EU MDR and its impact on existing Registrations

#1
Hi

Wanted to have opinions on the Medical device services required for already registered MD, after the MDR regulations being applicable 26 May 2021, where do you foresee challenges for registered medical devices?

Few challenges that I have enlisted are
UDI requirements for different class of devices which need implementation.
Up classification of registered Medical device

I am looking for responses from core regulatory submissions and registration requirements not from PV perspective. Will be happy to know your thoughts on the kind of services the MD industry would need in near future.
 
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