Legal analysis: -, must use quality verification of qualified disposable medical supplies.
Two, strengthen the management of - disposable medical supplies, correctly stored to prevent moisture, breakage, pollution.
Three, in the use of disposable medical supplies before, must check the expiration date and there is no damage.
Four - disposable medical supplies must be sterilized, soaked, disfigured according to the requirements of the treatment by the designated unit of unified recovery.
V. When receiving disposable medical supplies, there must be a signature of the head nurse. The number of receiving to maintain a certain base, the department shall not be stored in excess, in order to prevent expiration or contamination.
Sixth, in the use of disposable infusion (blood), syringe infection, pyrogenic reaction or related medical errors, must be registered in accordance with the provisions.
VII, all disposable items in accordance with the provisions of the use, the packaging shows disposable shall not be reused. No products may be tried in the clinic without approval.
Legal basis: "Medical Device Supervision and Administration Regulations" Article 49 of the medical device using units of reuse of medical devices, shall be in accordance with the provisions of the State Council competent department of health to develop the disinfection and management.
Disposable medical devices shall not be reused, the used shall be destroyed and recorded in accordance with relevant state regulations. Disposable medical device catalog by the state council drug supervision and management department in conjunction with the state council health department to develop, adjust and publish. Included in the directory of single-use medical devices, should have sufficient evidence that can not be reused reasons. Repeated use can ensure the safety and effectiveness of medical devices, not included in the directory of single-use medical devices. For the design, production process, sterilization technology and other improvements in repeated use can ensure the safety and effectiveness of medical devices, should be adjusted out of the single-use medical device directory, allowing repeated use.