(a) — Regulation (EU) 2022/123 of the European Parliament and of the Council of 25… · Lexiara

(a)

Regulation (EU) 2022/123 of the European Parliament and of the Council of 25 January 2022 on a reinforced role for the European Medicines Agency in crisis preparedness and management for medicinal products and medical devices (Text with EEA relevance) · European Union

the name of the manufacturer of the medical device and, if applicable, the name of its authorised representative;

← art_25__para_3__text_1 · All articles · art_25__para_3__point_a__text_1 →

Source: EUR-Lex (Cellar) · retrieved 2026-11-06 · Text as adopted (Official Journal); later amendments are not incorporated in this text.