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Tender Notice for Sterile Hypodermic Needles for Single use (V2) in BHARUCH, GUJARAT

Bid Publish Date

05-Jun-2026, 1:52 pm

Bid End Date

15-Jun-2026, 2:00 pm

Location

BHARUCH , GUJARAT

Progress

Issue05-Jun-2026, 1:52 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

20000

Bid Type

Two Packet Bid

N/a announces a tender for Sterile Hypodermic Needles for Single use (V2) (Q2) in BHARUCH, GUJARAT. Quantity: 20000. Submission Deadline: 15-06-2026 14: 00: 00. Last date to apply is approaching fast!

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Sterile Hypodermic Needles for Single use (V2) (Q2)

Authority Records

HEALTH AND FAMILY WELFARE DEPARTMENT
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Documents 3

GeM-Bidding-9426322.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

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 Product Description Hypodermic Needle
GENERAL FEATURES Sterility Sterile
GENERAL FEATURES Usage Single-Use
CONFORMITY TO STANDARD Conformity to specifications IS 10654 (Latest Revision)
PRODUCT INFORMATION Material of Needle Tube (As per ISO 9626) Stainless Steel
PRODUCT INFORMATION Needle Cap Yes
PRODUCT INFORMATION Lubricated Needle Tube Yes
PRODUCT INFORMATION Sharps injury protection feature Yes
PRODUCT INFORMATION Color coded for size identification as per IS 16004 / ISO 6009 Yes
PRODUCT INFORMATION Needle Hub Material Pigmented
PRODUCT INFORMATION Designated Metric Size of Needle 0.55 mm
PRODUCT INFORMATION Nominal Length of Needle Tube 25 mm
PRODUCT INFORMATION Tolerance on length of needle tube shall be as per Table 1 IS 10654 (Latest) Yes
PACKING Packaging & Marking shall be as per IS 10654 (Latest) Yes
CERTIFICATIONS AND REPORTS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS AND REPORTS Availability of valid drug/ 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 AND REPORTS Manufacturing unit certification ISO:13485 (Latest)
CERTIFICATIONS AND REPORTS Availability of Test Report for each supplied batch/product as per Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS AND REPORTS Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission and/or along with supplies as per buyer requirement Yes
SHELF LIFE Shelf life in months from the date of manufacture 36 Or higher

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Required Documents

1

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

2

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

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