LiKAMED is MDR-ready

The MDR audit carried out by TÜV Süd Product Service has been successfully completed. The MDR audit confirmed the new requirements of the European Medical Device Regulation (MDR) (EU) 2017/745, which are to be implemented on May 26, 2021.

Now we are ready for you!
Parallel to the MDR audit, the quality management audit according to EN ISO 13485 and ISO 9001 were also successfully passed.