Philips Avalon FM20, Service Manual

Page: 246 / 260

12 Specifications
246
Radio Compliance Notice
Avalon CL with WMTS
Operation of this equipment requires the prior coordination with a frequency coordinator designated
by the FCC for the Wireless Medical Telemetry Service.
This device complies with Part 15 of the FCC Rules and RSS-210 of Industry Canada. Operation is
subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this
device must accept any interference received, including interference that may cause undesired
operation. Any changes or modifications to this equipment not expressly approved by Philips Medical
Systems may cause harmful radio frequency interference and void your authority to operate this
equipment.
Radio Information Canada
Installation of this telemetry device is permitted in hospitals and health care facilities only. This device
shall not be operated in mobile vehicles (including ambulances and other vehicles associated with
health care facilities). The installer/user of this device shall ensure that it is at least 80 km from the
Dominion Radio Astrophysical Observatory (DRAO) near Penticton, British Columbia. The
coordinates of DRAO are: latitude N 49E 19' 15", longitude W 119° 37
′ 12 ″ . For medical telemetry
systems not meeting this 80 km separation (e.g. the Okanagan Valley, British Columbia) the installer/
user must coordinate with, and obtain the written concurrence of, the Director of DRAO before the
equipment can be installed or operated. The Director of DRAO may be contacted at 250-497-2300
Surge
IEC 61000-4-5
±1 kV differential
mode
±2 kV common
mode
±1 kV differential mode
±2 kV common mode
Mains power quality should be that of a
typical commercial and/or hospital
environment
Voltage dips, short
interruptions and voltage
variations on power
supply input lines
IEC 61000-4-11
<5% U
T
(>95%
dip in U
T
) for
0.5 cycles
<5% U
T
(>95% dip in U
T
)
for 0.5 cycles
Mains power quality should be that of a
typical commercial and/or hospital
environment. If the user of the device
requires continued operation during
power mains interruptions, it is
recommended that the device is
powered from an uninterruptible power
supply.
40% U
T
(60% dip
in U
T
) for 5 cycles
40% U
T
(60% dip in U
T
) for
5 cycles
70% U
T
(30% dip in U
T
) for
25 cycles
70% U
T
(30% dip in U
T
) for
25 cycles
< 5% U
T
(>95% dip in U
T
)
for 5 sec
< 5%U
T
(>95% dip in U
T
)
for 5 sec
Power frequency (50/
60 Hz) magnetic field
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic fields should
be at levels characteristic of a typical
location in a typical commercial and/or
hospital environment
Key: U
T
is the AC mains voltage prior to application of the test level.
Table 2 - Guidance and Manufacturer's Declaration: Electromagnetic Immunity
Immunity Test IEC 60601-1-2
Test Level
Compliance Level Electromagnetic Environment
Guidance