imito AG

The conformity of the devices is appropriately checked, in accordance with the QMS, before a device is released. The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Post-market surveillance obligations are complied with (MDR Art. 10(10)). Report to top management on the effectiveness of the QMS. Reporting obligations (vigilance) are fulfilled (MDR Art. 87-91). The QMS is maintained and internal audits are organized.