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Indian Air Force Semi Automated Coagulation Analyzer Tender Betul MP 2026 MDR 2017 ISO Standards

Bid Publish Date

02-Jul-2026, 10:03 am

Bid End Date

09-Jul-2026, 11:00 am

Location

BETUL , MADHYA PRADESH

Progress

Issue02-Jul-2026, 10:03 am
AwardPending
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Quantity

1

Bid Type

Two Packet Bid

Categories 3

Tender Overview

The Indian Air Force, Department of Military Affairs, invites bids for a Semi Automated Coagulation Analyzer (V2) (Q2) to support hospital diagnostics at 3 AIR FORCE HOSPITAL AMLA DEPOT, BETUL, MP. The procurement scope includes a programmable test menu with multi-channel capability, factor assays, and an incubation heating block. Expected delivery and installation are implied at the designated military facility, with OEM/authorized reseller participation and mandatory OEM certifications. A key differentiator is the emphasis on MDR 2017 compliance, drug license validity, and electrical safety alongside comprehensive certification packages. The bidding process requires OEM authorization where applicable and installation/commissioning by OEM-certified personnel. The project scope emphasizes system interoperability via LIS and a UPS-backed operation. Procurement favors suppliers with prior government deployments and strong post-sales support. This tender presents a structured, regulation-forward medical device purchase with clear conformity and delivery expectations.

Technical Specifications & Requirements

  • Product/Class: Semi Automated Coagulation Analyzer (V2) (Q2) with programmable test menu and coagulation capability
  • Configuration Model: documented configuration; includes incubation heating block and incubation Wells/Temperature controls
  • Core Features: Number of Channels, Factor Assay Included, Flagging for upper linearity, LIS Interface, built-in Printer, and Display (Type) for operator feedback
  • Electrical/Power: Power input (VAC) and verified UPS provision with specified backup time; ensure compatibility with hospital supply
  • Regulatory/Quality: MDR 2017 compliance, valid drug license under Drug and Cosmetic Act, Manufacturing unit certification, MDR test reports, Electrical Safety Standards; supplier must submit certifications at bid and with supply
  • Warranty: optional comprehensive warranty through bidding; if chosen, supersedes standard catalogue warranty
  • Delivery/Installation: on-site delivery and commissioning at the Betul address; installation/commissioning by OEM-certified personnel or OEM-authorized resellers
  • Documentation: bid must include all certifications, licenses, and test reports; GST/PAN and vendor registration details are required in bid submission

Terms, Conditions & Eligibility

  • EMD: amount not disclosed in current data; bidders should anticipate standard bid security requirements
  • Experience: OEM or bidder must have 3+ years of regular supply/manufacture of similar medical devices to Central/State Govt or PSUs; provide contract copies for each year
  • Delivery/Installation: delivery and installation at Commanding Officer, 3 Air Force Hospital, Betul, MP; timelines anchored to delivery orders with option for quantity variation up to 25%
  • Payment Terms: GST applicability to be determined by bidder; reimbursement as per actuals or applicable rates; bid must include EFT/payment documentation; no explicit payment schedule provided
  • Documentation: PAN, GSTIN, Cancelled Cheque, EFT Mandate; bank-certified; supplier must upload these with bid
  • Authorization: OEM authorization form/certification required when bidding through distributors; include full OEM contact details
  • Warranty/Support: optional comprehensive warranty; ensure post-installation support and service terms are defined; penalties or SLAs not detailed in current data

Key Specifications

  • Product/service names: Semi Automated Coagulation Analyzer (V2) with programmable test menu

  • Quantities/Volume: not explicitly provided; includes incubation wells and temperature controls

  • EMD/Estimated value: not disclosed in tender data

  • Experience: 3+ years supplying similar Category Products to Govt/PSU

  • Quality/standards: MDR 2017 compliance, Drug license under Drugs & Cosmetic Act, Manufacturing unit certification

  • Delivery/installation: on-site at 3 Air Force Hospital, Betul, MP; OEM-certified Installation & Commissioning

  • Testing/Certification: MDR test reports, Electrical Safety Standards, LIS interface compatibility

  • Warranty: option for comprehensive warranty via bid; supersedes catalogue warranty if selected

  • Power/UPS: UPS back-up time specified; power input in VAC

Terms & Conditions

  • Option clause allows ±25% quantity variation with extended delivery calculations

  • Delivery and installation at 3 Air Force Hospital, Betul, MP; OEM/authorized personnel required

  • Mandatory regulatory certifications: MDR 2017, Drug license, Manufacturing unit certification, electrical safety

Important Clauses

Payment Terms

GST handling on actuals or applicable rates; payment terms not precisely defined in data

Delivery Schedule

Delivery commencement linked to original delivery order; option to extend with formula ((Increased quantity/Original quantity) × Original delivery period) with minimum 30 days

Penalties/Liquidated Damages

No explicit LD rate provided in data; standard govt procurement penalties may apply per contract but not specified here

Bidder Eligibility

  • 3+ years of supplying same or similar medical devices to Govt/PSU

  • OEM authorization or OEM-certified reseller capability

  • Financial standing with non-liquidation and acceptable GST/PAN documentation

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Semi Automated Coagulation Analyzer (V2) (Q2)

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENT

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Documents 4

GeM-Bidding-9425615.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
GENERAL Product Description Semi Automated Coagulation Analyzer
GENERAL Purpose Coagulation Analyser rapidly and accurately measures blood clotting parameters, aiding in diagnosing and monitoring bleeding and clotting disorders.
PRODUCT INFORMATION Configuration Model Benchtop
PRODUCT INFORMATION Method Used Opto-Mechanical LED Photometric, Mechanical Mixing, Viscosity based Mechanical, Optical Light Scatter
PRODUCT INFORMATION Sample Type Plasma
PRODUCT INFORMATION Minimal usage volume for clotting assay ≤ 100 microlitre Or higher
PRODUCT INFORMATION Number of Channels 4
PRODUCT INFORMATION Test Menu Programmable PT, APTT, FIB
PRODUCT INFORMATION Factor Assay Included Yes
PRODUCT INFORMATION Flagging when values exceed upper linearity limits Yes
PRODUCT INFORMATION Incubation Heating block Yes
PRODUCT INFORMATION Incubation number of Wells 16
PRODUCT INFORMATION Incubation Temperature 37(±1) Degree Celsius
SYSTEM FEATURES LIS Interface Yes
SYSTEM FEATURES Printer Built-in thermal, External
SYSTEM FEATURES Calibration Automatic, Manual
SYSTEM FEATURES Display Built in LCD/LED
SYSTEM FEATURES Type of Display Touch Screen
Power requirements Power input, VAC 220-240VAC, 50Hz fitted with Indian plug
Power requirements UPS provided Yes, No
Power requirements UPS Back up Time in Minutes 15 Mins, NA
CERTIFICATION AND REPORTS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATION AND REPORTS Availability of valid drug license for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules made there under as amended till date Yes
CERTIFICATION AND REPORTS Manufacturing unit certification ISO:13485 (Latest)
CERTIFICATION AND REPORTS Availability of Test Report for product as per Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATION AND REPORTS Electrical Safety Standards IEC 60601-1 or equivalent BIS Standard
CERTIFICATION AND REPORTS Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission and/or along with supplies as per buyer requirement Yes
WARRANTY Warranty (Option of comprehensive warranty is available through bidding only, which if opted will supersede normal warranty in the catalogue) 2, 5

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Required Documents

1

Experience Criteria

2

Past Performance

3

Bidder Turnover

4

Certificate (Requested in ATC)

5

OEM Authorization Certificate

6

OEM Annual Turnover

7

Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria

8

the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

Frequently Asked Questions

How to bid for the coagulation analyzer tender in Betul MP

Bidders must meet eligibility: 3+ years supplying similar govt/PSU devices, provide OEM authorization and full GST/PAN documentation, and submit MDR 2017 compliance, drug license, manufacturing unit certification, and MDR test reports. Include on-site installation capability by OEM-certified personnel and UPS-backed power readiness with detailed delivery plan.

What documents are required for Indian Air Force coagulation analyzer bid

Required documents include PAN, GSTIN, cancelled cheque, EFT mandate, OEM authorization, proof of experience with govt contracts, manufacturing certificates, MDR compliance reports, and electrical safety certificates. Also attach current drug license and vendor registration details for submission.

What are the technical specifications for the coagulation analyzer in this tender

Specification highlights: programmable test menu, multiple channels, factor assay included, flagging for upper linearity, incubation heating block, defined incubation wells and temperature, LIS interface, built-in printer, display type, and UPS-backed operation; ensure MDR compliance and safety standards.

When is delivery and commissioning expected for the Betul facility

Delivery is on-site at Commanding Officer, 3 Air Force Hospital, Betul, MP. The option clause allows quantity variation up to 25% with delivery time calculation; ensure installation by OEM-certified personnel with training where applicable.

What is required for warranty and post-sales support

Bidders may offer a comprehensive warranty as an option; if selected, it supersedes the standard catalogue warranty. Include scope, duration, response times, and service levels in the bid; ensure availability of spare parts and annual maintenance options.

How does MDR 2017 compliance impact this coagulation analyzer bid

The product must comply with MDR 2017 as amended, with valid Drug License under Drugs and Cosmetic Act, and MDR test reports; provide these certifications at bid submission and with deliveries. This ensures regulatory acceptance for government use.

What is the role of OEM authorization in this bid

OEM authorization is mandatory when bidding through distributors; include a formal authorization form with OEM details (name, designation, address, email, phone). This confirms direct or certified support for installation, maintenance, and validation.

Are there specific power requirements or UPS needs for the analyzer

The tender requires a defined power input in VAC and a UPS backup specification; the bidder must confirm UPS capacity and runtime, ensuring uninterrupted operation during power fluctuations at the Betul facility.

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