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CE Mark

The CE mark is a mandatory European marking for certain product groups to indicate conformity with the essential health and safety requirements set out in European Directives. The letter 'CE' is an abbreviation of Conformité Européenne, French word for European conformity. The CE mark must be affixed to a product if it falls under the scope of 'New Approach' Directives of European union.

Without the CE marking, and thus without complying with the provisions of the Directives, the product may not be placed in the market or put into service in the fifteen member states of the European Union and Norway, Iceland and Liechtenstein. However, if the product meets the provisions of the applicable European Directives, and the CE mark is affixed to a product, these countries may not prohibit, restrict or impede the placing in the market or putting into service of the product.


KEY DIRECTIVES

  • Machinery Safety – 98/37/EEC
  • EMC – 2004/108/EC
  • Low Voltage Equipment – 2006/95/EC
  • Pressure Equipment – 97/23/EC
  • Medical Devices General – 93/42/EEC
  • Construction Products Directive – 89/106/EEC
  • Equipment – 99/5/EC
  • Packaging & Packaging Waste. – 94/62/EC

Benefits of Certification

  • Inclination of efficiency
  • Inclination of revenue
  • Employee of Morale
  • International Recognition
  • Factual approach to decision making
  • Supplier Relationship
  • Documentation
  • Customer Satisfaction

How we can help you?

  • Determination and compliance with the directives applicable to the product.
  • Determination of the extent to which the product complies with the essential requirements for design and manufacturing in the applicable directive(s).
  • Choosing of the conformity assessment procedure from the options called out by the directive for the product.
  • Selecting the applicable product standards and test methods for the product and selecting an independent lab If the product testing is to be done externally.
  • Establishing an authorized representative for regulatory affairs in the European Union for the product.
  • Preparation of a declaration of conformity that includes a list of the directives and standards that the product conforms to; product identification, the manufacturer's name, address and signature.
  • Affixing the CE Marking to your product.