Only comply with the relevant provisions of the European Directive the main requirements and to confirm that the product has passed the corresponding conformity assessment procedures and / or the manufacturer's qualified statement in order to truly become a product was allowed to enter the European Community market permits. CE mark has been affixed to enter the market and found that do not meet safety requirements and should be ordered to recover from the market, continuing to direct the CE mark in violation of the provisions will be restricted or prohibited from entering the EU market or be forced out of the market.
"CE" mark is a mandatory certification, whether the European Union and non-EU enterprise products in free circulation on the EU market, it is necessary to add "CE" standards in order to show that the products meet the EU's "technical coordination and standardization of new methods of" command the basic requirements. Why
products for CE certification?
A need to apply for CE certification
CE certified products for all countries to trade in the European market provides a unified technical specification, to simplify trade procedures. Products of any country to enter the European Union, the European Free Trade Area of the need for CE certification, in the product affixed CE mark. Therefore CE certified products into the European Union and the European free trade area of the permit markets. CE certification that the product has reached the security of the EU directive requirements; is a commitment to consumers to increase consumer confidence in the product; affixed with a CE marked product in Europe will reduce the risk of the market.
These risks include:
detained by customs and dealt with the risks;
investigated and dealt with by the market risk oversight bodies;
competition was for the purpose of peer risk charges.
Second, to apply for the benefits of CE certification
EU laws, regulations and standards is not only a large number of co-ordination, but also very complex, designated agencies to help achieve the EU is a time-saving, labor-saving, and reduces the risk of the wise ;
designated by the European Union CE Certification bodies can maximize access to consumer and market confidence in the oversight bodies;
to be effective in preventing irresponsible allegations from happening;
in the face of litigation, the EU designated CE Certification bodies will be legally binding technical evidence;
once punished by the European Union countries, certification bodies and enterprises to the risk-sharing, thus reducing the corporate risks.
Third, the application procedures for CE certification
application by enterprises;
the two sides signed the contract certification;
provide samples and technical documentation testing;
sample testing and technical documentation assessment;
issuance of compliance certificates;
qualified enterprises to issue a statement;
products from enterprises in the CE marking attached.
Provide information, samples
Customer requirements in accordance with the engineers to provide product information, such as product manuals, exploded diagram, circuit schematic, parts list, bill of materials, etc., according to the number of test items provide samples of products with the same ship.
BEL received samples of the product to make a preliminary analysis, based on advanced detection and rich experience of product certification, in accordance with testing standards, and strictly carry out the test.
In the detection process, discovered by product design, component selection, manufacturing issues such as product defects caused by the light of the actual product design information and response to reform, the reform program is part of a one-stop testing services, professionals and senior years counseling experience in a variety of product certification, equipment, strong support, coupled with technology and the certification body interaction, discussions of technical communication at any time. To ensure that customers find the best solutions to customers the full product, give full consideration to the cost of product manufacturing.
Quantity: At least two machine
CE prepared ：
1）International Certification Application Form
3) circuit schematic
5) Note the difference (when the application of a number of models)
6) a list of key components (the proposed international certification mark use of the components)
7) specification of some components (such as transformers, filters, fuses, capacitors, switches, etc.)
The above information must be written in english!
Test cycle: complete information, products, under the premise of no improvement for the five business days!
CE Certification scope
|EC implementation of CE marking of industrial products related to the implementation of Directive Table|
EU Directive No. (with amendments to the directive #)
|Simple Pressure Vessels||87/404/EEC,#90/488/EEC,#93/68/EEC||Civil explosives||93/15/EEC|
|Toy Safety||88/378/EEC,#93/68/EEC||Medical devices||93/42/EEC|
|Construction products||89/106/EEC ,#93/68/EEC||Low-voltage Electrical Products||2006/95/EC|
|EMC products||2004/108/EC||Easy to use in explosive environment of equipment and protection systems||94/9/EC|
|Machinery||2006/42/EC||Telecommunications by satellite earth station||93/97/EEC|
|Personal protective equipment||89/686/EEC,#93/68/EEC,93/95/EEC||With a lift by||95/16/EEC|
|Non-automatic weighing instrument||90/384/EEC,#93/68/EEC||Playground equipment||94/25/EC|
|Active implantable medical devices||90/385/EEC,#93/68/EEC||Pressure device||97/23/EC|
|Fuel gas combustion devices||90/396/EEC,#93/68/EEC||Dangerous goods transported on the road||94/55/EC,96/86/EC|
|Telecommunications terminal equipment||91/263/EEC,#93/68/EEC||Medical device testing||98/79/EC|
|Hot water boiler equipment||92/42/EEC,#93/68/EEC|
Add: A112~114,Qinye Business Center，Xin’an Sixth Road,82th District,Bao’an,Shenzhen,China.