According to the query 3618 medical devices network shows: medical DR manufacturers can monitor. As DR is a Class II medical device, its production, sales and use are strictly regulated by the relevant state departments. In the production link, medical DR manufacturers need to comply with relevant national regulations, accept the approval and supervision of the national drug regulatory authorities. In the sales process, medical DR manufacturers need to apply for a registration certificate from the national drug regulatory authorities and comply with the relevant sales regulations. In the use of the link, medical DR manufacturers need to comply with the relevant provisions of the use, to ensure the safety and effectiveness of medical devices.
In addition, medical DR manufacturers also need to accept social and public supervision. For example, Nanjing Leon Medical Equipment Manufacturing Co., Ltd. is a well-known Nanjing medical equipment manufacturers, specializing in the production of flat-panel DR and other medical equipment, its production, sales and use of the links are subject to the relevant departments of regulation and supervision.