ntr41-C_2022247EN.01000101-E0041

COMMISSION NOTICE The ‘Blue Guide’ on the implementation of EU product rules 2022 · European Union

(41) See Article 2 (1) and recital 19 of Regulation (EU) 2017/745 on medical devices and Article 2 (1) and recital 17 of Regulation (EU) 2017/746 on in vitro diagnostic medical devices.

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Source: EUR-Lex (Cellar) · retrieved 2026-09-25 · Text as adopted (Official Journal); later amendments are not incorporated in this text.