In accordance with EU law, non-EU countries included in the following four instructions requires not only the CE mark the product as a management, but also requires manufacturers in the 15 EU Member States and the European Free Trade between the Allies of the three members of a specified authorized agency. The four commands are:

      - Medical Device Directive (MDD)
      - Personnel Protection Equipment Directive (PPE)
      - Low Voltage Electrical Equipment Directive (LVD)
      - Electromagnetic Compatibility Directive (EMC)

      Authorized agency responsible for dealing with CE mark related matters;
      The functions of authority is different from the importers and wholesalers, and similar to the lawyer.
      Authorized agency in the EU have a can, and can have a number of importers and wholesalers.
      EU law requires non-EU countries, the product must be in the packaging / product licensing agency as stated on the name, address and contact information for any of the products have CE mark problems and authorized agents to contact.