Fukuda Denshi DS-8200, Руководство по обслуживанию

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Precautions for Using the Equipment
This System
D A N G E R
When connecting to other equipments, contact Fukuda Denshi.
Danger such as electric shock may result to the patient and operator.
W A R N I N G
Warnings about the System
z Do not connect any damaged / unspecified equipment or cable to any I/O
connector. If done so by mistake, the device cannot deliver its maximum
performance and the connected units may be damaged, resulting in a safety
hazard.
z If this equipment is used under an environment not fulfilling the specified
condition, not only that the equipment cannot deliver its maximum
performance, the equipment may be damaged and safety cannot be ensured. If
using the equipment under condition other than specified, contact Fukuda
Denshi.
z Use only the supplied 3-way AC power cable. Use of other cables may result
in electric shock to the patient and the operator.
z The power cable must be connected to a hospital grade outlet.
z When using multiple ME equipment simultaneously, perform equipotential
grounding to prevent potential difference between the equipments. Even a
small potential difference may result in electric shock to the patient and the
operator.
z Carefully route cables to reduce the possibility of patient entanglement and
strangulation.
z When lifting this equipment, hold it by the handle or the bottom part of the
main unit.
Warnings about the Monitoring
z The patient classification selection influences the precision of the QRS
detection and NIBP measurement. Make sure the correct selection is made.
z The pacemaker use selection influences the precision of the QRS detection
and arrhythmia analysis. Make sure the correct selection is made.
z If the QRS pace mask function is set to [OFF], [10ms] or [20ms], the pace
pulse may be erroneously be detected as a QRS complex and HR, Asystole
alarms may not generate due to incorrect HR (counting pace pulse as QRS
complex). Select [OFF], [10ms], or [20ms] only if you are sure that pacing
failure will not occur, or when the patient can be constantly monitored.
z When measuring the SpO
2
of patient with high fever or peripheral circulatory
insufficiency, check the sensor attachment periodically and change the
attachment site. The temperature of the attachment site will rise 2 to 3°C due to
the sensor heat which may result in burn injury.
z For the following case, accurate measurement of SpO
2
may not be possible.
y Patient with excessive abnormal hemoglobin (COHb, MetHb)
y
Patient with the pigment injected to the blood
y Patient receiving CPR treatment
y When a sensor is applied to a limb with NIBP cuff, arterial catheter, or
intracatheter
y
When measuring at site with venous pulse
y Patient with body motion
y Patient with small pulse
z Before the NIBP measurement, make sure the patient classification
([Adult]/[Child]/[Neonate]) is properly selected. Otherwise, correct
measurement cannot be performed, and congestion or other injury may result.
z When the system alarm is suspended, all the alarms will be suspended even if
the parameter alarm is set to [ON]. Also, the alarms will not be stored as recall
events.
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