Philips IntelliVue X2 Instructions For Use Manual page 85

Multi-measurement module
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Technical Alarm Messages (INOPs)
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INOP Message, Indication
<SO
Label>LIGHT INTENS
2
Numeric is replaced by -?-
INOP tone.
<SO
Label> LOW LIGHT
2
Numeric is replaced by -?-
INOP tone.
<SO
Label> NO OPTMOD
2
Numeric is replaced by -?-
INOP tone.
<SO
Label> OPTMOD MALF
2
<SO
Label> PRE-INS CAL
2
Numeric displays -?-
INOP tone
<SO
Label> UNPLUGGED
2
Numeric displays -?-.
INOP tone
SO
UPGRADE
2
INOP tone
<SO
Label> WARMUP
2
Numeric is displayed with ?
SOME ECG ALRMS OFF
Speaker Malfunct.
INOP tone
SPIRO MALFUNCTION
SPIRO INCOMPATIBLE
SPIRO UPGRADE
SPIRO CANNOT MEAS
SPIRO PURGE FAILED
SPIRO UNKN. SENSOR
SPIRO ALARMS SUPPR
SPIRO PURGING
SPIRO NO SENSOR
or call
1-800-674-3655
Source
What to do
SO
The intensity changed considerably since the last light intensity
2
calibration. This may indicate that the catheter tip is positioned
against a blood vessel wall or that there is low blood flow.
Reposition the catheter (and perform a Light Intensity
Calibration).
SO
The optical signal levels are too low. Check that the catheter is
2
either in the optical reference or inserted into the patient.
Check the catheter-to-Optical Module connection. If INOP
persists, try another catheter and Optical Module.
SO
Connect the Optical Module. If the INOP persists, try another
2
Optical Module. Silencing this INOP switches the
measurement off.
SO
The Optical Module memory is faulty, and calibration data
2
cannot be stored for transport or during power failure. If this
capability is needed, use another Optical Module.
SO
The pre-insertion calibration is running. This typically takes
2
one minute. During this time alarms are switched off. Wait
until the calibration is complete.
SO
Measurement switched on and SO
2
from the rack.
SO
The SO
module is currently in upgrade mode.
2
2
Monitoring is not possible in this mode.
SO
The Optical Module has not yet reached the operating
2
temperature. Wait a few minutes until warm-up is finished.
Arrhythmia This message appears (if configured to do so) when the on/off
settings of the yellow arrhythmia alarms differ from the current
Profile.
Monitor
Contact your service personnel to check the speaker and the
connection to the speaker.
Spirometry
Module failure detected. Contact your service personnel.
Spirometry
Module revision not compatible with the host monitor
software revision. Contact your service personnel.
Spirometry
The module is running a firmware upgrade. Wait until upgrade
is completed before resuming monitoring.
Spirometry
Measurement is at its limit, e.g. ambient pressure out of range.
Spirometry
The purge operation could not be completed successfully.
Check for kinked sensor tubings, hard occlusions and make
sure that the pump is running and all valves are switching.
Spirometry
An unknown sensor ID code was detected. Use only the sensors
listed in the Accessories chapter.
Spirometry
Alarming is suppressed for the spirometry module.
Spirometry
A purge operation is in progress - no data update on the screen.
Wait until purge is complete.
Spirometry
No sensor detected. Make sure the correct sensor is attached to
the breathing circuit.
5 Patient Alarms and INOPs
/SvO
module unplugged
2
2
77

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