Contact Us
Introduction Services Fees Medical Devices Other Products Questions & Answers European Authorised Representative Service
medical devices Let Wellkang be your EU/EC European Authorized Representative! Click here to learn more/continue ...

As of 21 March 2010, a Single EEA European Authorised/Authorized Representative must be designated by a non-EEA manufacturer of medical devices as required by directive 2007/47/EC, are you ready?
Register/Notify your MD-Medical Devices & IVD-In Vitro Diagnostic Medical
Devices with MHRA & other EEA authorities by world-leading CE Marking
Specialists based in London/UK. Click here to get FREE Guide Now!


AIMD-Active Implantable Medical Devices: Conformity Assessment Routes

Flow Chart of AIMD


Go to Top

FAQ/Q&A: Questions and Answers about CE Marking of Medical Devices About CE Marking:

 Home | About Us | Contact Us | Copyright & Disclaimer | Privacy | Log-in | Order Now |