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Invitation to Bid - Blood Bags as per IS 15102 in IMPHAL WEST, MANIPUR

Bid Publish Date

08-Jun-2026, 12:24 pm

Bid End Date

18-Jun-2026, 4:00 pm

EMD

โ‚น1,39,500

Value

โ‚น46,50,000

Progress

Issue08-Jun-2026, 12:24 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

15000

Bid Type

Two Packet Bid

A tender has been published for Regional Institute Of Medical Sciences Imphal Manipur Blood Bags as per IS 15102 (Q2) in IMPHAL WEST, MANIPUR. Quantity: 15000 by. Submission Deadline: 18-06-2026 16: 00: 00. Check eligibility and apply.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Blood Bags as per IS 15102 (Q2)

Authority Records

MINISTRY OF HEALTH AND FAMILY WELFAREHEALTH AND FAMILY WELFARE DEPARTMENT

BID & GeM Expert Consultancy

End-to-end support โ€” bid preparation, GeM registration, document filing & compliance by industry experts.

Bid Preparation GeM Registration Document Filing

Free consultation ยท 24h response

Documents 4

GeM-Bidding-9306218.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Buyer uploaded ATC document

ATC

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL FEATURES Disposable Yes
PRODUCT INFORMATION Conformity to standard for Blood Bag ISO 3826/IS 15102: Latest Revision
PRODUCT INFORMATION Type of blood bag Triple
PRODUCT INFORMATION Capacity of blood Bag 350 ml
PRODUCT INFORMATION Material of Bag (Medical grade) DEHP Plasticized PVC
PRODUCT INFORMATION Flexible pre-sterilized and pyrogen free Yes
PRODUCT INFORMATION Non toxic, non haemolytic, biocompatible material Yes
PRODUCT INFORMATION There should be no risk of contamination and air embolism (closed system) with all leak proof seals (Disposable bags) Yes
PRODUCT INFORMATION Slit on both sides of the bags should be enough to accommodate 5 -10 ml volume test tubes Yes
PRODUCT INFORMATION The capacity of the bag should be enough to prevent any bollooning/ripture of the abg from the seam when it is filled up with the requisite volume of blood Yes
TUBING OF BAG Flexible kink resistant tubing Yes
TUBING OF BAG Non sticking Yes
TUBING OF BAG Transparent Yes
TUBING OF BAG Leak Proof Yes
TUBING OF BAG The tubes should have multiple printed ID/segment numbers Yes
TUBING OF BAG Clamp provided for closed system Yes
NEEDLE Needle Size 16 G
NEEDLE Ultra thin walled and straight to reduce penetration force and enable painless vein puncture Yes
NEEDLE Sharp, regular and smooth margins and bevelled tip Yes
NEEDLE Rust proof Yes
NEEDLE Tightly fixed with hub covered with sterile guard Yes
NEEDLE Hermetically sealed Yes
NEEDLE The needle should not separate from the tube at any point of time, especially while removing it from the vein for donor safety Yes
NEEDLE The needle must confirm to ISO 1135-3 standard Yes
EXTERNAL PORT Easily accessible Yes
ANTICAOGULANT AND PRESERVATIVE SOLUTION Type of anticoagulant present CPDA-1
ANTICAOGULANT AND PRESERVATIVE SOLUTION Solution should be clear and colorless Yes
ANTICAOGULANT AND PRESERVATIVE SOLUTION There should be no discoloration of solution on storage at room temperature Yes
ANTICAOGULANT AND PRESERVATIVE SOLUTION Additive soultion present Yes
ANTICAOGULANT AND PRESERVATIVE SOLUTION Type of additive solution SAGM
ANTICAOGULANT AND PRESERVATIVE SOLUTION Quantity of Additive solution(ml) 80, 100, NA
ANTICAOGULANT AND PRESERVATIVE SOLUTION Anticoagulant and/or additive solution should be sterile and pyrogen free Yes
ANTICAOGULANT AND PRESERVATIVE SOLUTION Availability of anticoagulant/additive quality check certificate from manufacture (proof of same to be submitted to buyer) Yes
LABEL Non-peel off Yes
LABEL Heat sealed/ Pressure embossed label Yes
CERTIFICATIONS & REPORTS Manufacturer certifications (Proof of the same to be submitted to the buyer on demand) ISO 13485, GMP, WHO GMP
CERTIFICATIONS & REPORTS Product Certifications (Proof of the same to be submitted to buyer on demand) ISO, BIS, EU-CE, US-FDA
SHELF LIFE Shelf Life from the date of manufacture (in months) 24
SHELF LIFE Stability report from a recogniozed laboratory must be submitted to the buyer at the time of supply Yes

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Historical Data

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) *In case any bidder is seeking exemption from Experience / Turnover Criteria

9

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

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