
F5
4
HIGH
25
PENET
PENET
3.75MHz
F4
12.4
F3
6.2
MID
HIGH
#5
5
HIGH
34
2.3
3.3
n/a
4.9
8.3
8.5
3.7
2.6
64
52
n/a
n/a
n/a
n/a
Yes
0.85
contact
899
100
3.75MHz
F5
4
HIGH
25
PENET
PENET
3.75MHz
F4
24.9
F5
12.4
MID
HIGH
#5
5
HIGH
42
2.6
2.8
n/a
7.8
10
8.5
3.7
1.9
62
54
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
n/a
n/a
n/a
n/a
n/a
n/a
n/a
34
49
3.0
45
78
n/a
n/a
n/a
n/a
n/a
n/a
n/a
31
(mW)
(MPa)
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(Hz)
(Hz)
(mm)
(mm)
(̲)
(⊥)
(mm)
(̲)
(⊥)
(%)
(cm/sec)
wpb6
prr(PRF)
srr(SRF)
Output beam dimensions
Mp
8.3
3.0
7.5
190
13
2.2
12
263
MIspta
3.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.0
3.3
n/a
93
11
10
n/a
n/a
n/a
n/a
n/a
n/a
n/a
33
2.3
3.3
1002
n/a
11
10
2.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+M)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
31
2.0
3.3
1000
n/a
11
10
3.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+M)
12
3.1
n/a
93
16
10
3.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
(mW/cm 2)
(mW/cm 2)
(%)
100
100
100
100
(MHz) THE3.0MHz THE3.0MHz THE3.0MHz THE2.5MHz
F2
F7
F2
F2
(cm)
4
4
4
4
HIGH
HIGH
n/a
n/a
(%)
25
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
(MHz)
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
(cm/sec)
n/a
n/a
n/a
n/a
76
1.9
48
127
Bp
Mode
16. APPENDIX
16-47
lP
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
parameter
Maximum power
BIspta
Convex / Abdominal, Gynecological, Fetal
Acoustic power is controllable by the user.
UST-9123
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
1.8
3.0
610
n/a
11
10
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
1.8
3.0
1628
n/a
11
10
n/a
n/a
n/a
n/a
n/a
n/a
n/a
34
78
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F2
16.6
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F2
6.2
n/a
n/a
n/a
n/a
n/a
n/a
n/a
34
56
3.0
51
1680
DIspta
36
3.8
33
1079
Dp
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
1.8
3.0
2441
n/a
11
10
F2
24.9
n/a
n/a
n/a
n/a
n/a
34
98
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
56
3.0
51
1661
Mflowp
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.4
3.5
9766
n/a
16
10
F3
99.6
n/a
n/a
n/a
n/a
n/a
53
93
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
100
1.7
62
1717
MflowIspta
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
1.8
3.0
n/a
6.1
11
10
n/a
n/a
n/a
n/a
n/a
n/a
n/a
34
100
THE3.0MHz
F7
4
HIGH
25
n/a
PENET
3.75MHz
F2
10.0
52
3.8
46
1398
(B+D)p
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
1.8
3.0
n/a
16
11
10
n/a
n/a
n/a
n/a
n/a
n/a
n/a
34
95
THE3.0MHz
F4
4
HIGH
25
n/a
PENET
3.75MHz
F2
132.8
58
1.5
52
1689
(B+D)Ispta
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
1.8
3.0
n/a
34
11
10
F2
6.2
MID
HIGH
#5
5
n/a
34
100
THE3.0MHz
F7
24
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
61
3.1
54
487
(B+Bflow)p
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
11
2.8
n/a
21
16
10
F7
6.2
MID
HIGH
#5
5
n/a
39
100
THE3.0MHz
F7
4
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
106
1.8
66
972
(B+Bflow)Ispta
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
1.8
3.0
n/a
2.7
11
10
F2
6.2
MID
HIGH
#5
5
HIGH
34
100
5MHz
F1
4
HIGH
25
PENET
PENET
3.75MHz
F3
12.4
101
3.8
69
1387
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
1.8
3.0
n/a
3.5
11
10
F8
12.4
MID
HIGH
#5
5
HIGH
34
84
3.75MHz
F7
4
HIGH
25
PENET
PENET
3.75MHz
F2
24.9
70
2.7
59
1709
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-48
(mm)
(mm)
(mm)
(mm)
l ts
Inclusive modes
(%)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(⊥)
(̲)
(%)
contact
contact
2.2
n/a
134
7.0
5.7
4.6
n/a
n/a
n/a
n/a
Yes
0.97
n/a
n/a
n/a
n/a
n/a
n/a
n/a
24
3.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
1.6
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
2.6
n/a
134
6.2
5.7
5.5
n/a
n/a
n/a
n/a
Yes
0.97
100
5MHz
F5
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
100
6MHz
F4
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
11
2.0
28
26
(mW)
(MPa)
BIspta
Bp
8.7
2.2
25
22
Mode
l tt
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
Acoustic power is controllable by the user.
contact
(B+M)
2.6
1002
n/a
6.2
5.7
5.5
n/a
n/a
n/a
n/a
Yes
0.97
n/a
n/a
n/a
n/a
n/a
n/a
n/a
20
1.6
100
6MHz
F4
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
1.0
2.2
2.9
43
Mp
1.1
2.1
3.2
46
MIspta
contact
(B+M)
2.5
1002
n/a
6.2
5.7
4.7
n/a
n/a
n/a
n/a
Yes
0.97
n/a
n/a
n/a
n/a
n/a
n/a
n/a
21
1.7
100
5MHz
F4
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
Convex / Endovaginal Gynecological, Fetal
16. APPENDIX
UST-9124
contact
(B+D)
2.4
1572
n/a
6.2
5.7
5.9
n/a
n/a
n/a
n/a
Yes
0.97
n/a
n/a
n/a
n/a
n/a
n/a
n/a
22
1.6
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
6MHz
F4
10.0
7.0
2.6
20
320
Dp
contact
(B+D)
2.0
2170
n/a
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
0.97
n/a
n/a
n/a
n/a
n/a
n/a
n/a
25
1.8
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F4
16.6
11
2.1
32
440
DIspta
contact
2.4
2604
n/a
6.2
5.7
5.9
n/a
n/a
n/a
n/a
Yes
0.97
F4
16.6
n/a
n/a
n/a
n/a
n/a
22
1.6
100
n/a
n/a
4
n/a
n/a
n/a
PENET
6MHz
n/a
n/a
10
2.5
29
467
Mflowp
contact
2.0
4340
n/a
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
0.97
F4
33.2
n/a
n/a
n/a
n/a
n/a
25
1.8
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
13
1.6
37
512
MflowIspta
contact
2.4
n/a
27
6.2
5.7
5.9
n/a
n/a
n/a
n/a
Yes
0.97
F4
19.9
MID
HIGH
#5
5
n/a
22
1.6
100
5MHz
F5
17
HIGH
25
PENET
n/a
6MHz
n/a
n/a
8.7
2.4
25
93
contact
2.0
n/a
24
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
0.97
F4
33.2
MID
HIGH
#5
5
n/a
25
1.8
100
5MHz
F5
4
HIGH
25
PENET
n/a
5MHz
n/a
n/a
13
1.7
35
123
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
contact
2.4
n/a
10
6.2
5.7
5.9
n/a
n/a
n/a
n/a
Yes
0.97
F4
6.2
MID
HIGH
#5
5
HIGH
22
1.6
100
5MHz
F5
4
HIGH
25
PENET
PENET
6MHz
F4
12.4
17
2.6
47
484
contact
2.0
n/a
12
6.2
5.7
4.9
n/a
n/a
n/a
n/a
Yes
0.97
F4
10.0
MID
HIGH
#5
5
HIGH
25
1.8
100
5MHz
F5
4
HIGH
25
PENET
PENET
5MHz
F4
19.9
20
1.9
57
526
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
3.4
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+M)
2.3
3.6
1000
n/a
16
10
4.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+M)
13
3.5
n/a
113
19
10
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
(̲)
(⊥)
3.9
n/a
n/a
n/a
n/a
Yes
1.3
contact
(mm)
(mm)
(%)
(MHz)
(%)
(mm)
(mm)
(Hz)
(Hz)
(mm)
(mm)
prr(PRF)
srr(SRF)
Output beam dimensions
(mm)
(̲)
(⊥)
wpb6
(%)
4.0
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.3
3.6
n/a
113
16
10
n/a
n/a
n/a
n/a
n/a
n/a
n/a
53
n/a
n/a
n/a
n/a
n/a
n/a
n/a
45
n/a
n/a
n/a
n/a
n/a
n/a
n/a
53
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
100
5MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
2.4
3.8
1000
n/a
16
10
n/a
n/a
n/a
n/a
n/a
n/a
n/a
53
100
3MHz
F3
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
4.5
1.7
2.9
73
100
3.75MHz
F8
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
MIspta
100
5MHz
F3
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
Mp
26
2.0
17
28
(mW)
(MPa)
4.3
2.0
2.8
71
39
1.3
20
55
Bp
Mode
16. APPENDIX
16-49
lP
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
parameter
Maximum power
BIspta
Convex / Abdominal, Gynecological, Fetal
Acoustic power is controllable by the user.
UST-979-3.5
(B+D)
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.1
3.9
1628
n/a
9.6
10
n/a
n/a
n/a
n/a
n/a
n/a
n/a
36
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F2
16.6
20
2.2
21
477
Dp
(B+D)
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.2
3.6
3906
n/a
16
10
n/a
n/a
n/a
n/a
n/a
n/a
n/a
55
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F3
39.8
60
2.0
38
1080
DIspta
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.1
3.9
1628
n/a
9.6
10
F2
16.6
n/a
n/a
n/a
n/a
n/a
36
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
25
2.5
26
602
Mflowp
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.2
3.6
3255
n/a
16
10
F3
33.2
n/a
n/a
n/a
n/a
n/a
55
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
73
2.3
47
1300
MflowIspta
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.1
3.9
n/a
36
9.6
10
F2
6.2
MID
HIGH
#5
5
n/a
36
100
3.75MHz
F8
24
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
42
2.5
41
289
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
12
3.6
n/a
22
19
10
F8
6.2
MID
HIGH
#5
5
n/a
53
100
3.75MHz
F8
4
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
93
1.3
49
605
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.1
3.9
n/a
13
9.6
10
F2
12.4
MID
HIGH
#5
5
HIGH
36
100
3.75MHz
F8
4
HIGH
25
PENET
PENET
3.75MHz
F3
24.9
71
2.2
54
1010
3.7
n/a
n/a
n/a
n/a
Yes
1.3
contact
2.2
3.6
n/a
13
16
10
F8
12.4
MID
HIGH
#5
5
HIGH
55
100
3.75MHz
F8
4
HIGH
25
PENET
PENET
3.75MHz
F3
24.9
91
2.2
53
1120
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-50
(mm)
(mm)
(mm)
(mm)
l ts
Inclusive modes
(%)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(⊥)
(̲)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
contact
2.0
n/a
71
7.7
8.0
4.5
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
2.0
1002
n/a
7.7
8.0
4.5
n/a
n/a
n/a
n/a
Yes
1.0
100
5MHz
F6
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
30
2.5
100
5MHz
F6
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
30
2.5
(mW)
(MPa)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
1.7
2.2
2.7
57
B
10
2.2
16
30
Mode
l tt
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
parameter
Maximum power
Mp
contact
(B+M)
2.0
1002
n/a
6.3
8.0
4.6
n/a
n/a
n/a
n/a
Yes
1.0
100
5MHz
F5
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
25
2.1
1.4
2.2
2.8
58
MIspta
Dp
1.9
3255
n/a
6.3
8.0
4.9
n/a
n/a
n/a
n/a
Yes
1.0
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F5
24.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
26
2.0
18
2.4
36
705
contact
(B+D)
(B+Bflow+D)
Convex / Endovaginal Gynecological, Fetal
Acoustic power is controllable by the user.
UST-984-5
16. APPENDIX
contact
(B+D)
(B+Bflow+D)
1.9
7440
n/a
7.7
8.0
4.9
n/a
n/a
n/a
n/a
Yes
1.0
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F6
56.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
33
2.3
23
1.6
37
784
DIspta
contact
1.9
2170
n/a
6.3
8.0
4.9
n/a
n/a
n/a
n/a
Yes
1.0
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
F5
16.6
n/a
n/a
n/a
n/a
n/a
26
2.0
15
2.6
30
593
Mflowp
contact
1.9
3255
n/a
7.7
8.0
4.9
n/a
n/a
n/a
n/a
Yes
1.0
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
F6
24.9
n/a
n/a
n/a
n/a
n/a
33
2.3
22
2.3
35
749
MflowIspta
contact
1.9
n/a
12
6.3
8.0
4.9
n/a
n/a
n/a
n/a
Yes
1.0
100
5MHz
F6
17
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F5
24.9
MID
HIGH
#5
5
n/a
26
2.0
17
2.6
33
248
contact
1.9
n/a
17
6.3
8.0
4.9
n/a
n/a
n/a
n/a
Yes
1.0
100
5MHz
F6
4
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F5
33.2
MID
HIGH
#5
5
n/a
26
2.0
20
2.5
40
297
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-51
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
pIob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
Bp
6.5
2.2
11
21
100
7.5MHz
F4
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
32
1.4
1.9
n/a
128
9.5
6.0
6.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
Mode
8.2
1.6
12
39
100
7.5MHz
F8
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
25
7.3
1.9
n/a
128
11
6.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
16. APPENDIX
parameter
Maximum power
BIspta
0.75
2.2
1.3
32
100
7.5MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
32
1.4
1.9
1002
n/a
9.5
6.0
6.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
Mp
MIspta
0.76
2.1
1.3
33
100
6MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
29
1.4
1.9
1002
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
Convex / Intraoperative, Neonatal Cephalic
Acoustic power is controllable by the user.
UST-987-7.5
5.5
2.3
9.6
291
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
6MHz
F4
10.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
31
1.3
1.8
1572
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+D)
Dp
8.1
1.8
14
429
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
6MHz
F4
24.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
31
1.3
1.8
3906
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+D)
DIspta
6.9
2.5
12
367
100
n/a
n/a
3
n/a
n/a
n/a
PENET
6MHz
n/a
n/a
F4
10.0
n/a
n/a
n/a
n/a
n/a
31
1.3
1.8
1572
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
Mflowp
8.7
2.1
15
464
100
n/a
n/a
3
n/a
n/a
n/a
PENET
6MHz
n/a
n/a
F4
19.9
n/a
n/a
n/a
n/a
n/a
31
1.3
1.8
3125
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
MflowIspta
8.0
1.9
14
143
100
7.5MHz
F8
3
HIGH
25
PENET
n/a
6MHz
n/a
n/a
F4
24.9
MID
HIGH
#5
5
n/a
31
1.3
1.8
n/a
20
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
9.4
1.3
14
202
100
7.5MHz
F8
3
HIGH
25
PENET
n/a
6MHz
n/a
n/a
F7
24.9
MID
HIGH
#5
5
n/a
28
6.5
1.8
n/a
20
11
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
14
2.3
23
516
100
7.5MHz
F8
3
HIGH
25
PENET
PENET
6MHz
F4
12.4
F7
6.2
MID
HIGH
#5
5
HIGH
31
1.3
1.8
n/a
10
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+Bflow+D)
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-52
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
parameter
Maximum power
100
5MHz
F7
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
39
13
2.0
n/a
111
19
10
4.3
n/a
n/a
n/a
n/a
Yes
1.3
contact
100
5MHz
F2
4
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
36
1.8
2.2
n/a
111
9.6
10
4.2
n/a
n/a
n/a
n/a
Yes
1.3
contact
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
37
2.0
19
77
18
2.7
19
33
(mW)
(MPa)
BIspta
Bp
Mode
Acoustic power is controllable by the user.
Dp
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
5MHz
F2
10.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
38
1.7
2.0
1310
n/a
9.6
10
4.8
n/a
n/a
n/a
n/a
Yes
1.3
contact
(B+D)
(B+M)
22
3.4
23
761
100
5MHz
F2
4
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
36
1.8
2.2
1002
n/a
9.6
10
4.2
n/a
n/a
n/a
n/a
Yes
1.3
contact
3.0
2.7
3.2
93
M
Convex / Abdominal, Gynecological, Fetal
16. APPENDIX
UST-990-5
(B+D)
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
3.75MHz
F2
24.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
36
2.0
2.1
2441
n/a
9.6
10
3.8
n/a
n/a
n/a
n/a
Yes
1.3
contact
37
2.9
38
1270
DIspta
100
n/a
n/a
4
n/a
n/a
n/a
PENET
5MHz
n/a
n/a
F2
16.6
n/a
n/a
n/a
n/a
n/a
38
1.7
2.0
2170
n/a
9.6
10
4.8
n/a
n/a
n/a
n/a
Yes
1.3
contact
37
3.4
38
1260
Mflowp
100
n/a
n/a
4
n/a
n/a
n/a
PENET
3.75MHz
n/a
n/a
F2
33.2
n/a
n/a
n/a
n/a
n/a
36
2.0
2.1
3255
n/a
9.6
10
3.8
n/a
n/a
n/a
n/a
Yes
1.3
contact
41
2.6
42
1410
MflowIspta
100
5MHz
F7
19
HIGH
25
PENET
n/a
5MHz
n/a
n/a
F2
19.9
MID
HIGH
#5
5
n/a
38
1.7
2.0
n/a
31
9.6
10
4.8
n/a
n/a
n/a
n/a
Yes
1.3
contact
35
3.4
33
272
100
5MHz
F7
4
HIGH
25
PENET
n/a
3.75MHz
n/a
n/a
F8
6.2
MID
HIGH
#5
5
n/a
44
14
2.2
n/a
22
19
10
3.8
n/a
n/a
n/a
n/a
Yes
1.3
contact
73
1.5
38
745
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
100
5MHz
F7
4
HIGH
25
PENET
PENET
5MHz
F2
12.4
F6
6.2
MID
HIGH
#5
5
HIGH
38
1.7
2.0
n/a
10
9.6
10
4.8
n/a
n/a
n/a
n/a
Yes
1.3
contact
75
3.4
53
1440
100
5MHz
F7
4
HIGH
25
PENET
PENET
3.75MHz
F2
24.9
F8
12.4
MID
HIGH
#5
5
HIGH
36
2.0
2.1
n/a
13
9.6
10
3.8
n/a
n/a
n/a
n/a
Yes
1.3
contact
92
2.9
67
1820
(B+Bflow+D)p (B+Bflow+D)Ispta
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16-53
l tt
l ts
Inclusive modes
fawf
Acoustic Power-up fraction
Power-up mode
Acoustic Initialization fraction
Initialization mode
Acoustic output freeze
prr(PRF)
srr(SRF)
Output beam dimensions
lP
wpb6
Iob
Ispta
DVA%
B/W Frequency Select
B/W Focus
B/W-Range
B/W Line Density
B/W Scan Area
Color Image Select
Doppler Image Select
Doppler Frequency Select
Doppler Focus
Doppler Velocity Range
Flow Focus
Color Velocity Range
Color Line Density
Color Average
Flow Filter
Flow Scan Area
Triplex Velocity Range
p-
100
7.5MHz
F8
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
25
7.3
1.9
n/a
128
11
6.0
6.6
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
100
7.5MHz
F4
3
HIGH
25
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
32
1.4
1.9
n/a
128
9.5
6.0
6.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+M)
(mW)
(MPa)
(mm)
(mm)
(%)
(mm)
(mm)
(mm)
(Hz)
(Hz)
(̲)
(mm)
(⊥) (mm)
(MHz)
(%)
(̲)
(⊥)
(%)
(cm/sec)
(cm/sec)
(MHz)
(%)
(cm)
(mW/cm 2)
(mW/cm 2)
(%)
(MHz)
8.2
1.6
12
39
Bp
6.5
2.2
11
21
Mode
16. APPENDIX
parameter
Maximum power
BIspta
100
7.5MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
32
1.4
1.9
1002
n/a
9.5
6.0
6.4
n/a
n/a
n/a
n/a
Yes
1.0
contact
0.75
2.2
1.3
32
Mp
100
6MHz
F4
3
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
29
1.4
1.9
1002
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
0.76
2.1
1.3
33
MIspta
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
6MHz
F4
10.0
n/a
n/a
n/a
n/a
n/a
n/a
n/a
31
1.3
1.8
1572
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+D)
5.5
2.3
9.6
291
Dp
Convex / Intraoperative, Small parts, Peripheral Vascular
Acoustic power is controllable by the user.
UST-995-7.5
100
n/a
n/a
n/a
n/a
n/a
n/a
PENET
6MHz
F4
24.9
n/a
n/a
n/a
n/a
n/a
n/a
n/a
31
1.3
1.8
3906
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
(B+D)
8.1
1.8
14
429
DIspta
100
n/a
n/a
3
n/a
n/a
n/a
PENET
6MHz
n/a
n/a
F4
10.0
n/a
n/a
n/a
n/a
n/a
31
1.3
1.8
1572
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
6.9
2.5
12
367
Mflowp
100
n/a
n/a
3
n/a
n/a
n/a
PENET
6MHz
n/a
n/a
F4
19.9
n/a
n/a
n/a
n/a
n/a
31
1.3
1.8
3125
n/a
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
8.7
2.1
15
464
MflowIspta
100
7.5MHz
F8
3
HIGH
25
PENET
n/a
6MHz
n/a
n/a
F4
24.9
MID
HIGH
#5
5
n/a
31
1.3
1.8
n/a
20
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
8.0
1.9
14
143
100
7.5MHz
F8
3
HIGH
25
PENET
n/a
6MHz
n/a
n/a
F7
24.9
MID
HIGH
#5
5
n/a
28
6.5
1.8
n/a
20
11
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
9.4
1.3
14
202
(B+Bflow)p (B+Bflow)Ispta
Acoustic output data in accordance with IEC 61157/4.2.2, accompanying literature
100
7.5MHz
F8
3
HIGH
25
PENET
PENET
6MHz
F4
12.4
F7
6.2
MID
HIGH
#5
5
HIGH
31
1.3
1.8
n/a
10
9.5
6.0
6.0
n/a
n/a
n/a
n/a
Yes
1.0
contact
14
2.3
23
516
(B+Bflow+D)
MN1-5099 Rev.0
16-3. Acoustic Output Tables
MN1-5099 Rev.0
16-3. Acoustic Output Tables
16. APPENDIX
16-54
MN1-5099 Rev.0
MN1-5099 Rev.0
MANUFACTURER
ALOKA CO.,LTD.
Aloka Co., Ltd.
22-1, Mure 6-chome, Mitaka-Shi, Tokyo, 181-8622 Japan
Tel: +81-422-45-6049
Fax: +81-422-45-4058
Overseas Offices:
ALOKA GmbH: Authorized EU-representative
Mollsfeld 5, 40670 Meerbusch, Germany
Aloka Co., Ltd. Shanghai Office
Room 824, Jin Jiang Tower, 161, Changle Road.
Shanghai, 200020, P.R. China
Aloka Co., Ltd. Singapore Office
75, Bukit Timah Road, #06-02/03,
Boon Siew Building, Singapore, 229833
Distributor
MN1-5099 Rev.0 '02.10.04