MARKET ACCESS & RESOURCES

European Union · Medical device market access

Browse market access information and professional services, then explore related medical exhibitions and business connections.

European Union medical device registration resources

These summaries come from existing site resources. Rules, fees and timelines may change; check current requirements for each project.

Medical devices CE Marking Process

I. CE Marking Introduction The CE marking is a safety certification mark and is considered a passport for manufacturers to open and enter the European market. ‘CE marking of conformity’ or ‘CE marking’ of Medical Devices means a marking by which a manufacturer indicates that a device is in conformity with the applicabl

Source date: 2023-10-23
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