Orthopedic Implants Supply

This contract involves the supply of orthopedic implants, specifically endoprostheses, as detailed in the attached document. The supplier must ensure that the products meet Polish standards that align with European norms or those of other EEA member states. Additionally, the products must have valid documentation for market approval in Poland, in accordance with the Medical Devices Act of April 7, 2022, and EU Regulation 2017/745 on medical devices, if applicable. The supplier is required to provide current documents confirming compliance with the medical devices law and that the products are approved for use in healthcare, including CE certificates or declarations of conformity, as necessary. These documents must be submitted with the first delivery and updated as required throughout the contract duration.