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CE Marking
Enter the European Market ?
The ascertain a homogenous standard of product safety and compliance,
the European Union has issued several directives stating the basic
requirements that a certain product has to comply to be admitted on
the European market.
What is CE Marking?
The letters 'CE' on a product are the manufacturer's claim that
the product meets the requirements of all relevant European Directives.
CE Marking is mandated by New Approach Directives. Many products
are covered by these directives, and to be placed on the market
in the EU, some must bear CE marking - it's a legal requirement.
CE marking is the manufacturer's claim that the product meets the
essential requirements of all relevant European Directives.
Application of the CE Marking :
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Medical devices |
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Active implantable medical devices |
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Telecommunications terminal equipment |
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Gas appliances |
Benefits of the CE Marking on a product:
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indicates to governments that the product
can be legally sold within the European Union (EU) and the European
Free Trade Area (EFTA), |
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indicates to customers that the product meets
designated minimum safety standards and therefore a minimum
level of quality, |
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promotes public health and safety, |
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enhances product credibility, |
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leads to improve sales and greater customer
satisfaction. |
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