CE

   Among the products sold in the markets of the European Economic Area (European Union, European Free Trade Association, except Switzerland), the use of the CE mark is increasing, and the goods bearing the CE mark indicate that it meets safety, health, environmental protection and consumption. Protects the requirements of a series of European directives.

   The CE acronym is used to indicate that the product bearing the CE mark complies with the relevant requirements of the European Directive and is used to verify that the product has passed the corresponding conformity assessment procedure and/or the manufacturer's declaration of conformity. Become a pass to allow products to enter the European Community market. For industrial products that require the CE mark to be affixed to the Directive, if there is no CE mark, it shall not be listed for sale. Products that have been affixed with the CE mark to enter the market. If they fail to meet the safety requirements, they shall be ordered to recover from the market and continue to violate the CE marking requirements of the Directive. Will be restricted or prohibited from entering the EU market or forced to withdraw from the market.

Module A (internal production control):

1. For simple, high-volume, non-hazardous products, only for manufacturers applying European standards.

2. The factory conducts self-assessment and self-declaration.

3. The technical documents are submitted to the national agency for ten years. On this basis, the review and inspection can be used to determine whether the product complies with the instructions, and the producer must even provide the product design, production and assembly process for inspection.

4. There is no need to declare that the production process will always ensure that the product meets the requirements.