The significance of CE certification is: Let the CE certified products in accordance with the requirements of the European Directives with the Essential Requirements. And confirmed that the product has been passed the appropriate conformity assessment procedures and manufacturer's qualification statement, it can truly become the product is allowed to enter the European Community market. Relevant directives require the industrial products that if the devices fail of the CE certification by the time, they may not be listed for sale. They must to meet the requirements of CE certification and CE certification mark can enter the EU market. If the product does not meet the requirements of the market, it will be ordered to recover from the market, and continuing to violations of the provisions of the relevant CE certification, will be restricted or prohibited to enter the EU market or forced to withdraw from the market!
 
The targets of the CE certification are the Member states of the European Community and the National regulatory authorities which responsible for the safety control of market products, rather than customers. When a product had CE certification, the authorities responsible for the safety supervision of the member states shall assume that they are in compliance with the requirements of the directives and may freely in the European Community market.
 
Which aspects that CE certification to ensure?
Products must not interfere with health, and not endanger the environment and consumers, that can be sale in the market.
 
Products that are Legal listing in a European Union country can also sales in other member states.
 
Manufacturers can through the products with the CE logo, to indicating the products fully comply with the relevant provisions of the EU directives. If required, CE mark can also be marked on the packaging or accompanying documents. The CE logo was not the test mark; just indicate the manufacturer to declare their products comply with all relevant laws and regulations. At present, there are various assessment model that mark accord with the basic requirements, These regulations may involve a number of units, such as manufacturers, importers and distributors, etc.. Besides, In order to indicate the compliances, certification work may also be performed by independent agencies, Such as the third party certification bodies, etc. Testing and certification bodies must also have a formal authorization, or certification under the supervision of authorized institutions. Products that do not conform to the relevant instructions may cause a lot of problems, so we suggest that need the third party certification body to certificate.
 
Through the CE certification, it prove the quality of the products qualified for the European Directives on the core of the "main demand", there are some specific definition to the "main demand" in The resolution of the new method of technical coordination and standard (May 7, 1985 [5/C136/01] of the European Community), that is the products are not endanger in human, animal and goods and accord the basic safety requirements, rather than the general quality requirements, coordination directives only provides the main requirements, General command requirements are standard tasks. The products can add CE logo when it accord with the main requirements of the related instruction. CE logo is a safe and qualified symbol, but not a mark of quality