Bid Publish Date
11-May-2026, 11:21 am
Bid End Date
22-Jun-2026, 12:00 pm
Location
Progress
RAPublic procurement opportunity for Employees State Insurance Corporation Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others (Q2), Rapid Test Kit for HIV / Syphilis / Hepatitis B Virus (HBV) / Hepatitis C Virus (HCV) (Q2), Rapid Pregnancy Test Kit (Q2), Blood Collection Tube (Q2), Blood Collection Needles (V2) (Q2) in BAREILLY, UTTAR PRADESH. Quantity: 27048 issued by. Submission Deadline: 22-06-2026 12: 00: 00. View full details and respond.
These are the final prices after the reverse auction event. Prices may be lower than initial bids.
| Rank | Seller | Final Price | Item |
|---|---|---|---|
| L1 | STERI SOL MEDITRADE(MII) Under PMA Winner | ₹4,35,470 | Item Categories : Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others,Point of Care Rapid |
| L2 | ATHARVA HEALTHCARE TRADERS (MII) Under PMA | ₹4,36,980 | Item Categories : Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others,Point of Care Rapid |
🎉 L1 Winner
STERI SOL MEDITRADE(MII) Under PMA
Final Price: ₹4,35,470
Start
12-Sep-2026, 3:00 pm
End
17-Sep-2026, 10:00 am
Duration: 115 hours
Reverse Auction Document
✅ RA concluded. Check financial results for final rankings.
Quantity
27048
Category
Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others
Bid Type
Two Packet Bid
Bid Validity
180 (Days)
Bid Type
Service
Evaluation
Total value wise evaluation
Inspection Required
No
RA Qualification Rule
H1-Highest Priced Bid Elimination
Tech Clarification Time
3 Days
Min. Avg. Annual Turnover
1
OEM Avg. Turnover
11
Past Performance
10 %
Experience Required
1 Year (s)
Arbitration Clause
No
Mediation Clause
No
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others (Q2) , Rapid Test Kit for HIV / Syphilis / Hepatitis B Virus (HBV) / Hepatitis C Virus (HCV) (Q2) , Rapid Pregnancy Test Kit (Q2) , Blood Collection Tube (Q2) , Blood Collection Needles (V2) (Q2)
End-to-end support — bid preparation, GeM registration, document filing & compliance by industry experts.
Free consultation · 24h response
Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS
Extended Deadline
22-Jun-2026, 6:30 am
Opening Date
22-Jun-2026, 7:00 am
Extended Deadline
15-Jun-2026, 6:30 am
Opening Date
15-Jun-2026, 7:00 am
Extended Deadline
08-Jun-2026, 6:30 am
Opening Date
08-Jun-2026, 7:00 am
Experience Criteria
Past Performance
Bidder Turnover
Certificate (Requested in ATC)
OEM Authorization Certificate
OEM Annual Turnover
Additional Doc 1 (Requested in ATC)
Compliance of BoQ specification and supporting document *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
| Category | Specification | Requirement |
|---|---|---|
| PRODUCT INFORMATION | Type of Test Kit | Malaria Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) Antigen Rapid Test Kit |
| PRODUCT INFORMATION | Detection Type | Qualitative |
| PRODUCT INFORMATION | Sample Type | Whole Blood |
| PRODUCT INFORMATION | Result Time | ≤ 15 minutes |
| PRODUCT INFORMATION | Sensitivity (%) | ≥ 98, ≥ 99 Or higher |
| PRODUCT INFORMATION | Specificity (%) | ≥ 98, ≥ 99 Or higher |
| PRODUCT INFORMATION | Positive and negative controls provided with each pack of kit | No |
| PACKAGING | Number of Tests per Pack | 50 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 |