User guide

32
ReSound Forza Wireless RIE
These two pages provide information about wireless
connectivity.
FCC ID: X26MRIE
STATEMENT
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.
Note: This equipment has been tested and found to com-
ply with the limits for a Class B digital device, pursuant
to part 15 of the FCC Rules. These limits are designed to
provide reasonable protection against harmful interference
in a residential installation. This equipment generates, uses
and can radiate radio frequency energy and, if not installed
and used in accordance with the instructions, may cause
harmful interference to radio communications. However,
there is no guarantee that interference will not occur in a
particular installation. If this equipment does cause harmful
interference to radio or television reception, which can be
determined by turning the equipment off and on, the user is
encouraged to try to correct the interference by one or more
of the following measures:
• Reorientorrelocatethereceivingantenna.
• Increase the separation between the equipment and
receiver.
• Connecttheequipmentintoanoutletonacircuitdifferent
from the one in which the receiver is connected.
• Consultthedealeroranexperiencedradio/TVtechnician
for help.
Changes or modifications can void the user’s authority to
operate the equipment.
INTENDED USE
Generic air conduction hearing instruments are wear-
able sound amplifying devices intended to compensate
for impaired hearing. The fundamental operating principle
of hearing instruments is to receive, amplify, and transfer
sound to the ear drum of a hearing impaired person.
LIST OF COUNTRIES
Products without wireless functionality are intended for
worldwide sales.
Products with wireless functionality are intended for sale
in countries within the European Economic Area as well as
Switzerland.
Specification of restrictions: You are not allowed to operate
the equipment within 20 km of the centre of Ny Ålesund,
Norway.
The products are in compliance with the following regulatory
requirements:
• InEU:thedeviceconformstotheEssentialRequirements
according to Annex I of Council Directive 93/42/EEC
for medical devices (MDD) and essential requirements
and other relevant provisions of Directive 1999/5/EC
(R&TTE). The declaration of conformity may be consulted
at www.resound.com.
• InUS:FCCCFR47Part15,subpartC,section15.249
• Other identied applicable international regulatory
requirementsincountriesoutsideEUandUS.Pleaserefer
to local country requirements for these areas.
• ProductsarecategorizedasClass2receiveraccordingto
EN 300 440.
IC:6941C-MRIE
This Class B digital apparatus complies with Canadian
ICES-003.
Cet appareil numérique de la classe B est conforme à la
norme NMB-003 du Canada.