Medical device CE marking

MDCG 2021-26 Q&A on re-packaging and re-labelling activities


The MDCG has issued MDCG 2021-26 – a set of questions and answers about re-packaging and re-labelling obligations introduced by Article 16(2) to (4) under Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR).

The document can be downloaded in our library

Source: European Commission