SYMATESE SAS

-Control of medical devices batches conformity before release, -Technical Documentation and EU declaration of conformity, -PMS activities as per Art 10(10) of MDR, -Vigilance as per Art 87-91 of MDR, -Statement as per Section 4.1 of Chapter II of Annex XV of MDR in the case of investigational devices.

-Control of medical devices batches conformity before release (back-up), -Technical Documentation and EU declaration of conformity, -PMS activities as per Art 10(10) of MDR (back-up), -Vigilance as per Art 87-91 of MDR (back-up), -Statement as per Section 4.1 of Chapter II of Annex XV of MDR in the case of investigational devices.