Sterilization log sheet public health ontario 2025

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  1. Click ‘Get Form’ to open the sterilization log sheet in the editor.
  2. Begin by entering the 'Sterilizer Model' and 'Serial Number' at the top of the form. This information is crucial for tracking specific equipment.
  3. In the 'Load Details' section, document the contents of each pouch being sterilized. Ensure you note down the load number for reference.
  4. Fill in the 'Sterilizer Readings Met' fields, including temperature and pressure readings. Use checkboxes to indicate if quality indicators passed or failed.
  5. Record operator initials next to each entry to maintain accountability. Include dates and times for each sterilization cycle.
  6. If any readings are marked as 'No' or 'Fail', ensure to follow up with system failure documentation as required.
  7. Finally, have all operators print their names, sign, and initial at the bottom of the form for verification purposes.

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How should sterilization indicators be stored? A. In a cool, dry area.
Sterilization indicators, such as spore strips and indicator tape, enable routine monitoring, qualification,and load monitoring of the steam sterilization process. They indicate whether the conditions during a steam autoclave cycle were adequate to achieve a defined level of microbial inactivation.
8 Sterilizer maintenance and repairs should be documented in a paper or electronic record keeping system. 9 Sterilization records should be kept for seven years. facilities: Safety and effectiveness (ANSI/AAMI ST41) document recommends the use of a BI PCD in every other ethylene oxide sterilization cycle.
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Table-top Steam Sterilizers. The purpose of this document is to record process parameters for steam sterilization in community health care settings. This will assist with tracking of medical devices used on clients/patients/residents in the event of a recall or follow-up investigation.
For each sterilization cycle, record the type of sterilizer and cycle used; the load identification number; the load contents; the exposure parameters (e.g., time and temperature); the operator's name or initials; and the results of mechanical, chemical, and biological monitoring.
The effectiveness and proper performance of a sterilizer must be confirmed through a combination of three types of monitoring: physical or mechanical, chemical and biological. Use of one type of indicator does NOT replace the need to use the other two types.
How often should biological monitoring (spore testing) be done? A spore test should be used on each sterilizer at least weekly. Users should follow the manufacturer's directions for how to place the biological indicator in the sterilizer. A spore test should also be used for every load with an implantable device.
Completed autoclave use logs must be retained by laboratory staff for 3 years. Autoclave record keeping will be confirmed during yearly laboratory safety surveys.

public health sterilization monitoring log