Safety regulations for medical alcohol storage

Medical alcohol storage safety regulations are as follows:

1. The medical alcohol storage room is strictly forbidden to be attached to civil buildings.

2. The maximum allowable number of layers of medical alcohol warehouse is one layer, and the fire resistance rating should not be lower than the second level.

3, medical alcohol warehouse should be set up to prevent liquid diaspora facilities.

4. Fire extinguishers should be set around the medical alcohol warehouse.

5. Evacuation walkways with a length greater than 40m in the medical alcohol warehouse should be equipped with smoke exhaust facilities.

6. Medical alcohol needs to be sealed and stored in a cool and dark place, away from fire and power.

Medical alcohol has the following uses:

1, usually the highest concentration is 95% alcohol, which is only used to wipe the ultraviolet lamp and the combined equipment used for disinfection.

2. The most commonly used medical alcohol is 75% alcohol, which is usually used to disinfect the coated epidermis, because excessive alcohol will form a protective film on the surface of bacteria, preventing it from entering the bacteria, and it is difficult to completely sterilize. When the concentration is too low, bacteria can enter, but the protein in the body cannot be completely solidified. 75% alcohol is the most commonly used alcohol for disinfection and sterilization.

3. Alcohol with a concentration of 40%-50% can prevent bedsores, and the back, waist and buttocks of patients who stay in bed for a long time will be squeezed and cause bedsores. When massaging, you can pour a little 40%-50% alcohol on your hands and massage the patient evenly. Pressing the parts can promote local blood circulation and prevent the formation of bedsores.

4. 25% alcohol can be used for physical antipyretic, which can be wiped when the patient has a high fever to achieve the effect of physical cooling.

Legal basis: Article 35 of the Regulations of People's Republic of China (PRC) Municipality on the Supervision and Administration of Medical Devices.

Medical device registrants, filers and entrusted production enterprises shall, in accordance with the quality management standards for medical device production, establish and improve the quality management system suitable for the medical devices produced, and ensure their effective operation; Organize production in strict accordance with the technical requirements of registered or filed products, and ensure that the medical devices delivered from the factory meet the mandatory standards and the technical requirements of registered or filed products.

Medical device registrants, filers and entrusted production enterprises shall regularly conduct self-inspection on the operation of the quality management system, and submit self-inspection reports in accordance with the provisions of the drug supervision and administration department of the State Council.

Article 36

If the production conditions of medical devices change and no longer meet the requirements of the quality management system of medical devices, the medical device registrant, the filing person and the entrusted production enterprise shall immediately take corrective measures; May affect the safety and effectiveness of medical devices, should immediately stop production activities, and report to the original production license or production record department.

Article 37

Medical devices should use common names. The generic name shall conform to the naming rules for medical devices formulated by the drug supervision and administration department of the State Council.