Introduction

CE certification is the “major requirement” that forms the core of the European Directive. It is required to be developed and implemented in the European Community’s Resolution (85/C136/01) of May 7, 1985, on the New Approach to Technical Coordination and Standards. The “main requirements” of the purpose of the directive have a specific meaning, that is, the product only does not endanger the basic safety requirements of the safety aspects of humans, animals and goods, rather than the general quality requirements. The coordination directive only specifies the main requirements, and the general directive requirements are standard tasks. . If the product meets the relevant requirements of the relevant directives, the CE mark can be attached, and the CE mark cannot be determined according to the general quality requirements of the relevant standards.