ABComfort Sp. z o.o.

a) adequately checking the conformity of devices, in accordance with the quality management system b) preparation and ongoing updating of technical documentation and EU declaration of conformity; c) compliance with the post-market surveillance obligations pursuant d) compliance with the reporting obligations referred to in Art. 87–91; e) in the case of test devices, issuing the statement referred to in Section 4.1 of Chapter II of Annex XV.