EU REP - EUROPEAN REPRESENTATIVE.
In the event that the manufacturer does not have a registered place of business in the European Community, the manufacturer shall appoint an Authorized Representative in the EU (EC REP) as required by Article 14.2* of the Directive Council 93/42/EEC as amended by Directive 2007/47/EC. CMC is an authorized EC REP with an office in Spain, CMC signs an official cooperation with WonMed based in Korea and also an authorized representative of Europe. The definition of an authorized representative in Regulation 765/2008/EC states that: “Authorized representative” on behalf of the manufacturer to perform specific duties related to the manufacturer’s obligations according to the relevant Community law.
Therefore, Wonmed can completely sponsor and support all businesses to carry out certification activities, assess and handle related issues, helping businesses to trade and the European market. .
Especially for medical products, this is one of the products that we have the most experience in, the biggest advantage, which ensures that all medical device manufacturers we can support the best.