CE is an abbreviation of the French COMMUNATE EUROPEIA, English meaning EUROPEAN CONFORMITY, that is, the European **** the same body, in fact, CE is also the European **** body of many countries in the language of the "European **** the body" of the abbreviation of this phrase, the original use of English phrases EUROPEAN COMMUNITY abbreviated to EC, after the European *** body in French is COMMUNATE EUROPEIA, Italian COMUNITA EUROPEA, Portuguese COMUNIDADE EUROPEIA, Spanish COMUNIDADE EUROPE, etc., so change EC for CE.
In the EU market The "CE" mark is a mandatory certification mark, whether it is within the EU enterprise production of products, or products produced in other countries, in order to be free to circulate in the EU market, must be affixed with the "CE" mark to indicate that the product complies with the European Union "technical harmonization and standardization of new methods" directive basic requirements. New Approaches to Technical Harmonization and Standardization" directive of the European Union, the basic requirements. This is a mandatory requirement for products under EU law.
CE certification is the core of the European Directive constitutes the "main requirements", that is, limited to the product does not jeopardize the safety of human beings, animals and goods in terms of the basic safety requirements, rather than the general quality requirements, coordination of the Directive only provides for the main requirements of the general requirements of the Directive is the task of the standard. Therefore, the precise meaning is: CE mark is a safety mark of conformity rather than quality mark of conformity.
Medical devices exported to the EU must be CE marked and safety tested.