CCC certification

The name of China's national compulsory product certification mark is "China Compulsory Certification", the English abbreviation is "CCC", and it can also be abbreviated as "CCC" mark. As a common international practice, it mainly implements compulsory certification for products related to human health and safety, animal and plant life and health, and environmental protection and public safety, determines national standards, technical rules, and implementation procedures for uniform use, and develops uniform signs. Set uniform fees. All products listed in the catalog must be qualified by a nationally designated certification body, obtain relevant certificates and apply the certification mark before they can be shipped, imported, sold and used in business service places.

1.CCC certification catalog 2.CCC logo categories and logo patterns 3.CCC certification fees 4.CCC certification related regulations

China Quality Certification Center (CQC) has also launched a voluntary product certification business for product categories other than compulsory certification, which aims to protect the safety of consumers' personal and property and safeguard the interests of consumers; improve the product quality of domestic enterprises, and enhance Competitiveness in the international market; it also allows products of foreign companies to enter the domestic market more smoothly.

The scope of CQC voluntary product certification covers household and similar electrical appliances, electrical products, automobiles, motorcycles, tires, safety glass, audio and video products, information products, medical equipment, safety products, daily hardware, ceramics, cement, machine tools, Toys, valves and seals, materials, small gasoline engines, dozens of categories, hundreds of products.

1. CQC Mark Certification Catalog 2. CQC Mark Certification General Application Guide 3. CQC Voluntary Product Certification General Requirements (pdf) More

CCC Compulsory Certification

CQC mark certification

China Radio Transmission Equipment Type Approval (also known as SRRC)

SRMC (State Radio Monitoring Center)

In order to strengthen the management of imported radio transmitting equipment, the former National Radio Management Commission, the National Economic and Trade Commission, the Ministry of Foreign Trade and Economic Cooperation, and the General Administration of Customs, on July 24, 1995 "And the" Interim Measures for the Administration of the Import of Mechanical and Electrical Products "formulated the" Regulations on the Administration of Imported Radio Transmission Equipment ", which stipulates that all imported radio transmission equipment must comply with this regulation. In this regulation, radio transmission equipment is defined as: radio communication, navigation, Positioning, direction finding, radar, remote control, telemetry, broadcasting, television and other equipment that emit radio waves do not include industries, scientific research, medical equipment, electrified transportation systems, high-voltage power lines and other electrical devices that can radiate electromagnetic waves. At the same time, it is clearly stated that for any radio transmission equipment exported to China, foreign investors must hold the "type approval certificate for radio transmission equipment" issued by the Office of the State Administration of Radio Regulatory Commission (hereinafter referred to as the Office of the State Non-Commission), and the equipment must be marked with the code for the approval of the type of radio transmission equipment .

1. SRRC necessary information and instructions 2. SRRC charging standards and number of samples 3. SRRC testing basis and technical requirements More

SFDA (State Food and Drug Administration)

In order to regulate the registration management of medical device products and ensure the safety and effectiveness of medical devices, according to the "Regulations on the Supervision and Management of Medical Devices", the State Food and Drug Administration has formulated medical device registration management measures. The measures require that medical device products sold and used in China shall be declared and registered in accordance with the provisions of these Measures, and medical devices that have not been approved for registration shall not be sold for use. The measures require the state to implement classified registration of medical devices. The first class of medical devices produced by domestic enterprises shall be reviewed by the drug regulatory department in the district and city, and a product registration certificate shall be issued after approval. The second category of medical devices produced by domestic enterprises is reviewed by the provincial drug regulatory authority and a product registration certificate is issued after approval; the third category of medical devices produced by domestic enterprises is reviewed by the State Drug Administration and a product registration certificate is issued after approval ; Medical devices produced by overseas enterprises are reviewed by the State Drug Administration, and a product registration certificate is issued after approval.

1. Preparation for the initial registration of imported medical device products 2. Registration process for Class II and III medical device products