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Procurement Opportunity: Pressure Extension Tubes for Medical Purpose in SOUTH DELHI, DELHI

Bid Publish Date

09-Feb-2026, 11:50 am

Bid End Date

03-Mar-2026, 11:00 am

Location

SOUTH DELHI , DELHI

Progress

Issue09-Feb-2026, 11:50 am
AwardPending
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Quantity

19600

Bid Type

Two Packet Bid

Categories 1

POLYMERASE CHAIN REACTION PCR

All India Institute Of Medical Sciences (aiims) has released a public tender for Pressure Extension Tubes for Medical Purpose (Q2) in SOUTH DELHI, DELHI. Quantity: 19600. Submission Deadline: 03-03-2026 11: 00: 00. Download documents and apply online.

Documents 3

GeM-Bidding-8913865.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 Pressure Extension Tubes for Medical Purpose
GENERAL FEATURES Sterilized Yes
GENERAL FEATURES Single Use(Disposable) Yes
PRODUCT INFORMATION Type Low pressure (For pressure upto 5 bar or 80 psi), High pressure (For pressure upto 55 bar or 800 psi)
PRODUCT INFORMATION Material of Tube PVC
PRODUCT INFORMATION Non-Phthalate, Non-DEHP and Biocompatible Material Yes
PRODUCT INFORMATION Non-Toxic, Latex Free and Pyrogen Free Yes
PRODUCT INFORMATION Resistant to Radiation Yes
PRODUCT INFORMATION Radio Opaque Yes
PRODUCT INFORMATION 100% Leak Proof and No Blockage Yes
PRODUCT INFORMATION High Mechanical Strength and Kink Resistant Yes
PRODUCT INFORMATION Male Luer Lock at One End and Female Luer Lock Adaptor with Cap at the Other End Provided Yes
PRODUCT INFORMATION Tube Length (in cm) 200.0, 400.0
PACKING Packing Type Packed in sterile polyethene sealed pouch
CERTIFICATIONS & REPORTS Compliance to Medical Device Rule (MDR) 2017 as amended till date Yes
CERTIFICATIONS & REPORTS Availability of valid drug 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 each supplied batch/product as per Medical Device Rule (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 or along with supplies as per buyer requirement Yes
SHELF LIFE Shelf life in months from the date of manufacture 36 Or higher
SHELF LIFE Minimum shelf life of the product at the time of delivery to the consignee 3/4 th of Total Shelf Life

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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

Additional Doc 1 (Requested in ATC)

7

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

8

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