VIDAVO SA

(a) ensuring that the post-market surveillance obligations are complied with in accordance with Article 10(10) of MDR; (b) ensuring that the reporting obligations referred to in Articles 87 to 91 of MDR are fulfilled.

(a) ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (b) ensuring that the conformity of the medical software is appropriately checked, in accordance with the QMS under which the medical software are manufactured, before it is released;