Swiss AR Deadline: Class IIb non-implantable/IIa
11 May 2023Swiss-EU MRA Lapses for IVDs
11 May 2023All devices new to the market must be CE Marked to the IVDR.
All Class A non-sterile IVD devices require IVDR CE Marking as of 26 May 2022.
A transition period is granted for all other IVD devices. Certain conditions apply. Please see the rest of the timeline chart for the other IVDR compliance dates.