This page lists all published expert decisions and opinions in the context of the Clinical Evaluation Consultation Procedure (CECP) according to Article 54 of Regulation (EU) 2017/745).
The consultation procedure might be relevant to you, if you are a manufacturer of one of the following devices (exceptions, see Article 54 (2) MDR):
(a) class III implantable devices, or
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Orhopaedics – Traumatology – Rehabilitation – Rheumatology