MEXICO | The Secretary of Health, Salomon Chertorivski announces Equivalence Agreement with Japan for Medical Devices

•  The goal is to expand the supply of Japanese leading-edge medical

10th Apr 2012

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European Authorized Representative

All Non-European manufacturers of medical devices who wish to market their products in the EU market under their own name must designate a Regulatory Authorized Representative in order to meet the CE requirements.

Appointing a proper Regulatory Authorized Representative is one of the most important decisions a device manufacturer has to make.

Arazy Group European Authorized Representative is Medes Limited UK. Located in Radlett, Hertfordshire, Medes is a qualified and recognized Authorized Representative. We have been serving hundreds of companies worldwide since 1996.

From the very moment you appoint us as your Authorized Representative, we will take care of your device registration along with all correspondences. We will also manage complaint handling and reporting to European Authorities.

For more information about our European Authorized Representative services or an instant 24 hours standard contract application or special “Universal Authorized Representative™” package, please submit your inquiry or choose to consult our online experts right now. 



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