Certification

CE certification (Conformité Européenne) is a passport for products to enter the European market. It indicates that the product meets the basic requirements of the EU’s “New Approach to Technical Harmonization and Standardization” directive, including safety, health, environmental protection and consumer protection. Products with the CE mark can be sold in all European member states without having to meet the individual requirements of each member state, realizing the free circulation of goods within the EU member states.

FDA (US Food and Drug Administration) certification is one of the most stringent food and drug regulatory agencies in the world. Obtaining FDA certification means that the product has been strictly reviewed by the US Food and Drug Administration and meets its safety and efficacy standards, which is of great significance for the product to enter the US and even the global market.

RoHS (Restriction of the Use of Certain Hazardous Substances Directive) certification is a mandatory standard established by EU legislation to limit the use of hazardous substances in electronic products to protect the environment and human health. RoHS certification requires that the content of substances such as lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls (PBB) and polybrominated diphenyl ethers (PBDE) in electronic products shall not exceed certain limits to ensure that the products are more environmentally friendly and safe.

ISO certification is a series of standards developed by the International Organization for Standardization (ISO). ISO standards cover products, services and management systems in various fields. ISO system certifications mainly include ISO9001 quality management system certification, ISO14001 environmental management system certification, ISO45001 occupational health and safety management system certification, etc.