-checking the conformity of the devices in acc. with the quality management system before a device is released
-drawing and keeping up-to date the technical documentation and the EU declaration of conformity
-compling the post-market surveillance obligations with in acc. with Art. 10(10) of2017/745
-fulfilling the reporting obligations referred to in Art. 87 to 91 of2017/745
-issuing the statement referred to in Annex XV, Chapter II, Section 4.1 of 2017/745 in the case of investigational devices
Masqué
KABZIŃSKA Katarzyna
-checking the conformity of the devices in acc. with the quality management system before a device is released
-drawing and keeping up-to date the technical documentation and the EU declaration of conformity
-compling the post-market surveillance obligations with in acc. with Art. 10(10) of2017/745
-fulfilling the reporting obligations referred to in Art. 87 to 91 of2017/745
-issuing the statement referred to in Annex XV, Chapter II, Section 4.1 of 2017/745 in the case of investigational devices