Medical device CE marking

MDCG 2021-13 Q&A on Actor ID


On June 23 the European Commission published MDCG 2021-13: Questions and answers on obligations and related rules for the registration in EUDAMED of actors other than manufacturers, authorised representatives and importers subject to the obligations of Article 31 MDR and Article 28 IVDR.

The document can be downloaded in our library

Source: European Commission

Update (Rev. 1) on July 12, 2021