Users Manual Part 1

22
Safety precautions
1�3�3 Precautions regarding
electromagnetic waves
EMC Statement
This device has been tested and found to comply with the
limits for medical devices in IEC 60601-1-2: 2007 or IEC
60601-1-2: 2014.
These limits are designed to provide reasonable protec-
tion against harmful interference in a typical medical
installation. The device generates, uses and can radiate
radio frequency energy and, if not installed and used in
accordance with the instructions, may cause harmful in-
terference to other devices in its vicinity. However, there is
no guarantee that interference will not occur in a particular
installation.
Whether this device does cause harmful interference to
other devices can be determined by turning this device o󰀨
and on. If it causes harmful interference, the user is en-
couraged to try to correct the interference by 1 or more of
the following measures:
• Reorient or relocate the receiving device.
• Increase the separation between the devices.
• Connect this device into a wall outlet on a circuit di󰀨er-
ent from that to which the other devices are connected.
• Contact Konica Minolta technical representatives.
WARNING
• Do not use mobile RF communication devices such as
mobile phones or pocket pagers in the vicinity of this
device. Use of such RF devices near this device can
cause errors in operation due to electromagnetic wave
interference. When using a mobile RF device, ensure
that the distance between the RF device in use and this
device is at least 30 cm (12 inches).
• The use of accessories, transducers and cables other
than those sold by Konica Minolta, Inc. as internal
components, may result in increased emissions or de-
creased electromagnetic immunity of this device, pos-
sibly causing malfunction.
• Do not use this device adjacent to or stacked with other
devices. If adjacent or stacked use is necessary, con-
rm normal operation in the conguration in which this
device will be used.
Supplementary information regarding IEC
60601-1-2:2007andIEC60601-1-2:2014
(1) Take precautions against this device especially re-
garding EMC. Install and put into service according
to the electromagnetic compatibility (EMC) informa-
tion provided in the manual (Table 1 - Table 5).
(2) This device is suitable for use in medical institu-
tions such as hospitals and clinics. However, this
device is not suitable for use in environments with
high degree of electromagnetic wave interference
(such as near an electric operation device in use
for output, or near a high frequency treatment de-
vice).
(3) Cable list
• Power cable (3.048 m/3-Wire/No Shielding)
• Ethernet cable (max 30 m/Shielding)
• Non-shielded Ethernet cable can be used for con-
necting to the AeroDR Battery Charger and the
AeroDR Battery Charger2
(4) Specications regarding RF transmitters frequency:
• Frequency
— AeroDR SYSTEM:
5150 MHz to 5350 MHz, 5470 MHz to
5850 MHz
— AeroDR SYSTEM 2:
2412 MHz to 2472 MHz
5180 MHz to 5320 MHz, 5500 MHz to
5825 MHz
— SKR 3000:
2412 MHz to 2472 MHz
5180 MHz to 5320 MHz, 5500 MHz to
5825 MHz
• Modulation
— AeroDR SYSTEM:
OFDM
— AeroDR SYSTEM 2:
2412 MHz to 2472 MHz: DSSS/CCK/OFDM
5180 MHz to 5320 MHz, 5500 MHz to 5825
MHz:OFDM
— SKR 3000:
2412 MHz to 2472 MHz: DSSS/CCK/OFDM
5180 MHz to 5320 MHz, 5500 MHz to 5825
MHz:OFDM
• Maximum effective radiation power
— AeroDR SYSTEM:
+15 dBm
— AeroDR SYSTEM 2:
+10 dBm
— SKR 3000:
+15 dBm
• This device may be interfered with by other devices
that conform to CISPR emission requirements.