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Contract Bidding Open For Automated Blood Culture System in CHURACHANDPUR, MANIPUR

Bid Publish Date

09-Feb-2026, 2:58 pm

Bid End Date

23-Feb-2026, 3:00 pm

EMD

₹1,00,000

Progress

Issue09-Feb-2026, 2:58 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

1

Bid Type

Two Packet Bid

Categories 1

Public procurement opportunity for Directorate Of Health Services Automated Blood Culture System (Q2) in CHURACHANDPUR, MANIPUR. Quantity: 1 issued by. Submission Deadline: 23-02-2026 15: 00: 00. View full details and respond.

Documents 3

GeM-Bidding-8935509.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

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 Automated Blood Culture System
PRODUCT INFORMATION Technology Fluorometric technology / Colorimetric technology / Non-radiometric technology
PRODUCT INFORMATION Patient usage Adult and Pediatric
PRODUCT INFORMATION Type of Culture Bottles Supported Aerobic, Anaerobic, Fungal
PRODUCT INFORMATION Sample Capacity (Minimum) 40 bottles or more, 80 bottles or more, 120 bottles or more, 200 bottles or more, 360 bottles or more Or higher
PRODUCT INFORMATION Visual and audible alarms for positive cultures Yes
PRODUCT INFORMATION Every cell (bottle position) have its own optics and detection device Yes
PRODUCT INFORMATION Barcode Reader Built-in / External
DATA MANAGEMENT SYSTEM Type of monitor Inbuilt / PC Based
DATA MANAGEMENT SYSTEM Type of monitor display LCD / LED
DATA MANAGEMENT SYSTEM Touch screen display Yes
DATA MANAGEMENT SYSTEM UPS provided for Power Backup facility Yes
DATA MANAGEMENT SYSTEM UPS Back up time in minutes 30 minutes or more
DATA MANAGEMENT SYSTEM Availability of external printer Yes
CERTIFICATIONS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS Availability of valid 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
CERTIFICATIONS Certification for manufacturing unit ISO:13485 (Latest)
CERTIFICATIONS Availability of Test Report for each supplied batch/product as per Medical Device Rule (MDR) 2017 as amended till date Yes
WARRANTY Warranty in years (Option of comprehensive warranty is available through bidding only, which if opted will supersede normal warranty in the catalogue) 1, 2, 5

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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

OEM Annual Turnover

7

Additional Doc 1 (Requested in ATC)

8

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

9

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

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