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Indian Air Force Rapid Pregnancy Test Kit Tender 2026 - IS/CDCGI MDR 2017 Compliance, Medical Device License, GST 2026

Bid Publish Date

20-Jun-2026, 1:57 pm

Bid End Date

30-Jun-2026, 2:00 pm

Value

โ‚น14,400

Progress

Issue20-Jun-2026, 1:57 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

90

Bid Type

Single Packet Bid

Categories 1

Tender Overview

The Indian Air Force (Department of Military Affairs) seeks a Rapid Pregnancy Test Kit under a government procurement tender with an estimated value of โ‚น14,400. Key procurement scope includes detection type, sample type, and kit packaging details with specified shelf-life constraints. Mandatory certifications include ** Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017** compliance and a valid Medical Device license. Bid submissions require vendor registration data, including PAN, GSTIN, cancelled cheque, and an EFT mandate. Emphasis on data-sheet alignment with product specifications and OEM authorization for distributors. The tender allows a quantity option of up to 50% increase/decrease, with delivery timelines tied to the original delivery period. Bidders must ensure non-toxicity and provide MSDS for hazardous materials if applicable. GST invoice generation must be in the consigneeโ€™s name with the consignee GSTIN, and GST payments must be supported by portal screenshots.

Technical Specifications & Requirements

  • Product category: Rapid pregnancy test kit
  • Product information fields: Detection type, sample type, sensitivity, specificity, packaging details (tests per pack)
  • Shelf life: Minimum two years per DCGI/CDSCO shelf-life norms; on supply date, at least five-sixth of usable shelf life must remain
  • Certifications: Compliance to Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017; valid Medical Device license from competent authority
  • Quality: Non-toxic and harmless to health; provide MSDS for toxic components
  • Data alignment: Data sheet must match bid technical parameters; mismatch may lead to rejection
  • OEM/Authorization: Manufacturer authorization form required for distributors/agents with full details
  • Invoicing: Invoice to be issued in the consigneeโ€™s name with GSTIN; upload GST invoice and payment confirmation on GeM portal

Terms, Conditions & Eligibility

  • EMD/Deposits: Not explicitly stated; GST and regulatory compliance mandatory
  • GST: Bidder bears applicable GST; reimbursements as actuals or capped, per quoted rate
  • Documents: Submit PAN, GSTIN, cancelled cheque, EFT mandate; data sheet alignment; OEM authorization Form
  • Delivery/Option Clause: Quantity can vary by ยฑ50% with execution tied to original/extended delivery periods
  • Shelf life requirement: Minimum two years with minimum remaining shelf life at supply; non-toxic labeling
  • Invoicing: Invoice issued in consignee name with GSTIN; GST portal screenshot required
  • Compliance: Ensure product packaging and data sheets precisely reflect offered specs; non-compliant bids may be rejected

Key Specifications

  • Product: Rapid pregnancy test kit

  • Standards/Regulations: Drugs and Cosmetic Act 1940; Medical Device Rules (MDR) 2017; DCGI/CDSCO shelf-life norms

  • Shelf life: Minimum two years; at supply, minimum five-sixth of shelf life remaining

  • Licensing: Valid Medical Device license from competent authority

  • Packaging: Number of tests per pack as specified in data sheet

  • Non-toxicity: Product should be non-toxic; MSDS for toxic components to be provided

  • Invoicing: GSTIN of consignee; GST invoice and GST portal payment screenshot required

  • Authorization: OEM authorization form required for distributors

Terms & Conditions

  • GST applicable to bidders; reimbursement as actuals or capped by quoted rate

  • Option clause allows ยฑ50% quantity changes with proportional delivery implications

  • Shelf life minimum two years; ensure remaining shelf life at delivery is adequate

Important Clauses

Payment Terms

GST will be reimbursed as per actuals or the quoted rate, whichever is lower; bidder bears GST responsibility

Delivery Schedule

Delivery period linked to the last delivery order date; option for extended period with proportionate time calculation

Penalties/Liquidated Damages

Not explicitly stated; ensure compliance to delivery and data sheet alignment to minimize risk

Bidder Eligibility

  • Submit PAN and GSTIN

  • Provide OEM authorization for distributors

  • Demonstrate data-sheet alignment with offered product specifications

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Rapid Pregnancy Test Kit (Q2)

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENTINDIAN AIR FORCE

BID & GeM Expert Consultancy

End-to-end support โ€” bid preparation, GeM registration, document filing & compliance by industry experts.

Bid Preparation GeM Registration Document Filing

Free consultation ยท 24h response

Documents 4

GeM-Bidding-9443175.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Buyer uploaded ATC document

ATC

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 Detection Type Semi Quantitative
PRODUCT INFORMATION Sample Type Urine
PRODUCT INFORMATION Sensitivity โ‰ฅ25 milli I.U/ ml
PRODUCT INFORMATION Specificity โ‰ฅ99%
PACKAGING Number of Tests per Pack 10 Tests, 25 Tests, 50 Tests, 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

PAN Card copy

2

GSTIN copy

3

Cancelled Cheque

4

EFT Mandate certified by bank

5

Product Data Sheet corresponding to bid offerings

6

OEM manufacturer authorization certificate (for authorised distributors)

7

Data sheet alignment confirmation

8

GST invoice draft/format and GST portal payment confirmation

9

Medical Device license validity details

10

DCGI/CDSCO shelf-life documentation (as applicable)

Frequently Asked Questions

How to bid for the rapid pregnancy test kit tender in Delhi IAF 2026?

Bidders must submit PAN, GSTIN, cancelled cheque, EFT mandate, product data sheet, OEM authorization (if applicable), and Medical Device license. Ensure data sheet matches offered parameters; comply with MDR 2017 and DCGI/CDSCO shelf-life requirements; GST considerations follow actuals or quoted rate.

What documents are required for the pregnancy test kit procurement in India IAF?

Required documents include PAN, GSTIN, cancelled cheque, EFT mandate, product data sheet, OEM authorization certificate, and DCGI/CDSCO shelf-life evidence; GST invoice format and consignee GSTIN details must be provided for invoicing through GeM.

What are the essential technical specifications for the rapid tests?

Specifications include detection type, sample type, requested sensitivity and specificity, tests-per-pack packaging, and shelf-life details; ensure data sheet reflects exact numbers and match product performance against declared parameters.

When is the delivery timeline and how does the option clause work?

Delivery period is defined from the last date of the original delivery order; option to increase or decrease quantity up to 50%; extended delivery time calculated as (increased quantity/original quantity) ร— original period, minimum 30 days, with possible further extension.

What standards must the pregnancy test kit comply with for this IAF tender?

Products must comply with Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017, along with a valid Medical Device license from the competent authority; non-toxicity and MSDS for toxic components are required.

How should invoicing be processed for the IAF supply contract?

Invoices must be raised in the consigneeโ€™s name with the consigneeโ€™s GSTIN; bidders should upload scanned GST invoices and GST portal payment confirmation on the GeM portal.

What happens if the data sheet does not align with offerings?

Mismatched or unexplained technical parameters can lead to bid rejection; ensure the data sheet precisely reflects the offered productโ€™s specifications and performance metrics prior to submission.

What is the shelf-life requirement for the rapid test kits?

Shelf-life must be minimum two years per DCGI/CDSCO; at the time of supply, a minimum of five-sixth of usable shelf life must remain, ensuring product viability on delivery.

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