Aulisa Guardian Angel Rx GA1000, Инструкция по эксплуатации

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5
Cautions
1. This equipment complies with International
Standard IEC 60601-1-2: 2014 for electromagnetic
compatibility for medical electrical equipment
and/or systems. This standard is designed to
provide reasonable protection against harmful
interference in a typical medical installation.
However, because of the proliferation of
radio-frequency transmitting equipment and other
sources of electrical noise in healthcare and other
environments, it is possible that high levels of
interference due to close proximity or strength of
a source might disrupt the device's performance.
2. If Aulisa GA1000 Digital Vital Sign Monitoring
System fails to respond as described, discontinue
use until the situation is corrected by qualified
personnel.
3. Cardiogreen and other intravascular dyes may
affect the accuracy of SpO measurements.
2
4. The sensor probe might not work on cold
extremities due to reduced circulation. Warm or rub
the finger to increase circulation, or reposition the
sensor probe.
5. Aulisa GA1000 Digital Vital Sign Monitoring
System might misinterpret motion as good pulse
quality. Minimize motion of the monitored site.
6. Excessive ambient light may affect the accuracy
of the measurement.
7. Some nail polish colors or artificial nails can
reduce light transmission and affect SpO
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accuracy.
8. Inspect and relocate the sensor probe application
site at least every 6 to 8 hours to ensure correct
sensor probe alignment and skin integrity. Patient
sensitivity to a sensor probe may vary due to
medical status or skin condition.
9. Do not place liquids on top of the device.
10. Do not immerse the device or any of the
components in any liquids.
11. Do not use caustic or abrasive cleaning agents on
the device.
12. Do not gas sterilize or autoclave this pulse
oximetry system.