Specification for Syringe Infusion Pump
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Syringe pump should be programmable, user friendly and safe to use.
Demo of equipment is must.
Must accommodate any standard make of syringe 10, 20, 50ml.
Flow rate programmable from 0.1 – 999ml/Hr.
Accuracy of +/- 2 % is required.
Bolus rate should be programmable to 400 – 500 ml/Hr or more with infused volume display.
Save the last bolus rate.
Display of the drug name with provision of memorizing 10 -15 names by operator
Keep vein open option must be available
Selectable occlusion pressure trigger levels selectable from 300/500/900mm Hg +/- 100mm Hg.
Should have automatic detection of syringe size, proper fixing and provide alarm for wrong loading.
Antibolus system to reduce pressure or sudden release of occlusion.
Should have alarm package including,
a. Occlusion limit exceed alarm
b. Near end of infusion prealarm & alarm
c. Volume limit prealarm & alarm
d. Low battery prealarm & alarm
e. AC power failure
f. Drive disengaged
g. Air in line.
Rechargeable battery with a backup time of 5hrs or more.
Power supply of 220-240V AC, 50Hz
Shall meet IEC 60601-1-2:2001 or equivalent BIS general requirements of safety for Electromagnetic
compatibility.
Should operate in ambient temp 5-40 degree and humidity of 10-90% with no condensation and
should be amenable for storage at the same settings
Accessories, spares & consumables such as monitoring devices supplied shall be mentioned.
Should have a light & compact design.
Should have key lock function during infusion.
Should be FDA or CE approved product
Electrical safety conforms to standards for electrical safety IEC- 60601-1 General Requirements.
Manufacturer should be ISO certified for quality standards.
Certified for meeting IEC60601-2-24: Particular requirements for the safety of infusion pumps and
controllers
Should meet IEC 529 Level 3 and 4 (IP3X)(spraying and splashing water) for enclosure protection,
water ingress.
Electrical Safety Classification Class I/II, Type CF and Internally powered equipment.
Certified for meeting IEC 60601-1-4 Medical electrical equipment - Part 1-4: General requirements
for safety - Collateral Standard: Programmable electrical medical systems.
28. Comprehensive warranty for 3 years and provision of AMC for next 5 years.
29. Should have local service facility .The service provider should have the necessary equipments
recommended by the manufacturer to carry out preventive maintenance test as per guidelines
provided in the service/maintenance manual.
30. Certificate of calibration and inspection from factory.
31. List of Equipments available for providing calibration and routine maintenance support as per
manufacturer documentation in service / technical manual.
32. User Manual in English.
33. Service manual in English.
34. Log book with instructions for daily, weekly, monthly and quarterly maintenance checklist. The job
description of the hospital technician and company service engineer should be clearly spelt out.
35. List of important spare parts and accessories with their part number and costing.
36. User list to be provided with performance certificate.
37. Performance report in the last 5 years from major hospitals should be enclosed.