CE Mark certification for Pressure Equipment
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
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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
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CE marking on machinery 2006-42-EC Directive Make sure that the machine is not falling under Annex IV of the machinery Directive. If it does involve a Notified Body . Apply most specific standard or EN 60204 if no machine specific standard is available. Remember to choose the latest version of the applicable safety standard
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