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GEM

Open Tender for Spinal Needle (V2) in SOUTH DELHI, DELHI

Bid Publish Date

09-Feb-2026, 10:31 am

Bid End Date

02-Mar-2026, 4:00 pm

Location

SOUTH DELHI , DELHI

Progress

Issue09-Feb-2026, 10:31 am
AwardPending
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Quantity

4000

Bid Type

Two Packet Bid

Categories 2

INOCULATING DEVICES ANESTHESIA NEEDLES

A tender has been published for All India Institute Of Medical Sciences (aiims) Spinal Needle (V2) (Q2) in SOUTH DELHI, DELHI. Quantity: 4000 by. Submission Deadline: 02-03-2026 16: 00: 00. Check eligibility and apply.

Documents 4

GeM-Bidding-8911793.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Other Documents

OTHER

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 Product description Spinal Needle
GENERAL Sterility Sterile
GENERAL Usage Single-Use
STANDARD Conforming to Indian Standard IS 7350 : Latest
PRODUCT INFORMATION Point of Needle Quincke Bevel
PRODUCT INFORMATION Cannula Material (Medical Grade) Stainless Steel
PRODUCT INFORMATION Stilette Wire Brazed to Hub, Silver Soldered to Hub
PRODUCT INFORMATION Stilette Wire Material Stainless Steel Wire
PRODUCT INFORMATION Material of Hub conforming to IS 319 Yes
PRODUCT INFORMATION Hub Transparent hub with notch, Translucent Hub
PRODUCT INFORMATION Stilette should have smooth movement and well fitting Yes
PRODUCT INFORMATION Conical Fitting Luer Type
PRODUCT INFORMATION Length of Cannula (mm) 90 mm
PRODUCT INFORMATION Needle Size (G) 18G, 20G, 23G
PACKAGING Packing Individually Packed
CERTIFICATIONS & REPORTS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS & 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 & REPORTS Manufacturing unit certification ISO:13485 (Latest)
CERTIFICATIONS & REPORTS Availability of Test Report for product as per Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS & 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 from the date of manufacture in months 36 Or higher
SHELF LIFE Minimum shelf life of the product at the time of delivery to the consignee 3/4th of the total shelf life
ADVANCE SAMPLE Agree to provide advance sample of the product for buyer's approval before commencement of supply in case of bidding Yes

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Required Documents

1

Experience Criteria

2

Past Performance

3

Certificate (Requested in ATC)

4

OEM Authorization Certificate

5

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

6

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