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Procurement Opportunity: ELISA Test Kits (V2)

Bid Publish Date

11-Jun-2026, 4:23 pm

Bid End Date

22-Jun-2026, 5:00 pm

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Progress

Issue11-Jun-2026, 4:23 pm
AwardPending
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Quantity

384

Bid Type

Two Packet Bid

Directorate Of Medical Education & Research invites bids for ELISA Test Kits (V2) (Q2). Quantity: 384. Submission Deadline: 22-06-2026 17: 00: 00. Submit your proposal before the deadline.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

ELISA Test Kits (V2) (Q2)

Authority Records

MEDICAL EDUCATION AND RESEARCH DEPARTMENT

BID & GeM Expert Consultancy

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Documents 3

GeM-Bidding-9455577.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

ELISA Test Kits (V2)

N/a

LUCKNOW, UTTAR PRADESH

Posted: 9 January 2025
Closed: 10 March 2025
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ELISA Test Kits (V2)

Employees State Insurance Corporation

Posted: 18 July 2025
Closed: 28 July 2025
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ELISA Test Kits (V2)

Employees State Insurance Corporation

Posted: 21 May 2025
Closed: 31 May 2025
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ELISA Test Kits (V2)

N/a

NEW DELHI, DELHI

Posted: 29 March 2025
Closed: 14 April 2025
GEM

ELISA Test Kits (V2)

N/a

SOUTH ANDAMAN, ANDAMAN & NICOBAR

Posted: 14 July 2025
Closed: 24 July 2025
GEM

Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL Product Description ELISA Test KIt
PRODUCT INFORMATION Type of ELISA Kit Scrub Typhus IgM ELISA KIT
PRODUCT INFORMATION Type of Sample Serum, Plasma
PRODUCT INFORMATION Time to Result ≤ 180 minutes
PRODUCT INFORMATION Sensitivity ≥ 98% Or higher
PRODUCT INFORMATION Specificity ≥ 98% Or higher
PRODUCT INFORMATION Positive and negative controls provided with the kit Yes
CERTIFICATIONS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS Availability of valid 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
SHELF LIFE Minimum shelf life of the product at the time of delivery to the consignee 3/4th of Total Shelf Life

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Historical Data

Required Documents

1

Certificate (Requested in ATC)

2

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

3

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

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