Guidance on standardisation for medical devices Appendix: Transition to the ‘EU REP’ symbol in EN ISO 15223-1

The European Commission has published a new appendix to MDCG 2021-5 Rev. 1 – Guidance on standardisation for medical devices:

📄 Appendix: Transition to the “EU REP” symbol in EN ISO 15223-1
📅 Published: June 2026

This follows the publication in the Official Journal of the European Union (OJEU) of EN ISO 15223-1:2021/A1:2025, introducing the new symbol: EU REP → to identify the Authorised Representative