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Verfügbare Sprachen
Verfügbare Sprachen
DEVICE SPECIFICATIONS
This device complies with part 15 of the FCC Rules.
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.
This transmitter is authorized by rule under the Medical
Device Radio communication Service (in part 95 of the
FCC Rules) and must not cause harmful interference to
stations operating in the 400.150–406.000 MHz band in
the Meteorological Aids (i.e., transmitters and receivers
used to communicate weather data), the Meteorological
Satellite, or the Earth Exploration Satellite Services
and must accept interference that may be caused by
such stations, including interference that may cause
undesired operation. This transmitter shall be used only
in accordance with the FCC Rules governing the Medical
Device Radio Communication Service. Analog and
digital voice communications are prohibited. Although
this transmitter has been approved by the Federal
Communications Commission, there is no guarantee
that it will not receive interference or that any particular
transmission from this transmitter will be free from
interference.
Note: FCC Compliance information can be accessed on the CP in the
Clinician Programmer Settings screen.
IC Compliance
This device complies with Industry Canada license‐
exempt RSS standard(s). Operation is subject to the
following two conditions: (1) this device may not cause
interference, and (2) this device must accept any
interference, including interference that may cause
undesired operation of this device.
FCC and IC Compliance
This device may not interfere with stations operating in
the 400.150–406.000 MHz band in the Meteorological
Aids, Meteorological Satellite, and Earth Exploration
Satellite Services and must accept any interference
received, including interference that may cause
undesired operation.
Note: Changes and modifications to the Clinician Programmer are
not authorized by Axonics and could void FCC and IC certification
and negate the user's authority to use the product.
Note: The USB port on Clinician Programmer is used for the purpose
of transferring (copying) the session reports to a USB flash drive. Do
not plug any other devices into this port. Some examples of devices
that are prohibited are: USB with WiFi or Bluetooth, USB Data
Transfer Cable, USB mouse, USB keyboard, or USB flash drives with
autorun executables.
Note: The USB port is disabled in all screens except Reports List
screen (see section Reports). In this screen the session reports
can be transferred to a USB flash drive. In the Reports List screen,
the stimulation functions are not accessible and are disabled.
The reports are transferred (copied) in PDF format.
Note: A Wireless connection through the USB port is not an intended
use. This wireless functionality is disabled in the Clinician Programmer.
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