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Important information
The tinnitus masker generates sounds
that are used as part of your personalized
temporary tinnitus management program
to provide relief from tinnitus. It should
always be used as prescribed by a hearing
care professional who is familiar with the
diagnosis and treatment of tinnitus.
Good health practice requires that a person
reporting tinnitus have a medical evaluation
by a licensed ear physician before using
a sound generator. The purpose of such
an evaluation is to ensure that medically
treatable conditions, which may be causing
tinnitus, are identified and treated prior to
using a sound generator.
The tinnitus masker is intended for adults
18 years of age or older who have both
hearing loss and tinnitus.
13.
Information and explanation of
symbols
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With the CE symbol, Sonova AG confirms that
this product – including accessories – meets the
requirements of the Medical Devices Regulation (EU)
2017/745 as well as the Radio Equipment Directive
2014/53/EU. The numbers after the
CE symbol correspond to the code of certified
institutions that were consulted under the above-
mentioned regulation and directive
.
This symbol indicates that the products described in
these user instructions adhere to the requirements for
an applied part of Type B of EN 60601-1. The surface of
the hearing aid is specified as applied part of Type B.
IIndicates the medical device manufacturer, as
defined in Medical Devices Regulation (EU) 2017/745
Indicates the Authorized representative in the
European Community. The EC REP is also the importer
to the European Union.
This symbol indicates that it is important for the user to
read and take into account the relevant information in
these user guides.
This symbol indicates that it is important for the user to
pay attention to the relevant warning notices in this user
guide.
Important information for handling and product safety.
