Certification IntroductionCE is abbreviated from the French "Communate Europpene", which means the European Community, referred to as the European Union. The CE mark is a legally mandatory mark in the EU market. Whether it is a product produced by an enterprise within the EU or a product produced in other countries, in order to circulate freely in the EU market, the CE mark must be affixed to indicate that the product complies with the EU's "New Approach to Technical Harmonization and Standardization" (The New Approach to Standardization). The basic requirements of the technical harmonization and standardization) directive.Those without the CE mark shall not be sold on the market. If the products that have been affixed with the CE mark and entered the market are found to fail to meet the safety requirements, they shall be ordered to be withdrawn from the market. Those who continue to violate the CE mark regulations of the directive will be restricted or prohibited from entering the EU market or forced to withdraw from the market.basic information of CE certification is mandatory: mandatory + self-declaration certificate validity period: no validity period factory inspection requirements: no requirements certificate holder requirements: no requirementsTechnical information: Voltage and frequency AC 230V, 50Hz /60Hz, plug European standard CEE 7/7 & 7/16 or national standard CE Compulsory Certification and CE Self-Declaration InstructionsMost products can be affixed with the CE mark if the manufacturer adopts a self-declaration of conformity; some products with relatively higher risks need to be assessed by a third-party agency authorized by the EU, that is, a Notified Body. Only then can the CE mark be affixed.Applicable areaCE certification can be found in 33 special economic zones in Europe, including: 27 countries in EU, 4 countries in the European Free Trade Zone, and the United Kingdom and Turkey. Products with the CE mark can circulate freely in the European Economic Area (EEA).The specific EU 27 countries list is: Belgium, Bulgaria, Czech Republic, Denmark, Germany, Estonia, Ireland, Greece, Spain, France, Croatia, Italy, Cyprus, Latvia, Lithuania, Luxembourg, Hungary, Malta, Netherlands, Austria, Poland, Portugal, Romania, Slovenia, Slovakia, Finland, Sweden.Applicable product scopeIf you want to understand the product scope of CE, you must understand the NLF regulations of CE certification. NLF stipulates which products within its scope need to be certified by CE. There are currently 22 directives in the new EU legislative framework NLF, which are as follows: 1. Toy safety - Directive 2009/48/EU 2, Mobile Pressure Equipment - Directive 2010/35/EU 3, Restriction of Hazardous Substances in Electrical and Electronic Equipment - Directive 2011/65/EU 4, Construction Products - No. Regulation 305/2011 (EU) 5. Pyrotechnic articles - Directive 2013/29/EU 6. Recreational and personal watercraft - Directive 2013/53/EU 7. Explosives for civil use - Directive 2014/28/EU Directive 8, Simple Pressure Vessels - Directive 2014/29/EU 9, Electromagnetic Compatibility - Directive 2014/30/EU 10, Non-automatic Weighing Instruments - Directive 2014/31/EU 11, Measuring Instruments - Directive 2014/32/EU 12, Lifts - Directive 2014/33/EU 13, Equipment and protective systems for potentially explosive atmospheres - Directive 2014/34/EU 14, Radio equipment - 2014/53 /EU Directive 15, Low Pressure - Directive 2014/35/EU 16, Pressure Equipment - Directive 2014/68/EU 17, Marine Equipment - Directive 2014/90/EU 18, Ropeway Installations - Regulations (EU ) 2016/424 19, Personal Protective Equipment - Regulation 2016/425 20, Gas Appliances - Regulation (EU) 2016/426 21, Medical Devices - Regulation 2017/745 22, In Vitro Diagnostic Medical Devices, Regulation (EU) ) 2017/746 Note: NLF refers to the EU's new legislative framework, the full name "New Legislative Framework" is the EU's regulations to strengthen the market supervision framework and recognition system for products. In 2008, the "New Legislative Framework" was passed to the original New Method Directive. In addition to the unified definition of the relevant concepts in the system, specific provisions are made on national accreditation bodies and accreditation systems, the European Community market supervision framework, product market access control, general rules for the use of signs, and European Community funding. After you are familiar with the regulatory framework, you can classify the corresponding products. The scope of CE certification is very wide. Generally speaking, most products exported to the EU require CE certification. For electronic products and toys exported to Europe, CE certification is mandatory, such as: Power supply: communication power supply, charger, display power supply, LCD power supply, UPS, etc.; lamps and lanterns: chandeliers, track lights, garden lights, portable lights, downlights, light strings, table lamps, grille lights, aquarium lights, street lights, energy saving Lamps, T8 lamps, etc.; Household Appliances: fans, electric kettles, stereos, televisions, mice, vacuum cleaners, etc.; electronics: earplugs, routers, mobile phone batteries, laser pointers, vibrators, etc.; communication products: telephones, Wired telephone wireless main and auxiliary machines, fax machines, answering machines, modems, data interface cards and other communication products. Wireless products: Bluetooth BT products, wireless keyboards, wireless mice, wireless readers, wireless transceivers, wireless microphones, remote controls, wireless network devices, wireless image transmission systems and other low-power wireless products, etc.; wireless communication: 2G mobile phone, 3G mobile phone, 3.5G mobile phone, DECT mobile phone (1.8G, 1.9G frequency band), etc.; Machinery: gasoline engine, electric welding machine, CNC drilling machine, tool grinder, lawn mower, washing equipment, bulldozer, elevator, punching machine , dishwashers, water treatment equipment, gasoline welding machines, printing machinery, woodworking machinery, rotary drilling rigs, lawn mowers, snow blowers, excavators, printing presses, printers, cutting machines, road rollers, trowels, cutting machines Irrigation machines, hair straighteners, food machinery, lawn machines, etc.;Medical equipment and toys, etc. Common electrical and electronic products are:Low Voltage Directive: Household Appliances, IT/AV Products, Lighting Products, etc. Electromagnetic Compatibility Directive: Household Appliances, IT/AV Products, Lighting Products, etc. Mechanical Directive: All Related Products Radio Frequency and Communication Terminal Equipment Directive: Wireless or Communication Terminal Productsapplication process1. The applicant company fills in the application form and provides information, application form, product instruction manual and technical documents. 2. The institution evaluates CE certification inspection standards and CE certification inspection items and quotes. 3. The applicant company confirms the project and sends samples. 5. The laboratory arranges product testing and reviews and evaluates the integrity of technical documents. 6. After the product test meets the requirements, provide the product test report or technical construction document to the applicant company, and issue the CE certificate after the test is passed. 7. The applicant company signs the CE guarantee self-declaration and affixes the CE mark on the product.Application documents1. Name and address of the manufacturer (EU authorized representative (EU authorized agent)), product name, model, etc.; 2. Product instruction manual; 3. Safety design documents (including key structural diagrams, which can reflect the climbing distance, 4. Product technical conditions (or enterprise standards), establish technical data; 5. Product electrical schematic diagram, block diagram and circuit diagram, etc.; 6. List of key components or raw materials (please Select products with European certification marks); 7. Testing Report; 8. Relevant certificates issued by EU authorized certification body NB (for other modes other than Mode A); 9. Product registration certificate in the EU (for Some products such as: Class I medical devices, general IVD in vitro diagnostic medical devices); 10. CE Declaration of Conformity (DOC);Meaningness of CE certification1. The necessity of applying for CE certification, the export of products to Europe must be handled. CE certification is a passport for products to enter the European Union and European Free Trade Zone countries. CE certification means that the product has reached the safety requirements specified in the EU directives; CE certification is a commitment of enterprises to consumers, which increases consumers' trust in products; products bearing the CE mark will reduce sales in the European market. risk. 2. The benefits of applying for CE certification The EU's laws, regulations and harmonized standards are not only numerous, but also very complex in content. Therefore, it is a wise move to obtain the help of an EU-designated agency that saves time and effort and reduces risks; The CE certification certificate of the designated agency can maximize the trust of consumers and market supervision agencies; it can effectively prevent the occurrence of irresponsible allegations; it will become a technical evidence with legal effect.