MDCG guidance
MDCG 2025-10: Guidance on post-market surveillance of medical devices and in vitro diagnostic medical devices
MDCG guidance · Post-Market Surveillance and Vigilance (PMSV) · December 2025
Key facts
| Reference | MDCG 2025-10 |
|---|---|
| Title | Guidance on post-market surveillance of medical devices and in vitro diagnostic medical devices |
| Topic | Post-Market Surveillance and Vigilance (PMSV) |
| Published | December 2025 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- MDCG 2025-10 (December 2025) 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.