HYGIENX DOO BEOGRAD-RAKOVICA

-the conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before release -the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date -the post-market surveillance obligations are complied with in accordance with MDR -the reporting obligations (Articles 87-91) are fulfilled -in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued