SECTION 4: PULSE OXIMETRY (OPTIONAL FEATURE)
Part No. 715-0080, Rev. B
- 49 -
TEST OF OPERATIONAL ALARMS
To ensure the pulse oximeter is generating the proper alarm indications, the following instructions
should be followed:
1.
After the sensor is attached to the patient, verify the patient alarms are functional by setting the
SpO
2
and pulse rate high and low alarm limits beyond the patient readings.
a.
An audible alarm should sound.
b.
A “HI” or “LO” visual indicator should flash on the appropriate display screen.
2.
Verify the sensor alarms are functional.
a.
Remove the sensor from the patient.
i.
An audible alarm should sound.
ii.
Error code “E6” should flash on the %SpO
2
display screen.
b.
Disconnect the sensor from the incubator.
i.
An audible alarm should sound.
ii.
Error code “E9” should flash on the %SpO
2
display screen.
PULSE OXIMETRY SENSORS
The incubator has been validated to be used with Masimo LNCS sensors and Nellcor OxiMax sensors.
Refer to SECTION 13, PARTS AND ACCESSORIES, for vendor contact information to request sensor
technical data. Before using any sensor, carefully read the sensor’s instructions for use. When
selecting a sensor, consider the patient’s weight, the adequacy of perfusion, the available sensor sites,
and duration of monitoring.
WARNING:
If using pulse oximetry during full body irradiation, keep the sensor out of the
irradiation field. If the sensor is exposed to irradiation, the reading might be
inaccurate or the unit might read zero for the duration of the active irradiation
period.
CAUTION:
Oxygen sensor and pulse oximetry cables must be contained within cart or otherwise
secured when not in use.
Содержание AirBORNE A750i
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