Homologation Certificate
Introduction
The CE marking[1] comes from French and means "Conformité Européenne" (in Spanish, "European Conformity"), and is the certificate given by the European Commission to certain products that are marketed in the internal market of the European Union and that certifies that said good complies with community legislation on health, safety and sustainability. It is based on Directive 93/68/EEC of the European Parliament and the Council.
It was established by the then European Community and is the manufacturer's testimony that its product complies with the minimum legal and technical safety requirements of the European Union. It should be kept in mind that the CE marking does not imply the quality of the product; It only declares certain benefits in accordance with a certain format and that meets health, safety and sustainability standards.
The CE marking must be affixed to a product if it falls within the scope of the approximately 20 so-called "New Approach" Directives[2] (in Spanish, "de Enfoque Nuevo") and can be legally sold and put into service within the Single Market of the European Union. If the product complies with the provisions of the Directives and the CE marking is affixed to the product, Member States cannot prohibit, restrict or prevent the placing on the market or putting into service of the product. The CE marking can be considered as the passport for the trade of the product within the Single Market of the European Union.
Meaning
The CE marking represents that the manufacturer "declares that its product complies with the applicable European harmonization legislation" (EU declaration of conformity), allowing the free circulation of products within the European Economic Area. By affixing the CE marking to a product, "the manufacturer assumes responsibility for the conformity of said product" with all the legal requirements required to achieve the CE marking and ensures the validity of the product to be sold throughout the EEA (the 28 EU Member States and EFTA countries Iceland, Norway, Liechtenstein), as well as in Turkey. This also applies to products manufactured in third countries that are sold in the EEA and Türkiye.
The CE marking does not indicate that a product has been manufactured in the European Economic Area; It merely states that the product "is evaluated before being placed on the market" and therefore satisfies the legal requirements (for example a harmonized level of safety) to be sold on the market. This means that the manufacturer has verified that the product complies with all relevant essential requirements (for example safety, health and environmental protection requirements) of the applicable European Directives or Regulations. In some cases, before affixing the CE marking, it must undergo evaluation by a Notified Body.