MDCG guidance
Q&A rev.1: Q&A Obligation to inform in case of interruption or discontinuation of supply
MDCG guidance · Article 10a - interruption or discontinuation of supply · December 2024
Key facts
| Reference | Q&A rev.1 |
|---|---|
| Title | Q&A Obligation to inform in case of interruption or discontinuation of supply |
| Topic | Article 10a - interruption or discontinuation of supply |
| Published | December 2024 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- Q&A rev.1 (December 2024) 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.