Health & Family Welfare Department Jammu & Kashmir Dengue Malaria Rapid Test Kits Tender Baramulla 2026 MDR 2017 Compliant
N/a
BARAMULLA, JAMMU & KASHMIR
Bid Publish Date
15-Jun-2026, 8:52 am
Bid End Date
06-Jul-2026, 10:00 am
Value
₹29,388
Progress
Quantity
1206
Category
Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others
Bid Type
Two Packet Bid
Indian Air Force invites bids for Point of Care Rapid Test Kits for Humans covering Dengue, Malaria, Typhoid and others, and a Rapid Test Kit panel for HIV / Syphilis / HBV / HCV (Q2). Estimated value: ₹29,388.0 with potential quantity adjustments up to 50% under the option clause. Delivery scope includes data sheets, OEM authorization, and compliance with Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended. Bidders must provide product data sheets, and ensure Medical Device license validity. Shelf life minimum: 2 years with at least 5/6 remaining on supply date. Positive/negative controls must be included per pack. GST considerations will follow actuals or applicable rates. The tender requires data sheet alignment and manufacturer authorization when bidding through authorized distributors. The vendor code creation documents include PAN, GSTIN, cancelled cheque, and EFT mandate. An option to scale up to 50% in quantity and adjust delivery accordingly is clearly stated, with delivery timelines tied to the original order period.
Point of Care rapid test kits for Dengue, Malaria, Typhoid and HIV/Syphilis/HBV/HCV
DCGI/ CDSCO compliant; Medical Device license valid
Positive and negative controls included per pack
Minimum shelf life: 2 years with substantial remaining shelf life at supply
Data sheet must reflect exact sensitivity, specificity, sample type, and result time
GST charged as per actuals; invoice in consignee name with GSTIN
Option to increase/decrease quantity up to 50% with corresponding delivery adjustments
Data Sheet alignment required; mismatches may lead to bid rejection
GST applicability as actuals; invoicing in consignee name with GSTIN; GST portal payment confirmation required
Delivery period linked to original delivery order; extended period governed by option clause and proportional calculation
Not explicitly described in provided data; subject to standard procurement terms as per GeM/buyer terms
Must provide PAN, GSTIN, and EFT mandate
Must supply OEM/Manufacturer Authorization if bidding through distributor
Data Sheet must precisely reflect offered product specifications and be consistent with tender data
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)
End-to-end support — bid preparation, GeM registration, document filing & compliance by industry experts.
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Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
N/a
BARAMULLA, JAMMU & KASHMIR
N/a
SOUTH ANDAMAN, ANDAMAN & NICOBAR
N/a
ETAH, UTTAR PRADESH
N/a
LUCKNOW, UTTAR PRADESH
Directorate Of Medical Education And Training
PILIBHIT, UTTAR PRADESH
Tender Results
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| 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, Whole Blood, Serum and Plasma |
| PRODUCT INFORMATION | Result Time | ≤ 15 minutes |
| PRODUCT INFORMATION | Sensitivity (%) | ≥ 99 Or higher |
| PRODUCT INFORMATION | Specificity (%) | ≥ 99 Or higher |
| PRODUCT INFORMATION | Positive and negative controls provided with each pack of kit | Yes, No |
| PACKAGING | Number of Tests per Pack | 10 Tests, 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 |
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PAN Card copy
GSTIN copy
Cancelled cheque copy
EFT mandate certified by bank
Product Data Sheet (data sheet uploaded and matched with offered parameters)
Manufacturer Authorization / OEM authorization (if bidding via Authorized Distributor)
Extended Deadline
06-Jul-2026, 10:00 am
Opening Date
06-Jul-2026, 10:30 am
Extended Deadline
02-Jul-2026, 10:00 am
Opening Date
02-Jul-2026, 10:30 am
Extended Deadline
29-Jun-2026, 10:00 am
Opening Date
29-Jun-2026, 10:30 am
Bidders must submit PAN, GSTIN, cancelled cheque, and EFT mandate; upload the product Data Sheet aligned with offered specs; provide OEM authorization if bidding via distributor; ensure DCGI/MDR compliant status and a valid Medical Device license to participate.
Required documents include PAN card, GSTIN, cancelled cheque, EFT mandate, Product Data Sheet, OEM authorization, and GST invoice readiness; data sheet must map exactly to tender technical parameters to avoid rejection.
Kits must be DCGI/MDR compliant with valid medical device licenses; include positive/negative controls; specify sensitivity, specificity, sample type, and result time per pack as per data sheet; shelf life must be at least 2 years.
EMD amount is not disclosed in the provided data; quantity may be adjusted by up to 50% under the option clause, with delivery timelines recalculated accordingly, minimum 30 days for added quantity.
Delivery schedule follows the original delivery period with possible extension via option clause; invoices must be raised in the consignee name, with GSTIN and GST portal payment confirmation; GST reimbursement follows actuals or applicable rates.
Mandatory certifications include compliance with Drugs and Cosmetic Act 1940 and Medical Device Rules 2017; a valid Medical Device license from the competent authority is required; data sheet must reflect compliance and testing parameters.
If bidding through an Authorized Distributor, submit an OEM authorization certificate detailing the distributor’s name, designation, address, email, and phone; this ensures traceability and compliance with manufacturer specifications.
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Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS