According to the query of Huaru, medical devices produced within the validity period of the product registration certificate and does not expire, in line with the relevant provisions of the regulations, can be sold and used. This is in accordance with the "supervision and management of medical devices regulations" and "medical equipment business management measures". These regulations mainly require that the production and sale of medical device products must comply with the statutory procedures and standards to ensure the quality and safety of the products. At the same time, the medical device industry is also a highly regulated industry, and the relevant authorities will strictly supervise and manage the production and sale of medical devices to ensure the safety and effectiveness of the products.
Medical devices are instruments, equipment, appliances, materials or other items, including the required software, that are used in the human body, either alone or in combination.