The registration of medical devices confronts the manufacturers with significant challenges. National and international regulatory requirements are getting more tightened and breaking down into more detailed categories of devices. In case of Medical Device industry, Non-European Medical Device manufacturers, who wish to place their products into European market, must designate an Authorized Representative established in the European Community to fulfill one aspect of the requirements for Medical device directives.

   So we, Aemi world which is located in Berlin, Germany, are here for help to non-European Medical device manufacturer for marketing their products in the member state of Europe without any barriers and to extend Medical device market by meeting the regulation and national requirements.