Beauty equipment FDA, CE certification

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　　FDA is the abbreviation of Food and Drug Administration (Food and Drug Administration). Authorized by the U.S. Congress, the federal government, the FDA is the highest law enforcement agency specializing in food and drug management. National health monitoring agency for government health control. Many other countries seek and receive FDA assistance to promote and monitor the safety of their domestic products.

　　The FDA international free sales license is not only the highest level of certification in the US FDA certification, but also the highest certification for food and drugs approved by the World Trade Organization (WTO). certification certificate. Once this certification is obtained, the product can enter any WTO member country smoothly, and even the marketing mode, the government of the host country shall not interfere.

　　CE certification:

　　The significance of the CE mark is that it means that the product affixed with the CE mark has passed the corresponding conformity assessment procedures and or the manufacturer's declaration of conformity, and is in line with the relevant EU directives, and this product is allowed to enter the European Community market. The relevant directives require industrial products to be affixed with the CE mark. 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 withdraw from the market and continue to violate the relevant CE mark regulations of the directive. , will be restricted or banned from entering the EU market or forced to withdraw from the market. The CE mark is not a quality mark, it is a mark that represents that the product has complied with the European safety/health/environmental protection/sanitation series of standards and directives. All products sold in the EU must be marked with the CE mark. Since the CE mark appeared in 1995, the CE mark has always symbolized that a product - no matter where in the world it is produced - complies with EU law and allows the free circulation of the product in the European Economic Area. CE marking is planned as a market surveillance measure and has enforcement authority.

　　CE certification provides a unified technical specification for the trade of products from various countries in the European market and simplifies the trade procedure. To enter the European Union and the European Free Trade Area, the products of any country must be CE certified, and the CE mark should be affixed to the product. Therefore, 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 met the safety requirements stipulated by the EU directives; it is a commitment of enterprises to consumers, which increases consumers' trust in the product; products affixed with the CE mark will reduce the risk of being sold in the European market.

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Beauty equipment FDA, CE certification

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