The European Commission has launched the UDI (Unique Device Identification) Helpdesk to provide assistance in implementing the UDI-related requirements of the MDR and IVDR and using the EMDN (European Medical Devices Nomenclature).
The UDI Helpdesk webpage is divided in 5 sections, each containing frequent questions and answers. Few are presented below:
- Definitions and basic information
- What are UDI-DI and UDI-PI?
- Specific questions
- What are the UDI and device data sets to be provided in Eudamed?
- EUDAMED-related questions
- Can I link my UDI-DI to more than one Basic UDI-DI?
- Dates and deadlines
- What is the mandatory deadline for a device to comply with the UDI requirements?
- Documents and links
You can find all UDI relevant and useful documents in our Library of Documents.
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