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Guidance on appropriate surveillance regarding the transitional provisions under Article 120 of the MDR with regard to devices covered by certificates according to the MDD or the AIMDD. MDCG 2022-4

Bozza dell’atto di implementazione relativo a specifiche comuni per i dispositivi medici senza destinazione d’uso medica elencati nell’Allegato XVI del Regolamento (UE) 2017/745

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