GEM

Contract Bidding Open For Fully Automatic Biochemistry Analyzer (V2) in BANGALORE, KARNATAKA

Posted

28 Oct 2025, 11:20 am

Deadline

18 Nov 2025, 12:00 pm

EMD

₹96,000

Value

₹48,00,000

Progress

Issue28 Oct 2025, 11:20 am
AwardPending
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Quantity

1

Bid Type

Two Packet Bid

Categories 1

A tender has been published for Sports Authority Of India (sai) Fully Automatic Biochemistry Analyzer (V2) (Q2) in BANGALORE, KARNATAKA. Quantity: 1 by. Submission Deadline: 18-11-2025 12: 00: 00. Check eligibility and apply.

Technical Specifications 1 Item

Item #1 Details

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Category Specification Requirement
GENERAL Product Description Fully Automatic Biochemistry Analyzer
PRODUCT INFORMATION System Type Fully Automated Random Access System
PRODUCT INFORMATION Type of Biochemistry Analyzer Floor Model Type
PRODUCT INFORMATION Sample Type Serum, Plasma, Whole Blood, Urine, CSF, Hemolyzed Blood, Any body fluid samples
PRODUCT INFORMATION Assay Type End point, Rate, Kinetic Turbidometric and Bi chromatic Assay
PRODUCT INFORMATION Throughput tests / hour Photometric Tests with ISE module 350 or more, 600 or more, 1000 or more Or higher
PRODUCT INFORMATION Throughput tests/hour Photometric Tests without ISE Module 200 or more, 350 or more, 600 or more, 1000 or more Or higher
PRODUCT INFORMATION Calibration Facility Factor, Linear (one, two and multi-point), Exponential, Logit-Log, Spline, Non-Linear
PRODUCT INFORMATION Equipment must have self diagnostic tests with error message and online display Yes
PRODUCT INFORMATION Equipment must be programmable for all test menus and state of the art work station should be up-gradable by addition of ISE module Yes
PRODUCT INFORMATION Sample loading type Continuous
PRODUCT INFORMATION Equipment should have both internal and external probe cleaning/washing capacity Yes
PRODUCT INFORMATION Repeat facility to be available for calibrator and control Yes
PRODUCT INFORMATION Reagent refill message and monitoring facility Yes
PRODUCT INFORMATION Minimum number of test parameters on board at a time ≥ 30 Or higher
PRODUCT INFORMATION Minimum sample capacity at a time 100 or more
PRODUCT INFORMATION Minimum number of STAT samples at a time ≥ 10 Or higher
PRODUCT INFORMATION Should have pre post and auto dilution of samples and return capability for out of range samples Yes
PRODUCT INFORMATION Probe dispensers Probe dispensers must have level detectors and must typically use between 2-25 µl of sample
PRODUCT INFORMATION Spectoral range in nm 340 to 800 nm
PRODUCT INFORMATION Wave length selection method Diffraction Grating
PRODUCT INFORMATION Light source Halogen lamp low cost with long life
PRODUCT INFORMATION Life of lamp in hrs ≥ 1000 Or higher
PRODUCT INFORMATION Power consumption of lamp in VA ≤ 1000 Or higher
PRODUCT INFORMATION Type of sample cups Primary Tube
PRODUCT INFORMATION Number of sample cups provided with machine 1000, 1500, 2000 Or higher
PRODUCT INFORMATION QC program QC Programme with L-J graphs, Print out of reports
PRODUCT INFORMATION Reaction Cuvette Reusable
PRODUCT INFORMATION System should have on board cooling system Refrigerated
PRODUCT INFORMATION DI water plant for the washing of the cuvettes/ to avoid carry over and contamination Yes
PRODUCT INFORMATION Compatible on line UPS Yes
PRODUCT INFORMATION Back up time 1 hour, 2 hour Or higher
PRODUCT INFORMATION Data management software Equipment to be provided with compatible programmable windows based comprehensive data processing and management system graphical user interface software, LM Capability complete back up of data base for calibration control and patient sample results, capability for Bi-directional interfacing with LIS
PRODUCT INFORMATION Patient result storage capacity 10000, 15000, 50000 or more Or higher
PRODUCT INFORMATION Onboard cuvette washing & drying facility Yes
PRODUCT INFORMATION Photometeric Checking of cuvettes before next reaction - Create Another field Yes
PRODUCT INFORMATION System should have facility for reading results on monitor and print out facility Yes
PRODUCT INFORMATION Reagents to be provided with machine Creatinine, Urea, Uric Acid, Triglycerides, Glucose, Cholesterol, Total Protein, Calcium, Albumin, SGOT, SGPT, Alkaline Phosphatase, Bilirubin (Total & Direct), Anti-Streptolysin O (ASO), Calibrator, Control (Normal), Control (Abnormal)
PRODUCT INFORMATION Quantity of Reagents provided (Number of Tests) 100 Tests or more, 500 Tests or more Or higher
PRODUCT INFORMATION Reports Prinout of reports and full patient demographics to be available
PRODUCT INFORMATION System to be provided with necessary pre requisites and start up kits normal and abnormal QC and calibrators Yes
PRODUCT INFORMATION Availability of RS 232 port/USB for data transfer Yes
PRODUCT INFORMATION Power supply 200-240V AC, 50Hz Single phase
PRODUCT INFORMATION Reagents position 30 or more
PRODUCT INFORMATION Bar code reader for reagents Yes
PRODUCT INFORMATION Bar code reader for samples Yes
PRODUCT INFORMATION Refrigerator provided with Analyzer No
PRODUCT INFORMATION Capacity of Refrigerator (Litres) 300 Litres, 500 Litres, NA Or higher
PRODUCT INFORMATION Type of Micro pipette provided Not provided
PRODUCT INFORMATION Variable Micro pipette provided No
PRODUCT INFORMATION Seller must provide original documentary proof of the date and place of manufacturing of provided equipment Yes
PRODUCT INFORMATION Sytem shall be provided with a compatible desktop PC Yes
PRODUCT INFORMATION Speed of processor in GHZ Greater than 3 GHZ
PRODUCT INFORMATION RAM in MB ≥ 512 MB
PRODUCT INFORMATION Hard disk drive capacity in GB ≥ 80 GB
PRODUCT INFORMATION Monitor TFT/LCD/LED/ Digital color monitor
PRODUCT INFORMATION Monitor size (inches) 17 inches or more
PRODUCT INFORMATION Compatible operating system provided in PC Yes
PRODUCT INFORMATION Printer provided Yes
PRODUCT INFORMATION Type of printer Laser Printer
PRODUCT INFORMATION Startup kit, Calibrators, consumables required in training the staff/Technician/Doctors should be provided at the time of installation &Training Yes
PRODUCT INFORMATION The reaction cuvettes should be replaced at free of cost when ever required during the warranty period No
CERTIFICATION AND REPORTS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATION AND REPORTS Availability of valid Drug/medical device 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
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 provided in English in hard and soft copy Yes
MISCELLANEOUS REQUIREMENTS Details of equipments and procedures required for local calibration and routine maintenance to be provided and advanced maintenance task documentation also to be furnished Yes
MISCELLANEOUS REQUIREMENTS List of important spares and accessories, with their part numbers to be provided 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
MISCELLANEOUS REQUIREMENTS Calibration certificates as per NABH requirement Yes
WARRANTY Warranty in years (including machine, DI Water Plant if provided , UPS, computer and printer) 3, 5 Or higher

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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

Additional Doc 1 (Requested in ATC) *In case any bidder is seeking exemption from Experience / Turnover Criteria

7

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