EU CE Certification Mandatory + Self-declaration LVD, EMC, R&TTE, MD and other directive

Description

In the EU market, "CE" is a mandatory certification directive and is regarded as a passport for manufacturers to open and enter the European market. Whether they are products produced by companies within the EU or products produced in other countries, if they want to circulate freely in the EU market, they must be affixed with the "CE" mark to show that the products comply with the basic requirements of the EU's "New Approach to Technical Coordination and Standardization" directive. Require. This is a mandatory requirement imposed by EU law on products. All products bearing the "CE" mark can be sold in each EU member state without having to meet the requirements of each member state, thus achieving the free circulation of goods within the EU member states. The significance of the CE mark is that the CE abbreviation is used as a symbol to indicate that the product with the CE mark complies with the essential requirements (Essential Requirements) stipulated in the relevant European directives, and is used to confirm that the product has passed the corresponding conformity assessment procedures and/or manufacturing The manufacturer's declaration of conformity truly becomes a passport for products to be allowed to enter the European Community market for sale. The relevant directives require industrial products to be affixed with the CE mark. If they do not have the CE mark, they shall not be put on the market for sale. If the products that have been affixed with the CE mark and enter the market are found to not meet the safety requirements, they shall be ordered to be withdrawn from the market. If they continue to violate the directive's provisions on the CE mark, , will be restricted or prohibited from entering the EU market or forced to withdraw from the market.

The CE mark indicates that the product complies with European regulations or differences. It can be self-declared by the manufacturer in accordance with EU laws and directives. Today, the CE mark is mandatory for entry into the European Economic Area (including the European Union, Norway, Iceland and Liechtenstein).

Directives
Directives are statutory requirements for the use of certain categories of products, including basic health and safety requirements. These directives must be met before CE marking can be posted, but manufacturers can choose how to evaluate. At present, the European Union has promulgated more than 20 CE directives (CE directives), affixing CE markings to products and providing technical documentation for the products. Only in this way can it be circulated in its market.

Harmonized Standards Harmonized Standards
The easiest way to demonstrate compliance with the directive is through harmonized European standards. If a particular product category complies with the harmonized standards, it also means that it complies with the corresponding directive specifications.

Declaring conformity
Many directives allow manufacturers to self-declare. Some directives require manufacturers to submit products to third-party certification agencies for testing and certification, or to have their quality systems audited by certification agencies.