State Bank of India Digital Blood Pressure Monitor Tender Munger Bihar MDR 2017 2026

Bidders must ensure MDR 2017 compliance and Drugs and Cosmetic Act alignment, submit Director Legal Metrology model approvals for each device, and provide regulatory certificates. Complete bid documents include regulatory conformity proofs, device specifications, and OEM authorizations where applicable. The procurement allows up to 25% quantity variation, impacting delivery planning and pricing.

Required submissions include MDR 2017 compliance evidence, Drugs and Cosmetic Act alignment, Director Legal Metrology model approval certificates, device technical specs, OEM authorizations for each model, and standard bid forms. Ensure GST registration and PAN information are ready for tender eligibility checks.

Standards include the Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017, as amended. Bidders must provide model approval certificates from Director Legal Metrology for each device model and show regulatory traceability for compliance and post-market support.

Delivery terms depend on the original delivery period; any additional time is calculated as (Additional quantity ÷ Original quantity) × Original delivery period, with a minimum extension of 30 days. The purchaser may extend delivery within the contracted rates under the 25% option clause.

EMD details are not disclosed in the available data; bidders should verify at bid launch. Payment terms are not specified here; bidders must obtain exact terms during bid clarification. Prepare EMD submission and financial documents as part of standard bid packet.

The purchaser may increase or decrease ordered quantity up to 25% at contract signing and during the currency of the contract at contracted rates. Delivery planning must accommodate potential surges or reductions, with scheduling adjusted per the 30-day minimum extension rule.