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CE-marking

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This is the regulatory European product marking allowing access to the EU/EEA member countries (and even some EU candidate countries in Eastern Europe), as dictated by EU Directives and corresponding national regulations.

It is required for a wide range of products, including:

  • Electrical consumer products
  • Medical equipment
  • Machinery

Other facts about the CE-marking:

  • The CE-marking is essentially based on the manufacturer’s own declaration of conformity with the relevant Directives.
  • In the case of some high risk products and where European product standards are not used, the involvement of an authorized Notified Body (or Competent Body) is required as a basis for the manufacturer’s Declaration of Conformity (DoC) and for CE-marking of the product.
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