What does Ce certification mean?

CE certification is limited to the basic safety requirements of products that do not endanger the safety of human beings, animals and goods, rather than the general quality requirements. The coordination instruction only specifies the main requirements, and the general instruction requirements are standard tasks. Therefore, the accurate meaning is that the CE mark is a safety qualified mark rather than a quality qualified mark. The "main requirements" constitute the core of the European directive. "CE" mark is a kind of safety certification mark, which is regarded as a passport for manufacturers to open and enter the European market. CE stands for obedient Europe. In the EU market, the "CE" mark is a compulsory certification mark. Whether products produced by enterprises within the EU or products produced by other countries want to circulate freely in the EU market, they need to be labeled with "CE" to show that the products meet the basic requirements of the EU's "New Method of Technical Coordination and Standardization" directive. This is a mandatory requirement for products under EU law. Meaning: safety conformity mark, not quality conformity mark. Objective: To prove that it has passed the international safety standard test. CE is the abbreviation of French, which means "European consistency" in English. In fact, CE is also the abbreviation of the word "European style" in many European languages. At first, it was abbreviated as EC by the English phrase "European Community", but later it was abbreviated as Commute Europe in French. Italian is the European Community, Portuguese is the European Community, and Spanish is the European Community, so EC is changed to CE. Of course, CE can also be regarded as conforming to Europe (demand), which constitutes the "main requirement" of the European directive core. In the resolution of 1985 on technical coordination and new methods of standards (85/C 136/0 1), the "main requirements" put forward for the formulation and implementation of this directive have a specific meaning, that is, they are only limited to the basic safety requirements that products do not endanger the safety of human beings, animals and goods. The product meets the main requirements of relevant directives, and the CE mark is a safety conformity mark rather than a quality conformity mark. In the 1940s, western European countries felt it necessary to unite to ensure their own security between the two great powers, improve their international status and accelerate economic development, thus promoting the process of European integration. European integration can be divided into five levels: the establishment of free trade area, customs union, unified big market, economic and monetary union and political union. The declaration of conformity/declaration of conformity independently issued by the enterprise is a self-declaration and should not be issued by a third-party institution (intermediary institution or testing and certification institution). Therefore, it can be replaced by an enterprise conformity statement in the EU format. Certificate of conformity/certificate of conformity is a declaration of conformity issued by a third party (intermediary or testing and certification institution), which must be accompanied by technical data such as testing report TCF, and the enterprise must sign the declaration of conformity. EC Conformity Attitude, which is a certificate issued by EU certification bodies. According to EU regulations, only NB is qualified to issue EC-type CE statements. Authentication procedure. It is confirmed that exporting countries may need CE certification if they export to any of the 30 member countries of the European Economic Area, including the European Union and the European Free Trade Area. Confirm product categories and related EU product directives. If a product belongs to more than one category at the same time, it must meet the requirements listed in the product specifications corresponding to all categories. Some products are sometimes listed in some product manuals, but these product manuals are not included. Authorized representative of the European Union In order to ensure that the above four requirements can be met when CE mark certification is implemented, the European Union law requires that manufacturers located outside the 30 EEA allies must appoint an authorized representative of the European Union to ensure the consistency of product "safety" in circulation and use after the products are put into the European market. Technical files must be kept in the European Union for inspection by supervisory bodies at any time; Remedial measures must be taken for products found by market supervision institutions that do not meet the requirements of CE, or products that have been labeled with CE during use. (such as temporary or permanent removal); After the CE mark product model is put into the European market, if the relevant EU laws change or change, the subsequent products of the same model must also be changed or modified accordingly to meet the new EU legal requirements.