MDCG guidance
MDCG 2019-6 Rev.4: Questions and answers: Requirements relating to notified bodies
MDCG guidance · Notified bodies · October 2022
Key facts
| Reference | MDCG 2019-6 Rev.4 |
|---|---|
| Title | Questions and answers: Requirements relating to notified bodies |
| Topic | Notified bodies |
| Published | October 2022 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- MDCG 2019-6 Rev.4 (October 2022), MDCG 2019-6 Rev.3 (October 2021) Revisions on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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.