Rheumatoid Factor Test Kit - RA Test Kit (V2)
North Eastern Railway
VARANASI, UTTAR PRADESH
Bid Publish Date
08-Jul-2026, 6:02 pm
Bid End Date
23-Jul-2026, 6:00 pm
Location
Progress
Quantity
3717
Category
Rheumatoid Factor Test Kit - RA Test Kit (V2)
Bid Type
Single Packet Bid
A tender has been published for North Eastern Railway Rheumatoid Factor Test Kit - RA Test Kit (V2) (Q2), Widal Test Kit - Agglutination Method for Human Samples (Q2), ASO (Anti Streptolysin-O) Test Kits (V2) (Q2) in VARANASI, UTTAR PRADESH. Quantity: 3717 by. Submission Deadline: 23-07-2026 18: 00: 00. Check eligibility and apply.
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
No
Item Category
Rheumatoid Factor Test Kit - RA Test Kit (V2) (Q2) , Widal Test Kit - Agglutination Method for Human Samples (Q2) , ASO (Anti Streptolysin-O) Test Kits (V2) (Q2)
Max Delivery Days
30
Delivery Locations
2
Delivery Cities
Gorakhpur, Varanasi
Delivery Pincodes
221002, 273012
| Consignee | Address | City | State | Pincode | Quantity | Delivery Days | Additional Requirement |
|---|---|---|---|---|---|---|---|
| Anand Kumar Singh | 221002,Divisional Railway Hospital, N.E.Railway, Varanasi | Varanasi | Uttar Pradesh | 221002 | 500 | 30 | - |
| Umesh Maurya | 273012,Lalit Narayan Mishra Railway Hospital, North Eastern Railway, Gorakhpur | Gorakhpur | Uttar Pradesh | 273012 | 2500 | 30 | - |
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Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS
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Tender Results
Loading results...
| Category | Specification | Requirement |
|---|---|---|
| General Features | Product Description | Rheumatoid Factor Test Kit (RA Test Kit) |
| Product Description | Result Type | Qualitative |
| Product Description | Sample Type Required | Serum, Plasma |
| Product Description | Testing Principle | Latex Agglutination Slide Method |
| Product Description | Sensitivity | ≥ 98% Or higher |
| Product Description | Specificity | ≥ 98% Or higher |
| Packaging | Pack Size | 100 Tests |
| 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 | 3/4 th of Total Shelf Life |
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Experience Criteria
Past Performance
Certificate (Requested in ATC)
OEM Authorization Certificate *In case any bidder is seeking exemption from Experience / Turnover Criteria
the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer
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Sign up now to access all documents
Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS