How should medical institutions dispose of disposable medical devices after use?

Disposable Medical Supplies Management System In order to protect the health of the people, prevent the spread of iatrogenic diseases, and strengthen the management of disposable sterile medical supplies, this system is formulated.

1. The person in charge of the clinic is responsible for the management of purchase, acceptance, use, destruction and other aspects.
2. When purchasing, you must purchase from an operating company with a “Medical Device Business Enterprise License”. After purchase, you must verify that the three acceptance certificates are complete (health license, production license, and medical device registration certificate number). Must obtain the “Medical Device Manufacturing Enterprise License”, “Industrial Product Production License” and “Medical Device Product Registration Certificate” issued by the drug supervision and administration department at or above the provincial level and the health license issued by the health administrative department or obtain the “Medical Device Business Enterprise” Business enterprises that have obtained the “License” purchase qualified products.
3. Store items on a cool, dry, well-ventilated shelf, ≥20cm from the ground and >5cm from the wall. Products with damaged, invalid or moldy packaging shall not be released for use.
4. Before use, check whether the packaging is damaged, invalid, mildewed, and whether the label is clear. Use it only if there are no suspicious phenomena. Otherwise, use is prohibited.
5. Destroy the shape immediately after use. After soaking and disinfecting in a fixed container, plastic items should be placed in a special recycling bag (yellow), and non-plastic items should be placed in a (black) medical waste recycling bag. Other medical waste must not be mixed. Burn it once a day and keep records. The medical waste storage room is managed by dedicated personnel and disinfected regularly. Prevent mosquitoes and flies in summer and autumn, and pay attention to fire prevention.
6. Hygienists should protect themselves. When working, you must wear isolation gown, mask, isolation cap and gloves. Wash your hands and disinfect your hands after each work.
7. If pyrogen reaction, infection or other abnormal conditions occur during use, samples must be collected in time and sent for inspection, recorded in detail according to regulations, and reported to the drug regulatory department.
8. When the clinic discovers substandard products or products of questionable quality, it should immediately stop using them and report them to the local drug regulatory department in a timely manner. It is not allowed to return or exchange the products on its own.