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Open Tender for Urine Culture Bottle (V2) in RAJKOT, GUJARAT

Bid Publish Date

05-Jun-2026, 11:56 am

Bid End Date

20-Jun-2026, 12:00 pm

Progress

Issue05-Jun-2026, 11:56 am
Corrigendum09-Jun-2026
AwardPending
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Quantity

45000

Bid Type

Two Packet Bid

N/a announces a tender for Urine Culture Bottle (V2) (Q2) in RAJKOT, GUJARAT. Quantity: 45000. Submission Deadline: 20-06-2026 12: 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

Yes

Item Category

Urine Culture Bottle (V2) (Q2)

Authority Records

HEALTH 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 3

GeM-Bidding-9316551.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Past Similar Tenders (Historical Results)

5 found

Urine Culture Bottle (V2)

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GANDHI NAGAR, GUJARAT

Posted: 8 January 2025
Closed: 18 January 2025
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Urine Culture Bottle (V2)

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Posted: 20 May 2025
Closed: 30 May 2025
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Posted: 10 January 2025
Closed: 24 January 2025
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Urine Culture Bottle (V2)

Nuclear Power Corporation Of India Limited

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Posted: 30 May 2025
Closed: 2 August 2025
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Urine Culture Bottle (V2)

Nuclear Power Corporation Of India Limited

Posted: 5 November 2024
Closed: 26 November 2024
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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL Product Description Urine Culture Bottle
GENERAL Sterility Sterile
GENERAL Usage Disposable
PRODUCT INFORMATION Material of Bottle Medical Grade Polypropylene
PRODUCT INFORMATION Type of Cap Plastic Screw Cap
PRODUCT INFORMATION Type of Mouth Wide
PRODUCT INFORMATION Capacity (ml) (ยฑ5 ml) 30 ml
PACKING Packing Individually packed
CERTIFICATIONS & REPORTS Compliance to Medical Device Rule (MDR) 2017 as amended till date Yes
CERTIFICATIONS & REPORTS Availability of valid medical device license / registration 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
SHELF LIFE Minimum shelf life of the product available at the time of delivery to the consignee 3/4 th of Total Shelf Life

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Historical Data

Required Documents

1

Certificate (Requested in ATC)

2

Additional Doc 1 (Requested in ATC)

3

Additional Doc 2 (Requested in ATC)

4

Additional Doc 3 (Requested in ATC) *In case any bidder is seeking exemption from Experience / Turnover Criteria

5

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

Corrigendum Updates

1 Update
#1

Update

09-Jun-2026

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