MDCG guidance
MDCG 2021-26: Q&A on repackaging & relabelling activities under Article 16 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746
MDCG guidance · Authorised Representatives, Importers, Distributors · October 2021
Key facts
| Reference | MDCG 2021-26 |
|---|---|
| Title | Q&A on repackaging & relabelling activities under Article 16 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746 |
| Topic | Authorised Representatives, Importers, Distributors |
| Published | October 2021 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- MDCG 2021-26 (October 2021) Revisions on file
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About MDCG guidance documents
The Medical Device Coordination Group (MDCG), made up of EU member-state experts, endorses guidance on applying the Medical Devices Regulation (EU) 2017/745 and the In Vitro Diagnostic Regulation (EU) 2017/746. Each page here covers one document and all of its revisions.