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Indian Air Force Digital Medical X-Ray Films Tender 2026 India - ISI/MDR 2017 Compliance and Medical Device License 2026

Bid Publish Date

10-Jun-2026, 8:01 am

Bid End Date

20-Jun-2026, 9:00 am

Progress

Issue10-Jun-2026, 8:01 am
AwardPending
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Quantity

11

Bid Type

Single Packet Bid

Key Highlights

  • Strict MDR 2017 and DCGI/CDSCO shelf-life compliance required
  • OEM/Authorised distributor authorization mandatory for non-OEM bidders
  • Delivery quantity flexibility up to 50% with adjusted timelines
  • GST handling and invoicing to consignee GSTIN only
  • Data Sheet must precisely match technical parameters
  • Two-year minimum shelf life; minimum remaining shelf life criteria

Categories 1

Tender Overview

The Indian Air Force invites procurement of Digital Medical X-Ray Films (V3) for medical imaging, with mandatory drugs and cosmetics act compliance and valid Medical Device license/registration. Key categories include Film Size (inches), Digital detectors for X-ray capture, pack size per piece, and residual shelf life requirements. The notice emphasizes linkage to a detailed product data sheet and OEM/authorised distributor authentication. A flexible quantity clause up to 50% increase/decrease during contract execution is included, with delivery periods aligned to last-order dates. This procurement is designed for robust, compliant radiology workflows within the Indian Air Force, with emphasis on safety, traceability, and regulatory conformity.

Technical Specifications & Requirements

  • Product category: Digital Medical X-Ray Films (V3) with associated digital detectors for X-ray image capture.
  • Film size: specify compatible film size in inches.
  • Pack details: number of pieces per pack to be delivered.
  • Shelf life: minimum shelf life requirements; must comply with DCGI CDSCO shelf life norms and maintain balance life at supply.
  • Regulatory compliance: Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended; valid Medical Device license/Registration number from competent authority.
  • Quality data: Data Sheet illustrating technical parameters; ensure consistency with offered product specs; non-toxic materials preferred with MSDS provided where applicable.
  • Authorization: OEM authorization if bidding via distributor, including full details of the OEM/Original Service Provider.
  • Delivery & warranty: Delivery terms tied to the contract’s final orders; warranty/AMC as applicable per MDR and DCGI guidelines.

Terms, Conditions & Eligibility

  • GST: GST invoicing as per consignee GSTIN; GST applicability to be determined at bid time.
  • Vendor code documents: PAN, GSTIN, cancelled cheque, and EFT mandate certified by bank.
  • Data Sheet: Tender requires verified product Data Sheet matching technical parameters.
  • Authorization: OEM authorization where applicable; provide distributor/authorisation details.
  • Quantity flexibility: up to 50% increase/decrease in order quantity; delivery period adjusted per clause, minimum 30 days.
  • Shelf life requirement: minimum two years as per DCGI/CDSCO; balance usable shelf life at delivery.
  • Invoicing: Invoice must be raised in the consignee name with GSTIN provided.
  • Contract law: No assignment/sub-contract without prior written consent from buyer.

Key Specifications

  • Digital Medical X-Ray Films (V3) with digital detectors for X-ray imaging

  • Exact Film Size (in inch) to be provided

  • Number of pieces per pack specification

  • Minimum residual shelf life per DCGI/CDSCO guidance

  • Compliance to Drugs and Cosmetics Act 1940 and Medical Device Rules (MDR) 2017

  • Valid Medical Device license/Registration number from competent authority

Terms & Conditions

  • GST payable per actuals or applicable rates to be reimbursed

  • 50% quantity variation rights for the purchaser

  • Two-year shelf life minimum with remaining life criteria

  • Invoices issued in consignee GSTIN only

Important Clauses

Payment Terms

GST conformity and reimbursement as per actuals; invoicing in consignee GSTIN.

Delivery Schedule

Delivery period linked to last date of original delivery order; extended time proportional to quantity variation (minimum 30 days).

Penalties/Liquidated Damages

Not specified in provided data; apply standard IAF procurement penalties as per contract.

Bidder Eligibility

  • Must hold valid DCGI/CDSCO registration for medical devices

  • OEM authorization if bidding via distributor

  • Financial stability evidenced by GST and bank EFT mandates

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Digital Medical X - Ray Films (V3) (Q2)

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENT

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Documents 4

GeM-Bidding-9359708.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
Performance and design Film Size(in inch) 10"x12"
Performance and design Digital detectors [to capture X-ray images] Computed Radiography (CR)
Packaging Number of pieces per pack 150
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
Certification Compliance to Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended till date Yes
Certification Availability of valid Medical Device license/ Registration number 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 copy

4

EFT Mandate certified by bank

5

Product Data Sheet aligned to offered specifications

6

OEM authorization or Distributor authorization with contact details

Frequently Asked Questions

How to bid for digital X-ray films tender in India Air Force

Respondents must submit PAN, GST, cancelled cheque, EFT mandate, and OEM/distributor authorization. Include a data sheet matching technical specs for Digital Medical X-Ray Films (V3), confirm MDR 2017 and DCGI compliance, and provide valid Medical Device license numbers. Ensure delivery terms align with 50% quantity variation clause.

What documents are required for IAF X-ray film procurement

Required documents include PAN, GSTIN, cancelled cheque, EFT mandate, OEM authorization (if applicable), and a detailed product data sheet. Data sheet must precisely reflect film size, pack quantity, shelf life, and digital detector specs, with MDR 2017 and DCGI compliance indicated.

What are the regulatory standards for X-ray film supply to IAF

Suppliers must comply with MDR 2017, DCGI shelf life norms, and have a valid Medical Device license/registration number. Ensure non-toxic materials and MSDS availability when applicable, with data sheet cross-checked against offered parameters.

When is delivery expected for Digital X-ray films in IAF tender

Delivery terms are tied to the last date of the original delivery order; if quantity increases by up to 50%, additional time is calculated as (Increased quantity / Original quantity) × Original delivery period, minimum 30 days.

What are the EMD and payment terms for IAF medical devices bid

EMD amount is not specified in the data provided; payment terms indicate GST reimbursement as actuals or as per applicable rates, whichever is lower, and invoicing in consignee GSTIN. Bidders should prepare for standard EMD as per IAF norms.

How to verify product data sheet alignment with offered X-ray film

Submit a Data Sheet that exactly matches the product's technical parameters: film size, pack quantity, detector type, shelf life, and regulatory licenses. Any mismatch can lead to bid rejection; ensure OEM authorization is included if required.

What documents prove OEM authorization for IAF bid

Provide a formal OEM authorization certificate detailing name, designation, address, email, and phone of the authorized distributor or service provider, ensuring alignment with the product data sheet and MDR/DCGI compliance.

What is the MC compliance requirement for X-ray film packaging

Packaging must reflect non-toxic, safe materials; include MSDS for toxic components if present, and ensure the number of pieces per pack aligns with the BOQ and data sheet specifications.

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