Officers and regulatory representatives of ALLEGRE CHIRURGIE
PIERREFEU Claude
a) the conformity of the devices (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) the post-market surveillance obligations (d) the reporting obligations referred (e) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued (d) local medical device vigilance correspondents