Management of disposable medical supplies

With the rapid development of medical business, to reduce the incidence of nosocomial infection, disposable medical supplies are widely used in hospitals. In order to prevent the inflow of disposable medical supplies into society or reuse, prevent cross infection and ensure medical safety, our hospital manages the whole process of disposable medical supplies from purchase, storage, use and after use.
Strict control of the purchase of 1 disposable medical supplies
Before the purchase of disposable medical supplies, the written application report is written by the Department of use, and then the centralized procurement office organizes the review and review by the centralized purchasing office to see whether the manufacturer's three certificates are complete, and the manufacturer must be determined by the state. Finally, it was purchased by the medical equipment department. The hospital procurement of disposable sterile medical supplies must be issued by the Department of drug supervision and management at the provincial level, the license for the production of medical instruments, the industrial product production license, the registration certificate for medical equipment products, and the medical equipment issued by the health administration department. The operating enterprises of the license of the equipment management enterprise purchase the qualified products; the imported disposable catheter and other aseptic medical supplies should have the medical instrument product registration certificate issued by the drug supervision and Management Department of the State Council. We must strictly control the purchase, warehousing and warehousing, and confirm that the latter can be used.
2. Disposable medical supplies are kept and put out strictly.
If the items purchased are in conformity with the contract, the three certificates are identical, and the warehouses shall be kept in warehouses after checking the goods. According to the manufacturer's production date, product name, shelf layer classification. The shelf is 20 cm away from the ground, 10 cm away from the wall, and maintained at room temperature from 18 to 20 C. After the product is purchased, the biological test report is required, and the clinical use can be released after verification. It is found that leakage and breakage are not allowed to be used. And timely contact with the relevant departments to change or terminate the contract.
3 strictly enforce the hygienic standard for disposable medical products (GB19580-1995)
_3.1 Microbiological Standard requires that no microorganism should be detected in sterile products, and no pathogenic microorganism should be detected in disinfected medical products. The number of bacteria is less than 20 cfu/m3.
3.2 product packaging sign small package sign: Manufacturer's name, address, trademark. Product name and type, hygiene license number, instructions for use, sterilization method and validity period, date of production. Medium package marks: Manufacturer's name, trade mark, product type and quantity, production date and factory number. Big package marks: product name, model and quantity, manufacturer name, address, health license number, product factory batch number, sterilization date, sterilizing certificate and effective date.
4 the supply room seriously records the purchase of disposable items.
Each purchase time, manufacturer, specification, model, batch number, batch number, sterilizing batch number, failure date, and every batch of biological testing reports provided by the manufacturer, and the use of the Department, the distributor, and the head of the Department to be signed and registered to confirm that the unmistakable side can be used for clinical use, so that the use of disposable articles is traceable. Sex, so as to ensure medical safety. The supply room should be sent to the ward in a small package according to the clinical needs.
5 the use of disposable medical products is based on the principle of "first in first out".
_tomake warning signs for medical supplies with red cards within 6 months of validity, contact clinical use in time, so as to avoid waste caused by expiration.