The CE certification constitutes the "major requirement" of the core of the European Directive. It was formulated and implemented as required in the European Community's Resolution of the New Method for Technical Coordination and Standards (85/C136/01) of May 7, 1985. The "main requirement" of the directive has a specific meaning, that is, it is limited to the basic safety requirements of products that do not endanger the safety of humans, animals and goods, rather than the general quality requirements. The coordination directive only stipulates the main requirements. The general directive requirements are the standard tasks. . Products comply with the relevant requirements of the relevant directives, can be attached CE mark, not according to the relevant standards for the general quality of the provisions of the use of the CE mark.

Therefore, the exact meaning is: CE mark is a safety mark rather than a quality mark. It is regarded as a passport for manufacturers to open and enter the European market. Any product bearing the "CE" mark can be sold in the EU member states without having to meet the requirements of each member country, thereby realizing the goods in the EU member states. Free circulation within.