Declaration of conformity and CE / EU marking
Most industrial products require a CE MARKING to be marketed in the European Union, regardless of their country of origin. The CE Mark for Medical Devices or CE Certificate of Conformity should not be confused with the Declaration of Conformity.
The CE Certificate of Conformity or CE Marking is the result of making a product comply with all the technical requirements demanded by each of the applicable directives (documentation, tests, and implementation of quality systems in some cases).
