On February 16, 2023, the European Parliament voted in favour of the Proposal to prolong the transitional provisions for certain medical devices and in vitro diagnostic medical devices.
The decision passed with a majority of 537 votes.
This Proposal, adopted in January 2023, foresees more time to certify medical devices under the Regulations on Medical Devices (MDR) and In Vitro Diagnostic Medical Devices (IVDR). This decision affects legacy devices, i.e., those devices certified under the previous Directives and meeting legacy requirements.
You can find all Commission and other relevant documents in our Library of Documents.