C.E. Sign Application

C.E. The mark application is a necessary application to maintain the validity of the products that will be sold abroad. This application, also known as the European Union certificate of conformity, ensures that products can operate in European Union countries.

CE Mark Conformité Européenne means European Conformity. It is a mandatory certification mark for all products placed on the market in the European Economic Area. This certificate; It indicates that the product complies with high safety, health and environmental protection requirements. However, not all products require CE marking. Only products that meet EU specifications require CE marking. More than 20 product sectors EU requirements for “New Approach” which include but are not limited to: It is stated in the directives.

  • Gas Appliances Regulation (GAR)
  • Construction Products Regulation (CPR)
  • Low Voltage Directive (LVD)
  • Pressure Equipment Directive (PED)
  • Electromagnetic Compatibility Directive (EMC)
  • Equipment for potentially explosive atmospheres (ATEXS)

C.E. Why is the sign important?

If a product falls within the scope of any of the product sectors, it must undergo conformity assessment. It is possible for a product to fall within the scope of more than one directive or regulation. In this case it must comply with everything that applies. The New Approach Directives set out the basic requirements that a product must meet before being placed on the EU market. However, technical details outlining the minimum requirements are generally not found in the Directive itself.

Nowadays, some European standards have been adopted for specific products targeting certain essential requirements within the scope of directives in order to provide a technical solution in meeting the essential requirements. This means that if harmonized European standards exist for a product and the manufacturer follows them in the production process, it will be assumed that the product complies with the requirements targeted by these standards in the relevant EU directive. Using standards is optional, though. This gives manufacturers the flexibility to choose other technical solutions found in general engineering and scientific literature to evaluate suitability. References to harmonized standards can be found in the Official Journal of the European Union (OJEU) available for each directive.

C.E. Sign Application Scope

C.E. We can state that within the scope of the sign application, manufacturers are responsible for the following.

  • Identify applicable directives and standards
  • Verify product requirements
  • Determine whether an independent conformity assessment (by a notified body) is required
  • üproductü test and check suitability
  • Have the necessary documents ready for the presentation
  • Attach the CE marking and issue a declaration of conformity

Importers or distributors buy a product While marketing under their own names, they assume the responsibilities of the manufacturer. However, for some products where security risks are higher, conformity assessment may require an independent third party. It must be done by the individual. Organizations approved by EU countries will carry out product type tests and a declaration of conformity is published.

Professional Services

You too C.E. If you want to have the mark certificate and ensure that your products are offered for sale and used in the best way in Europe, you are at the right place. You can get detailed information about this subject by contacting our company.