Regulation (EU) 2023/607 of the European Parliament and of the Council of 15 March 2023 amending the MDR and the IVDR as regards the transitional provisions for certain medical devices and in vitro diagnostic medical devices.
In line with this, some timelines of the related factsheet or guidance are modified, including but not limited to:

2. 1.    Factsheet for authorities in non-EU/EEA states on medical devices and in vitro diagnostic medical devices
3. 2.    COMMISSION IMPLEMENTING REGULATION (EU) 2023/1194 of 20 June 2023

For the concrete timeline, please consult the reference.

 

 

Reference: 
Factsheet for authorities in non-EU/EEA states on medical devices and in vitro diagnostic medical devices

COMMISSION IMPLEMENTING REGULATION (EU) 2023/1194 of 20 June 2023