What are the disposable medical devices in Du Ya industry?

Definition of disposable sterile infusion set: medical devices (mainly consumables) that need to be destroyed (including destroyed) after one-time use in order to ensure the safety and effectiveness of medical device consumables in clinical use and avoid cross-infection.

The basic uses of disposable sterile infusion sets are: mainly used in medical institutions to prevent, diagnose, treat, monitor and alleviate diseases; Diagnosis, treatment, monitoring, mitigation and compensation of injury or disability; Research, substitution, adjustment, etc. Anatomical or physiological process.

Alcohol cotton pad, iodine cotton swab, infusion disinfection package, etc. According to the management of a class of medical devices; Reusable protective clothing, isolation clothing, protective cap and protective shoe cover, medical mask, medical isolation cabin, surgical clothing, etc. According to the second class medical device management; Disposable interventional therapy instrument probes are managed according to Class III medical devices, among which, the Catalogue of National Key Monitoring Class III Medical Devices:

He' nan Du Ya industrial disposable sterile medical equipment

1, disposable sterile syringe;

2. Disposable infusion set;

3. Disposable blood transfusion device;

4. Disposable anesthesia puncture kit;

5. Disposable intravenous infusion needle;

6. Disposable sterile injection needle;

7. Disposable plastic blood bag;

8. Disposable blood sampler;

9. Disposable burette infusion set.

The use of disposable medical devices requires strict compliance with the following six systems:

1. Establish the procurement and acceptance system of sterile instruments, strictly implement it and make records. The purchase acceptance record shall at least include: enterprise name, product name, model specification, product quantity, production batch number, sterilization batch number, product validity period, etc. According to the records, the procurement source of each batch of sterile instruments should be traced back.

2. Purchase sterile instruments from production or business enterprises, and fulfill the necessary documents of production or business enterprises (production license, product registration certificate, business license) and the legal identity certificate of sales personnel.

3. Establish a system for the destruction of sterile instruments after use. Used sterile instruments must be destroyed according to regulations, and the parts that no longer have the function of use should be disinfected and treated harmlessly, and records should be made.

4. If the small package is found to be damaged and the label is unclear, it should be stopped immediately and sealed, and the manufacturer should be contacted for replacement in time.

5. If unqualified sterile instruments are found, they should be stopped immediately and sealed, and the manufacturer should be contacted for replacement in time.

6. When a suspicious adverse event occurs when using sterile devices, it shall be reported to the provincial medical device adverse event monitoring center in a timely manner as required.