CE-Marking

CE Marking

The CE marking is a key indicator (but not proof) of a product’s compliance through European Union (EU) health, safety and environmental protection directives and regulations.If your product comes under the scope of a directive requiring CE marking you must ensure the product complies with the applicable requirements or fulfil the requirement of harmonized standard and affix the CE mark(Standard logo) before placing it in the market in the European Economic Area (EEA). Often the CE marking is described as a trade passport because it enables the free movement of products within the European market.

KBS has collaboration with Applus+ Laboratory, Spain (Notify Body No. 0370) to provide CE marking and training services in India/Abroad. Applus+ is one of the world’s leading testing, inspection and certification companies which have more than 20,000 employeesaround the world. Applus+operates a network of more than 350 offices and laboratories in more than 70 countries across the globe.

KBS can assist you togain easier access into the European market by ensuring your product meets all the CE mark requirements. If you manufacture or import products which falls under the scope of one or more of the New Approach Directives then you will need professional guidance on how to meet all the essential requirements of these directives. KBS has the capabilities and technical expertise for professional guidance –

  • Review of product specification(s)
  • Identification of Directive(s)&applicable Harmonized standard(s)
  • Testing of products by NABL/Notified body lab etc.
  • Review of Technical File
  • GAP analysis and pre-certification audit
  • Performing Audit
  • Affix CE marking

Products and Directives in which KBS Certifies

  • Machinery Directive (2006/42/EC)
  • Low Voltage Directives –2006/95/EC
  • EMC Directive – 2004/108/EC
  • Construction Products Regulation – Regulation (EU) No 305/2011
  • Personal Protective Equipment Directive (89/686/EEC)
  • Pressure Equipments Directive(PED) -97/23/EC
  • Medical Devices Directives -93/42/EEC
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