Delivery of Enteral and Parenteral Nutrition Preparations and Modified Milk with Accessories
Delivery of enteral and parenteral nutrition preparations and modified milk with accessories. For the offered products, current and valid market approval documents must be submitted: for medical devices (Declaration of Conformity, CE Certificate, notification/registration according to the Medical Devices Act of May 9, 2022), for medicinal products (market approval certificates according to the Pharmaceutical Law of September 6, 2001, and CHPL), for cosmetic products (registration confirmation in the CPNP according to the Cosmetic Products Act of October 4, 2018), for biocidal products (market approval in Poland according to the Biocidal Products Act of October 9, 2015), and for products containing hazardous substances (current safety data sheets according to the Chemical Substances and Mixtures Act of February 25, 2011). Furthermore, descriptions and photographs (catalogs) of the products in Polish, reflecting their parameters, must be submitted. If required, positive opinions from IMiD or equivalent documents, as well as evidence of the required biocidal spectrum and exposure time through laboratory tests from accredited EU research institutions compliant with medical standards, must be provided. Each document must be assigned to the respective task from Annex 1 of the SWZ.
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