Dear Partners,
Please find here attached a summary of the European UDI process,
From UDI-DI that will have to feature on DoC asap, and be obtained even for "Legacy Devices" within EUDAMED gets live
(any vigilance event shall concern a device with its UDI to be able to reported for instance) ;
till labelling and UDI on devices times.
Hoping it will be of help to you,
We remain at your disposal for any question you may have on these topics.
Best regards,
MediMark Europe Team
