The commission and the IMDRF-group have published the final guidelines for the filling of the EUDAMED-DBase.
Look for more details under the item; EUDAMED.
The "Basic UDI-DI" is defined in the european medical device and in-vitro diagnostica regulations. It is further specified in the guidance document "Draft guidance on basic UDI-DI and changes to UDI-DI".
The "Basic UDI-DI" describes a modell of products. HIBC members may create their Basic UDI-DI identifiers on their own using the guideline below.
Click here to view the details for creation!