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CE MARKING is the symbol. The letters "CE" are the abbreviation of French phrase "Conformity European" which literally means "European Conformity". The term initially used was "EC Mark" and it was officially replaced by "CE MARKING" in the Directive 93/68/EEC in 1993. "CE MARKING" is now used in all EU official documents. CE MARKING on a product is a manufacturer's declaration that the product complies with the essential requirements of the relevant European health, safety and environmental protection legislation, in practice by many of the so-called Product Directives. CE mark approval, CE testing and CE mark requirements: There are a series of steps outlined below for CE mark approval. Depending upon your product and the nature of the risks it presents:  
Determine if any directives apply to your product. If more than one applies you will have to comply with all of them.
Determine the extent to which your product complies with the essential requirements for design and manufacturing in the applicable directive(s).
Choose the conformity assessment procedure called out by the directive for your product.
 
 
The CE Mark is a mandatory European MARKING for certain product groups to indicate conformity with the essential heath and safety requirements set out in European Directives. The letters ‘CE’ are an abbreviation of Conformite Europeenne, French for European conformity. The CE MARKING of products as “passport” which can allow a Manufacturer to freely circulate their products within the European market place. . The CE Mark declares that your product complies with the Essential Requirements of the applicable EU Directives.

Applicable requirements are set forth in various European Directives that replace individual country safety standards. The Directives apply to products manufactured within but also exported to the European Union.

The CE Mark is placed on a product as the manufacturer’s visual identifier that the product meets the requirements of relevant European Directives. It is mandatory for a wide range of products sold within or exported to the European market.

To facilitate free trade and ensure the safety of certain products, European countries have developed a series of standards, or Directives as they are called. Compliance is mandatory. It is a legal obligation on the part of the manufacturer or his agent. Penalties for failing to get CE-MARKING for a product can be severe.

If you wish to sell your products within the European Union member states and the European Economic Area, the product in question must comply with the Directive(s). This also applies if you are a manufacturer who wants to export products into the European Member countries.

The Directives replace individual country standards as they relate principally to the safety of these products.

What products do the Directives cover? The Directives apply to a wide range of products. The most notable products that likely need CE-MARKING are:
 
Pressure equipment
Machinery of almost any description
Electrical and electronic equipment
Medical devices and equipment
Personal protective equipment
Equipment for use in potentially explosive environments.


 

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