How to CE mark an Accessory for a Medical Device?

Within EU MDR 2017/745 there is a definition for Accessory for a Medical Device. But how can we CE mark these products?
For that, we propose you look at this LinkedIn Live with Erik Vollebregt who is a lawyer at Axon Lawyers, and Martin Witte who is working for the Notified Body TÜV SÜD.
We have collected some questions from the audience and we will answer them. I hope that with this you can understand clearly how to manage your accessories to a Medical Device.
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