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Indian Army Oxygen Concentrator (V2) Tender 2026 Gujarat Rajasthan MDR 2017 Compliance

Bid Publish Date

08-Jul-2026, 9:53 am

Bid End Date

17-Jul-2026, 11:00 am

Value

โ‚น1,14,500

Location

THIRUVANANTHAPURAM , KERALA

Progress

Issue08-Jul-2026, 9:53 am
AwardPending
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Quantity

5

Bid Type

Two Packet Bid

Tender Overview

The Indian Army, Department Of Military Affairs, seeks bids for an Oxygen Concentrator (V2) with MDR 2017 compliance and drug license validation. Estimated value: โ‚น114,500.00. Key requirements include 5-year OEM warranty, 10-year spare part availability, English manuals (hard & soft copy), and installation with training. A direct presence or approved Indian service center for the principal manufacturer is mandatory. The bid specifies an option to adjust quantity by ยฑ25% and to extend delivery timelines accordingly. This tender emphasizes post-sale support, calibration procedures, and a toll-free technical assistance channel, with emphasis on supplier readiness to demonstrate at installation and training on acceptance.

Technical Specifications & Requirements

  • Product: Oxygen Concentrator (V2)
  • Core features: General product description; maximum flow rate; oxygen concentration monitor; operation type
  • Standards/Certifications: MDR 2017 compliance, valid drug license under Drugs and Cosmetics Act; manufacturing unit certification; product test reports per MDR 2017
  • Documentation & Deliverables: certifications, licenses, and test reports at bid submission and with supplies; spare parts catalog; detailed maintenance manuals; local calibration procedures; advanced maintenance documentation; list of critical spares with part numbers
  • Support & Training: toll-free technical support; installation, commissioning, and operator/training post-supply; service center presence in India; English manuals; calibration & maintenance guidance
  • Lifecycle: uninterrupted 10-year spare part availability; 5-year warranty from final acceptance; commissioning if included in scope
  • OEM/Reseller: must ensure uninterrupted availability of spares for 10 years and direct OEM service presence in India

Terms, Conditions & Eligibility

  • Option Clause: quantity may increase/decrease by up to 25% at contract placement or during currency at contracted rates
  • Warranty: 5-year warranty from final acceptance; OEM warranty certificates required at delivery; ensure defect rectification during warranty; dedicated service personnel per SLA
  • Service & Support: broad after-sales network, toll-free support, installation, training, and maintenance services in India; spares and service coverage validated before acceptance
  • Documentation: submit all certifications, licenses, and MDR-compliant test reports; provide manuals in English; present part numbers and spares list; show local service capabilities
  • Compliance: adhere to MDR 2017 amendments; ensure drug license validity; provide manufacturing unit certification and product test reports
  • Delivery: delivery timeline aligned with option clause; reference to original delivery order dates; extended time rules apply
  • Acceptance: installation, demonstration, and training completed prior to acceptance; after-sales service alignment with consignee location

Key Specifications

  • Product/service names and category: Oxygen Concentrator (V2)

  • Estimated value: โ‚น114,500.00

  • Core requirements: MDR 2017 compliance; drug license; manufacturing unit certification

  • Performance: maximum flow rate; oxygen concentration monitor

  • Warranty: 5-year standard; optional comprehensive warranty via bidding

  • Spare parts: 10-year availability; OEM service centers in India

  • Documentation: MDR test reports, licenses, manuals in English

  • Training: installation, commissioning, operation and maintenance training

  • Delivery: option/extension clauses up to 25% quantity; extended timelines rules

Terms & Conditions

  • Delivery flexibility up to 25% quantity change with contract terms

  • 5-year warranty from final acceptance; OEM service presence in India

  • MDR 2017 compliance and drug license validity required

Important Clauses

Payment Terms

Not specified in data provided; bidders should verify in bid terms and supplier contract

Delivery Schedule

Delivery period linked to original order; option for extended delivery with 30+ days minimum when quantity changes

Penalties/Liquidated Damages

Not explicitly listed; ensure SLA alignment and performance penalties per bid conditions

Bidder Eligibility

  • Presence of direct OEM service center in India or approved service network

  • MDR 2017 compliance with product testing and drug licensing

  • English user/maintenance manuals and training capability

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Oxygen Concentrator (V2) (Q2)

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENT

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 3

GeM-Bidding-9566650.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

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 Oxygen Concentrator
PRODUCT INFORMATION Maximum Flow Rate 5 LPM
PRODUCT INFORMATION Oxygen Concentration monitor available Yes
PRODUCT INFORMATION Type of operation Continuous Flow Type
WARRANTY Warranty in years (Option of comprehensive warranty is available through bidding only, which if opted will supersede normal warranty in the catalogue) 3 Or higher
WARRANTY Spare part availability Yes
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 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
MISCELLANEOUS REQUIREMENTS OEM/Reseller shall ensure uninterrupted availability of all spares for 10 years Yes
MISCELLANEOUS REQUIREMENTS Availability of toll free facility for technical support maintened by OEM or authorized agencies Yes
MISCELLANEOUS REQUIREMENTS User/Technical/Maintenance manuals to be supplied in English in hard and soft copy Yes
MISCELLANEOUS REQUIREMENTS Details of equipments and procedures required for local calibration and routine maintenance to be supplied and advanced maintenance task documentation also to be furnished Yes
MISCELLANEOUS REQUIREMENTS List of important spares and accessories, with their part numbers to be supplied to the buyer at the time of supplying the equipment Yes
MISCELLANEOUS REQUIREMENTS Installation and Demonstration of equipment and training to be provided after completing supplies before acceptance Yes
MISCELLANEOUS REQUIREMENTS The Principal Manufacturer must have direct Presence/approved service center In India Yes

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Required Documents

1

GST Registration Certificate

2

Permanent Account Number (PAN) Card

3

Experience certificates for prior oxygen concentrator supply

4

Financial statements (latest) and proof of turnover

5

EMD documents (as applicable by tender terms)

6

Technical bid documents demonstrating MDR 2017 compliance

7

OEM authorization or approved reseller agreement

8

Manufacturing unit certification

9

Test reports per MDR 2017

10

Drug license under Drugs and Cosmetic Act 1940

11

Maintenance manuals (English) โ€“ hard and soft copies

12

Spare parts list with part numbers and 10-year availability plan

13

Installation, commissioning, and training plan

14

Service center details and toll-free support information

Frequently Asked Questions

How to bid for the Indian Army oxygen concentrator tender in India 2026

Bidders must meet MDR 2017 compliance, provide drug license, manufacturing unit certification, and MDR test reports. Submit OEM authorization, 5-year warranty plan, and 10-year spare parts availability. Include English manuals and installation/maintenance plan. Delivery terms may include a 25% quantity option with extended timelines.

What documents are required for oxygen concentrator bid in India

Submit GST, PAN, experience certificates, financial statements, MDR-compliant test reports, drug license, manufacturing unit certification, OEM authorizations, and installation/maintenance manuals in English. Include spare parts catalog with part numbers and service center details, plus training plan and toll-free support information.

What MDR 2017 standards apply to oxygen concentrator procurement

Bidders must provide MDR 2017 compliant certification and test reports, along with a valid drug license under the Drugs and Cosmetic Act. Ensure manufacturing unit certification is current, and furnish all MDR-related documentation at bid submission and with delivery.

What is the warranty period and service terms for the oxygen concentrator

A 5-year warranty from final acceptance or after installation is required, with OEM certificates at delivery. The seller must maintain service personnel in India for timely servicing under SLA, and provide installation, commissioning, and training post-supply.

What is the impact of quantity option on delivery for this tender

The purchaser may adjust quantity by up to 25% at contract placement or during the contract period at contracted rates. Delivery timelines extend proportionally, with a minimum extension of 30 days when additional quantity is exercised.

Which certifications and manuals must accompany the oxygen concentrator bid

Include MDR compliance reports, drug license, manufacturing unit certification, English user/maintenance manuals (hard & soft copy), and a detailed maintenance/calibration procedure. Provide a spare parts list with part numbers and a toll-free support plan.

Who must have a direct presence for service in India for this tender

The principal manufacturer or an approved service center must have a direct Presence/approved service center in India, ensuring uninterrupted spare parts availability for 10 years and prompt post-sales support.

What installation and training are required after supply

Installations must be demonstrated and training provided on site before acceptance. Deliver maintenance task documentation, local calibration details, and operator training. Training should cover operation, troubleshooting, and routine maintenance.

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