MDCG guidance
MDCG 2021-5 rev.1 - Appendix: Transition to the "EU REP" symbol in EN ISO 15223-1
MDCG guidance · Standards · June 2026
Key facts
| Reference | MDCG 2021-5 rev.1 - Appendix |
|---|---|
| Title | Transition to the "EU REP" symbol in EN ISO 15223-1 |
| Topic | Standards |
| Published | June 2026 |
| Document | health.ec.europa.eu |
At a glance
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- MDCG 2021-5 rev.1 - Appendix (June 2026) 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.