Arterial Blood Gas Analyzer (V2)
Employees State Insurance Corporation
VALSAD, GUJARAT
Progress
Quantity
1
Bid Type
Single Packet Bid
The Hospital Medical Education under the Health And Family Welfare Department, Mizoram invites bids for an Arterial Blood Gas Analyzer (V2) for delivery to the District Hospital, Kolasib, Mizoram. The procurement focuses on a modern blood gas analyzer capable of neonatal and cardiac parameter analysis, patient bar code support, LIS/HIS data transfer, and compatible with room-temperature reagents (2-30°C). The tender emphasizes OEM/authorized service presence in India, comprehensive calibration, and NABH-compliant documentation. Delivery terms include potential quantity variation up to 25%, and installation/commissioning to occur at the Kolasib address. The scope covers training, manuals in English, and a robust maintenance framework. The estimated value and EMD are not disclosed in the data, but the emphasis is on MDR 2017 compliance and long-term support.
Arterial Blood Gas Analyzer (V2) with multi-panel capability
Neonatal and cardiac parameter measurement support
LIS/HIS data transfer capability
Patient barcode facility and wide-range panel support
Room-temperature reagent stability 2-30°C
Power supply with battery backup
MDR 2017 compliance and NABH calibration certificates
On-board reagent shelf life and cartridge maintenance details
Mandatory OEM direct presence in India for service and calibration
Delivery quantity may vary by ±25% with extended delivery calculations
Must supply MDR 2017 compliance, NABH calibration, drug license, and manufacturing certification
Installation, training, and maintenance to be performed by OEM or authorized personnel
Not disclosed in data; ensure compliance with standard govt terms and OEM support during delivery
Delivery to District Hospital, Kolasib; base period with option-based extension as per clause 1
Not specified; implied through delivery delays and non-compliance with MDR/NABL calibrations
3 years of supply/manufacture history of similar arterial blood gas analyzers to govt or PSU
OEM direct presence or approved Indian service center
Compliance with MDR 2017, NABH calibration and drug licensing
Main Document
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS
Employees State Insurance Corporation
VALSAD, GUJARAT
National Animal Resource Facility For Biomedical Research
Office Of Dg (ls)
NORTH DELHI, DELHI
Office Of Dg (ls)
NORTH DELHI, DELHI
Employees State Insurance Corporation (esic)
INDORE, MADHYA PRADESH
Tender Results
Loading results...
| Category | Specification | Requirement |
|---|---|---|
| PRODUCT INFORMATION | Type of blood gas analyser | Bench Top |
| PRODUCT INFORMATION | Type of Technology | Cartridge (Multiple-Use) |
| 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, Hct |
| 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 |
| PRODUCT INFORMATION | Battery backup provided | 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 | 5.0 |
| WARRANTY & SHELF LIFE | Shelf life of the reagent / cartridges as applicable in months | 6 |
| WARRANTY & SHELF LIFE | On-board shelf life of reagent in weeks | 8 |
| 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 |
Discover companies most likely to bid on this tender
GST registration certificate
Permanent Account Number (PAN) card
Experience certificates showing 3 years of similar Govt/PSU supply
Financial statements demonstrating financial stability
EMD/Security deposit documents (if applicable)
Technical bid documents and OEM authorization (if bidding through distributors)
MDR-related certifications, NABH calibration certificates
Drug license for the product under Drugs and Cosmetic Act
Manufacturing unit certification and product test reports as per MDR 2017
Installation, calibration procedures, and maintenance manuals (English)
Key insights about MIZORAM tender market
This Mizoram procurement requires MDR 2017 compliance, NABH calibration certificates, and OEM direct presence in India. Submit 3 years of govt/PSU supply contracts, OEM authorization, and English manuals. Include installation, training plans, and calibration procedures with your bid package, plus spares list and data interoperability features.
Required submissions include GST and PAN, experience contracts proving 3 years of similar govt work, MDR/ NABH certificates, drug licenses, manufacturing certification, calibration reports, and OEM authorization. English user manuals and maintenance procedures must accompany the bid and be supplied with the equipment.
Bidders must meet MDR 2017 compliance, electrical safety standards, NABH calibration certificates, and drug licensing requirements. The product should enable LIS/HIS data transfer, patient barcode, and 2-30°C reagent storage, with origin OEM service available in India.
The buyer may increase or decrease quantity by up to 25% at contract award and during currency. Delivery time extensions follow the specified formula, with a minimum extension of 30 days, beginning after the original delivery date.
Installation, commissioning, and training must be conducted by OEM or an authorized reseller. Provide an installation plan, training schedule, and advanced maintenance documentation; ensure service availability via toll-free OEM support.
Key certifications include MDR 2017 compliance, NABH calibration certificates, and Drugi license under the Drugs and Cosmetic Act. Also required are manufacturing unit certification and product test reports as per MDR guidelines.
Yes. The tender mandates direct presence or an approved service center in India to ensure warranty support, calibration, and maintenance. An OEM authorization certificate is also needed when bidding through distributors.
The system must support LIS/HIS data transfer and patient barcode capability, enabling seamless integration with existing hospital information systems and flexible panel configurations on a single analyzer system.
Indian Army
📍 UDHAMPUR, JAMMU & KASHMIR
Kamdhenu University
📍 NAVSARI, GUJARAT
Gujarat Medical Services Corporation Limited (gmscl)
Sign up now to access all documents
Main Document
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS