C-16 Starling Monitor - User Guide
SpO
2
Module (Optional)
Warnings and Precautions
Substitution of a component different from that supplied may result in measurement
error. Repairs should be undertaken only by personnel trained or authorized by Baxter.
All SpO
2
sensors used to connect the patient to the Starling SpO
2
Module must be
approved by Baxter. Unauthorized SpO
2
sensors may cause the module to perform in
an improper fashion. Authorized SpO
2
sensors are offered as accessories from Baxter.
Do not use an NIBP cuff or constricting devices on the same appendage as that used
for the sensor.
The SpO
2
Module may not operate correctly if used or stored outside the relevant
temperature or humidity ranges listed in Table C-5.
Do not immerse sensors in liquids.
WARNING
DO NOT use theSpO
2
Module for any purpose other than specified in this manual without
written consent and approval from Baxter.
Intravascular dyes (such as indocyanine green, methylene blue, etc.) and darkly
pigmented skin can adversely affect SpO
2
readings.
Significant amounts of dysfunctional hemoglobins (such as carboxyhemoglobin,
methemoglobin, etc.) may adversely affect oximetry performance.
Oximetry performance may be impaired when patient perfusion is low or signal
attenuation is high.
Long cables (such as the sensor or extension cable) may cause patient strangulation if
routed incorrectly.
Electromagnetic interference which includes devices such as MRI imaging devices, or
electro-surgical units, may adversely affect SpO
2
readings.
When using the SpO
2
Module, observe the precautions outlined below.