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Government Tender Published for Apheresis Machine (V2) in PONDICHERRY, PUDUCHERRY

Bid Publish Date

18-Dec-2025, 3:58 pm

Bid End Date

15-Jan-2026, 4:00 pm

EMD

₹1,80,000

Location

PONDICHERRY , PUDUCHERRY

Progress

Issue18-Dec-2025, 3:58 pm
AwardPending
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Quantity

1

Bid Type

Two Packet Bid

Categories 1

MACHINE

Public procurement opportunity for Jawaharlal Institute Of Postgraduate Medical Education And Research (jipmer) Apheresis Machine (V2) (Q2) in PONDICHERRY, PUDUCHERRY. Quantity: 1 issued by. Submission Deadline: 15-01-2026 16: 00: 00. View full details and respond.

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL Product Name Apheresis Machine
GENERAL Parameters available in machine Leucodepleted Platelets + Plasma, Therapeutic Plasma Exchange, Peripheral Blood stem cell collection, Red Blood cell exchange, Lymphoplasma exchange, Platelet and white blood cell depletions, Granulocyte Collection, Mononuclear Cell Collection, Bone Marrow Processing
PRODUCT INFORMATION Controller Type Microprocessor Controlled
PRODUCT INFORMATION Display Type LCD/LED
PRODUCT INFORMATION Touch Screen Display Yes, No
PRODUCT INFORMATION Technology Continuous flow with single and double needle
PRODUCT INFORMATION Capable to connect bar code reader if desired Yes Or higher
PRODUCT INFORMATION Inbuilt cuff pressures and prompts grip for donor comfort and adequate blood flow. Yes
PRODUCT INFORMATION Inlet and return flow rates Upto 100 ml/min
PRODUCT INFORMATION Facility to use platelets additive solution and / or normal Saline for re-suspension and storage fluid in place of plasma Yes Or higher
PRODUCT INFORMATION Auto elutriation separation technique to be able to collect platelets Yes
PRODUCT INFORMATION In single needle procedure the equipment should continue to process the whole blood during the return cycle to reduce the procedure time and increase the efficiency Yes
PRODUCT INFORMATION Peripheral blood stem cell (MNC) collection should be fully automatic Yes Or higher
PRODUCT INFORMATION Capable of dong prime with normal Saline and / or mixture or Normal Saline and ACD Yes
PRODUCT INFORMATION Should be able to collect single and / or double needle platelet aphaeresis along with concurrent plasma and / or RBC Yes
PRODUCT INFORMATION Built in data storage capacity Minimum 100 Procedures
PRODUCT INFORMATION Rechargeable battery to store data and restart in case of power failure Yes
PRODUCT INFORMATION Capable of collecting various single donor blood components including peripherals blood stems cells (MNC) Yes
PRODUCT INFORMATION The separation of blood should be able to automatically maintain a constant hematocrit to improve collection efficiency and reduce contaminations Yes
PRODUCT INFORMATION Other Features Yield estimator to help decide yield, Optical sensor at PRP line for online monitoring of component collection against the desired yield, Advance help menu at any time during alarm conditions, Continuous monitoring of collection to avoid any contamination through Interface detector, Programmable Haematocrit and Plasma Volume, Haemolysis monitoring for plasma line, Built in safety features such as access and return pressure sensors, air bubble detectors, Built in automated interface monitoring using CCD camera, Highly Mobile and Transportable, Prints and Exports Data
PRODUCT INFORMATION Extra corporeal volume 200 to 250 ml
PRODUCT INFORMATION Blood Flow Range 5-140 ml/min
ELECTRICAL REQUIREMENTS Power Input 220-240VAC, 50Hz
ELECTRICAL REQUIREMENTS UPS Provided Yes
ELECTRICAL REQUIREMENTS UPS Battery Backup 30 min
WARRANTY Warranty in Years (Option of comprehensive warranty is available through bidding only, which if opted will supersede normal warranty in the catalogue) 2, 3, 5 Or higher
CERTIFICATIONS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS Availability of valid Medical Device license for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules made there under as amended till date Yes
CERTIFICATIONS Certification for manufacturing unit ISO:13485 (Latest)
CERTIFICATIONS Availability of Test Report for each supplied batch/product as per Medical Device Rule (MDR) 2017 as amended till date Yes
CERTIFICATIONS Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission or along with supplies as per buyer requirement Yes
CERTIFICATIONS Electrical Safety IEC 60601-1-2 or Equivalent BIS

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Required Documents

1

Experience Criteria

2

Past Performance

3

Bidder Turnover

4

Certificate (Requested in ATC)

5

OEM Authorization Certificate

6

OEM Annual Turnover

7

Additional Doc 1 (Requested in ATC)

8

Additional Doc 2 (Requested in ATC)

9

Additional Doc 3 (Requested in ATC)

10

Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria

11

the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer