The significance of CE certification is that the product with CE certification meets the main Requirements stipulated in the relevant European directives, and confirms that the product has passed the corresponding conformity assessment procedure and/or the manufacturer's conformity declaration, and truly becomes the passport for the product to be allowed to enter the European Community market. The relevant directive requires that industrial products that have passed the CE certification shall not be marketed when they have not passed the CE certification. Must first meet the requirements of CE certification and attach the CE certification mark to enter the EU market. If the products found in the market do not meet the requirements, will be ordered to withdraw from the market, continuous violation of the relevant CE certification provisions, will be restricted or prohibited to enter the EU market or forced to withdraw from the market!

 

CE certified products are accepted for the European Community member States or responsible for the implementation of market product safety control of the national regulatory authorities, rather than customers, when a product has been attached to the CE mark, the Member States responsible for sales safety supervision authorities should assume that it meets the main requirements of the directive, can circulate freely in the European Community market.

 

What does CE certification ensure?

 

Products must not be harmful to health, the environment and consumers before they can be circulated on the market.

 

Products legally listed in one EU country may also be sold in other Member States.

 

Manufacturers label their products with the CE mark to indicate that the products fully comply with the relevant provisions of the EU directive. If permitted by regulations, the CE marking may also be displayed on the packaging or accompanying documents. The CE mark is not a test mark, but only indicates that the manufacturer has declared that its products comply with all relevant regulations. At present, there are various compliance assessment models to mark compliance with the basic requirements, which may involve several entities, such as manufacturers, importers and distributors. In addition, certification may have to be performed by an independent body, such as a third-party certification body, in order to demonstrate compliance. Testing and certification bodies must also be formally authorized or certified under the supervision of an accredited accrediting body. Products that do not comply with the relevant directives may cause many problems, so we recommend certification by a third party certification body.

 

Through the CE certification, whether it proves that the quality of the product meets the "core of the European Directive"; Main requirements" In the EC Decision of 7 May 1985 (85/C136/01) on New methods of technical harmonisation and standards, "the need for the purpose of formulating and implementing the Directive". Main requirements" There is a specific definition, that 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 harmonization directive only specifies the main requirements, the general directive requirements are standard tasks. Products meet the main requirements of the relevant directives, can be attached to the CE mark, and not according to the provisions of the relevant standards for general quality to determine whether the CE mark can be used. Therefore, the accurate meaning is that the CE mark is a safety conformity mark rather than a quality conformity mark.