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Canada PHSA Laboratories AVOXimeter 1000E: Quality Control Record Sheet 2018-2025 free printable template

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PSA Laboratories CW Site Point of Care Title: CPC AVON 0115 Oximeter 1000 Quality Control Record SheetAVOXimeter 1000E: Quality Control Record Sheet Note: Weekly open a new vial and liquor Levels
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How to fill out Canada PHSA Laboratories AVOXimeter 1000E: Quality Control

01
Gather your AVOXimeter 1000E device and ensure it is calibrated.
02
Connect the device to a power source, if necessary.
03
Prepare the control samples necessary for quality control testing.
04
Follow the manufacturer’s instructions to input control sample information into the device.
05
Insert the control samples into the device’s designated chamber.
06
Press the start button to initiate the quality control test.
07
Wait for the test to complete and record the results as displayed on the screen.
08
Compare results with the expected quality control ranges provided by PHSA.
09
Complete any necessary documentation or forms to report your quality control results.
10
Store all records in compliance with your facility’s quality assurance procedures.

Who needs Canada PHSA Laboratories AVOXimeter 1000E: Quality Control?

01
Healthcare professionals utilizing the AVOXimeter for patient care.
02
Laboratory technicians performing blood gas analysis.
03
Quality assurance personnel responsible for equipment maintenance.
04
Clinical laboratories ensuring compliance with quality control protocols.
05
Medical facilities that prioritize accuracy in patient oxygenation assessments.
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The Canada PHSA Laboratories AVOXimeter 1000E is a device used for measuring carboxyhemoglobin and methemoglobin levels in blood samples. Quality control refers to the procedures and standards implemented to ensure the accuracy and reliability of the measurements obtained from this device.
Laboratories and medical facilities that utilize the AVOXimeter 1000E for clinical assessments or research purposes are required to implement and file quality control measures. This includes technicians, laboratory managers, and any personnel involved in blood analysis.
To fill out the quality control documentation for the AVOXimeter 1000E, users must record the date and time of the test, the calibrator lot number, the results of control tests, and any corrective actions taken if results are out of acceptable ranges. Proper signatures and verification by supervisory staff may also be required.
The purpose of quality control for the AVOXimeter 1000E is to ensure that the device is functioning correctly and producing accurate, reliable results. This process helps to identify any errors or inconsistencies before patient testing, ensuring patient safety and optimal diagnostic accuracy.
The information that must be reported includes the date and time of testing, control levels (e.g., high, low, normal), batch numbers of control materials, results obtained, and any deviations or corrective actions taken. Additionally, technician and supervisor signatures may be required to validate the quality control process.
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