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Bids are Invited For Uterine Balloon Tamponade Device (V2) in NORTH DELHI, DELHI

Bid Publish Date

24-Jun-2026, 1:26 pm

Bid End Date

04-Jul-2026, 2:00 pm

Value

₹2,40,000

Progress

Issue24-Jun-2026, 1:26 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

60

Bid Type

Two Packet Bid

A tender has been published for Municipal Corporation Of Delhi (mcd) Uterine Balloon Tamponade Device (V2) (Q2) in NORTH DELHI, DELHI. Quantity: 60 by. Submission Deadline: 04-07-2026 14: 00: 00. Check eligibility and apply.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Uterine Balloon Tamponade Device (V2) (Q2)

Authority Records

URBAN DEVELOPMENT DEPARTMENT

BID & GeM Expert Consultancy

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Bid Preparation GeM Registration Document Filing

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Documents 4

GeM-Bidding-9514094.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 Product Description Uterine Balloon Tamponade Device
GENERAL FEATURES Usage Single Use
GENERAL FEATURES Sterility Sterile
PRODUCT INFORMATION Balloon Material Latex
PRODUCT INFORMATION Balloon Capacity 300 ml to 500 ml
PRODUCT INFORMATION Inflation Mechanism Manual Syringe Inflation
PRODUCT INFORMATION Syringe Provided Yes
PRODUCT INFORMATION Connector provided Yes
PRODUCT INFORMATION Tube Length 50 cm or longer
PRODUCT INFORMATION Other Features Allows for Contraction and Retraction of Uterus, Provides Visual Indicator, Allows for Intra-Uterine Pressure Control, Free Flow Open System, Separate drainage port for monitoring of blood loss
PACKAGING Type of Packing Moisture Proof Packing
CERTIFICATIONS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS 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 Manufacturing unit certification ISO:13485 (Latest)
CERTIFICATIONS Availability of Test Report for each supplied batch/product as per Medical Device Rules (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 and/or along with supplies as per buyer requirement Yes
SHELF LIFE Shelf life in months from the date of manufacture 24 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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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

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

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