Regulatory guidance
Transition to the "EU REP" symbol in EN ISO 15223-1
Published Jun 1, 2026
Reference
MDCG 2021-5 rev.1 - Appendix
Source
MDCG
Topic
Standards
Published
Jun 1, 2026
Languages
EN
© European Union — European Commission, DG SANTE. Reuse under CC BY 4.0.
Guidance on standardisation for medical devices
Published Jul 1, 2024
Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746
Published Sep 1, 2026
Position Paper: UDI assignment between manufacturers and distributors
Published Jul 1, 2026
MDCG Position Paper: Management of SS(C)P in EUDAMED after mandatory use
Published Jun 1, 2026