Sensors And Cables - Cardinal Health Alaris Directions For Use Manual

WARNINGS
• Inspect the p
S O
2
correct sensor positioning, application and site integrity.
Tissue damage could occur over prolonged time periods,
depending on the patient profile (such as neonates) and
method of application. Reference the sensor instructions
for additional information.
• Do not use a sensor, cable or connector that appears
damaged. Do not use a sensor with exposed optical
components.
• The sensor disconnect error message and associated
alarm indicate the sensor is either disconnected or the
wiring is faulty Check the sensor connection and, if
necessary, replace the sensor.
• Model :
8210
Use only approved O
pulse oximetry cables.
OC–3
Model :
8220
Use only approved Masimo
cables.
Use of sensors, transducers, cables and accessories
other than those specified may cause improper
Module performance resulting in inaccurate readings,
increased emission and/or decreased immunity, and
degraded electromagnetic compatibility performance of
the p Module. For a list of compatible sensors and
S O
2
cables, reference the Sensor and Cable Compatibility Card
(provided separately).
• Carefully route patient cabling to reduce the possibility of
patient entanglement or strangulation.
• Before use, read the sensor directions for use, including
all warnings, cautions and instructions.
CAUTION
Do not immerse or dampen the sensor or cable. Clean per
manufacturer's instructions.
4-16
General Information
Warnings and Cautions

Sensors and Cables

sensor site regularly to ensure
M sensors, and
XI AX
® sensors and patient
(Continued)
and
DOC–10
p
S O
2
Alaris
®
System (with v9 Model 8000) DFU
SpO Modules Section
2