The "CE" mark is a safety certification mark and is regarded as a passport for manufacturers to open and enter the European market. CE stands for CONFORMITE EUROPEENNE. In the EU market, the “CE” mark is a compulsory certification mark. Whether it is a product produced by an EU enterprise or a product produced in another country, if you want to circulate freely on the EU market, you must affix the “CE” mark to indicate the product It complies with the basic requirements of the EU Directive "New Methods of Technical Coordination and Standardization". This is a mandatory requirement of EU law on products.
CE is the abbreviation of French, and the English meaning is "European Conformity, which is the European Community. In fact, CE is also the abbreviation of the phrase "European Community" in many languages of the European Community. The original English phrase EUROPEAN COMMUNITY was abbreviated as EC. Because the European Community is COMMUNAUTE EUROPEENNE in French, COMUNITA EUROPEA in Italian, COMUNIDADE EUROPEIA in Portuguese, and COMUNIDADE EUROPE in Spanish, the EC is changed to CE.
Of course, you may wish to regard CE as CONFORMITY WITH EUROPEAN (DEMAND) (in line with Europe (requirements)), which constitutes the "main requirements" at the core of the European Directive, which was published in the European Community on May 7, 1985 (85/C136/01) No. "Resolution on New Methods of Technical Coordination and Standards" has a specific meaning for the "main requirements" that need to be used as the purpose of formulating and implementing instructions, that is, it is limited to the basic safety requirements of products that do not endanger the safety of humans, animals and goods. It is not a general quality requirement. The coordination directive only specifies the main requirements, and the general directive requirements are standard tasks.
Products comply with relevant directives and relevant main requirements, the CE mark is a safety conformity mark rather than a quality conformity mark. In the 1940s, Western Europe felt that in order to guarantee its own security, improve international status, and accelerate economic development between the two major powers of the United States and the Soviet Union, it was necessary to unite, and therefore pushed forward the process of European integration. European integration can be divided into five levels: the establishment of a free trade zone, a customs union, a unified large market, an economic and monetary union, and a political union.
Issuing authorityedit
(1) The Declaration of conformity / Declaration of compliance issued by the company itself. This certificate is a self-declaration and should not be issued by a third-party agency (intermediary or testing certification agency). Therefore, the EU format can be used Replaced by the Enterprise "Declaration of Conformity".
(2) Certificate of compliance / Certificate of compliance "Certificate of Compliance", this is a declaration of compliance issued by a third-party agency (intermediary or testing certification agency), must be accompanied by technical data TCF such as test reports, and at the same time, the company must also sign "Declaration of Conformity."
(3) EC Attestation of conformity "Certificate of Conformity to EU Standards", this is a certificate issued by the EU Notified Body (Notified Body abbreviated as NB). According to EU regulations, only NB is eligible to issue a CE declaration of EC Type.
Certification programedit
Confirm export
If the export to the EEA of the European Economic Area includes any of the 30 member states of the European Union EU and the European Free Trade Agreement EFTA, CE certification may be required.
Confirm the product category and relevant 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 directives corresponding to all categories. Note: Some product directives sometimes list some products that are excluded from the directive.
Authorized Representative
In order to ensure that the aforementioned four requirements in the implementation of CE Marking (CE Marking) certification are met, EU law requires manufacturers located outside the 30 EEA allies to appoint an EU authorized representative (Authorized Representative) within the EU. ) To ensure the consistency of the product's "safety" during the circulation and use period after the product is put on the European market;
Technical files (Technical Files) must be stored in the EU for inspection by the supervisory authority at any time; remedial measures must be taken for products found by market supervisory authorities that do not meet CE requirements, or products that have an accident during use but have been labeled with CE.
(For example, temporarily removed from the shelf, or removed from the market); after the product model that has been affixed with the CE label is put on the European market, if it encounters the relevant legal changes or changes in the European Union, the subsequent production of the same model product It must also be changed or amended accordingly in order to comply with the new legal requirements of the European Union.
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