Unique Device Identifier - UDI - Public Health The unique device identification (UDI) is a unique numeric or alphanumeric code related to a medical device It allows for a clear and unambiguous…
MDCG endorsed documents and other guidance - Public Health This page provides a range of documents to assist stakeholders in applying: Regulation (EU) 2017 745 on medical devices (MDR) and Regulation (EU) 2017 746 (IVDR) on in vitro diagnostic medical devices The majority of documents on this page are endorsed by the Medical Device Coordination Group (MDCG) in accordance with Article 105 of the MDR and Article 99 of the IVDR They are drafted in
UDI Device registration - Public Health - European Commission UDI Device registration Regulation (EU) 2017 745 on medical devices and Regulation (EU) 2017 746 on in vitro diagnostic medical devices introduce a device identification system based on a unique device identifier (UDI) allowing easier traceability of medical devices
Unieke identificatiecode voor medische hulpmiddelen (UDI) De Basic UDI-DI is het belangrijkste element in de databank en in de documentatie (bv certificaten, conformiteitsverklaringen, technische documentatie en samenvattingen van veiligheids- en klinische prestaties) en is ook de sleutel tot informatie over elk hulpmiddel in de toekomstige Europese databank voor medische hulpmiddelen
Identificador único del producto (UDI) - Public Health El sistema de identificación única del producto (UDI) es un código numérico o alfanumérico único relacionado con un producto sanitario Permite una clara e inequívoca