Home | ¤¤¤å


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 :

Medical devices
Active implantable medical devices
Telecommunications terminal equipment
Gas appliances

Benefits of the CE Marking on a product:

indicates to governments that the product can be legally sold within the European Union (EU) and the European Free Trade Area (EFTA),
indicates to customers that the product meets designated minimum safety standards and therefore a minimum level of quality,
promotes public health and safety,
enhances product credibility,
leads to improve sales and greater customer satisfaction.