PLAN 1 HEALTH S.r.l.

MDR 2017/745 Article 15 (a) the conformity of the devices is appropriately checked.....;” “(b) the technical documentation and the EU declaration of conformity are drawn up.....” “(c) the post-market surveillance obligations are complied............;” “(d) the reporting obligations referred to in Articles 87 to 91 are fulfilled;” “(e) in the case of investigational devices, the statement ......is issued”