CE Marking
CE marking is a declaration by the manufacturer that the product meets all the appropriate provisions of the relevant legislation implementing certain European Directives. CE marking gives companies easier access into the European market to sell their products without adaptation or rechecking. The initials "CE" do not stand for any specific words but are a declaration by the manufacturer that his product meets the requirements of the applicable European Directive(s).
The European Commission refers to the CE Marking of products as a "passport" which can allow a manufacturer to freely circulate their products within the European marketplace. The marking applies only to products regulated by the European Commissions health, safety and environmental protection legislation (product directives) but this is estimated to include more than 50% of the goods currently exported from the U.S. to Europe.
Notified bodies are authorized by European countries to serve as independent test labs and perform the steps called out by product directives, only in cases where self-certification is not possible. They must have the necessary qualifications to meet the testing requirements set forth in the directives. Notified bodies may be a private sector organization or a government agency. Manufacturers may choose a notified body in any member state of the European Union
We provide you both notified & non-notified certificates. We have strategic tie-up with different notified bodies to issue CE mark certificate.
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Appliances burning gaseous fuels
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Cableway installations designed to carry persons
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Electromagnetic compatibility
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Equipment and protective systems in potentially explosive atmospheres
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Explosives for civil uses
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Medical devices: Active implantable
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Medical devices: In vitro diagnostic
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New hot-water boilers fired with liquid or gaseous fluids (efficiency requirements)
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Non-automatic weighing instruments
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Packaging and packaging waste
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Personal protective equipment
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Radio and telecommunications terminal equipment
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