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CE MARK CERTIFICATE

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CE MARK CERTIFICATE

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

CE Mark means Conformité Européenne, that is, 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. EU requirements for more than 20 product sectors are set out in “New Approach” Directives, which include but are not limited to:

  • * 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 its sectors, it must undergo conformity assessment. It is possible for a product to be covered by more than one directive or regulation. It must comply with everything that applies in this case. 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 during the production process, the product will be assumed to comply 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 available 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
  • * Test the product and check its suitability
  • * Have the necessary documents ready for the presentation
  • * Attach the CE marking and issue a declaration of conformity

Importers or distributors assume the responsibilities of the manufacturer when marketing a product under their own name. However, for some products where security risks are higher, conformity assessment must be carried out by an independent third party. 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 sold 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.

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About Us

Performans Customs Consultancy; It has been operating in the foreign trade sector since 2004 with its understanding of transparency, publication and quality service. Click for detailed information...

  • www.pfr.com.tr
  • info@pfr.com.tr
  • Aydınevler, Amiral Orbay Cd. No:5, 34854 Maltepe/İstanbul - Türkiye

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