The IECEE/CB Scheme is an international mutual recognition system that enables the safety of electrical and electronic products and coordination between national and international standards to obtain national certification without redundant testing. The IECEE/CB scheme allows various countries, safety standards, conformity marks, etc. to be treated as a single test procedure.

Electrical/electronic devices, information office equipment, batteries, lighting devices, instruments, switches, insulation transformers, parts and capacitors are designated as target items.

Accredited Certification Agency by CNCA : CVC, COC. CTC, CEPRE, CGC etc.

Unlike compulsory certification, certificates are issued for about 500 kinds of products by proving themselves that the quality, safety, environmental protection, and performance of the products meet the relevant standards. In the case of foreign companies, it is a plan to enter the Chinese market smoothly.

Specific electrical appliances: 116 items, such as wires, fuses, wiring equipment, heating appliances, electrical therapy equipment, etc.
Other electrical appliances: 341 items, such as electric heating appliances, power application machinery equipment, light source and light source appliances, electronic application machinery equipment, etc.

CVC (Certainty Value-added Credibility)
CQC (China Quality Certification Centre)

From 1 June 1999, the Ministry of Information Industry (MII) implemented a compulsory certification system for telecommunications products under compulsory certification for specific wireless or wireless devices. As this prevents unauthorized telecommunications products from being sold to China, wireless products sold or used in China must be SRRC certified.

27 types of devices for navigation, radar, remote control, mobile phone, navigation, telemetry, broadcasting and television.

State Radio Regulatory Commission of the People's Republic of China ([Link])

Medical device grades are classified into grades 1, 2, and 3, and in the case of overseas medical devices when obtaining CFDA medical device certification, foreign manufacturers shall assign designated equipment in China as their representatives.
In addition, overseas manufacturers should entrust medical device sales and follow-up services to corporate organizations or Chinese companies with corresponding qualifications in China. All medical device products sold and used in China through the medical device registration system must obtain CFDA certification.

Medical device system, coral saturation meter, myoconduction and induced response diagnostic, endoscopy, respiratory tract, high-pressure steam sterilizer, respiratory gas monitor, blood pressure meter, fluid pump, etc.

National Medical Products Administration ([Link])