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EAST CAROLINA UNIVERSITYINFECTION CONTROL POLICYAutoclave Use and MonitoringDate Originated: 2/26/08Date Reviewed: 3.04.08; 9.13.11; 3. Date Approved: 3/4/086.2.15-Page 1 of 5Approved by: Vice Chancellor
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How to fill out autoclave use and monitoring

01
Make sure the autoclave is clean and free of any debris before use.
02
Place the items to be sterilized in autoclave-safe bags or containers.
03
Close the autoclave door securely and ensure it is properly sealed.
04
Set the appropriate sterilization parameters such as temperature, pressure, and time.
05
Start the autoclave and allow it to reach the desired temperature and pressure.
06
Monitor the autoclave throughout the sterilization process to ensure it is functioning correctly.
07
Once the sterilization cycle is complete, allow the autoclave to cool down before opening the door.
08
Carefully remove the sterilized items from the autoclave and store them appropriately.

Who needs autoclave use and monitoring?

01
Autoclave use and monitoring is necessary for anyone involved in medical or laboratory settings where sterilization of equipment and materials is critical.
02
This includes healthcare professionals, laboratory technicians, and researchers.
03
Autoclaves are also commonly used in tattoo and piercing studios, nail salons, and beauty spas to maintain proper hygiene and prevent the spread of infections.

What is Autoclave Use and Monitoring Form?

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Autoclave use and monitoring is the process of sterilizing equipment and monitoring its effectiveness to ensure proper sterilization.
Anyone using an autoclave for sterilization purposes is required to file autoclave use and monitoring.
Autoclave use and monitoring forms can be filled out by providing information about the sterilization process, equipment used, monitoring results, and any corrective actions taken.
The purpose of autoclave use and monitoring is to ensure that sterilization processes are effective in killing microorganisms and preventing contamination.
Information such as autoclave settings, sterilization cycle information, temperature and pressure readings, monitoring results, and any deviations from the set standards must be reported on autoclave use and monitoring.
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