About 50 results
Open links in new tab
  1. Unique Device Identifier - UDI - Public Health

    Jul 30, 2024 · The unique device identification (UDI) is a unique numeric or alphanumeric code related to a medical device. It allows for a clear and unambiguous…

  2. Identificazione unica dei dispositivi - Public Health

    L'identificazione unica dei dispositivi (UDI) è un codice numerico o alfanumerico unico associato a un dispositivo medico che permette di identificare in modo chiaro e inequivocabile...

  3. Identificativo unico del dispositivo (UDI) / Registrazione dei ...

    Helpdesk UDI L' helpdesk UDI fornisce sostegno agli operatori economici nell'attuazione degli obblighi e dei requisiti introdotti dal nuovo sistema UDI, comprese l'assegnazione, l'etichettatura e la …

  4. The manufacturer is responsible for complying with all UDI related requirements. This includes the assignment of the UDI (and Basic UDI-DI), the UDI (and Basic UDI-DI) registration in the Eudamed …

  5. UDI/Device registration - Public Health - European Commission

    UDI Helpdesk The UDI helpdesk provides support to economic operators in the implementation of the obligations and requirements introduced by the new UDI system, including UDI assignment, labelling …

  6. 2. Are the UDI-DIs of single-use reprocessed devices the same as the original devices? l assume the obligations incumbent on manufacturers, including the ones referred to in Chapter III of the MDR. …

  7. The main features of the UDI system and relevant obligations for operators will be provided in a dedicated Q/A paper to be published by the Commission in spring 2018. This guidance is intended to …

  8. Identifiant unique des dispositifs (UDI) - Public Health

    L’identifiant unique des dispositifs (UDI) est un code numérique ou alphanumérique unique lié à un dispositif médical qui permet l'identification claire et formelle...

  9. Einmalige Produktkennung (Unique Device Identifier – UDI)

    Die UDI ist ein eindeutiger numerischer oder alphanumerischer Code für ein Medizinprodukt. Sie ermöglicht eine klare und eindeutige …

  10. The EUDAMED four first modules will be mandatory to use as from 28 …

    Nov 27, 2025 · In accordance with the transitional provisions set out in Regulation (EU) 2024/1860, this publication triggers a transition period of 6 months; Therefore, as from 28 May 2026 the first four …