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Full service company for entering EU Medical device market.

At MEDeviCE Group, we understand that change is not always easy. Since 2018, we’ve been helping companies from Singapore, China, Russia, Ukraine, Latvia, Estonia etc. respond to industry transitions in order to stay competitive and encounter new markets. Our experience have taught us to always make your goals our priority.


CE registration in EU - from 98/79/EC to IVDR,  from 93/42/EEC to MDR - our specialists will help you perform smooth and easy transition, suggest the best solution and assist you on the way of implementation avoiding months of headaches and mountains of papers. 


If you are preparing MD manufacturing, keep in mind the necessities of corresponding to ISO 13485 - our highly knowledgeable professionals with years of experience in field, will advise, suggest and prepare all required documentation for 100% successful audit and obtaining the certificate.  


Looking for a reliable Authorized representative and partner within EU - MEDeviCE Group is your #1 choice. Your interest and success is our priority. We will prepare all required documents and will ensure up-to-date information about changes, aftermarket surveillance and feedback. 


Our team of experts is ready to help you develop strategies for thriving in the future. Get in touch with us today to set up your first consultation.


MEDeviCE Group Ltd. 


Andrejs Gaivoronskis

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