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Contract Bidding Open For C-Reactive Protein (CRP) Test Kit - Latex Agglutination Method for Human Samples in LUCKNOW, UTTAR PRADESH

Bid Publish Date

08-Jul-2026, 5:53 pm

Bid End Date

23-Jul-2026, 6:00 pm

Location

LUCKNOW , UTTAR PRADESH
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Progress

Issue08-Jul-2026, 5:53 pm
AwardPending
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Quantity

31

Bid Type

Single Packet Bid

Categories 1

BDV KIT

North Eastern Railway announces a tender for C-Reactive Protein (CRP) Test Kit - Latex Agglutination Method for Human Samples (Q2) in LUCKNOW, UTTAR PRADESH. Quantity: 31. Submission Deadline: 23-07-2026 18: 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

No

Item Category

C-Reactive Protein (CRP) Test Kit - Latex Agglutination Method for Human Samples (Q2)

Delivery Details

Max Delivery Days

30

Delivery Locations

2

Delivery Cities

Gorakhpur, Lucknow

Delivery Pincodes

226006, 273012

Delivery Locations

ConsigneeAddressCityStatePincodeQuantityDelivery DaysAdditional Requirement
Vijay Narayan Mishra226006,Central Pathology Laboratory, Divisional Hospital, North Eastern railway, Badshahnagar, Balmikinagar, Lucknow-226006LucknowUttar Pradesh226006430-
Umesh Maurya273012,Lalit Narayan Mishra Railway Hospital, North Eastern Railway, GorakhpurGorakhpurUttar Pradesh2730122530-

Authority Records

MINISTRY OF RAILWAYS

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Documents 3

GeM-Bidding-9578476.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
PRODUCT INFORMATION Result Type Qualitative
PRODUCT INFORMATION Sample Type Serum
PRODUCT INFORMATION Positive and Negative controls provided Yes
PRODUCT INFORMATION Slide with applicator sticks provided Yes
PACKAGING Number of Tests per Pack 100 Tests
SHELF LIFE Residual shelf life of the product Agree to provide residual shelf life of atleast 75% of total shelf life at the time of delivery to the consignee
CERTIFICATIONS Compliance to Drugs and Cosmetic Act 1940 and 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 Yes

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Required Documents

1

Experience Criteria

2

Past Performance

3

Certificate (Requested in ATC)

4

OEM Authorization Certificate *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

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