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product certification
 
 
CE-marking

To be sold within the European market, certain products require CE-marking. The CE mark declares that your product complies with the Essential Requirements of the applicable EU Directives.

Applicable requirements are set forth in various European Directives that replace individual country safety standards. The Directives apply to products manufactured within but also exported to the European Union.

On this CE-marking homepage, we will help you understand the what and why of CE-marking what it is and why your product may need to be CE-marked.

Partner with DNV for:
CE-marking of your product(s) to the requirements of various EU Directives. Applicable to a wide range of products sold within or exported to countries in the European Union and European Economic Area.

DNV offers certification worldwide, and holds a wide range of national accreditations. With our global network of local resources, we can provide you with the certification most suitable to your needs, type of business, and company location. Wherever you are, our auditors make it a point to know the business you are in.



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RELATED INFO
  links:
Medical Devices Directive 93/42/EEC (pdf)
Directive 2003/32/EC on devices containing tissue of animal origin (pdf)
Guidelines on medical devices (pdf)
Information on MEDDEVs (pdf)
How to reproduce the CE mark (pdf)
  downloads:
Helpful links for Directives (pdf)
The Medical Device Directive brochure (pdf)
   
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