The virtual event, which was attended by about 100 participants, aimed at updating information on UDI implementation in accordance with the Medical Devices Act. The topics ranged from UDI-compliant marking to the required product registrations in the UDI database EUDAMED to the practice at the manufacturer site. The summary provides an overview on UDI and its implementation specialities for Europe. Additional information can be found in the UDI book published by Beuth-Verlag, second edition, for details on UDI (see link below).
Technical questions can be sent to the speakers by email: This email address is being protected from spambots. You need JavaScript enabled to view it..
Link for access and trial reading of the UDI book II:https://www.beuth.de/de/publikation/udi-unique-device-identification/320019099