1.3 Other important information
Persons with pacemakers or other medical devices should ALWAYS
consult their physician or the manufacturer of their device BEFORE using
the device. The use of the device with a pacemaker or other medical de-
vices should ALWAYS be in accordance with the safety recommendations
of the physician responsible for your pacemaker or the pacemaker ma-
nufacturer.
Device collects and stores internal technical data. This data may be read
by a authorized service center in order to check the device, as well as to
help you use your device correctly.
The digital signal sent from the device to a connected receiver cannot
be overheard by other devices which are not in the transmitter network.
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Declaration of Conformity
In body worn operation, the devices have been found in compliance with
the requirements of EN 62209-2, FCC rule paragraph 2.1093, the ANSI/
IEEE C95.1:1999, the NCRP Report Number 86 for uncontrolled environ-
ment, according to the Health Canada's Safety Code 6 and the Industry
Canada Radio Standards Specification RSS-102 for General Population/
Uncontrolled exposure.
Hereby, Phonak Communications AG, Länggasse 17, CH-3280 Murten, de-
clares that these Phonak products are in compliance with the essential
requirements and other relevant provisions of Directive 2014/53/EU. To
obtain a copy of the Declaration of conformity, please contact the manu-
facturer or the local Phonak representative whose address can be taken
from the list on www.phonak-communications.com (worldwide locations).
This device complies with Part 15 of the FCC Rules and with Industry
Canada's license - exempt RSSs. 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
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