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Importer & Authorized Representation for
Medical Device & IVD Manufacturers Exporting to Europe


For compliance with Article 13 of the EU MDR and IVDR.

Great Britain
UK Importer

For compliance with new MMDA  requirements from UK MHRA.


For compliance with new  requirements from Swissmedic.

Authorized Rep

New requirement for all manufacturers exporting to Switzerland.

Helping Manufacturers Meet New Requirements in the EU, UK and Switzerland While Maintaining Commercial Control, Independence and Flexibility

New medical device regulations in the European Union, UK and Switzerland impose strict new requirements on device manufacturers and elevate the role of the importer in placing devices on these markets. 


While a local distributor could act as your importer, there are many reasons to select an independent, professional importer service company such as MedEnvoy to act as your single independent importer for all European markets.

100% Focused on Medical Devices & IVDs

We are no strangers to the medical device industry. Our seasoned executive team has been working with device and IVD companies worldwide for decades. MedEnvoy fully understands the complexities of managing and controlling your European supply chain along with the new regulatory requirements imposed by the European Commission, UK MHRA and Swissmedic. We are ready to help you maintain compliance and the seamless flow of your products into Europe.  

Experienced in
medical devices & IVDs
Offices in EU, UK
and Switzerland
European regulatory