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Our services
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.
LIST OF DIRECTIVES
Directive No.
Directive Title
2006/95/EC
Low voltage equipment
90/396/EEC
Appliances burning gaseous fuels
2000/9/EC
Cableway installations designed to carry persons
89/106/EEC C
Construction products
2004/108/EC
Electromagnetic compatibility
94/9/EC
Equipment and protective systems in potentially explosive atmospheres
93/15/EEC
Explosives for civil uses                         
95/16/EC
Lifts
98/37/EC
Machinery safety
2004/22/EEC
Measuring instruments
90/385/EEC
Medical devices: Active implantable
93/42/EEC
Medical devices: General
98/79/EC
Medical devices: In vitro diagnostic
92/42/EEC
New hot-water boilers fired with liquid or gaseous fluids (efficiency requirements)
90/384/EEC
Non-automatic weighing instruments
94/62/EC
Packaging and packaging waste
89/686/EEC
Personal protective equipment
97/23/EC
Pressure equipment
1999/5/EC
Radio and telecommunications terminal equipment
94/25/EC
Recreational craft
87/404/EEC
Simple pressure vessels
88/378/EEC
Toys safety
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