ACTIMI GmbH

the conformity of the devices is appropriately checked, 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 Article 10(10);the reporting obligations referred to in MDR Articles 87 to 91 are fulfilled;in the case of investigational devices, the statement referred to in MDR Section 4.1 of Chapter II of Annex XV is issued