No three certificates of ultraviolet phototherapy medical devices out of the problem to complain about suing

In accordance with the relevant provisions, where the therapeutic function of the instrument, equipment (including the product you mentioned), should belong to the medical device, by the drug regulatory department for approval, to obtain a production license and product registration certificate, but now the situation is not so, some of the products belonging to the medical device, some other departments are irresponsible, unauthorized approval, some of the products were approved by the health sector as health care, and some were approved as industrial products by the technical supervision department, causing confusion in the market. Some products are approved as health care products by the health department, and some are approved as industrial products by the technical supervision department, resulting in market confusion. You mentioned no three certificates of the product, may be that there is no production license, medical device product registration certificate and business license, you can take a look at the packaging, product specifications, take a look at which product belongs to the health care products to the health department, belongs to the industrial products to the technical supervision department. In accordance with the principle of who approves who regulates, where the registration of medical device products by the supervision of the drug administration department, for the approval of other departments of the product drug administration department has no right to deal with, that is, to report to the drug administration department they can do nothing about it. If the product is not approved by any department, you can report to the drug administration department. According to the above, you can refer to, see how to make your complaint more effective.