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CE marking is a mandatory conformity marking for certain products sold within the European Economic Area (EEA) since 1985. The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in. more...
CE Marking For Medical Device Directive is one of the most complex directive and one which involves strict vigilance by the European Authorities. Steps for CE marking for Medical Devices of Class 1s , IIa, IIb and III are as follows more...
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 "c more...
For many products to be sold in the EU, CE labelling is necessary. When a product bears the CE label, it means that the maker has evaluated it and determined that it complies with EU standards for environmental, health, and safety protection. It is necessary for any goods created anywhere in the world that ar more...
CE Marking is a mandatory requirement for products to be sold in the European Economic Area (EEA). CE marked products shall meet the set of regulations published by the European Union (EU) known as directives. By complying with relevant directives and harmonised standards one can make sure that his prod more...
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