CE certification is the core of the European Directive constitutes the "main requirements" in the European **** body on May 7, 1985 (85/C136/01) "technical harmonization and standards of the new approach to the resolution" on the need for the development and implementation of the Directive as the purpose of the "main requirements" has a specific meaning, that is, is limited to the product does not jeopardize the safety of human beings, animals and the safety of the goods aspects of basic safety requirements, rather than general quality requirements, the harmonization of directives only stipulate the main requirements. Instead of general quality requirements, the harmonized directives only provide for the main requirements, and the general directive requirements are the task of the standards. The product meets the main requirements of the relevant directives, can be attached to the CE marking, but not according to the general quality of the standard provisions of the ruling on the use of CE marking. The precise meaning is: CE marking is a safety mark of conformity rather than quality mark of conformity. It is regarded as the manufacturer to open and enter the European market passport, where the "CE" marking of the product can be affixed to the EU members of the domestic sales, without the need to comply with the requirements of each member state, so as to achieve the free flow of goods in the EU member states within the scope of the free flow of goods.
Simply put, CE marking is a mandatory certification for products entering the European market.
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