CE MARK CERTIFICATION

EUROPEAN CONFORMITY (CE) PRODUCT CERTIFICATION

The European Conformity (Conformitè Europëenne) CE Mark is a Product Certification mark defined by the European Union to ensure the products’ safety, security, and quality to meet the requirements set by Union for the products sold within the EU. The CE Mark represents the declaration from the manufacturer that the product meets the requirements and complies with the EU directives.

The Ce mark Certification is mandatory for manufacturers who want to sell their products in the EU Countries. The Mark is also mandatory for manufacturers and exporters outside the EU to sell their products within EU Countries. 

EU Directives for the CE Certification

• Machinery Directive – 2006/42/EC
• Low Voltage Directive – 2014/35/EU
• EMC Directive – 2014/30/EU
• Medical Devices Directive – 93/42/EEC
• Personal Protective Equipment Directive – 89/686/EEC (as of 21 April 2018 replaced by the Personal Protective Equipment Regulation (Regulation (EU) 2016/425)
• Construction Products Regulation – Regulation (EU) No 305/2011
• Pressure Equipment Directive – 2014/68/EU
• REACH – Regulation (EC) No 1907/2006
• RoHS – Restriction of Hazardous Substances – Directive – 2011/65/EU
• Waste Electrical and Electronic Equipment Directive – 2012/19/EU
• ATEX Directive – 2014/34/EU
• Toy Directive – 2009/48/EU
• Radio Equipment Directive – 2014/53/EU
• Recreational Craft Directive – 2013/53/EU
• Active Implantable Medical Devices Directive – 90/385/EEC
• Explosive for Civil Use Directive – 93/15/EEC
• Noise Emission in the Environment Directive – 2000/14/EC
• Gas Appliances Directive – 2009/142/EC
• Lifts Directive – 2014/33/EU
• Pyrotechnic Directive – 2007/23/EC
• Measuring Instruments Directive – 2004/22/EC