MDCG guidance
MDCG 2020-3 Rev.1: Guidance on significant changes regarding the transitional provision under Article 120 of the MDR with regard to devices covered by certificates according to MDD or AIMDD
MDCG guidance · Notified bodies · May 2023
Key facts
| Reference | MDCG 2020-3 Rev.1 |
|---|---|
| Title | Guidance on significant changes regarding the transitional provision under Article 120 of the MDR with regard to devices covered by certificates according to MDD or AIMDD |
| Topic | Notified bodies |
| Published | May 2023 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- MDCG 2020-3 Rev.1 (May 2023), MDCG 2020-3 (March 2020) 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.