Bempu ApneBoot, Operation Manual, Page: 31 / 48

31 www.bempu.com
BEMPU ( may result in increased emission and/or decreased immunity of this
device.
24. Do not use a damaged sensor. If the sensor is damaged in any way, dis -
continue use immediately and replace the sensor.
25. The accuracy of the SpO
2
measurement may be affected if the total sen -
sor cable length (including extension cables) is greater than 3 meters.
26. Follow local, state, or national governing ordinances and recycling in -
structions regarding disposal or recycling of the device and device compo -
nents.
27. In compliance with the European Directive on Waste Electrical and Elec -
tronic Equipment (WEEE) 2002/96/EC, do not dispose of this product as un -
sorted municipal waste. This device contains WEEE materials; please contact
your distributor regarding take-back or recycling of the device.
28. This pulse oximeter module is designed to determine the percentage of
arterial oxygen saturation of functional hemoglobin. Significant levels of dys
-
functional hemoglobin, such as methemoglobin, might affect the accuracy
of the measurement. Factors that may degrade pulse oximeter performance
or affect the accuracy of the measurement include the following: exces
-
sive ambient light, excessive motion, electrosurgical interference, blood
flow restrictors (arterial catheters, blood pressure cuffs, infusing lines, etc.),
moisture in the sensor, improperly applied sensor, incorrect sensor type, poor
pulse quality, venous pulsations, anemia or low hemoglobin concentrations,
cardiogreen or other intravascular dyes, carboxyhemoglobin, methemoglo
-
bin, dysfunctional hemoglobin, artificial nails or fingernail polish, or a sensor
not at heart level.
29. This device has motion tolerant software that minimizes the likelihood of
motion artifact being misinterpreted as good pulse quality. In some circum
-
stances, however, this device may still interpret motion as good pulse quality.
30. This product complies with IEC EN 60601-1-2 for electromagnetic com -
patibility 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 ra
-
dio-frequency transmitting equipment and other sources of electrical noise
in healthcare and other environments, it is possible that high levels of such
interference due to close proximity or strength of a source might disrupt
the performance of this device. Medical electrical equipment needs special