Gain market access in Europe

CE marking approval and certification

CE marking certification

A medical device can only be sold in Europe with a CE mark. By placing the CE mark on a product, the manufacturer declares that it complies with all applicable European Directives and Regulations.

As a full-scope Notified Body for medical devices and in-vitro diagnostic medical devices, BSI The Netherlands (2797) issues CE certificates for MDR and IVDR devices, when required by the legislation.

Class I medical devices that are non-sterile, non-reusable or with no measuring function, do not require a certificate from a Notified Body. The same applies for Class A non-sterile IVDs.


Clinical Masterclass Series

Our webinar series is back!

Join us for part 2 of our Clinical Masterclass Series in 2023 and listen to our experts discuss various aspects of the MDR. From preparing a Clinical Evaluation Plan, to supporting you with preparing a Clinical Evaluation Report, advice on PMCF and SSCP and much more.