Hello, according to the following relevant regulations: The production enterprise should purchase packaging materials or small packages that contact with st《生产实施细则》, and establish management systems for the purchase, storage, distribution and use of product packaging. Unqualified aseptic instruments and discarded and expired aseptic instrument product packages or parts must be destroyed or destroyed in the factory, and shall not flow out of the factory. Fortieth medical device trading enterprises and users shall not operate or use medical devices that are not registered according to law, have no certificates or expired, invalid or eliminated. Article 41 When transferring medical devices in use between medical device users, the transferor shall ensure that the transferred medical devices are safe and effective, and shall not transfer expired, invalid, obsolete or unqualified medical devices. Article 66 Under any of the following circumstances, the food and drug supervision and administration department at or above the county level shall order it to make corrections and confiscate the medical devices illegally produced, operated or used; If the value of medical devices illegally produced, operated or used is less than 10,000 yuan, a fine ranging from 20,000 yuan to 50,000 yuan shall be imposed; If the value of the goods is more than 10,000 yuan, a fine of more than 5 times and less than 10 times the value of the goods shall be imposed; If the circumstances are serious, it shall be ordered to stop production and business until the original issuing department revokes the registration certificate, production license and business license of medical devices: (1) producing, operating and using medical devices that do not meet the mandatory standards or the technical requirements of registered or filed products; (2) The medical device manufacturing enterprise fails to organize production in accordance with the technical requirements of the registered or filed products, or fails to establish a quality management system and maintain effective operation in accordance with the provisions of these Regulations; (three) the operation and use of medical devices without certificates, expired, invalid or obsolete, or the use of medical devices that are not registered according to law; (four) the food and drug supervision and management department ordered it to recall or stop operating in accordance with the provisions of these regulations, but still refused to recall or stop operating medical devices; (5) Entrusting an enterprise that does not meet the requirements stipulated in these Regulations to produce medical devices, or failing to manage the production behavior of the entrusted party. Article 6 In any of the following circumstances, the food and drug supervision and administration department at or above the county level shall order it to make corrections and impose a fine of not less than 10,000 yuan but not more than 30,000 yuan; If the circumstances are serious, it shall be ordered to stop production and business until the original license-issuing department revokes the medical device production license and medical device business license: (1) The production conditions of the medical device production enterprise have changed, which no longer meets the requirements of the medical device quality management system, and fails to rectify, stop production and report in accordance with the provisions of these Regulations; (two) the production and operation instructions and labels of medical devices do not meet the requirements of these regulations; (3) Failing to transport or store medical devices according to the instructions and labels of medical devices; (four) the transfer of expired, invalid, obsolete or unqualified medical devices in use. It can be known that the sale of expired medical devices is not allowed and can only be destroyed.