How do consumers claim for out-of-range medical devices?

Consumers can sue, and after investigation, the enterprise will compensate, fine or even revoke its business license, and the market supervision department will confiscate the machinery. The practice beyond the scope of medical institutions generally refers to the fact that their diagnosis and treatment behavior is beyond the scope of diagnosis and treatment registered in the Practice License of Medical Institutions and the Application for Practice Registration of Medical Institutions.

Article 44 of the Measures for the Supervision and Administration of Online Sales of Medical Devices is under any of the following circumstances, the local food and drug supervision and administration department at or above the county level shall order it to make corrections and impose a fine of 1 10,000 yuan but not more than 30,000 yuan:

(1) Enterprises engaged in online sales of medical devices sell beyond their business scope;

(2) Medical device wholesale enterprises sell to unqualified operating enterprises and users.

Medical device retail enterprises that sell medical devices that are not used by consumers themselves to individual consumers shall be punished in accordance with the provisions of the first paragraph of the preceding paragraph.

Article 76 of the Regulations on the Supervision and Administration of Medical Devices, if the medical devices that may contain harmful substances or change the design, raw materials and production process of medical devices without authorization and have potential safety hazards cannot be inspected according to the inspection items and methods specified in the national standards and industry standards of medical devices, the medical device inspection institution may use the supplementary inspection items and methods approved by the drug supervision and administration department of the State Council to conduct inspection; The inspection conclusions obtained by supplementary inspection items and inspection methods can be used as the basis for drug supervision and management departments to determine the quality of medical devices.