Tender Details
Description / Scope of Work
SIUT, a 1500-bedded tertiary care teaching hospital in Karachi, Sindh, is inviting pre-qualification proposals from well-established and reputed importers, authorized distributors, and sole agents for the supply of GI endoscopic disposable and consumable items for the financial year 2026–27. The procurement aims to ensure the highest standards of transparency and quality in medical supplies. Interested vendors must be Sales Tax and Income Tax registered and remain active tax payers for the year 2025–26. Pre-qualification documents can be obtained from the CRS Department, Ground Floor, Gate No. 3, Transplant Tower, SIUT, Karachi, on payment of a non-refundable fee of Rs. 3000 in the form of a Pay Order made payable to the Director SIUT, valid between 04-08-2026 and 17-08-2026. Sealed proposals for pre-qualification are required to be submitted by 11:00 am on 18-08-2026 (Tuesday) and will be opened at 11:30 am the same day at SIUT Trust Hospital, Shahrah e Faisal, Karachi. The pre-qualification process shall be conducted in accordance with SPP Rules, 2010. Tender documents are available for download from www.siut.org/join-us/tenders.
For Bidders: Our Analysis PAKISTANTENDER INSIGHT
Independent analysis by PakistanTender — not part of the official notice. Always confirm details against the original tender document.
SIUT seeks pre-qualified suppliers of GI endoscopic consumables for an ongoing institutional requirement. This is a recurring annual procurement for a major teaching hospital, indicating substantial volume and long-term engagement potential. Vendors must be tax-registered and active filers. The tight submission window (04–18 August 2026) and pre-qualification gate suggest SIUT values compliance and financial standing. This is a qualification stage only; financial bid details are not yet visible.
Who can bid: Bidders must be established importers, authorized distributors, or sole agents with valid Sales Tax and Income Tax registration and active tax-filer status for 2025–26. Typically, medical device suppliers require PEC registration or equivalent healthcare authority recognition, though not explicitly stated here.