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Open Tender for Haematology Analyzer Reagents (V2),Haematology Analyzer Reagents (V2),Haematology Analyzer Reagents in SURAT, GUJARAT

Bid Publish Date

16-Jul-2026, 4:26 pm

Bid End Date

27-Jul-2026, 2:00 pm

Location

SURAT , GUJARAT
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Progress

Issue16-Jul-2026, 4:26 pm
AwardPending
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Quantity

45

Category

Haematology Analyzer Reagents (V2)

Bid Type

Single Packet Bid

Categories 5

ANALYZER LABORATORY MATERIAL LABORATORY CHEMICAL LABORATORY SUPPLIES HAEMATOLOGY

Nuclear Power Corporation Of India Limited has released a public tender for Haematology Analyzer Reagents (V2) (Q2) in SURAT, GUJARAT. Quantity: 45. Submission Deadline: 27-07-2026 14: 00: 00. Download documents and apply online.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Haematology Analyzer Reagents (V2) (Q2)

Payment Timelines

Payments shall be made to the Seller within 10 days of issue of consignee receipt-cum-acceptance certificate (CRAC) and on-line submission of bills (This is in supersession of 10 days time as provided in clause 12 of GeM GTC)

Delivery Details

Max Delivery Days

30

Delivery Locations

1

Delivery Cities

Tapi

Delivery Pincodes

394651

Delivery Locations

ConsigneeAddressCityStatePincodeQuantityDelivery DaysAdditional Requirement
Anurag Pushp394651,KAPS PLANT SITE, PO ANUMALA, DISTRICT TAPI, GUJARATTapiGujarat394651530-

Authority Records

DEPARTMENT OF ATOMIC ENERGY

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Documents 6

GeM-Bidding-9605426.pdf

Main Document

Other Documents

OTHER

CATALOG-Specification-1

CATALOG Specification

CATALOG-Specification-2

CATALOG Specification

CATALOG-Specification-3

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Technical Specifications 3 Items

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Reactivity Human
PRODUCT INFORMATION Type of Reagent Cleaner 1
PACKAGING Total Volume of Reagent per Pack 50 ml
CERTIFICATIONS & REPORTS Compliance to Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS & REPORTS Availability of valid Medical Device license for the product issued from the competent authority Yes

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Required Documents

1

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

2

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

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