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Government Tender Published for Hematology Analyzer (Fully-Automated) in VADODARA, GUJARAT

Bid Publish Date

02-Sep-2026, 4:00 pm

Bid End Date

12-Sep-2026, 4:00 pm

Progress

Issue02-Sep-2026, 4:00 pm
AwardPending

Public procurement opportunity for Indian Army Hematology Analyzer (Fully-Automated) (Q2) in VADODARA, GUJARAT. Quantity: 1 issued by. Submission Deadline: 12-09-2026 16: 00: 00. View full details and respond.

Tender Data

Bid Details

Quantity

1

Bid Type

Two Packet Bid

Bid Validity

30 (Days)

Bid Type

Service

Evaluation

Total value wise evaluation

Inspection Required

No

Tech Clarification Time

2 Days

Preference & Exemptions

EMD Required

No

MII Purchase Preference

No

MSE Purchase Preference

Yes

MSE Preference Band

L1+15%

MSE Exemption/Relaxation

Yes

Startup Exemption/Relaxation

Yes

Bid Splitting Applied

No

Requirements

Min. Avg. Annual Turnover

8

OEM Avg. Turnover

5

Past Performance

40 %

Experience Required

1 Year (s)

Arbitration Clause

No

Mediation Clause

No

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Hematology Analyzer (Fully-Automated) (Q2)

Delivery Details

Max Delivery Days

15

Delivery Locations

1

Delivery Cities

Vadodara

Delivery Locations

ConsigneeAddressCityStatePincodeQuantityDelivery DaysAdditional Requirement
-VadodaraVadodara--115-

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENT

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Free consultation · 24h response

Documents 3

GeM-Bidding-9837718.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Authority & Contact

Organization

Indian Army

Office Name

Not disclosed yet

Grievance Contact

[email protected]

Categories 4

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Historical Data

Required Documents

1

Experience Criteria

2

Past Performance

3

Bidder Turnover

4

Certificate (Requested in ATC)

5

OEM Authorization Certificate

6

OEM Annual Turnover

7

Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria

8

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

Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
ANALYSIS PARAMETERS Type 3-Part
ANALYSIS PARAMETERS WBC Differential (Reportable) 3-Part (Lymphocytes, Mid-Cells/Mixed Cells, Granulocytes/Neutrophils)
ANALYSIS PARAMETERS Core CBC Parameters (Reportable) WBC, RBC, HGB, HCT, MCV, MCH, MCHC, RDW-SD, RDW-CV, PLT, MPV Or higher
ANALYSIS PARAMETERS Reticulocyte Count No
ANALYSIS PARAMETERS NRBC (Nucleated Red Blood Cells) No
ANALYSIS PARAMETERS Immature Platelet Fraction (IPF) No
ANALYSIS PARAMETERS Body Fluid (Reportable) No
ANALYSIS PARAMETERS Minimum Throughput (Samples/hour) 50.0 Or higher
SAMPLE Modes available for sample running Open Tube, Capillary/Pre-diluted
SAMPLE Sample Loading Mode Manual Loading
SAMPLE Minimum Autosampler Capacity 0.0 Or higher
SAMPLE STAT Capability No
SAMPLE Cap-Piercing Function No
REAGENT On board reagent facility and automatic reagent inventory management No
CALIBRATION & QUALITY CONTRAOL Calibration Type Automatic and Manual Both Or higher
CALIBRATION & QUALITY CONTRAOL Quality Control Type Manual, Automatic, Automatic and Manual Both Or higher
CALIBRATION & QUALITY CONTRAOL QC Levels (Minimum) 2 Levels Or higher
CALIBRATION & QUALITY CONTRAOL QC Trend Analysis Levey-Jennings Charts / Westgard Rules
DISPLAY & INTERFACE Inbuilt Screen Size ≥ 5 inch
DISPLAY & INTERFACE Printer Type In-built Thermal Printer
DISPLAY & INTERFACE Connectivity USB, LAN, LIS/HIS Integration
DISPLAY & INTERFACE Data Storage Capacity (Number of results storable) ≥ 50000 Or higher
DISPLAY & INTERFACE Barcode Reader Yes
OTHER FEATURES Features Abnormality Flagging Capability, Clogging detection, overflow protection, Reagent level monitor, Error Detection & Alerts, Automatic Cleaning Cycles, System self-check on startup
CERTIFICATIONS Availability of valid medical device license (CDSCO License) for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules as amended till date Yes