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The world's product testing certification marks list which products your products pass through.
What are the safety certification codes that foreign trade export products need to pass in other countries? What are the meanings of these certification marks? Let us look at the current 20 internationally recognized certification marks and their meanings, and see if your products are currently passed. The following certifications. 1, CE
The CE mark is a safety certification mark and is regarded as a passport that the manufacturer opens and enters the European market. CE stands for CONFORMITE EUROPEENNE. Products bearing the "CE" mark can be sold in EU member states without meeting the requirements of each member state, thus realizing the free circulation of goods within the EU member states.
ROHS is the abbreviation of "The Restriction of the use of certain hazardous substances in electrical and electronic equipment". ROHS lists a total of six hazardous substances, including: lead Pb, cadmium Cd, mercury Hg, hexavalent chromium Cr6+, polybrominated diphenyl ether PBDE, polybrominated biphenyl PBB. The EU began implementing ROHS on July 1, 2006. Electrical and electronic products that use or contain heavy metals and PBDEs such as polybrominated diphenyl ethers and PBBs are not allowed to enter the EU market. ROHS is for all electrical and electronic products that may contain the above six hazardous substances in all production processes and raw materials, including: white goods, such as refrigerators, washing machines, microwave ovens, air conditioners, vacuum cleaners, water heaters, etc., black appliances, such as audio and video products. , DVD, CD, TV receiver, IT products, digital products, communication products, etc.; power tools, electric electronic toys, medical electrical equipment.
Remark: When the guest asks if there is no rohs, he has to ask whether he wants the finished rohs or the raw materials rohs. Some factories can't do the finished rohs, and the price of rohs is generally about 10%-20% higher than the ordinary products.
UL is a shorthand for Underwriter Laboratories Inc. The UL Safety Laboratory is the most authoritative in the United States and a large private institution engaged in safety testing and identification. It is an independent, non-profit, professional organization that tests for public safety. It uses scientific testing methods to determine the extent to which various materials, devices, products, equipment, buildings, etc. are hazardous or harmful to life and property; to determine, prepare, and issue appropriate standards and to help reduce and prevent life. The property is subject to loss of information, and at the same time, the fact-finding business is carried out. In short, it is mainly engaged in product safety certification and business safety certification business, and its ultimate goal is to obtain a fairly safe product for the market and contribute to the protection of personal health and property safety. Regarding product safety certification as an effective means of eliminating technical barriers to international trade, UL also plays an active role in promoting the development of international trade.
Remark: It is not mandatory for UL to enter the United States.
4. FDA The US Food and Drug Administration referred to the FDA. The FDA is one of the executive agencies established by the US government in the Department of Health and Human Services (DHHS) and the Department of Public Health (PHS). The FDA's role is to ensure the safety of food, cosmetics, pharmaceuticals, biologics, medical devices and radioactive products produced or imported in the United States. After the "9.11" incident, people in the United States believed that it was necessary to improve the safety of food supply. After the US Congress passed the Public Health and Safety and Bioterrorism Prevention and Countermeasures Act of 2002 in June last year, it allocated US$500 million to authorize the FDA to formulate specific rules for implementing the bill. The regulation stipulates that the FDA will assign a registration number to each registration applicant. The food exported by the foreign institution to the United States must be notified to the US Food and Drug Administration 24 hours before arriving at the US port, otherwise it will be refused entry. And detained at the port of entry.
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