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Directorate Of Purchase And Stores Hematology Analyser Tender Kota Rajasthan ISI/ MDR Compliant 2026

Bid Publish Date

16-Jun-2026, 10:20 am

Bid End Date

29-Jun-2026, 11:00 am

Location

CHITTORGARH , RAJASTHAN

Progress

Issue16-Jun-2026, 10:20 am
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

1

Bid Type

Two Packet Bid

Key Highlights

  • Technical standards: MDR 2017 compliance and NABH calibration certificates
  • Warranty: 5 years with option for comprehensive warranty through bidding
  • Service availability: OEM direct presence in India and 10-year spares lifecycle
  • Data management: LJ Plot, LIS integration, online QC, workload recording
  • Power: UPS rating and backup time clearly defined, power supply specs
  • Make in India: mandatory declaration with Annexure-XI
  • Training: 7 days on-site training at NFC Kota for 1 trainee
  • Post-supply inspection: not permitted; ensure compliance without external inspection

Categories 2

Tender Overview

The procuring entity is the Directorate Of Purchase And Stores for the Department Of Atomic Energy, issuing a tender for a 5 Part Automated Hematology Analyser (V2) (Q2) to be deployed at NFC Kota, Rajasthan. The scope emphasizes a fully automated system with startup/shutdown and sample analysis, multi-channel capability, and extensive data management features. The BOQ shows a comprehensive feature set spanning analysis methods, WBC/RBC/PLT measurements, reticulocyte analysis, linearisations, and advanced cytopenia options. The package requires integration readiness with lab information systems, on-board reagent inventory, and a robust warranty framework, including a 5-year OEM-backed warranty. Uniquely, the contract includes training for one person at NFC Kota and post-delivery service considerations with India-based support. The tender's differentiator lies in its exhaustive specification list covering calibration, QA programs, and remote data handling, with a strong emphasis on MDR compliance and service continuity for 10 years through spares availability.

Technical Specifications & Requirements

  • System should support automatic start-up/shut-down, sample analysis, and multi-channel WBC/PLT/RBC analysis with direct capillary blood aspiration.
  • Required parameters include CSF, synovial, serous body fluids with WBC-BF, RBC-BF, MN#, MN%, PMN%, and additional indices like IPF, PLT-0, PLT-F, RET-HE, HFR, LFR, MFR, IRF.
  • Throughput metrics, linearity checks (platelet, RBC, Hb, retic, WBC), and direct MCV measurement must be specified; include auto-dilution, clot detection, auto probe wiping, and extended cytopenic analyses.
  • Data management must feature on-board HDD/RAM, integrated LCD, PC with latest processor, USB ports, network/LIS compatibility, workload recording, QC/Delta checks, online QC, and LJ Plot, with auto-cleaning software.
  • POWER: UPS rating, backup time, and power supply details; temperature/humidity operating ranges; and sufficient consumables with 2/3rd shelf-life.
  • CERTIFICATION: MDR 2017 compliance, drug license under Drugs and Cosmetic Act, NABH calibration certificates, electrical safety, and OEM/authorized service presence in India.

Terms & Eligibility

  • Warranty: 5-year warranty from final acceptance or post-installation completion, with OEM certificates provided at delivery. Comprehensive warranty option may supersede catalogue terms.
  • EMD/PBG: Bid security via DD payable at Hyderabad; post-award delivery of original DD within 15 days; PSDBG/PSDDD submission as specified.
  • Training: 7-day training for 1 trainee at NFC, Kota, included in scope; supplier to furnish service centers and toll-free technical support; Make in India declaration required.
  • After-sales: 10-year spare availability, local calibration procedures, English manuals, and OEM direct presence in India.

Key Specifications

  • Type of configuration: 5 Part Automated Hematology Analyser (V2) with multi-channel analysis

  • Automation: automatic startup/shutdown, sample analysis, auto-dilution, auto probe wipe

  • Measurements: WBC, RBC, Hb, Platelets, Retic, MCV, IPF, LINEARITY checks

  • Body fluids parameters: WBC-BF, RBC-BF, MN#, MN%, PMN%, PMN#

  • Data management: LIS interoperability, on-board storage, LJ Plot, online QC, workload recording

  • Calibration/QA: multiple QC programs, NABH calibration certificates, calibration per MDR

Terms & Conditions

  • EMD via DD with 15-day delivery of original; PSDBG/PSDDD submission required

  • Warranty: 5 years; options for comprehensive warranty via bidding

  • Post-delivery service: India-based OEM service centers and 10-year spares

Important Clauses

Payment Terms

DD-based EMD submission, PBG optional; final payment terms to be as per GeM terms and buyer ATC

Delivery Schedule

Delivery and installation timelines to be provided; post-supply inspection not permitted

Penalties/Liquidated Damages

LDs for late delivery or non-compliance to MDR/NABH calibration; details to be specified

Bidder Eligibility

  • Direct presence of OEM or authorized service centers in India

  • Experience in supplying and supporting hematology analysers with MDR compliance

  • Financial capability to sustain 5-year warranty and 10-year spares lifecycle

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

5 Part Automated Hematology Analyser (V2) (Q2)

Authority Records

DEPARTMENT OF ATOMIC ENERGYDIRECTORATE OF PURCHASE AND STORES

BID & GeM Expert Consultancy

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

Bid Preparation GeM Registration Document Filing

Free consultation · 24h response

Documents 4

GeM-Bidding-9458073.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
PRODUCT INFORMATION Type of Configuration Benchtop
PRODUCT INFORMATION Type of system offered Closed system
PRODUCT INFORMATION Type of automation Fully Automatic
PRODUCT INFORMATION Equipment should have automatic start up,shut down and sample analysis Yes
PRODUCT INFORMATION Analysis principle Based on principle of counting and sizing
PRODUCT INFORMATION Type of cell counting 5 part WBC differential without Retic and NRBC enumeration capability
PRODUCT INFORMATION Should have multi channel analysis for better resolution and reproductability Yes
PRODUCT INFORMATION NRBC% No
PRODUCT INFORMATION Availability of body fluid (CSF, synovial, serous) parameters like WBC-BF, RBC-BF, MN#, MN%, PMN%, PMN#,TC-BF# No
PRODUCT INFORMATION IPF analysis No
PRODUCT INFORMATION PLT-0 Analysis No
PRODUCT INFORMATION PLT-F Analysis No
PRODUCT INFORMATION RET-HE analysis No
PRODUCT INFORMATION HFR analysis No
PRODUCT INFORMATION LFR analysis No
PRODUCT INFORMATION MFR analysis No
PRODUCT INFORMATION IRFanalysis No
PRODUCT INFORMATION Discrete analysis modes available CBC,CBC+DIFF
PRODUCT INFORMATION Analysis method for WBC Dual differential count
PRODUCT INFORMATION Method for platelet measurement Electrical impedance
PRODUCT INFORMATION RBC Measurement method Electrical Impedance
PRODUCT INFORMATION Hb measurement Cyanide free colorimetry
PRODUCT INFORMATION Retic measurement Not provided
PRODUCT INFORMATION Number of sample racks to cater to different tube sizes 1
PRODUCT INFORMATION Maximum sample Aspiration volume needed in all modes 100 µl or less
PRODUCT INFORMATION Minimum sample volume required in all modes 20µl or less
PRODUCT INFORMATION Throughput capacity in CBC/Differential 50-60
PRODUCT INFORMATION Throughput capacity in Retic mode NA
PRODUCT INFORMATION Type of modes of sample running Open vial
PRODUCT INFORMATION Linearity of Platelet 0 to 3000 * 10 3 cells/ micro litres
PRODUCT INFORMATION RBC Linearity 0 to 8 x 10^6 per micro litre or more
PRODUCT INFORMATION Hemoglobin linearity 0 to 25 gm per litre
PRODUCT INFORMATION Retic linearity NA
PRODUCT INFORMATION WBC linearity 0 to 300 * 1000 cells/ micro litres
PRODUCT INFORMATION Directly measures MCV Yes
PRODUCT INFORMATION Time taken by the analyser to produce the test results(Analysis time) in seconds 40-60
PRODUCT INFORMATION Availability of Auto dilution Yes
PRODUCT INFORMATION Clot detection facility Yes
PRODUCT INFORMATION Automatic probe wipe Yes
PRODUCT INFORMATION Extended Analyses for cytopenic samples Yes
PRODUCT INFORMATION Quality assurance system with calibration and controls Yes
PRODUCT INFORMATION Number of quality control programs Atleast 3
PRODUCT INFORMATION Type of Calibration Both manual and automatic
PRODUCT INFORMATION Direct aspiration for capillary blood from finger prick No
PRODUCT INFORMATION Floating discriminator for platelets and RBC counting for reliable RBC and PLT data Yes
PRODUCT INFORMATION Separate diluting nozzles for RBC and WBC Yes
PRODUCT INFORMATION Double bathing mechanism Yes
PRODUCT INFORMATION Upgradable to integrate with attachment No
Data Management and Display Type of data management In-built system
Data Management and Display Display LCD, LED Or higher
Data Management and Display PC hard disk NA
Data Management and Display Inbuilt monitor size in inches NA (for PC based)
Data Management and Display Processor of PC Provided with system NA (If PC not provided)
Data Management and Display RAM NA (If PC not provided)
Data Management and Display HDD NA (If PC not provided)
Data Management and Display The processor and RAM of the board system should be latest version Yes
Data Management and Display Type of external storage SD Card
Data Management and Display Number of USB Port provided 2
Data Management and Display Type of printer unit Inbuilt
Data Management and Display Printer type Black and White Laser Printer
Data Management and Display Display and print provided Scatter plot and histograms
Data Management and Display Auto loader facility Yes
Data Management and Display Database capability of storing sets of results and graphics ≥ 2000 to 5000
Data Management and Display L J Plot facility Yes
Data Management and Display Delta check for cumulative review Yes
Data Management and Display On-line QC option Yes
Data Management and Display Patient moving average Yes
Data Management and Display QC File management Yes
Data Management and Display Facility for workload recording Yes
Data Management and Display Flagging in event of unacceptable control data Yes
Data Management and Display Ability to transmit results to host computer Yes
Data Management and Display Type of user Interface or data entry Touchscreen, Handheld barcode reader facility, Manual
Data Management and Display Have auto cleaning function in the analyser’s software Yes
POWER REQUIREMENTS Type of power supply 100-240 VAC,50-60 Hz
POWER REQUIREMENTS Power Backup facility UPS
POWER REQUIREMENTS Type of UPS Online
POWER REQUIREMENTS Rating of UPS in KVA 0.5
POWER REQUIREMENTS Back up time in minutes 30, 60, 90, 120 Or higher
POWER REQUIREMENTS Availability of Sufficient Number of Quality control files which store 100 or more XB Analysis Yes
ACCESSORIES, SPARE PARTS AND CONSUMABLES Offered equipment unit to be supplied with sufficient consumables (with at least 2/3rd of total shelf life) required for, sufficient to carry out haematological testing of samples" 500
ACCESSORIES, SPARE PARTS AND CONSUMABLES Should have on board reagent facility and automatic reagent inventory management Yes
ACCESSORIES, SPARE PARTS AND CONSUMABLES Net work integration with lab information system feature Yes
ACCESSORIES, SPARE PARTS AND CONSUMABLES Operating temperature and humidity Capable of operating continuously in ambient temperature of 10 to 35 deg C and relative humidity of 15 to 85% in ideal circumstances
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 Warranty in years (Option of comprehensive warranty is available through bidding only, which if opted will supersede normal warranty in the catalogue) 5 Or higher
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 The Principal Manufacturer must have direct Presence/approved service center In India Yes
MISCELLANEOUS REQUIREMENTS Calibration certificates as per NABH requirement Yes
MISCELLANEOUS REQUIREMENTS Time to attend breakdown calls within 48 hrs

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Historical Data

Required Documents

1

GST registration certificate

2

PAN card

3

Experience certificates for similar hematology analyser supplies

4

Financial statements demonstrating stability

5

EMD submission document (DD payable at Hyderabad) and PSDBG/PSDDD documents

6

OEM authorization or direct manufacturer presence proof in India

7

Technical compliance certificates (MDR, electrical safety, NABH calibration)

8

Drug license under the Drugs and Cosmetic Act (as applicable)

9

Calibration certificates and maintenance manuals in English (hard/soft copy)

10

Make in India declaration (Annexure XI)

Frequently Asked Questions

How to bid for Kota hematology analyser tender 2026?

Bidders must submit GST, PAN, experience certificates, financial statements, and EMD via DD payable at Hyderabad. Include OEM authorization, MDR compliance certificates, NABH calibration, and Make in India declaration. Attach training plan for NFC Kota and service center details to enable after-sales support.

What documents are required for this hematology analyser bid in Kota?

Required documents include GST certificate, PAN, vendor qualification, company financials, experience in similar projects, MDR and electrical safety certificates, NABH calibration, OEM authorization or proof of Indian service presence, and the Make in India declaration. Also provide post-delivery maintenance manuals.

What are the essential technical specifications for this analyser in Kota?

System must support automatic startup/shutdown, multi-channel analysis, direct capillary blood aspiration, WBC/RBC/PLT/Retic measurements, and LIS compatibility. Include throughputs, linearity for Hb/RBC/PLT/Retic, and QA programs; ensure MDR and NABH documentation is attached.

When is the bid submission deadline for the NFC Kota tender?

Exact submission dates are not provided in the data; bidders should monitor GeM portal and the NFC tender notices for bid opening timelines, required submission windows, and post-delivery inspection policies.

What are the payment terms for the NFC Kota hematology analyser supply?

Payment terms will align with buyer ATC; DD-based EMD, and PBG options exist; post-award payment timing and milestones will be defined in the contract and GeM terms, including delivery acceptance and installation milestones.

What warranty and after-sales support are required for this tender?

A 5-year warranty from final acceptance or post-installation is required, withOEM certificates provided at delivery. Ensure India-based service centers, toll-free support, and 10-year spare availability; consider comprehensive warranty if bidding accordingly.

What certifications must be submitted with the bid for MDR compliance?

Submit MDR 2017 compliance certificates, NABH calibration certificates, Electrical Safety certificates, drug license per Drug and Cosmetic Act, and NABH calibration reports. Include Make in India Annex XI declaration and OEM authorization if applicable.

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