By today’s publication in the official European database NANDO we have reached the final designation under Regulation (EU) 2017/745 (MDR).
After a preparation, assessment and approval time of three years we are proud that we have reached this important goal not only for ourselves but also for our clients. The corporate management of mdc thanks all employees for their contribution to this milestone in the company’s history and all the clients for their confidence during this long application period.
We are looking forward to being your competent partner for the CE-marking of your medical devices under the new regulations and are at your disposal for respective inquiries.