DEADLINE MDR Application Notified Body Transition periods
Regulation (EU) 2023/607 has extended the transitional periods for placing medical devices on the market under certain conditions. This affects so-called legacy devices, i.e. medical devices that may be placed on the market in accordance with the provisions of Directive 93/42/EEC or Directive 90/385/EEC if certain conditions are met - after the MDR comes into force - in accordance with the transitional provisions of Art. 120 MDR. However, the extension of the TRANSITIONAL PERIODS is EXCLUDED if the conformity assessment has not been APPLIED for at a NOTIFIED BODY by 26.05.2024.