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Document 32025R1920

Legal basis:
32017R0745 - A27P10PTB)
Initiative summary:
EU rules provide for a Unique Device Identification (UDI) system to make the traceability of medical devices easier. However, the wide variety of types and clinical parameter combinations for certain highly individualised devices means that a disproportionately high number of identifiers are being assigned, with few regulatory and safety benefits. This initiative aims to group highly individualised devices with clear clinical similarities under the identifier called ‘Master UDI-DI’.
EuroVoc thesaurus:
health policy; marketing standard; EC conformity marking; harmonisation of standards; health legislation; optical industry; medical device; safety standard; market supervision; quality standard; market approval
See the lifecycle of this act on the Interinstitutional register of delegated acts