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ntr214-C_2022247EN.01000101-E0214

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

(214) In the medical devices sector, the product must also bear the authorised representative’s name and address.

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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.