EU Representative
In order to improve the overall efficiency of market regulation, the European Commission requires all member states to meet the minimum legal requirements. The Commission cooperates with customs and cooperates with relevant parties (manufacturers, EU authorized representatives, importers, distributors) to establish a comprehensive product traceability system. The European Commission first focuses on high-risk areas, such as medical devices.The EU's medical device directives: 93-42-EEC, 98-79-EC, and 90-385-EC cover all medical device products, all of which require non EU manufacturers to have an EU authorized representative.EU Authorized Representative/EU Representative (European Authorized Representative or European Authorized Representative) refers to a natural or legal person specifically designated by a manufacturer located outside the European Economic Area (EEA) (including EU and EFTA). The natural or legal person may represent a manufacturer outside of EEA to fulfill specifi...
2018
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04
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12