Silicone products manufacturers want to develop their products in the international direction, to obtain more sales channels, but to open the international market is not easy, the following Cushion Electronics for you to briefly introduce the silicone products to the international market need to pass the following certification: 1.

1. ISO certification: translated into Chinese is "International Standards Organization". Founded on February 23, 1947, ISO is responsible for standardization activities in many important fields other than electrical and electronic fields and military, oil and shipbuilding.

ISO9001 refers to the international quality management system, which is introduced by converting international standards into national standards, and there are two types of conversion methods: equivalent adoption and equivalent adoption, which are adopted in China, that is, the standard is adopted without any changes. In order to facilitate the identification of the cited international standard we added "10000", so the correct way to write the cited quality management system standards: ISO9001: 2008 idt GB/T19001-2008. idt means equivalent to the meaning of the adoption, GB/T represents the meaning of the national recommended standards. 　　GB/T19000 family standards include

(a) GB/T19000 Quality Management System Basics and Terminology 　

(b) GB/T19001 Quality Management System Requirements 　

(c) GB/T19004 Quality Management System Performance Improvement Guide

(d) GB/T19011 Quality and/or Environmental Management System Audit Guide

2. FDA: is one of the executive agencies of the U.S. government within the Department of Health and Human Services (DHHS) and the Department of Public Health (PHS).

As a scientific regulatory agency, the FDA's responsibility is to ensure the safety of food, cosmetics, drugs, biologicals, medical devices, and radiological products manufactured or imported into the United States. It was one of the first federal agencies to have consumer protection as a primary function. The agency has a stake in the lives of every American citizen. Internationally, the FDA is recognized as one of the world's largest food and drug regulatory agencies. Many other countries seek and receive help from the FDA to promote and monitor the safety of their own products.

The Food and Drug Administration (FDA) is in charge of: food, drugs (including veterinary drugs), medical devices, food additives, cosmetics, animal food and drugs, wine beverages with an alcohol content of less than 7%, and the supervision and inspection of electronic products; products in the use or consumption of ionized, non-ionic radiation generated during the process of testing, inspection and certification of human health and safety programs. According to the regulations, the above products must be tested by the FDA to prove safety before they can be sold in the market, and the FDA has the right to inspect manufacturers and prosecute violators.

  3.RoHS (The Restriction of&nbs p;the use of Certain Hazardous Subs tances in Electrical and Electronic;Equipment), the directive was born in January 2003, the EU Parliament and the EU Council In 2005, the EU supplemented the 2002/95/EC with the resolution 2005/6 18/EC, which specifies the maximum limit values of six hazardous substances.

RoHS certification mark

The RoHS Directive lists a total of six hazardous substances, including: lead Pb, cadmium Cd, mercury Hg, hexavalent chromium Cr6+, polybrominated diphenyl ethers PBDE, and polybrominated biphenyls PBB.

The maximum allowable content of lead (Pb), mercury (Hg), hexavalent chromium (Cr6+), polybrominated biphenyls (PBB) and polybrominated diphenyl ethers (PBDE) in the RoHS Directive is 0. 1% (1000ppm) and cadmium (cd) is 0.01% (100ppm), and the limit value is the legal basis for developing products to comply with the RoHS Directive.

The EU has officially implemented RoHS on July 1, 2006, in the future where the use or contain heavy metals and PBDE, PBB and other flame retardants of electrical and electronic products will not be allowed to enter the EU market.

  4.LFGB: Germany's new Food and Catering Products Act

In September 2005, the new German Food and Catering Products Act LFGB replaced the Food and Household Products Act LMBG. It is also known as "Food, Tobacco Products, Cosmetics and Other Daily Products Act" is the most important basic legal document in the management of food hygiene in Germany, and is the guideline and core of other special food hygiene laws and regulations. However, it has been amended in recent years, mainly to match European standards. All foodstuffs and all food-related articles on the German market must comply with its basic regulations. Food contact products that have been tested and comply with Articles 30 and 31 of the German Food and Household Products Act can be sold on the German market with an LFGB test report issued by an authorized institution as a "product free of chemically toxic substances".