Sivantos BTE001 BTE hearing instrument User Manual Safety manual English

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Document ID	3486394
Application ID	2ceRvDQ4AenCj5a7i0LFtA==
Document Description	Safety manual English
Short Term Confidential	No
Permanent Confidential	No
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Document Type	User Manual
Display Format	Adobe Acrobat PDF - pdf
Filesize	142.28kB (1778473 bits)
Date Submitted	2017-07-28 00:00:00
Date Available	2017-11-13 00:00:00
Creation Date	2017-07-27 14:50:35
Producing Software	Adobe PDF Library 11.0
Document Lastmod	2017-07-27 14:50:41
Document Title	Safety manual English
Document Creator	Adobe InDesign CC 2014 (Windows)

Safety manual
for hearing instruments
for US and Canadian markets
Master
DRAFT 2017-07-27
Content
Safety information  
Intended use  
Explanation of symbols  
General warnings  
For certain instrument types  
For children under the age of 3 years  
For certain battery types  
When using remote control apps  
For Hearing Care Professionals  
12
13
14
15
16
Important information  
Operating, transport and storage conditions  
Disposal information  
Conformance information  
17
17
18
18
For US and Canadian markets only  
For prospective hearing instrument users  
For hearing instrument users  
Tinnitus feature  
For children with hearing loss  
Warranty and service  
21
21
22
30
33
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Safety information
This safety manual provides safety information and other
important information about your hearing instruments. It
covers several instrument types and optional features.
X Refer to the user guide of your hearing instruments, to
check the instrument type and the activated features.
Intended use
Hearing instruments are intended to improve the hearing
of hearing impaired persons. Diagnosis and prescription
of a hearing instrument must be performed by hearing
health specialists, e.g. acousticians, audiologists or
ENT doctors.
Use the hearing instruments and accessories only as
described in the respective user guides.
Explanation of symbols
Symbols used in this document
Points out a situation that could lead to serious,
moderate, or minor injuries.
Indicates possible property damage.
Information and warnings for children with hearing
instruments.
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Symbols on the device or packaging
CE compliance label, confirms compliance with
certain European Directives, refer to section
"Conformance information".
EMC and radio communications
compliance label Australia, refer to section
"Conformance information".
Optional symbol for custom models with
wireless functionality.
Indicates the legal manufacturer of the device.
Do not dispose of the device with general
domestic waste. Read more in section
"Disposal information".
Read and follow the instructions in the user
guide.
General warnings
WARNING
Risk of impairing the residual hearing of the user.
X Use only hearing instruments that have been
fitted especially for your needs.
WARNING
Risk of injury!
X Do not use obviously damaged devices and
return them to point of sale.
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WARNING
Note that any unauthorized changes to the product
may cause damage to the product or cause injury.
XX Use only approved parts and accessories. Ask
your Hearing Care Professional for support.
WARNING
Your hearing instruments may reduce certain
background sounds, potentially also traffic or
warning signals.
WARNING
Risk of explosion!
XX Do not use your hearing instruments in explosive
atmospheres (e. g. in mining areas).
WARNING
Choking hazard!
Your hearing instruments contain small parts which
can be swallowed.
XX Keep hearing instruments, batteries and
accessories out of reach of children and
mentally disabled persons.
XX If parts have been swallowed consult a physician
or hospital immediately.
If you have hearing instruments that are intended for the
fitting of children under the age of 3 years or persons
with a developmental age of under 3 years, refer also to
section "For children under the age of 3 years".
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NOTICE
XX Protect your hearing instruments from high
humidity. Do not wear them in the shower or
when you apply make-up, perfume, aftershave,
hairspray or suntan lotion.
NOTICE
XX Protect your hearing instruments from extreme
heat. Do not expose them to direct sunlight.
NOTICE
XX Do not dry your hearing instruments in the
microwave oven.
NOTICE
Different types of strong radiation, e. g. during
X-ray or MRI head examinations, may damage
hearing instruments.
XX Do not wear the hearing instruments during
these or similar procedures.
Weaker radiation, e. g. from radio equipment or
airport security, does not damage the hearing
instruments.
NOTICE
Your devices comply with international standards.
However, it cannot be guaranteed that all products
on the market work interference‑free, for example
some induction cookers may cause audible
interference.
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Contraindications
WARNING
Consult a Hearing Care Professional if you
experience any unusual side effects like skin
irritation, excessive accumulation of ear wax,
dizziness, change in your hearing, or if you think
there may be a foreign object in your ear canal.
WARNING
A Hearing Care Professional should advise a
prospective hearing instrument user to consult
a licensed physician before using the hearing
instrument if the Hearing Care Professional
determines that the prospective user has any of the
following conditions:
XX Visible congenital or traumatic deformity of the
ear.
XX History of active drainage from the ear within the
previous 90 days.
XX History of sudden or rapidly progressive hearing
loss within the previous 90 days.
XX Acute or chronic dizziness.
XX Unilateral hearing loss of sudden or recent onset
within the previous 90 days.
XX Audiometric air‑bone gap equal to or greater
than 15 dB at 500 Hz, 1,000 Hz, and 2,000 Hz.
XX Visible evidence of significant cerumen
accumulation or a foreign body in the ear canal.
XX Pain or discomfort in the ear.
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For hearing instruments with wireless functionality
In some countries restrictions for the usage of
wireless equipment exist.
XX Refer to local authorities for further information.
WARNING
Risk of affecting electronic equipment!
XX In areas where the use of electronics or wireless
devices are restricted, verify if your device has to
be turned off.
NOTICE
Your hearing instruments are designed to comply
with international standards on electromagnetic
compatibility but interference with nearby electronic
devices could occur. In this case, move away from
the source of interference.
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For hearing instruments with a tinnitus feature
Your hearing instrument may be equipped with a tinnitus
feature (e. g. with a tinnitus therapy signal, a tinnitus
noiser, or another special function). The use of the
tinnitus feature should be only on the advice and in
consultation with your Hearing Care Professional.
WARNING
Risk of further impairment to the user’s hearing
health.
The volume of the tinnitus feature can be set to
a level which could lead to permanent hearing
damage when used for a prolonged period of time.
XX The tinnitus feature should never be used at
uncomfortable levels.
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For hearing instruments with AutoPhone magnet
WARNING
Risk of affecting life support systems!
XX Use a magnet only when it is a safe distance
away from life support systems, such as
pacemakers or magnetic valves. For example,
the safe distance between pacemaker and
magnet should be at least 10 cm (4 inches).
NOTICE
Magnets can disturb electrical devices and delete
stored data.
XX Keep magnets away from computers, monitors,
television sets, storage media and other
electronic equipment/devices.
NOTICE
In close proximity, AutoPhone magnets can
damage receiver units of RIC hearing instruments.
XX Keep a minimum distance of 2 cm between the
RIC receiver and any magnet, including the
AutoPhone magnet.
For example, do not store your RIC hearing
instruments and a smartphone with attached
AutoPhone magnet together in a small pocket
or box.
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For hearing instruments with a magnet in the battery
compartment
WARNING
Risk of interference with active and non-active
implants!
If you wear an active or a non-active implant, e.g. a
brain implant:
XX Prior to use, have the electromagnetic
compatibility verified.
Consult the physician that implanted the device
before using your hearing instruments.
XX Keep a safe distance of about 1.6 inches (4 cm)
between the implant and hearing instruments.
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For certain instrument types
BTE models
Instruments that are worn behind the ear and that have a
tube.
CAUTION
Risk of injury!
X Always wear the tube with an ear piece.
X Make sure that the ear piece is completely
attached.
RIC models
The receiver is placed within the ear canal and connected
to the instrument via a receiver cable.
CAUTION
Risk of injury!
X Always wear the receiver cable with an ear
piece.
X Make sure that the ear piece is completely
attached.
NOTICE
X Do not pull the receiver connection
as this could damage your hearing
instruments.
Other models
For all other models, no model‑specific safety information
applies.
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For children under the age of 3 years
There are special hearing instruments for the fitting
of children under the age of 3 years or persons with a
developmental age of under 3 years. Ask your Hearing
Care Professional for further information.
WARNING
Choking hazard!
Your hearing instruments contain small parts which
can be swallowed.
XX Ensure adequate supervision if infants, small
children or mentally disabled persons need to
wear hearing instruments.
XX Check the completeness of the hearing
instruments regularly.
XX Ensure that your child or the mentally disabled
person does not detach the hearing instrument
from the earmold.
XX Consult your Hearing Care Professional if the
housing is deformed.
XX Keep the battery compartment locked. Verify the
proper function of the locking mechanism.
XX Keep batteries and accessories out of children's
or mentally disabled person's reach.
XX If swallowed consult a physician or a hospital
immediately.
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For certain battery types
For hearing instruments with built-in power cells
(lithium‑ion rechargeable batteries)
Read the safety information on power cells in the hearing
instrument's user guide.
For hearing instruments with replaceable batteries
NOTICE
Only use zinc‑air batteries or nickel‑metal hydride
(NiMH) rechargeable batteries.
Do not use e.g. silver‑zinc or lithium‑ion
rechargeable batteries.
NOTICE
Leaking batteries damage the hearing instruments.
XX Turn the hearing instruments off when not in use
to preserve the battery.
XX Remove batteries when the instruments are not
in use for a prolonged period of time.
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When using remote control apps
When using an app for controlling hearing instruments:
WARNING
Risk of hearing damage!
The device with the app for controlling hearing
instruments generates short control signals which
may be audible. If the device running the app has
a very high audio output there is the risk of hearing
damage.
While using the app:
XX Do not hold the loudspeaker of the device to
your ears or the ears of others.
XX Do not use the device with headphones,
headsets or other audio playback devices.
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For Hearing Care Professionals
WARNING
For hearing instruments with an output sound
pressure level of 132 dB SPL or more:
Risk of impairing the residual hearing of the user.
XX Take special care when fitting this instrument.
Tinnitus feature
The target population is primarily the adult population
over 21 years of age. The patient may have some control
of the level or volume of the signal and the patient should
discuss this adjustment as well as his or her comfort
level and sound of the signal with their Hearing Care
Professional.
WARNING
Risk of further impairment to the user’s hearing
health.
The volume of the tinnitus feature can be set to
a level which could lead to permanent hearing
damage when used for a prolonged period of time.
XX Should the tinnitus feature be set to such a level
in the hearing instrument, advise the user of
the maximum amount of time per day he or she
should use the tinnitus feature.
For example, occupational safety guidelines
restrict continuous noise exposure of
80 dBA SPL to 8 hours per day.
XX The tinnitus feature should never be used at
uncomfortable levels.
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Important information
Operating, transport and storage conditions
For hearing instruments with built-in power cells
(lithium‑ion rechargeable batteries)
Read the operating, transport and storage conditions in
the hearing instrument's user guide.
For hearing instruments with replaceable batteries
Operating conditions
Temperature
0 to 50 °C (32 to 122 °F)
Relative humidity
5 to 93 %
During extended periods of transport and storage, please
observe the following conditions:
Storage
Transport
Temperature
10 to 40 °C
(50 to 104 °F)
-20 to 60 °C
(-4 to 140 °F)
Relative humidity
10 to 80 %
5 to 90 %
For other parts, such as batteries, other conditions may
apply.
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Disposal information
XX Recycle hearing instruments, accessories and
packaging according to local regulations.
For hearing instruments with replaceable batteries
XX To avoid environmental pollution, do not throw
batteries into household trash.
XX Recycle or dispose of batteries according to local
regulations or return them to your Hearing Care
Professional.
Conformance information
The CE mark indicates conformity with the following
European directives:
■ 93/42/EEC concerning medical devices
■ 2011/65/EU RoHS concerning the restriction of
hazardous substances
■ Only for products with wireless functionality:
2014/53/EU RED concerning radio equipment
The full text of the declaration of conformity can
be obtained from www.signia-hearing.com/doc (for
hearing instruments manufactured by Signia GmbH) or
from www.sivantos.com/doc (for hearing instruments
manufactured by Sivantos GmbH).
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The ACMA compliance mark
indicates conformity
with the electromagnetic interference standards set by
the Australian Communications and Media Authority
(ACMA).
Devices with the FCC marking comply with the standards
of the FCC regarding electromagnetic interference (only
for products with wireless functionality).
Notices
This Class B digital apparatus complies with Canadian
ICES‑003.
Changes or modifications made to this equipment not
expressly approved by the legal manufacturer may void
the FCC authorization to operate this equipment.
This device complies with Part 15 of the FCC Rules and
with ISED's licence-exempt RSSs.
Operation is subject to the following conditions:
■ this device may not cause harmful interference, and
■ this device must accept any interference received,
including interference that may cause undesired
operation.
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This equipment has been tested and found to comply
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 to an outlet on a circuit
different from that to which the receiver is connected.
■ Consult the dealer or an experienced radio/TV
technician for help.
For body worn operation, this device has been tested
and meets the FCC RF exposure guidelines when used
with the legal manufacturer’s accessories supplied or
designated for this product. Use of other accessories may
not ensure compliance with FCC RF exposure guidelines.
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For US and Canadian markets only
For prospective hearing instrument users
Good health practice requires that a person with a hearing
loss have a medical evaluation by a licensed physician
(preferably a physician who specializes in diseases
of the ear) before purchasing a hearing instrument.
Licensed physicians who specialize in diseases of the ear
are often referred to as otolaryngologists, otologists or
otorhinolaryngologists. The purpose of medical evaluation
is to assure that all medically treatable conditions that may
affect hearing are identified and treated before the hearing
instrument is purchased.
Following the medical evaluation, the physician will give
you a written statement that states that your hearing
loss has been medically evaluated and that you may
be considered a candidate for hearing instruments. The
physician will refer you to a Hearing Care Professional for
a hearing instrument evaluation.
The Hearing Care Professional will conduct a hearing
instrument evaluation to assess your ability to hear with
and without hearing instruments. The hearing instrument
evaluation will enable the Hearing Care Professional to
select and fit hearing instruments to your individual needs.
If you have reservations about your ability to adapt to
amplification, you should inquire about the availability of
21
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a trial‑rental or purchase‑option program. Many Hearing
Care Professionals now offer programs that permit you
to wear hearing instruments for a period of time for a
nominal fee after which you may decide if you want to
purchase them.
U.S. federal law restricts the sale of hearing instruments
to those individuals who have obtained a medical
evaluation from a licensed physician. U.S. federal law
permits a fully informed adult to sign a waiver statement
declining the medical evaluation for religious or personal
beliefs that preclude consultation with a physician. The
exercise of such a waiver is not in your best health
interest and its use is strongly discouraged.
For hearing instrument users
Hearing instruments will not restore normal hearing and
will not prevent or improve a hearing impairment resulting
from organic conditions. In most cases infrequent use of
hearing instruments prohibits the wearer from attaining
the full benefit from it. The use of hearing instruments is
only part of hearing rehabilitation and may need to be
supplemented by auditory training and instruction in lip
reading.
Health considerations
If soreness or skin irritation develops, discontinue
wearing your hearing instruments, and bring the
instruments and earmolds to your Hearing Care
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Professional. Minor fit adjustments or earmold
modification can often correct this condition. If soreness
persists, discontinue wearing the hearing instrument and
see your physician. If excessive earwax accumulates
when wearing your hearing instruments, consult your
Hearing Care Professional.
Battery tips
If a battery is accidentially swallowed, seek medical
attention immediately, or call the National Battery Hotline
collect at (202) 625‑3333.
Identification information
Your hearing instruments have a serial number imprinted
on them. The location of the serial number will vary
according to the style of hearing instrument you have
chosen. Record the serial number in your user guide for
future reference.
The year of manufacture is incorporated into the serial
number.
For custom instruments, the year of manufacture
is derived from the first two digits. In the following
examples, the year of manufacture is 2016.
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➎ ➏
xxxx/xx R
56
16X01234
xxxx / xx
16X0123456R
➊➋ ➌
➎
➊
➏
➍
XXXXX/XXX
16X123456R
➋➌
➎
➍
➊ 16:
year manufactured
➋ X:
facility code where
instrument was
manufactured
➌ Serial number
➏
➍ L or R:
left or right ear instrument
➎ Manufacturer/Distributor
➊
XXXXX XX
16X123456R
Model
➍ ➏
➋ ➌
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For BTE and RIC instruments, the year of manufacture is
derived from the second digit:
Code (second digit)
Year
D, E, F
2013
G, H
2014
L, M
2015
N, P
2016
Q, R
2017
S, T
2018
Please note the warranty is based upon the date of
purchase, not the date of manufacture.
Your Audiologist or Hearing Care Professional can
answer any questions you may have about the identifying
code on your hearing instrument.
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Wireless functionality
The following tables summarizes the technical details of
the wireless technology:
Wireless technology Nearfield magnetic induction
Antenna type
Inductive antenna
Antenna dimensions BTE or RIC models:
Ø: 1.9 mm, L: 6.5 mm, respectively,
Ø: 2.3 mm, L: 5.7 mm, respectively,
Ø: 2.8 mm, L: 4.4 mm
Custom models:
Ø: 3.3 mm, L: 4.2 mm, respectively,
Ø: 2.0 mm, L: 6.7 mm
Modulation
PSK (Phase Shift Key)
Magnetic field
strength
0.07 A/m, (1 cm2 coil; average)
Output power (EIRP) 53 μW
EIRP = Equivalent isotropically radiated power
Range
< 20 cm between hearing instruments
Center frequency
3.28 MHz
Channel
Single channel radio
Bandwidth
BTE or RIC models: 140 kHz
Custom models: 138 kHz
Data rate
324 kbit/sec (raw channel capacity)
Data flow
Simplex or semi-duplex capability
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Protocol
Random access, no collision
avoidance
S.A.R.
2.36 nW/kg (BTE)
6.63 nW/kg (custom models)
S.A.R. = Specific Absorption Rate (S.A.R.) based on
10 g ICNIRP testing.
Bluetooth® low energy*
Wireless technology
Radio frequency Bluetooth low energy
Antenna type
Electromagnetic dipole antenna
Antenna dimensions BTE or RIC models:
H: approx. 4 mm, L: approx. 15 mm
Magnetic field
strength
not applicable
Output power (EIRP) 150 μW
EIRP = Equivalent isotropically radiated power
Range
< 10 m between smartphone/
accessory and hearing instruments
Center frequency
2.45 GHz
Channel
40 channel radio
Bandwidth
2 MHz per channel
* The Bluetooth word mark and logos are owned by the Bluetooth SIG, Inc., and any
use of such marks by the legal manufacturer of this product is under licenses. Other
trademarks and trade names are those of their respective owners.
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Data rate
1 Mbit/sec, respectively, 2 Mbit/sec
Data flow
Simplex or semi-duplex capability
Protocol
Bluetooth network FHSS (Frequency
Hopping Spread Spectrum)
S.A.R.
1.31 nW/kg
S.A.R. = Specific Absorption Rate (S.A.R.) based on
10 g ICNIRP testing.
EMI/EMC compliance
Wireless hearing instruments comply with the following
EMC/EMI standards:
Standard
Test Type
Note
47 CFR Part 15, RF emissions
Subpart C
U.S. FCC requirements
for intentional radiators.
EN 300 330-1/2
RF emissions
including
spurious
emission
EMC and radio
spectrum matters for
short range devices in
the frequency range
9 kHz ‑ 25 MHz.
EN 301 489-1/3
Immunity,
RF and ESD
Standard for low
power transmitters in
the frequency range
9 kHz ‑ 40 GHz.
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Standard
Test Type
Note
EN 300 328
Signal integrity
and emissions
Wideband transmission
systems; data
transmission equipment
operating in the 2.4 GHz
ISM band and using
wide band modulation
techniques
IEC 60118-13
RF immunity
International product
standard for hearing
instruments to ensure
adequate immunity to
radio interference from
mobile telephones.
ANSI C63.19
RF immunity
American National
Standard method
of measurement of
compatibility between
wireless communication
devices and hearing
instruments.
ANSI/AAMI
PC69
RF emissions
Implantable medical
device EMC immunity.
ISO 14117
RF emissions
Implantable medical
device EMC immunity.
EN 45502-2-1
RF emissions
Particular requirements
for pacemakers.
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Wireless security measures
Wireless signal security is assured through the device
system design that includes:
■ A built-in pairing table which specifies valid and
legitimate pairing among units.
■ A proprietary communication protocol which checks
the package numbers during each transmission.
■ A Cyclic Redundancy Check (CRC) to check data
validity.
■ A convolutional encoder/decoder (Viterbi) to correct
errors.
The Bluetooth low energy connection uses the security
measures that are defined in the Bluetooth low energy
standard.
Tinnitus feature
Your hearing instrument may be equipped with a tinnitus
feature. Many tinnitus patients also suffer from some
degree of hearing loss. Many hearing instruments can
be used alone or in combination with the tinnitus feature.
The tinnitus feature is fixed to a broadband noise that can
be adjusted by your Hearing Care Professional for your
tinnitus therapy.
The feature may provide temporary relief of your tinnitus.
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Prescription Use Only
U.S. federal law restricts this device to sale by or on the
order of a doctor or Hearing Care Professional licensed
to dispense hearing instruments in your state. The use of
any sound generating tinnitus therapy device should be
only on the advice and in consultation with your Hearing
Care Professional. Your Hearing Care Professional will
properly diagnose and fit the device to your personal
needs and requirements. This should include its use in a
prescribed tinnitus treatment program. Your Hearing Care
Professional will also be able to offer the appropriate
follow-up care. It is important that you follow your Hearing
Care Professional’s advice and direction regarding such
care.
There are some potential concerns associated with the
use of any sound generating tinnitus therapy device.
Discontinue use and seek medical evaluation if any of the
following conditions occur:
■ Chronic skin irritation on, near, or around the site of
device placement.
■ Unusual side effects (e.g., dizziness, nausea,
headaches, heart palpitations).
■ Perceived decrease in auditory function
(e.g., decreased loudness, speech not as clear).
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For Hearing Care Professionals
Indications for use
The tinnitus feature is a tool to generate sounds to be
used in a tinnitus management program to relieve patients
suffering from tinnitus. The target population is primarily
the adult population over 21 years of age. The tinnitus
feature is targeted for healthcare professionals treating
patients suffering from tinnitus, as well as conventional
hearing disorders. The fitting of the tinnitus feature should
be done by a Hearing Care Professional participating in a
tinnitus management program.
Device description
The tinnitus feature is a software function that generates
sound which is programmed into a hearing instrument.
Depending on the type of hearing instrument, the hearing
instrument may be used in up to three modes of operation:
as a hearing instrument, as a tinnitus treatment device, or
as a hearing instrument and tinnitus treatment device.
When enabled, the tinnitus feature generates the sound
and allows a patient’s Hearing Care Professional to design
and program appropriate settings for an individually
prescribed sound treatment plan. The treatment plan
should be used in a tinnitus management program for
relief of tinnitus.
The tinnitus feature generates a broadband noise
signal that varies in frequency and amplitude. These
characteristics are adjustable by the Hearing Care
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Professional and are specific to the prescribed therapy
designed by the professional for the patient’s needs and
comfort. The patient may have some control of the level
or volume of the signal and the patient should discuss
this adjustment as well as his or her comfort level and
sound of the signal with their Hearing Care Professional.
A Hearing Care Professional should advise a prospective
tinnitus feature user to consult promptly with a licensed
physician (preferably an ear specialist) before using
the tinnitus feature if the Hearing Care Professional
determines through inquiry, actual observation, or
review or any other available information concerning the
prospective user that the prospective user has any of the
following conditions:
■ Visible congenital or traumatic deformity of the ear.
■ History of active drainage from the ear within the
previous 90 days.
■ History of sudden or rapidly progressive hearing loss
within the previous 90 days.
■ Acute or chronic dizziness.
■ Unilateral hearing loss of sudden or recent onset
within the previous 90 days.
For children with hearing loss
In addition to seeing a physician for a medical evaluation,
a child with a hearing loss should be directed to an
audiologist for evaluation and rehabilitation since hearing
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loss may cause problems in language development
and the educational and social growth of a child. An
audiologist is qualified by training and experience to
assist in the evaluation and rehabilitation of a child with a
hearing loss.
Warranty and service
Your hearing instrument, with the exception of the
battery, is covered by a comprehensive warranty. All
covered instrument parts received for warranty service at
an authorized service center will be repaired or replaced
with new or reconditioned components, without charge, to
meet the performance specifications for that model.
This warranty does not cover malfunctions due to
unusual wear and tear or mistreatment of the instrument
such as physical shock, excessive wax build-up, or
tampering with the instrument, any of which voids all
warranties. Your Hearing Care Professional may charge
a service fee for processing warranty service.
Warranty service must only be performed by an
authorized service center. Service performed by
unauthorized service depots voids this warranty, and
repairs so necessitated will be done on a parts and labor
cost basis.
Please refer to the warranty card included with your
hearing instruments for warranty period effective dates.
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Your hearing instruments may have additional loss and
damage coverage. Please consult your Hearing Care
Professional to determine if this is applicable to your
hearing instruments.
Risk mitigations (for internal use only)
FCC RF exposure | use with accessories............................................................. 20
IFU101 | interference induction cooker | device...................................................... 6
M11 | explosion | HI................................................................................................. 5
M15 | choking | non-ped HI..................................................................................... 5
M18_2/2 | Battery type........................................................................................... 14
M20_1/4 | heat | HI.................................................................................................. 6
M20_2/4 | humidity | HI not Aquaris......................................................................... 6
M20_3/4 | microwave | HI........................................................................................ 6
M20_4/4 | X-Ray | HI............................................................................................... 6
M23 | wireless interference...................................................................................... 8
M28, M213 | environmental pollution..................................................................... 18
M29 | recycle HI..................................................................................................... 18
M31_1/3 | tube with ear piece................................................................................ 12
M35 | choking | pediatric........................................................................................ 13
M38_1/2 | autophone | interference....................................................................... 10
M38_2/2 | autophone | life support........................................................................ 10
M48_1/3 | cable with ear piece.............................................................................. 12
M78a | more than 132 dB...................................................................................... 16
M90 | only fitted | HI................................................................................................. 4
M91 | interference.................................................................................................... 8
M102 | magnet in HI.............................................................................................. 11
M105_2/2 | tinnitus D8 und D9................................................................................ 9
M106_1/2 | tinnitus dispenser................................................................................ 16
M107 | directionality................................................................................................. 5
M108 | app acoustic control signal........................................................................ 15
M109 | damaged device | HI.................................................................................... 4
M110 | unauthorized modifications.......................................................................... 5
M111 | contraindications dispenser (replaces M106_2/2) ab RA V29..................... 7
M112 | contraindications user (replaces M105_1/2) ab D9..................................... 7
35
DRAFT 2017-07-27
This document applies to hearing instruments manufactured by
Sivantos GmbH and by Signia GmbH.
Document No. 03341-99T##-#### ##
Order/Item No. ### ### ##
Master Rev01, 07.2017
© ##.2017, Sivantos GmbH. All rights reserved
0123

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