Philips DreamStation 2 User Manual page 62

Pressure and Flow Accuracy
If you suspect that the pressure and/or flow rate accuracy is affected by EMC interference
remove power and relocate the device to another area. If performance continues to be
affected discontinue use and contact your home care provider.
SpO and Pulse Rate Accuracy
2
The DreamStation 2 therapy device is designed to capture the SpO
data within the accuracy specification described in the sensor manufacturer's instructions
for use. When 4 hours of successful oximetry data have been achieved the device indicates
this to the user by displaying "Your pulse oximetry recording was successful". If you suspect
that your unit is affected by EMC interference, remove power and relocate the device to
another area. If performance continues to be affected discontinue use and contact your
home care provider.
Guidance and Manufacturer's Declaration - Electromagnetic Emissions – This device is
intended for use in the electromagnetic environment specified below. The user of this
device should make sure it is used in such an environment.
E T
missions EsT
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/Flicker
emissions
IEC 61000-3-3
Emission of Radio Frequency
Energy
RTCA/DO-160G Section 21
- 58 -
C E
omplianCE lECTromagnETiC
The device uses RF energy only for its internal
function. Therefore, its RF emissions are very low
Group 1
and are not likely to cause any interference in
nearby electronic equipment.
Class B
The device is suitable for use in all
Class A establishments, including domestic
establishments and those directly connected to
the public low-voltage power supply network.
Complies
This device is suitable for use onboard
Category M
commercial airplanes inside passenger cabin.
and pulse rate oximetry
2
E - g
nvironmEnT uidanCE