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Gujarat Panchayats And Rural Housing Dept Blood Gas Analyzer Tender Vadodara 2026 – MDR/Medical Device Standards

Bid Publish Date

19-Jun-2026, 5:33 pm

Bid End Date

29-Jun-2026, 6:00 pm

EMD

₹1,44,000

Progress

Issue19-Jun-2026, 5:33 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

6

Bid Type

Two Packet Bid

Key Highlights

  • Direct OEM/approved service center presence required in India
  • MDR 2017 compliance and NABH calibration certificates explicit
  • 25% quantity adjustment right during and after contract initiation
  • 10-year uninterrupted spare parts availability commitment
  • LIS/HIS data transfer capability and barcode patient identification
  • Room-temperature cartridge storage (2–30°C) and automatic calibration details

Categories 5

Tender Overview

The Gujarat Panchayats And Rural Housing Department seeks to procure an arterial blood gas analyzer (V2) for Vadodara, Gujarat. The project is positioned under general medical equipment procurement with an EMD of ₹144,000. The scope covers a complete blood gas analyzer system including sample handling, barcode capabilities, LIS/HIS data transfer, and room-temperature cartridge storage. The buyer emphasizes long-term spare availability (10 years), OEM service presence in India, English manuals, and installation training post-delivery. These factors define a comprehensive clinical analytics platform requiring strict MDR 2017 compliance and NABH calibration standards.

The tender emphasizes data interoperability, patient panel versatility, and robust maintenance documentation to support clinical workflows. A key differentiator is the requirement for direct OEM/approved service centers and toll-free technical support, with mandatory calibration and local maintenance procedures provided by the supplier. The procurement signals a regulated, hospital-grade instrument with lifecycle support and regulatory compliance.

Technical Specifications & Requirements

  • Product category: arterial blood gas analyzer system (V2)
  • Core capabilities: measures standard blood gas parameters, cardiac and neonatal panels, and wide patient panels; supports on-board barcoding; patient data transfer to LIS/HIS
  • Printer type and sample handling: built-in printer; cartridge/reagent storage 2–30°C; automatic calibration advisory
  • Data & interoperability: LIS/HIS interoperability; NABH-calibration certificates; advanced maintenance documentation
  • Compliance: MDR 2017 compliance; valid drug license under Drugs and Cosmetics Act; electrical safety standards; NABH calibration
  • Accessories/aftercare: spares availability for 10 years; toll-free technical support; English manuals; installation, training, and on-site demonstrations
  • OEM presence: principal manufacturer must have direct presence or approved Indian service center
  • Documentation: all certifications, licenses, and test reports to bidder at bid/submission time and with supplies
  • Warranty & shelf life: specify warranty duration; reagent cartridge shelf life; on-board reagent shelf life weeks
  • Miscellaneous: list of spares with part numbers; local calibration procedures; advanced maintenance task docs

Terms, Conditions & Eligibility

  • EMD: ₹144,000 (requirement not specified as refundable/deducted here; verify bid terms)
  • Delivery/term: option clause allows ±25% quantity; delivery period calculated per contract with minimum 30 days extension
  • Service centers: must have functional service center in-state; if not, establish within 30 days of award
  • Compliance: bidder must not be in liquidation; provide undertaking; submit all requested certificates/documents
  • Documentation: supply OEM authorizations, test reports, MDR compliance certificates, NABH calibration certificates, and installation/training manuals
  • Warranty/penalties: ensure warranty coverage including electrodes/membranes; define LD/penalty terms if specified; calibration certificates required
  • Presence in India: Principal Manufacturer must have direct presence or approved service center
  • Post-delivery: installation, demonstration, and operator training required before acceptance
  • Payment terms: not explicitly stated; verify in terms and conditions; typical procurement may include staged payments
  • Right to modify: purchaser may adjust quantities up to 25% during contract currency

Key Specifications

  • Arterial blood gas analyzer with LIS/HIS data transfer capability

  • Wide patient panels on a single system and patient barcode facility

  • Room-temperature cartridge/reagent storage 2–30°C

  • Automatic calibration functionality with supplier details at supply time

  • On-board reagent shelf life in weeks and cartridge shelf life in months

  • Electrical safety standards compliance and MDR 2017 adherence

  • 10-year spare parts availability and toll-free technical support

Terms & Conditions

  • Delivery quantity may vary up to ±25% with contract extension

  • Functional in-state service centers required; establishment within 30 days if absent

  • Submit MDR-related licenses, NABH calibration, and OEM authorizations with bid

Important Clauses

Payment Terms

Not explicitly defined; procurement typically follows staged payments; confirm with ATC

Delivery Schedule

Delivery period commences from last delivery order date; extension rules apply per option clause

Penalties/Liquidated Damages

Penalties not detailed; verify LD terms in bid ATC and supply agreement

Bidder Eligibility

  • Functional service center in Gujarat or documented plan to establish in 30 days

  • Demonstrated experience delivering MDR-compliant medical devices

  • Financial stability proof and non-liquidity certification

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Arterial Blood Gas Analyzer (V2) (Q2)

Authority Records

PANCHAYATS AND RURAL HOUSING DEPARTMENT

BID & GeM Expert Consultancy

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

Bid Preparation GeM Registration Document Filing

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Documents 4

GeM-Bidding-9494860.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 Arterial Blood Gas Analyzer
PRODUCT INFORMATION Type of blood gas analyser Bench Top
PRODUCT INFORMATION Type of Technology Liquid Reagent Based Calibration
PRODUCT INFORMATION Parameters measured by blood gas analyser pCO₂, pO₂, Na⁺, K⁺, pH and calculated parameters like HCO₃⁻, Base excess, TCO₂
PRODUCT INFORMATION Additional Parameters measurable by the blood gas analyser Cl-, iCa, Glu, Hct, Lacate
PRODUCT INFORMATION Cardiac Parameters measurable Not available
PRODUCT INFORMATION Neonatal Parameters Not available
PRODUCT INFORMATION Monitor type LCD, LED Or higher
PRODUCT INFORMATION Type of printer Inbuilt Printer
PRODUCT INFORMATION Cartridge / reagent to be used can be stored mostly at room temperature between 2-30 Degree C, Automatic calibration (hint: seller shall inform the exact details to buyer at the time of making the supplies) Yes
PRODUCT INFORMATION Shall have patient Bar Code facility, Ability to run a wide range of patient panels on one system Yes
PRODUCT INFORMATION Capability to transfer patient data to LIS/HIS Yes
PRODUCT INFORMATION Sample Volume in micro litre ≤ 200
PRODUCT INFORMATION Power source AC Mains + Rechargeable battery
PRODUCT INFORMATION Battery backup provided Through rechargeable battery for 30 mins, Through UPS for 30 mins
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/EN 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 & SHELF LIFE Warranty (including electrode and membrane etc as applicable for the analyzer offered) in years 2.0, 3.0
WARRANTY & SHELF LIFE Shelf life of the reagent / cartridges as applicable in months 3
WARRANTY & SHELF LIFE On-board shelf life of reagent in weeks 4
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 Principal Manufacturer must have direct Presence/approved service center In India Yes
MISCELLANEOUS REQUIREMENTS Calibration certificates as per NABH requirement Yes

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Required Documents

1

GST registration certificate

2

Permanent account number (PAN) card

3

Experience certificates for similar medical device supply

4

Financial statements or banker’s certificate

5

EMD payment receipt or proof of exemption

6

Technical bid documents and manufacturer authorization

7

OEM/Authorized service center proof (India presence)

8

MDR compliance certificates and NABH calibration certificates

9

Test reports and electrical safety certificates

10

User/Technical/Maintenance manuals (English) in hard and soft copy

Frequently Asked Questions

Key insights about GUJARAT tender market

How to bid for a blood gas analyzer tender in Vadodara Gujarat 2026

Bidders must submit GST, PAN, financials, MDR/compliance certificates, NABH calibration, OEM authorization, and evidence of a functional Indian service center. Include EMD of ₹144,000 and demonstrate 10-year spare parts availability. Ensure installation, training, and LIS/HIS interoperability details are provided.

What documents are required for Gujarat blood gas analyzer procurement

Submit: GST certificate, PAN, experience certificates for similar devices, financial statements, MDR compliance certificates, NABH calibration certificates, test reports, OEM authorization, and service center proof in India. Include installation and training manuals in English.

What are the key technical specifications for the blood gas analyzer

System must support wide patient panels, barcode facility, LIS/HIS data transfer, room-temperature reagent storage (2–30°C), built-in printer, automatic calibration, neonatal and cardiac parameter support, and NABH-calibrated NABH requirements with manufacturer calibration documentation.

What are the EMD and delivery terms for this procurement

EMD is ₹144,000. The option clause allows ±25% quantity changes with price protection. Delivery periods extend from the last original delivery date, with a minimum 30-day extension in extended periods. Confirm exact delivery schedule in ATC.

What warranties and maintenance terms are required for equipment

Warranty should cover electrodes and membranes as applicable, with on-board reagent shelf life details. Ten-year spare parts availability and toll-free service support expected. NABH calibration certificates must be maintained and provided.

How to verify OEM service presence in India for this bid

Bidder must provide direct OEM presence or approved Indian service center documentation. If not present, establish a service center within 30 days of award and supply evidence before payment release.

What training and installation obligations accompany delivery

installation and demonstration must occur after supplies and before acceptance. Training provided to users, with English manuals in hard and soft copy, and local calibration procedures documented for ongoing maintenance.

Which standards and certifications are mandatory for compliance

Must comply with MDR 2017 (as amended), electrical safety standards, NABH calibration, and Drug License under Drugs and Cosmetics Act. Provide manufacturing unit certification and test reports as part of bid submission.

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