WARNINGS
• The
p
Module is not to be used as an apnea monitor.
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• Pulse oximetry readings and pulse signal can be
affected by certain ambient conditions, sensor application
errors and certain patient conditions.
• The
p
Module is intended only as an adjunct in patient
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assessment. It must be used in conjunction with clinical
signs and symptoms.
• The
p
Module should be considered an early warning
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device. As a trend towards patient deoxygenation is
indicated, blood samples should be analyzed by a
laboratory CO-Oximeter to completely understand the
patient's condition.
• Interfering Substances: Carboxyhemoglobin and
methemoglobin may erroneously increase readings. The
level of increase is approximately equal to the amount of
carboxyhemoglobin present. Dyes, or any substance
containing dyes, that change usual arterial pigmentation
may cause erroneous readings.
• The
p
Module is not rated for defibrillation use.
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Disconnect the sensor from the patient or patient cable
from the module prior to defibrillation.
• Do not lift the
p
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O
disconnect from the instrument, causing it to drop on the
patient. Do not place the
may cause it to fall onto the patient.
• Respond immediately to system alarms; patient
monitoring may cease under certain alarm conditions.
Alaris
System Directions for Use
®
SpO
Modules Section
2
Warnings and Cautions
General
Module by the cable because it may
2
p
Module in any position that
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General Information
General Information
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