Medical device CE marking

MDCG 2021-25 report issued on transitional provisions


The MDCG ad hoc task-force on transitional provisions (‘legacy devices’ and devices placed on the market prior to 26 May 2021 in accordance with Directives 90/385/EEC or 93/42/EEC) has issued the MDCG 2021-25 report, which has been endorsed as an MDCG guidance.

The document can be downloaded in our library

Source: European Commission