Rourkela Steel Plant Hospital Consumables Tender 2026: ISI/Medical Device Standards for Micro CuVette Items - SBI Procurement

Tender Overview

Organization: Rourkela Steel Plant, a unit of Steel Authority of India Limited. Procurement scope: Life-science hospital consumables (micro cuvettes) with shelf-life integrity, including ancillary documentation such as guaranty certificates and batch/expiry details. Location: Rourkela, Odisha, with focus on hospital supply to government/PSU institutions. Estimated value/EMD: Not disclosed in provided data. Key differentiator: Mandatory compliance with drug and medical device regulations, and CDSCO-aligned documentation. Context: ATC terms emphasize non-discretionary adherence to tendered specification and rigorous inspection by HOD Pathology.

Technical Specifications & Requirements

• Product category: Hospital consumables (micro cuvettes) for pathology use; LVG: 23MM, HELENA C4-2806 listed in category metadata.
• Shelf life requirement: Leftover shelf life at receipt must be ≥ 80%.
• Documentation at supply: Guaranty certificate; invoice must include batch number, manufacturing date, expiry date.
• Regulatory alignment: Compliance with Drugs & Cosmetics Act 1940 & Rules and Medical Device Rules 2017; CDSCO notifications followed.
• Licensing & certifications: Bidder must provide a valid Medical Device License, product certification, and test report on demand.
• Inspection: Material will be inspected by HOD Pathology or their representatives.
• Eligibility context: Prior supply of similar hospital consumables to government/PSU hospitals (≥200 beds) within the last 7 years, withPO/PO references; alternative eligibility for bidders already known to IGH/RSP.

Terms, Conditions & Eligibility

• GST: Applicant to account for GST; invoice in consignee name with consignee GSTIN; GST reimbursement as actuals or lower applicable rates.
• Scope of supply: Bid price to include all costs; only supply of goods.
• EMD/PO docs: If applicable, maintain standard EMD as per GEM terms; attach relevant purchase orders or evidence of supply for similar work.
• Submission: Self-declaration accepting GEM terms; only relevant documents for technical/commercial evaluation; avoid extraneous uploads.
• Special clauses: Shelf-life integrity, compliance with CDSCO/MoHW/federal regulations, and verification via medical device licenses.
• Non-submission caveat: Preference for suppliers with IGH/RSP past orders; others must provide PO reference details.