mdi Europa GmbH was founded in March 2000 to provide medical device manufacturers world-wide with flexible and well adjusted service packages to assist its clients to comply with EU legislation.

mdi Europa GmbH acts as European Authorized Representative (as defined under „European Authorized Representative“) for a wide range of companies – from start-ups to established corporations throughout the world.

Our highly qualified regulatory affairs experts have hands-on experience and have registered hundreds of medical device manufacturers for CE-marking with the European competent authorities.

In addition, we have created a world-wide network of regulatory experts, thus enabling us to provide our clients with excellent regulatory services around the world.

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Many bad traps are hidden
in the EU regulatory jungle
We guide you safely

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