User's Manual

F Series Fetal & Maternal Monitor User Manual Maternal Monitoring Display
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ECG EQUIP
MALF
ECG
The ECG board can not
communicate with the system
successfully.
Restart the monitor and try
again, contact the
manufacturer if the
connection still fails.
HR EXCEEDS
MEASUREMENT
RANGE
ECG/
Pulse
The heart rate exceeds the
measurement limits.
Check the connection of the
ECG leads/SpO
2
sensor and
the patient’s condition.
NIBP EQUIP
MALF
NIBP
The NIBP board can not
communicate with the system
successfully.
Restart the monitor and try
again, contact the
manufacturer if the
connection still fails.
NIBP SYSTEM
FAILURE
NIBP The NIBP module defective.
Restart the monitor and try
again, contact the
manufacturer if the
connection still fails.
NIBP CUFF
LOOSE or OFF
NIBP
The cuff is loose or not
connected.
Wrap the cuff properly.
NIBP OVER
PRESSURE
NIBP
The pressure has exceeded the
specified upper safety limit.
Measure again, if failure
persists, stop using the
monitor for NIBP measuring
and contact the manufacturer
for service.
NIBP CUFF TYPE
ERROR
NIBP
A different cuff other than the one
supplied by the manufacturer is
used.
Use the cuff supplied by the
manufacturer.
NIBP LEAK NIBP
The cuff, hose and (or) connector
are (is) damaged.
Check and replace the
leaking part(s). Contact the
manufacturer for service if
required.
NIBP SIGNAL
LOSS
NIBP
Cuff is too loose or the patient
pulse is too weak.
Use other methods to
measure NIBP.
NIBP SIGNAL
INTERFERED
NIBP
Large signal noise or irregular
pulse rate caused by excessive
motions of the patient.
Keep the arm that is wrapped
with the cuff still.
NIBP EXCEEDS
MEASUREMENT
RANGE
NIBP
The blood pressure exceeds the
measurement limits.
Check the connection of the
cuff and the patient’s
condition.
NIBP TIME OUT NIBP
Measuring time has exceeded
120 seconds.
Start measuring again, or use
other measuring methods.
SpO
2
LOW
PERFUSION
SpO
2
The signal received by SpO
2
sensor is too weak, or the
measurement part has low
perfusion, and therefore the result
may be inaccurate.
Check the patient’s condition
and reposition the SpO
2
sensor. Contact the
manufacturer for service if
the problem persists.