European Union Medical Device Regulation (MDR)
Find out more about the key changes of the new MDR.
What is MDR
The regulation applies to all Medical Device manufacturers who intend to place their medical devices on the European market. The EU Medical Device Regulation (MDR) will replace the EU’s current Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC).
Key Changes due to New MDR
Explore and discover how the new MDR regulations impact your product lines. Set up one-on-one consultations with our experts and learn more MDR