No. According to the provisions of Article 23 of the "Regulations on the Administration of Medical Devices", it is learned that medical device manufacturers, operating enterprises and user units shall conduct acceptance, storage, withdrawal and use management of medical devices in accordance with the quality requirements stipulated by the state. Activities to ensure the safe and effective use of medical devices. Medical devices cannot be sold directly. They must be inspected and stored first, and then sold. Class II medical devices refer to medical devices that are defined as requiring supervision and management in the "Medical Device Classification Catalog" jointly issued by the Ministry of Industry and Information Technology, the Health Commission and the Food and Drug Administration. These devices include various medical materials, medical devices, medical electronic instruments, etc.