Supply of other medical materials

Supply of other medical materials: Offered medical devices must possess attestations, certificates, and be registered in accordance with legal requirements, and must be placed on the market and used in compliance with the Medical Devices Act of April 7, 2022 (Dz. U. z 2024r., item 1620). They must conform to applicable standards or technical specifications. If a medical device does not require notification to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, all necessary actions to fulfill legal requirements for placing the device on the market and its use in Poland must be carried out at the contractor's own expense. Equivalent solutions to specified trademarks, patents, or origins are permissible. Contract terms are defined in the tender documents. Goods supplied must not originate from the People's Republic of China (PRC) for more than 50% of the total contract value, if the order is subject to IZM measures according to Regulation (EU) 2025/1197 and Art. 8 para. 1 lit. b of Regulation (EU) 2022/1031. Subcontracting to entities from the PRC must not exceed 50% of the total contract value. No additional orders under Art. 214 para. 1 pts 7 and 8 of the Polish Public Procurement Law are foreseen. Offers will be evaluated based on the criteria of Price (80%) and Order Completion Term (20%).

Tender documents

Lots (3)

• LOT-0001Infusionsmanschetten
• LOT-0002Fixierungsgurte
• LOT-0003Untersuchungsliege

Additional details