Medical Devices CE marking EU directives
As a Notified Body under the Medical Devices Directives, BSI has one of the broadest scopes of any Notified Body.
- The Medical Devices Directive (MDD) - all products
- The Active Implantable Medical Devices Directive (AIMDD) - all products
- The In Vitro Diagnostics Directive (IVDD) 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.
