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Indian Air Force Rapid Test Kits Tender for Dengue Malaria Typhoid & HIV/HBV/HCV – IS 1940 MDR 2017 Compliant 2026

Bid Publish Date

15-Jun-2026, 8:52 am

Bid End Date

06-Jul-2026, 10:00 am

Value

₹29,388

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Progress

Issue15-Jun-2026, 8:52 am
Corrigendum02-Jul-2026
AwardPending
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Quantity

1206

Category

Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others

Bid Type

Two Packet Bid

Key Highlights

  • Critical brand/OEM requirements: Manufacturer Authorization where distributors bid
  • Mandatory certifications: DCGI Drug Act compliance, MDR 2017, valid Medical Device license
  • Shelf life requirement: minimum 2 years with balance remaining at supply
  • Packaging: positive and negative controls included per pack; tests per pack specified in data sheet
  • Option clause: quantity can vary ±50% at contract time with adjusted delivery periods
  • GST handling: bidder manages GST; invoicing to consignee with GSTIN; GST documentation via GeM
  • Submission prerequisites: PAN, GSTIN, cancelled cheque, EFT mandate, Data Sheet alignment
  • Delivery terms: timeline tied to original delivery period; extended delivery timelines only via option clause

Categories 2

Tender Overview

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.

Technical Specifications & Requirements

  • Type of Test Kit: Point of care rapid test kit for infectious diseases
  • Detection Type: Qualitative/rapid qualitative detection
  • Sample Type: Blood/serum or as specified in data sheet
  • Result Time: Within specified minutes per test
  • Sensitivity / Specificity: As per data sheet; must meet DCGI/MDR claims
  • Controls: Positive and negative controls provided with each pack
  • Tests per Pack: As per packaging information
  • Shelf Life: Minimum 2 years; remaining shelf life must be substantial at supply
  • Certifications: Compliant with Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 and valid Medical Device license
  • Testing Method / Standards: Data sheet alignment; OEM authorization if bidding via distributor
  • Brand/OEM: Manufacturer Authorization required if bid via authorized channels

Terms, Conditions & Eligibility

  • EMD: Not disclosed in tender data
  • GST: Bidder responsible for applicable GST; GST invoicing to consignee with GSTIN; reimbursement as actuals or as per rates
  • Documents Required: PAN card, GSTIN, cancelled cheque, EFT mandate; Data Sheet; OEM authorization where applicable
  • Delivery & Option Clause: Up to 50% increase/decrease in quantity; extended delivery time calculated based on additional quantity; minimum 30 days; adherence to original delivery period where applicable
  • Warranty/LS/Quality: Non-toxic materials; DCGI/CDSCO shelf life alignment; product should be harmless to health; MSDS may be provided for toxic materials
  • Payment Terms: Invoice in consignee name; GST-paid documentation required on GeM portal
  • Other Conditions: Data sheet must match technical parameters; bid may be rejected for mismatches; vendor code creation prerequisites

Key Specifications

  • 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

Terms & Conditions

  • 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

Important Clauses

Payment Terms

GST applicability as actuals; invoicing in consignee name with GSTIN; GST portal payment confirmation required

Delivery Schedule

Delivery period linked to original delivery order; extended period governed by option clause and proportional calculation

Penalties/Liquidated Damages

Not explicitly described in provided data; subject to standard procurement terms as per GeM/buyer terms

Bidder Eligibility

  • 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

Additional Tender Data

Commercial Details

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)

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENT

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Documents 6

GeM-Bidding-9351725.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

CATALOG-Specification-2

CATALOG Specification

CATALOG-Specification-3

CATALOG Specification

Buyer uploaded ATC document

ATC

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Technical Specifications 3 Items

Item #1 Details

View Catalog
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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Historical Data

Required Documents

1

PAN Card copy

2

GSTIN copy

3

Cancelled cheque copy

4

EFT mandate certified by bank

5

Product Data Sheet (data sheet uploaded and matched with offered parameters)

6

Manufacturer Authorization / OEM authorization (if bidding via Authorized Distributor)

Corrigendum Updates

3 Updates
#1

Update

02-Jul-2026

Extended Deadline

06-Jul-2026, 10:00 am

Opening Date

06-Jul-2026, 10:30 am

#2

Update

29-Jun-2026

Extended Deadline

02-Jul-2026, 10:00 am

Opening Date

02-Jul-2026, 10:30 am

#3

Update

25-Jun-2026

Extended Deadline

29-Jun-2026, 10:00 am

Opening Date

29-Jun-2026, 10:30 am

Frequently Asked Questions

How to bid for the Indian Air Force rapid test kit tender in 2026?

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.

What documents are required for the IAF rapid test kit procurement bid 2026?

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.

What are the key technical specifications for the rapid test kits in this tender?

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.

What is the EMD and quantity variation in this IAF tender?

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.

What are the delivery and payment terms for IAF rapid test kit supply?

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.

What certifications and licenses are mandatory for these rapid tests?

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.

How should OEM authorization be provided for this bidder qualification?

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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