Cogniguard Sp z o.o.

a) appropriate checking of the conformity of the products in accordance with the QMS, before the product is released; b) preparation and ongoing updating of technical documentation and EU declaration of conformity; c) compliance with the post-market surveillance obligations in accordance with Article 10; 10 sec. 10 MDR d) compliance with the reporting obligations referred to in Article 87-91 MDR; e) in the case of research devices - issuing the statement ref. Annex XV, Chapt.II, Sec.4.1 of MDR