CE mark For Pressure Equipment Directive ( 97/23/EC) is applicable to all those equipments which have a internal design pressure more than 1.5 bar. Design pressure is generally greater than maximum operating pressure...
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...
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....
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...
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