Stryker Altrix 8001, Operation Manual

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Alarm conditions
Patient probe malfunction alarm
This alarm notifies the operator that the probe is not providing information to the product during an active therapy.
Alarm generation:
When the primary patient probe is in a shorted, opened condition, or out of range for more than 30 seconds, the product
will display the Patient Probe Malfunction Alarm.
Note: The product will deactivate the heat exchange and keep the pump activated as requested by the Active Therapy.
Patient probe disconnect alarm
This alarm notifies the operator that the probe is not providing information to the product during an active therapy.
Alarm generation:
When the adapter cable for the primary probe is removed and the reading of the Primary Patient probe is out of range for
more than 30 seconds, the product displays the Patient Probe Disconnected alarm.
Patient temperature deviation medium alarm
This alarm notifies the operator that the patient is not responding as expected in the active therapy.
Alarm generation:
The product will display the Patient Temperature Deviation Medium Alarm, if after the initial achievement of the current
patient temperature target, the actual primary patient temperature becomes 0.5° C or more above, or below the Current
Target Temperature.
Patient temperature output deviation alarm
This alarm notifies the operator that the patient temperature output is out of range or their is a calibration error.
Alarm generation:
The product will display the Patient Temperature Output Deviation Alarm, if the calibration has failed, or the patient
temperature output is out of range.
Normothermia deviation alarm
This alarm notifies the operator of that the Primary Patient Temperature is out of range.
Alarm generation:
If the actual Primary Patient Temperat ure is lower or equal to 35.9° C or higher or equal to 38.1° C, the controller will
display the Patient Normothermia Deviation alarm.
Water temperature deviation alarm group
This alarm notifies the operator that the water is not responding as expected to the therapy. The product is at full power,
with the current mode and the temperature selection. The water temperature cannot remain within a range of ±0.8º C of
the selected Water Target Temperat ure.