As a Notified Body under the Medical Devices Directives, BSI has one of the broadest scopes of any Notified Body.
This means whatever type of device a manufacturer wishes to market in Europe, where CE marking is now a legal requirement, BSI has the technical expertise to assist and provide appropriate conformity assessment services.
For further information about CE marking of medical devices, please contact us.
CE Marking (CE Mark) gain compliance with BSI.Tel: +44 (0)8450 765600
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