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 "CE" mark is that the products comply with European directives (replace all national laws and regulations), the only sign, which means "CE" mark shall replace all signs comply with national regulations (such as the German GS mark). Member States should "CE" marking into their national legislation and administrative procedures. Products can be affixed to other signs, but must meet the following conditions: 

 The logo has the "CE" mark different functions, the signs provide added value to the other, for example, environmental issues not covered by instructions. 

 Affixed to the sign law is not easy to cause confusion, such as the protection of trademarks and other manufacturers. 

 CE marking mode 

 Currently, the EU approved the use of CE marking has the following eight kinds of models: 

 1 plant self-control and certification 

 Module A (internal production control): 

 a) simple, high-volume, non-hazardous product, only for the production of plants according to European standards 

 b) be qualified facility self-assessment, self-declaration 

 c) technical documents submitted to the State institutions than ten years, on this basis, can review and inspection to determine whether the product complies with Directive, producers and even to provide product design, production and assembly process for inspection 

 d) do not need to declare their production process to ensure that products consistently meet the requirements 

 Module B: 

 a) manufacturer fails to European standards 

 b) Testing agency special parts for the product of random testing 

 (2) assessment of the test bodies 

 Module B (EC type of review): 

 Samples and technical documents submitted to the selected testing agency for review, test certificate issued by the agency. Note: only B is insufficient to constitute use of CE 

 Module C + B (consistent with the type of sample + B): 

 Factory for conformance statement (consistent with the type certification) stating that ten years of 

 Module D + B (production process quality control + B): 

 This model concern the production process and final product control, factory approval in accordance with test method (quality system, EN29003) for production, on the basis of the type declaration and certification of its product line (Declaration of Conformity) 

 Module E + B (product quality control + B): 

 This model is concerned only with the final product control (EN29003), the other with Module D 

 Module F + B (product testing + B): 

 Factory to ensure the production process to ensure that products meet the requirements for declaration of conformity. Recognized testing organization through the entire inspection or sampling inspection to verify compliance of their products. Testing issues certificates. 

 Module G (individually tested): 

 Factory statement complies with Directive requirements, submit to the testing agency technical parameters of products, product testing agency to inspect the certificates. 

 Module H (comprehensive quality control): 

 This model concern the design, production process and final product control (EN29001). The other with Module D + Module E. 

 Among them, the mode of F + B, G mode for particularly high risk products. 

 Following these common general electronics mode in accordance with Module C + B certify that issued by the testing agency test reports and certificates, signed Declaration of Conformity plant (consistent with the type certification): 

 1 class information technology (IT), such as computers and peripherals 

 2 Class audio and video (AV), such as TV, DVD, CD, audio, amplifiers and other 

 3 appliances, such as air conditioners, refrigerators, washing machines, microwave ovens, etc. 

 4 Radio and telecommunications terminal products (R & TTE) 

 These signs shall not be in the meaning or form with the "CE" mark confusion 

 "CE" marking must be in by the manufacturer or a representative designated by the European Union plus posts. Manufacturers (or from outside the EU within the EU) is to make the product meets the essential requirements of Directive ultimately responsible, manufacturers can also designate a plenipotentiary in the European Union, is responsible for placing the product on the market should bear the responsibility of the manufacturer. 

 European Economic Area that the European Union, European Free Trade Association countries (except Switzerland). Before the implementation of the CE mark, as the EC countries for imports and sales requirements are different, so easy to form trade barriers between each other and hinder economic integration process. According to EC May 7, 1985 the (85/C136/01) No. "technical coordination and standards for new methods of resolution" (New Approach Directives), CE mark came into being. 

 Apply the CE mark on the product means that the manufacturer declares: This product complies with European health, safety, environmental and consumer protection under the law related to the basic requirements (in practice, these laws more directive approach to product release) . Apply the CE Marking, can legally enter the EU single market and free circulation within the EU single market. 

 CE certification and EU Directive 

 The EU has already implemented a system to protect the health of consumers and workers, the state of goods and the environment. Under this new system in the European Union and some European Free Trade Association countries, the development of the EC directive. To ensure that products meet safety and quality standards. 

 Through the reconciliation of standards, the application of uniform assessment procedures and acceptance criteria, test and was able to reduce the duplication of individual countries in the case to trial. 

 European Union / European Community and European Free Trade Association in 1994, jointly established the European Economic Area, this is the world's largest economic zone, participating countries include Austria, Belgium, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy , Luxembourg, Netherlands, Norway, Portugal, Spain, Sweden, and the United Kingdom. 

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