Medical equipment after ce certification still need dfda certification?

"CE" mark is a safety certification mark, is regarded as the manufacturer to open and enter the European market passport. CE represents the European unity (CONFORMITE EUROPEENNE). Where the "CE" marking of the product can be affixed to the EU members of the domestic sales, without having to meet the requirements of each member state, thus realizing the free flow of goods in the EU member states within the scope of the free flow of goods.

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 under EU law.

Medical equipment to do CE marking in accordance with the MDD directive.