Do ultraviolet products belong to medical devices? Do I need a license?

It depends on the purpose of the product. If it is used for medical treatment, medical devices must be considered. If you are not sure, you can do classification and identification first.

Medical device registration refers to the process of systematically evaluating the safety and effectiveness of medical devices to be marketed and used in accordance with legal procedures to decide whether to approve their sale and use. Divided into domestic medical device registration and overseas medical device registration. Overseas medical devices, whether Class I, Class II or Class III, must be handled by the State Food and Drug Administration of Beijing; domestic medical devices of Class I and Class II shall be handled by the local provincial or municipal food and drug administration, and medical devices of Class III shall be handled by the State Food and Drug Administration. Medical device registration certificate refers to the legal identity card of medical device products.