Gujarat Health & Family Welfare Department Haematology Analyzer Reagents (V2) Tender Banaskantha Gujarat 2026
N/a
BANASKANTHA, GUJARAT
Progress
Quantity
25
Bid Type
Two Packet Bid
The Gujarat Health & Family Welfare Department seeks procurement of Haematology Analyzer Reagents (V2) for Q2 for delivery to Surat, Gujarat 394101. The scope is supply-only for reagents with reactivity specification, reagent type, and total volume per pack defined. Key commercial terms include a quantity flexibility of ±25% and a delivery framework tied to the original delivery period. Approval of Detailed Design Drawings by the Buyer is required within 5 days of award, with modifications communicated within 5 days. The tender emphasizes regulatory compliance and licenses as core eligibility criteria, with price accounting for GST where applicable. The bid must align to the buyer’s drawings and delivery schedule without LD penalties if buyer delays approvals. The opportunity is location-specific to Gujarat and targets suppliers capable of delivering compliant, licenced reagents under the MDR 2017 framework.
Reactiveness of the reagent
Type of reagent
Total volume per pack
Compliance with Drugs and Cosmetic Act 1940
MDR 2017 compliance as amended
Availability of valid Medical Device license from competent authority
Option to increase/decrease quantity up to 25% with adjusted delivery.
Approval of Detailed Design Drawings within 5 days of award.
GST implications: bidder bears GST; reimbursement as actuals or as per rate, whichever lower.
GST and applicable rates to be reimbursed as actuals or as per quoted rate; bidders bear GST; no LD specified beyond standard contract terms.
Delivery aligned to approved drawings; additional time rules defined by option clause with minimum 30 days.
Not explicitly provided; LD would typically be governed by standard contract terms and delivery delays.
Eligible suppliers must meet regulatory requirements under MDR 2017 and Drugs and Cosmetic Act 1940
Possess valid Medical Device license for the reagents from a competent authority
Ability to submit Detailed Design Drawings within 5 days of award and obtain Buyer approval
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
No
Item Category
Haematology Analyzer Reagents (V2) (Q2)
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Main Document
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
N/a
BANASKANTHA, GUJARAT
N/a
BHAVNAGAR, GUJARAT
South Eastern Coalfields Limited
ANUPPUR, MADHYA PRADESH
Health Department
DARBHANGA, BIHAR
Employees State Insurance Corporation (esic)
JAMMU, JAMMU & KASHMIR
Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| PRODUCT INFORMATION | Reactivity | Human |
| PRODUCT INFORMATION | Type of Reagent | Diluent |
| PACKAGING | Total Volume of Reagent per Pack | 20000 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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Certificate (Requested in ATC) *In case any bidder is seeking exemption from Experience / Turnover Criteria
the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer
Key insights about GUJARAT tender market
Bidders should submit the goods-only proposal for Haematology Analyzer Reagents (V2) in Surat, ensuring MDR 2017 and Drugs and Cosmetic Act 1940 compliance. Include a valid Medical Device license and detailed design drawings within 5 days of award. Ensure GST handling per tender terms and respect the ±25% quantity variation clause.
Required documents include the organization’s GST registration, PAN, evidence of Medical Device license, product-specific compliance certificates, and demonstrated ability to deliver per approved drawings. Prepare technical bid detailing reagent type, reactivity, and total pack volume, plus financial statements and prior similar supply experience.
The procurement mandates compliance with Drugs and Cosmetic Act 1940 and MDR 2017 as amended. A valid Medical Device license from the competent authority is mandatory, along with batch-level traceability and quality assurance aligned to these regulatory standards.
Delivery timelines are governed by the original delivery period plus any extension under the option clause, with a minimum extension of 30 days. Additional time depends on quantity changes and approval of drawings; delays in buyer approval may shift the delivery schedule accordingly.
Post-award, the supplier must submit Detailed Design Drawings within 5 days. The buyer will approve or list modifications within 5 days. Delivered reagents must conform to the approved drawings, and any delay in approval postpones delivery as specified without LD penalties.
GST is the bidder’s responsibility; reimbursement will be provided as actuals or at the applicable rate, whichever is lower, limited to the quoted GST percentage. Ensure accurate GST documentation in the submission to avoid payment delays.
The purchaser may increase or decrease the ordered quantity up to 25% of the bid quantity at contract placement and during the contract at contracted rates. Delivery period adjusts proportionally, with a minimum extension of 30 days for increased quantity.
Bidders must hold a valid Medical Device license for the reagents and demonstrate compliance with MDR 2017 and Drugs and Cosmetic Act 1940. Documentation must be supported by regulatory approvals and batch-level traceability for all reagents.
N/a
📍 BANASKANTHA, GUJARAT
N/a
📍 BHAVNAGAR, GUJARAT
N/a
📍 RAJKOT, GUJARAT
N/a
📍 NAVSARI, GUJARAT
N/a
📍 NAVSARI, GUJARAT
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Main Document
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS