(2) buying and selling import and export licenses, import and export certificates of origin and other business licenses or approval documents stipulated by laws and administrative regulations;
(three) without the approval of the relevant competent departments of the state, illegally engaged in securities, futures, insurance business, or illegally engaged in fund payment and settlement business;
(four) other illegal business activities that seriously disrupt the market order.
Engaged in the operation of second-class medical devices, the operating enterprise shall file with the municipal food and drug supervision and administration department located in the district, and fill in the filing form for the operation of second-class medical devices. The food and drug supervision and administration department shall check the integrity of the information submitted by the enterprise on the spot, put it on record if it meets the requirements, and issue a record certificate for the operation of Class II medical devices.
Legal basis: Article 10 of the Regulations on the Supervision and Administration of Medical Devices.
For the filing of Class I medical device products, the filing person shall submit the filing materials to the food and drug supervision and administration department of the municipal people's government where the district is located. Among them, the product inspection report can be the self-inspection report of the filing person; Clinical evaluation data does not include clinical trial reports, but it can be data obtained through literature and clinical use of similar products to prove the safety and effectiveness of medical devices.