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Unofficial consolidated textConsolidated 2026-01-01English

Article 12

Reproduced from official EUR-Lex 1/1/2026.

Official catalogue · non-binding

Related guidance (3)

Current English catalogue entries that refer to Article 12. Guidance is non-binding and kept separate from the regulation text.

Browse topics
MDCG 2019-15 rev.1Guidance notes for manufacturers of class I medical devicesDecember 2019
MDCG 2022-16Guidance on Authorised Representatives Regulation (EU) 2017/745 and Regulation (EU) 2017/746October 2022
MDCG 2021-25 rev.1Application of MDR requirements to "legacy devices" and to devices placed on the market prior to 26 May 2021 in accordance with Directives 90/385/EEC or 93/42/EECOctober 2024

Reader references