Before purchasing disposable medical supplies, the following certificates must be obtained and accepted from the manufacturer: production license, product registration certificate, and product qualification certificate.

Establish a registration book to record the product name, quantity, specification, unit price, product batch number, disinfection date, delivery date, expiration date, supply and demand parties, and the name of the handler for each order and arrival.

Imported various disposable sterile medical supplies must have the "Medical Device Product Registration Certificate" issued by the Drug Administration Department of the State  Council.

Disposable sterile medical supplies must be purchased by the purchasing department through a unified bidding, and the user department must not purchase it by themselves.

Each purchase must undergo quality inspection, so that the order contract, shipping location and payment account number are consistent with the manufacturer, and each batch number, product inspection certificate, disinfection date, delivery date and validity period are checked.

Disposable infusion (blood) devices, syringes, puncture needles, etc. equipped with medicines, contrast media, etc., should be checked for various documents.

Large packages of single-use sterile instruments (such as infusion (blood) devices, syringes) should be stored in a clean warehouse, stored separately, and a dedicated person is responsible. Store in a cool, dry, well-ventilated shelf, ≧20cm from the ground and ≧5cm from the wall.

In order to further strengthen the management of disposable medical supplies, ensure the safety of patients, and improve the quality of medical care, according to the problems that occur in the procurement, acceptance, storage, distribution and use of disposable sterile medical supplies, this management system is reiterated and clarified. The tasks and responsibilities of each department.