CIC R NW Non Wireless Custom Hearing Aid User Manual
- May 15, 2024
- Custom Hearing Aid
Table of Contents
CIC R NW Non Wireless Custom Hearing Aid
Introduction
Non-Wireless Products
CIC R NW*
(Rechargeable Completely-in-Canal)
CIC NW (Completely-in-Canal)
IIC NW (Invisible-in-Canal)
P00003720
*The CIC R NW is a wireless hearing aid for regulatory purposes since it contains a radio transmitter.
The wireless functionality is only used during the programming of the hearing
aid.
Warnings, Cautions, & Notices
REQUIRED HEARING AID INFORMATION
The following additional information is provided in compliance with U.S. Food and Drug Administration (FDA) regulations:
WARNING : People younger than 18 should go to a doctor before using this.
People younger than 18 years old need specialized care, and using this without
a medical evaluation may worsen impairment or disability. A hearing aid user
who is younger than 18 should have a recent medical evaluation from a doctor,
preferably an ear-nose-throat doctor (an ENT). Before using this, a doctor
should determine that the use of a hearing aid is appropriate.
WARNING : to Hearing Aid Dispensers:
You should advise a prospective hearing aid user to consult promptly with a doctor, preferably an ear specialist such as an ENT, before dispensing a hearing aid if you determine through inquiry, actual observation, or review of any other available information concerning the prospective user, that the prospective user has any of the following conditions:
- Visible deformity of the ear, either congenital or traumatic
- Fluid, pus, or blood coming out of the ear within the previous 6 months
- Pain or discomfort in the ear
- History of excessive ear wax or suspicion that something is in the ear canal
- Dizziness, either recent or long-standing
- Sudden, quickly worsening, or fluctuating hearing loss within the previous 6 months
- Hearing loss or ringing (tinnitus) only in one ear or a noticeable difference in hearing between ears
- Audiometric air-bone gap equal to or greater than 15 dB at 500 Hz, 1000 Hz, and 2000 Hz
WARNING : to Hearing Aid Dispenser, Outputs over 132 dB SPL: You should
exercise special care in selecting and fitting a hearing aid with a maximum
output that exceeds 132 dB SPL because it may impair the remaining hearing of
the hearing aid user.
WARNING : If Portable Radio Frequency communications equipment is used
closer than 30 cm (12 inches) from your hearing aid, degradation of the
performance of your hearing aid could result. If this occurs, move away from
the communications equipment.
WARNING : The stability of the hearing aid is designed for normal use.
Avoid physical impacts to the ear when wearing a hearing aid that may cause
the device to break or component of the device to become detached. This may
lead to lacerations of the ear canal or perforation of the eardrum. If this
occurs, it is strongly recommended to see a physician for evaluation and safe
removal.
WARNING : If the hearing aid drops onto a hard surface, it could cause
the hearing aid to break or become damaged. This includes mechanical stress or
shock of the device. Ensure the hearing aid is intact before placing it in the
ear. If you find the device is damaged, discontinue use and see your hearing
professional.
WARNING : Repeated stress to the removal handle may cause it to break. If the removal handle breaks and you’re unable to remove the device carefully, it is recommended to see a physician for safe removal.
WARNING TO HEARING CARE PROFESSIONAL
A hearing care professional should advise a prospective sound generator (tinnitus masker) user to consult promptly with a licensed physician (preferably an ear specialist) before using a sound generator 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
WARNING : There are some potential concerns associated with the use of
any sound generating tinnitus therapy instrument. Among them are the potential
for worsening of tinnitus, a possible change in hearing thresholds, and
possible skin irritation at the point of contact with the hearing aid.
Multiflex Tinnitus Technology has been designed to minimize these concerns.
However, should you experience or notice any of the above conditions or any
dizziness, nausea, headaches or heart palpitations, you should immediately
discontinue use of the hearing aid and seek a consultation with a medical,
audiology or other hearing care professional.
As with any hearing aid, misuse of the tinnitus therapy instrument could
present some potentially harmful effects. Care should be taken to prevent the
unauthorized use and to keep the hearing aid out of the reach of children and
pets.
CAUTION : This is not hearing protection.
You should remove this device if you experience overly loud sounds, whether
short or long-lasting.
If you’re in a loud place, you should use the right kind of hearing protection
instead of wearing this device. In general, if you would use ear plugs in a
loud place, you should remove this device and use ear plugs.
CAUTION : The sound output should not be uncomfortable or painful.
You should turn down the volume or remove the device if the sound output is
uncomfortably loud or painful. If you consistent need to turn the volume down,
you may need to further adjust your device.
CAUTION : You might need medical help if a piece gets stuck in your ear.
If any part of your hearing aid, like the eartip, gets stuck in your ear, and
you can’t easily remove it with your fingers, get medical help as soon as you
can. You should not try to use tweezers or cotton swabs because they can push
the part farther into your ear, injuring your eardrum or ear canal, possibly
seriously.
NOTE : What you might expect when you start using a hearing aid.
A hearing aid can benefit many people with hearing loss. However, you should
know it will not restore normal hearing, and you may still have some
difficulty hearing over noise. Further, a hearing aid will not prevent or
improve a medical condition that causes hearing loss.
People who start using hearing aids sometimes need a few weeks to get used to
them. Similarly, many people find that training or counseling can help them
get more out of their devices.
If you have hearing loss in both ears, you might get more out of using hearing
aids in both, especially in situations that make you tired from listening—for
example, noisy environments.
NOTE : Tell FDA about injuries, malfunctions, or other adverse events.
To report a problem involving your hearing aid, you should submit information
to FDA as soon as possible after the problem. FDA calls them “adverse events,”
and they might include: skin irritation in your ear, injury from the device
(like cuts or scratches, or burns from an overheated battery), pieces of the
device getting stuck in your ear, suddenly worsening hearing loss from using
the devices, etc.
Instructions for reporting are available at
https://www.fda.gov/Safety/MedWatch, or call 1-800-FDA-1088. You can also
download a form to mail to FDA.
NOTE : Hearing loss in people younger than 18.
- People younger than 18 should see a doctor first, preferably an ear-nose-throat doctor (an ENT), because they may have different needs than adults
- The doctor will identify and treat medical conditions as appropriate
- The doctor may refer the person to an audiologist for a separate test, a hearing aid evaluation
- The hearing aid evaluation will help the audiologist select and fit the appropriate hearing aid
A person who is younger than 18 years old with hearing loss should have a
medical evaluation by a doctor, preferably an ENT, before buying a hearing
aid. The purpose of a medical evaluation is to identify and treat medical
conditions that may affect hearing but that a hearing aid won’t treat on its
own.
Following the medical evaluation and if appropriate, the doctor will provide a
written statement that the hearing loss has been medically evaluated and the
person is a candidate for a hearing aid. The doctor may refer the person to an
audiologist for a hearing aid evaluation, which is different from the medical
evaluation and is intended to identify the appropriate hearing aid.
The audiologist will conduct a hearing aid evaluation to assess the person’s
ability to hear with and without a hearing aid. This will enable the
audiologist to select and fit a hearing aid for the person’s individual needs.
An audiologist can also provide evaluation and rehabilitation since, for
people younger than 18, hearing loss may cause problems in language
development and educational and social growth. An audiologist is qualified by
training and experience to asset in the evaluation and rehabilitation of
hearing loss in people younger than 18.
IMPORTANT NOTICE FOR PROSPECTIVE Rx HEARING AID USERS
It is good health practice for a person with a hearing loss to have a medical evaluation by a licensed physician (preferably a physician who specializes in diseases of the ear) before purchasing a prescription hearing aid. Licensed physicians who specialize in diseases of the ear are often referred to as otolaryngologists, otologists or otorhinolaryngologists. The purpose of the medical evaluation is to assure that all medically treatable conditions that may affect hearing are identified and treated before the hearing aid 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 a hearing aid.
The physician will refer you to an audiologist or hearing aid dispenser, as
appropriate, for a hearing aid evaluation.
The audiologist or hearing aid dispenser will conduct a hearing aid evaluation
to assess your ability to hear with and without a hearing aid. The hearing aid
evaluation will enable the audiologist or dispenser to select and fit a
hearing aid to your individual needs.
If you have reservations about your ability to adapt to amplification, you
should inquire about the availability of a trial-rental or purchase option
program. Many hearing aid dispensers now offer programs that permit you to
wear a hearing aid for a period of time for a nominal fee after which you may
decide if you want to purchase the hearing aid.
In some geographies, you must have a medical evaluation before purchasing a
prescription hearing aid. Some States allow an adult to waive the medical
evaluation.
A hearing aid will not restore normal hearing and will not prevent or improve
a hearing impairment resulting from organic conditions. Use of a hearing aid
is only part of hearing habilitation and may need to be supplemented by
auditory training and instruction in lip reading. In most cases infrequent use
of a hearing aid does not permit a user to attain full benefit from it.
Some hearing instrument users have reported a buzzing sound in their hearing
instrument when they are using mobile phones, indicating that the mobile phone
and hearing instrument may not be compatible.
It is well-known that mobile phones are potential sources of noise for hearing
aids. Your Starkey Hearing Aids have been tested for compliance to two
standards that define hearing aid immunity to digital wireless devices and
meet the requirements of ANSI C63.19- 2019 as well as the criteria for user
compatibility as defined by IEC 60118-13:2019.
CAUTION : The following are potential physiological side effects from use
of hearing aids.
Consult a physician if the following occur:
- Worsening of hearing loss or tinnitus
- Pain or discomfort from heat (burns), abrasion (cuts and scratches), infection, shock
- Dermal allergic reaction (inflammation, irritation, swelling, discharge)
- Excessive production of cerumen (Earwax)
What’s Included
Congrats on your new hearing aids!
Use this helpful manual to get to know your new hearing aids – and get the
most out of your hearing experience.
After all, when you hear better, you live better.
Thanks to your new hearing aids.
Hearing aids covered in this user manual (select yours):
-
CIC R NW
-
CIC NW
-
IIC NW
My hearing aid uses a:
- 10 battery (CIC NW, IIC NW) – Yellow
- 312 battery (CIC NW) – Brown
Get To Know Your Hearing Aids
Meet your hearing aids
Overview
- Microphone and cover
- User control (optional on CICs)
- Charging contacts (CIC R NW only)
- Removal handle
- Vent
- Side indicator (location may vary) BLUE is for left ear, RED is for right ear
- Serial number
- Wax guard (included accessory) and sound outlet
- Programming slot for hearing care professional (CIC NW & IIC NW)
- Battery compartment (CIC NW & IIC NW)
- White dot indicates top of hearing aid (IIC NW only
Use your hearing aids
For CIC R NW
STEP 1 : Charge your hearing aids Select your charger:
- Star Link Custom Charger 2.0
- Star Link Premium Custom Charger 2.0
Before using your hearing aids for the first time, fully charge them.
See Your StarLink Charger 2.0 User Manual.
For CIC NW & IIC NW
STEP 1 : Insert hearing aid batteries
Your hearing aid is powered by a battery. Find your battery size by looking at the color code on the packaging – brown (312) or yellow (10).
To insert or replace the battery
- Using the finger pick, gently open the battery door.
- Remove the old battery.
- Remove the colored tab from the new battery. Wait 3–5 minutes.
- Insert the battery into the battery door, ensuring the “+” on the flat side of the battery is even with the “+” on the battery door.
- Close the battery door.
Helpful battery tips
- To avoid damage, try not to force the battery door shut or open it too far.
- If the battery door won’t close securely, check that you’ve inserted the battery correctly.
- Discard used batteries right away in the proper waste or recycling container.
- Batteries vary. Ask your hearing care professional any questions you may have on battery life, or the right battery size and type for your hearing aids.
WARNINGS
Batteries can be harmful if swallowed. To help prevent this:
- Keep batteries out of reach of children and pets.
- Double-check your medications before taking them. Batteries can be mistaken for pills.
- Do not put batteries in your mouth.
NATIONAL BATTERY INGESTION HOTLINE: 800-498-8666
STEP 2: Put on your hearing aids
-
Gripping the outer edge of your hearing aid, gently insert canal tip into your ear canal and rotate the hearing aid backward.
-
Gently press the hearing aid into place. Done!
STEP 3: Remove your hearing aids
-
Grip the outer edges of your hearing aid.
-
Rotate the hearing aid forward and pull outward.
OR
If your hearing aid has a removal handle: Grip this and gently remove the hearing aid from your ear. Done!.
For CIC R NW
| Turning ON| Turning OFF
---|---|---
Charger| Each hearing aid will turn ON when removed from the
charger.| Each hearing aid will turn OFF when placed in the charger.
User Control (optional)| If set up, press and hold the user control
for 3 seconds or more.| If set up, press and hold the user control for 3
seconds or more.
Battery door| Insert your battery and close the battery door securely.
A 3-second delay occurs before your hearing aid turns ON. This allows time to
place it in your ear.| Each hearing aid will turn OFF when you open the
battery door (and the battery is no longer touching the battery contacts).
Battery indicators
- Low battery: An indicator will sound when battery voltage is low. From there, you’ll have about 5 minutes of battery life left.
- Battery shutdown: An indicator may also sound just before the battery stops working.
Expected battery operating time Battery life varies based on usage.
- CIC R NW: Up to 30 hours
- CIC NW & IIC NW:
- 10 battery: Up to 7 days
- 312 battery: Up to 10 days
User control (optional)
Your hearing aid user control lets you control your hearing aids by hand. This is set up by your hearing care professional.
Your user control operates in 2 ways:
- Short press: Press the user control for 1 second and then release.
- Long press: Press and hold the user control for 3 seconds or more.
User control | Hearing aid function |
---|---|
Short press (1 second) | |
Long press (3 seconds) |
Questions? Your hearing care professional can help.
Care for your hearing aids
Keep your hearing aid clean at all times. Heat, moisture and foreign substances can result in poor performance.
Using the included cleaning tool:
-
Do not clean using water, solvents, cleaning fluids or oils.
Do not take your hearing aid apart or insert a cleaning tool inside of them. -
Wipe hearing aids daily over a soft cloth to prevent damage should they drop to a hard surface. If the hearing aid falls/drops onto a hard surface, it could cause the shell or casing to break and/or become damaged. This includes mechanical stress or shock of the device.
See your hearing care professional for more care and maintenance tips.
Storage tips
When you’re not wearing your hearing aids, protect them from damage using these storage tips:
- Choose a cool, dry location away from heat and moisture. Avoid direct sunlight if you can.
- Ensure you can easily find your hearing aids – and your kids and pets cannot. A nightstand or dresser spot is ideal.
See your hearing care professional for more storage tips.
Cleaning microphone cover
The custom microphone cover on your hearing aids protects the microphone from earwax and debris. Ask your hearing care professional for instructions on cleaning and maintaining it.
Replacing wax guards
The wax guards prevent earwax from building up in your hearing aid. It’s best to replace this if you notice built-up debris or poor sound from your hearing aids.
To replace your wax guards:
-
Insert the empty end of the application stick straight into the used wax guard of your hearing aid. Push firmly.
-
Pull the application stick straight out to remove the used wax guard. Do not twist.
-
Use the opposite end of the application stick to insert the new wax guard straight into the hearing aid. Push firmly.
-
Pull straight out to remove the application stick. Do not twist. Discard the application stick.
Done!
Troubleshooting Guide
If, for any reason, your hearing aid does not operate properly, do NOT attempt
to fix it yourself. Not only are you likely to violate any applicable
warranties or insurance, you could easily cause further damage.
Should your hearing aid fail or perform poorly, check this troubleshooting
guide for possible solutions. If problems continue, contact your hearing care
professional for advice and assistance. Many common problems may be solved in
your hearing care professional’s office or clinic.
Symptom | Possible causes | Solutions |
---|---|---|
Hearing aids are not loud enough. | Blocked microphone or wax guard and | |
sound outlet. |
- Clean your hearing aids.
- Replace the wax guards as needed.
Buildup of debris.| Clean the microphone, as well as the wax guard and sound
outlet with your cleaning tool.
Change in your hearing.| Contact your hearing care professional.
Low battery.| CIC R NW:
Charge your hearing aids.
CIC NW & IIC NW:
Replace the battery.
Inconsistent hearing aid performance.| Blocked microphone or wax
guard and sound outlet.|
- Clean your hearing aids.
- Replace the wax guards as needed.
A restart is needed.| CIC R NW:
- Place your hearing aids in the charger until charging begins.
- Remove when charging begins. This “power cycles” your hearing aids.
CIC NW & IIC NW:
- Open the battery door until the battery is no longer touching the battery contacts.
- Close the battery door securely.
Low battery.| CIC R NW:
Charge your hearing aids.
CIC NW & IIC NW:
Replace the battery.
Unclear and distorted hearing aid performance.| Blocked microphone or
wax guard and sound outlet.|
- Clean your hearing aids.
- Replace the wax guards as needed.
Blocked vent.| Clean the vent.
Defective hearing aids.| Contact your hearing care professional.
No sound coming from your hearing aids.| Blocked microphone or wax
guard.|
- Clean the microphone with your cleaning tool brush.
- Replace the wax guard as needed.
Dead battery.| CIC R NW:
Charge your hearing aids.
CIC NW & IIC NW:
Replace the battery.
Defective hearing aids.| Contact your hearing care professional.
Additional Guidance
Intended Use
Intended Use : Air conduction hearing aids are wearable sound-amplifying
devices that are intended to compensate for impaired hearing. The Multiflex
Tinnitus Technology is a tool to generate sounds to be used in a Tinnitus
Management Program to relieve patients suffering from tinnitus.
Indications for Use : Air conduction hearing aids are available in
multiple gain/output levels appropriate to treat patients with hearing losses
ranging from mild to profound. The Multiflex Tinnitus Technology is indicated
for patients suffering from tinnitus.
Intended Patient Population : Air conduction hearing aids are intended
for people (18 years of age or older) who have been diagnosed by a licensed
clinician or audiologist to have hearing loss. The Multiflex Tinnitus
Technology is targeted for patients suffering from tinnitus being treated by
healthcare professionals. The fitting of the Multiflex Tinnitus Technology
should be done by a hearing professional when participating in a Tinnitus
Management Program.
Intended User and User Environment: Lay persons in a home environment
Clinical Benefit: Clinical benefits include: (a) compensation for hearing
loss, (b) relief from Tinnitus symptoms (where applicable).
Adverse Event Reporting: Any serious incident that has occurred in relation to
your Starkey device should be reported to your local Starkey representative
and the Competent Authority of the Member State in which you are established.
A serious incident is defined as any malfunction, deterioration in the
characteristics and/or performance of the device, or inadequacy in the device
Operations Manual/ labeling which could lead to the death or serious
deterioration in the state of health of the user, OR could do so upon
recurrence.
Your hearing aids are designed to comply with the most stringent Standards of
International Electromagnetic Compatibility. However, it is still possible
that you may experience interference caused by power line disturbances,
airport metal detectors, electromagnetic fields from other medical devices,
radio signals and electrostatic discharges.
If you use other medical devices or wear implantable medical devices such as
defibrillators or pacemakers and are concerned that your hearing aids might
cause interference with your medical device, please contact your physician or
the manufacturer of your medical device for information about the risk of
disturbance.
Your hearing aids should not be worn during an MRI procedure or in a
hyperbaric chamber. Your hearing aids are not formally certified to operate in
explosive atmospheres such as coal mines or certain chemical factories. Your
hearing aids are classified as a Type B applied part under the IEC 60601-1
medical device standard.
Storage and Transportation : Your hearing aids are not formally certified to operate in explosive atmospheres such as may be found in coal mines or certain chemical factories.
Your hearing aids should be stored and transported within the temperature, humidity, and pressure ranges of -10°C (14°F) to +45°C (113°F), 10%-95% rH, and 70 kPa – 106 kPa (equivalent to altitudes from 1,200 ft (380 m) below sea level to 10,000 ft (3,000 m).
Your hearing aids are designed to operate from 0°C (+32°F) to +40°C (104°F).
The charging temperature range for the CIC R NW hearing aid is from +10°C
(+50°F) to +40°C (104°F).
The expected service life is 3 years.
CAUTIONS:
- If the product is hot, do not touch it until cool.
- If the product is not working, do not disassemble. Due to a shock hazard, please send in for repair.
- Keep out of reach from children. Do not ingest anything in the package, including desiccant, cleaning tool, etc.
Clinical benefit
The hearing aid is designed to provide better speech understanding to help ease communication with the aim of improving quality of life.
Clinical Study Summary
A clinical study, including adults aged 18 years and over with hearing losses ranging from mild to profound, assessed hearing aid performance and benefit. Over the course of 2-6 weeks of device wear, users completed various laboratory and field assessments to determine if the devices met clinical expectations. The results of the study confirm that the devices provide amplification appropriate for the users’ hearing losses, and that users perceive benefit from amplification consistent with normative data. There were no serious or lasting adverse events encountered during the study.
DO NOT OPEN HEARING AID, NO USER-SERVICEABLE PARTS INSIDE
Required Hearing Aid Information
The following additional information is provided in compliance with U.S. Food and Drug Administration (FDA) regulations:
IMPORTANT NOTICE FOR PROSPECTIVE HEARING AID 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 aid. Licensed physicians who
specialize in diseases of the ear are often referred to as otolaryngologists,
otologists or otorhinolaryngologists. The purpose of the medical evaluation is
to assure that all medically treatable conditions that may affect hearing are
identified and treated before the hearing aid 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 a hearing aid. The physician will
refer you to an audiologist or hearing aid dispenser, as appropriate, for a
hearing aid evaluation.
The audiologist or hearing aid dispenser will conduct a hearing aid evaluation
to assess your ability to hear with and without a hearing aid. The hearing aid
evaluation will enable the audiologist or dispenser to select and fit a
hearing aid to your individual needs.
If you have reservations about your ability to adapt to amplification, you
should inquire about the availability of a trial-rental or purchase-option
program. Many hearing aid dispensers now offer programs that permit you to
wear a hearing aid for a period of time for a nominal fee after which you may
decide if you want to purchase the hearing aid.
Federal law restricts the sale of hearing aids to those individuals who have
obtained a medical evaluation from a licensed physician. 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.
A hearing aid will not restore normal hearing and will not prevent or improve
a hearing impairment resulting from organic conditions. Use of a hearing aid
is only part of hearing habilitation and may need to be supplemented by
auditory training and instruction in lip reading. In most cases infrequent use
of a hearing aid does not permit a user to attain full benefit from it.
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 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.
Required Multiflex Tinnitus Information for Hearing Care Professionals
INDICATIONS FOR USE
The Multiflex Tinnitus Technology 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 18 years of age.
The Multiflex Tinnitus Technology is targeted for hearing care professionals, which are treating patients suffering from tinnitus, as well as conventional hearing disorders. The fitting of the Multiflex Tinnitus Technology must be done by a hearing care professional participating in a Tinnitus Management Program.
INSTRUMENT DESCRIPTION
Multiflex Tinnitus Technology is a software function that generates sound
which is programmed into a hearing aid. The hearing aid may be used in one of
three modes of operation: as a hearing aid, as a tinnitus treatment instrument
or as a hearing aid and tinnitus treatment instrument.
When enabled, the Multiflex Tinnitus Technology 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.
Multiflex Tinnitus Technology generates a broadband white noise signal that
varies in frequency and amplitude. These characteristics are adjustable by the
hearing care 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. For the Patient A
tinnitus therapy instrument is an electronic instrument intended to generate
noise of sufficient intensity and bandwidth to treat ringing in the ears. It
can also be used as an aid in hearing external sounds and speech.
Multiflex Tinnitus Technology is a tool to generate sounds. It is recommended
that this tool be used with appropriate counseling and/or in a tinnitus
management program to relieve patients suffering from tinnitus.
TINNITUS THERAPY CONCEPTS AND BENEFITS
Multiflex Tinnitus Technology can be used as a part of a tinnitus treatment
program.
Multiflex Tinnitus Technology plays a white noise through the hearing aid.
Multiflex Tinnitus Technology is programmed according to your hearing loss and
preference, and your hearing care professional can adjust the settings of
Multiflex Tinnitus Technology to meet your needs.
Multiflex Tinnitus Technology may provide temporary relief of your tinnitus.
PRESCRIPTION USE ONLY
CAUTION : Federal law restricts this hearing aid to sale by or on the order of a doctor, audiologist or other hearing care professional licensed to dispense hearing aids in your state.
The use of any sound generating tinnitus therapy instrument should be only on the advice and in consultation with your audiologist or hearing care professional. Your hearing care professional will properly diagnose and fit the hearing aid 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.
CAUTION : If set to the maximum output level and worn for periods of time exceeding the recommendations below, your exposure to sound energy has the potential to exceed noise exposure limits. You should not use your hearing aid for more than sixteen (16) hours a day if your hearing aid is set at the maximum output level, nor should you use your hearing aid if your hearing care professional has set the hearing aid at levels that exceed your comfort level.
Important Notice for Prospective Sound Generator Users
Good health practice requires that a person with tinnitus have a medical
evaluation by a licensed physician (preferably a physician who specializes in
diseases of the ear) before using a sound generator.
Licensed physicians who specialize in diseases of the ear are often referred
to as otolaryngologists, otologists or otorhinolaryngologists.
The purpose of a medical evaluation is to assure that all medically treatable
conditions that may affect tinnitus are identified and treated before the
sound generator instrument is used.
TINNITUS TECHNICAL DATA
Multiflex Tinnitus Technology Maximum Output = 87 dB SPL (typical) when
measured in a 2cc coupler per ANSI S3.22 or IEC 60118-7.
The following IEC 60601-1-2 conformance information does not apply to
tinnitus.
This hearing aid model has been tested to, and has passed, the following emissions and immunity tests:
- IEC 60601-1-2 radiated emissions requirements for a Group 1 Class B device as stated in CISPR 11.
- RF radiated immunity at a field level of 10 V/m between 80 MHz and 2.7 GHz as well as higher field levels from communications devices as stated in Table 9 of IEC 60601-1-2.
- Immunity to power frequency magnetic fields at a field level of 30 A/m, as well as proximity magnetic fields as defined in table 11 of 60601-1-2.
- Immunity to ESD levels of +/- 8 kV conducted discharge and +/- 15 kV air discharge.
CIC R NW WIRELESS TECHNICAL DESCRIPTION
Your CIC R NW hearing aids contain a radio transceiver utilizing Bluetooth Low Energy wireless technology operating in the 2.4-2.4835 GHz frequency band with a maximum effective radiated power of -8 dBm using GFSK transmission modulation. The receiver section of the radio has a bandwidth of 1.5 MHz.
FCC information
CIC R NW FCC ID: EOA-24GENCICLPO (left); EOA-24GENCICRPO (right)
IC: 6903A-24GENCICLPO (left); 6903A-24GENCICRPO (right)
These devices comply with part 15 of the FCC rules and with ISED Canada
license-exempt RSS standards.
Operation is subject to the following two conditions: (1) The device may not
cause harmful interference, and (2) this device must accept any interference
received, including interference that may cause undesired operation of the
device.
NOTE : The manufacturer is not responsible for any radio or TV
interference caused by unauthorized modifications to this equipment. Such
modifications could void the user’s authority to operate the equipment.
Hereby, Starkey Laboratories, Inc. declares that the CIC R NW is in compliance
with the essential requirements and other relevant provisions of Directive
2014/53/EU.A copy of the Declaration of Conformity can be obtained from the
address below or from
docs.starkeyhearingtechnologies.com.
Hereby, Starkey Laboratories, Inc. declares that the CIC R NW is in compliance
with the UK Radio Equipment Regulations SI 2017 as amended. A copy of the UK
Declaration of Conformity can be obtained from the following addresses and
from
docs.starkeyhearingtechnologies.com.
Regulatory information
For service or repair, please contact your hearing care professional first. If necessary, you can send your hearing aids to:
Starkey Laboratories, Inc. 6700 Washington Ave. South Eden Prairie, MN 55344 USA www.starkey.com
Starkey Laboratories (Germany) GmbH Weg beim Jäger 218-222 22335 Hamburg Germany Starkey UK Rep Address: Starkey UK William F. Austin House Pepper Rd, Hazel Grove Stockport SK7 5BX, UK www.starkey.co.uk
Class II Device
Waste from electronic equipment must be handled according to local regulations
Consult user manual
Keep dry
Instructions for Disposal of Old Electronics
Starkey Laboratories, Inc. encourages, the EU requires, and your local
community laws may require, that your hearing aids be disposed of via your
local electronics recycling/disposal process.
At the benefit of disposal/recycling personnel, please remove zinc air battery
from the battery compartment according to the instructions in the battery
section prior to recycling. In addition, please include this user manual when
disposing of your hearing aids.
Symbol | Symbol Meaning | Applicable Standard | Symbol Number |
---|---|---|---|
Manufacturer | BS EN ISO 15223-1:2021 | 5.1.1 | |
Authorized representative in the European Community | BS EN ISO | ||
15223-1:2021 | 5.1.2 | ||
Date of Manufacture | BS EN ISO 15223-1:2021 | 5.1.3 | |
Catalogue Number | BS EN ISO 15223-1:2021 | 5.1.6 | |
Serial Number | BS EN ISO 15223-1:2021 | 5.1.7 | |
Medical Device | BS EN ISO 15223-1:2021 | 5.7.7 | |
Keep Dry | BS EN ISO 15223-1:2021 | 5.3.4 | |
Temperature Limit | BS EN ISO 15223-1:2021 | 5.3.7 | |
Humidity Limitation | BS EN ISO 15223-1:2021 | 5.3.8 | |
Caution | BS EN ISO 15223-1:2021 | 5.4.4 | |
General warning sign | EC 60601-1, Reference no. Table D.2, Safety sign 2 |
ISO 7010-W001
| Refer to instruction manual/booklet| EC 60601-1, Reference no. Table D.2,
Safety sign 10| ISO 7010-M002
| Collect Separately| DIRECTIVE 201 2/19/EU (WEEE)| Annex IX
| Class II equipment| IEC 60417 Reference no. Table D.1| Symbol 9 (IEC 60417-
5172)
| Regulatory Compliance Mark (RCM)| AS/NZS 4417.1:2012| N/A
| Giteki Mark| Japanese Radio Law| N/A
| Direct current| IEC 60601-1 Reference no. Table D.1| IEC 60417-5031
| Recycling Symbol| European Parliament and Council Directive 94/62/EC| Annex
I-VII
Technical data
CIC R NW | L | M | P | UP |
---|---|---|---|---|
Measurement | ANSI/IEC 2cc Coupler | ANSI/IEC **2cc | ||
Coupler** | ANSI/IEC 2cc Coupler | ANSI/IEC 2cc Coupler | ||
Peak OSPL90 (dB SPL) | 110 | 114 | 117 | 125 |
HFA OSPL90 (dB SPL) | 105 | 110 | 113 | 122 |
Peak Gain (dB) | 40 | 49 | 59 | 67 |
HFA Full-On Gain (dB) | 36 | 47 | 53 | 62 |
Frequency Range (Hz) | <100-9400 | <100-8500 | <100-6600 | <100-5500 |
HFA Frequencies (kHz) | 1.0,1.6,2.5 | 1.0,1.6,2.5 | 1.0,1.6,2.5 | 1.0,1.6,2.5 |
Reference Test Gain (dB) | 28 | 33 | 36 | 45 |
Equivalent Input Noise (dB)1 | 25 | 25 | 25 | 25 |
Equivalent Input Noise (dB)2 | 14 | 14 | 14 | 14 |
Harmonic Distortion | ||||
500 Hz (%) | <3 | <3 | <3 | <3 |
800 Hz (%) | <3 | <3 | <3 | <3 |
1600 Hz (%) | <3 | <3 | <3 | <3 |
Estimated Battery Life | ||||
Lithium-ion battery (hrs) | Up to 30 | Up to 30 | Up to 30 | Up to 30 |
Battery Current (mA) | 0.9 | 0.9 | 0.9 | 0.9 |
Tinnitus Therapy Stimulus | ||||
Max RMS Output (dB SPL) | 87 | 87 | 87 | 87 |
Weighted RMS Output Level (dB SPL) | 87 | 87 | 87 | 87 |
Max 1/3 Octave Output (dB SPL) | 87 | 87 | 87 | 87 |
Matrices: L, M, P, UP
Battery: Lithium-ion
CIC NW | L | M | P | UP |
---|---|---|---|---|
Measurement | ANSI/IEC 2cc Coupler | ANSI/IEC **2cc | ||
Coupler** | ANSI/IEC 2cc Coupler | ANSI/IEC 2cc Coupler | ||
Peak OSPL90 (dB SPL) | 110 | 114 | 118 | 126 |
HFA OSPL90 (dB SPL) | 105 | 110 | 114 | 121 |
Peak Gain (dB) | 43 | 52 | 61 | 68 |
HFA Full-On Gain (dB) | 37 | 48 | 54 | 63 |
Frequency Range (Hz) | <100-9600 | <100-8300 | <100-6600 | <100-5900 |
HFA Frequencies (kHz) | 1.0,1.6,2.5 | 1.0,1.6,2.5 | 1.0,1.6,2.5 | 1.0,1.6,2.5 |
Reference Test Gain (dB) | 28 | 33 | 37 | 44 |
Equivalent Input Noise (dB)1 | 25 | 25 | 25 | 25 |
Equivalent Input Noise (dB)2 | 14 | 14 | 14 | 14 |
Harmonic Distortion | ||||
500 Hz (%) | <3 | <3 | <3 | <3 |
800 Hz (%) | <3 | <3 | <3 | <3 |
1600 Hz (%) | <3 | <3 | <3 | <3 |
Estimated Battery Life for 16-Hour Day | ||||
10 Zinc Air (days) | Up to 7 | Up to 7 | Up to 7 | Up to 6 |
312 Zinc Air (days) | Up to 10 | Up to 10 | Up to 10 | Up to 9 |
Battery Current (mA) | 1.1 | 1.2 | 1.2 | 1.3 |
Tinnitus Therapy Stimulus | ||||
Max RMS Output (dB SPL) | 87 | 87 | 87 | 87 |
Weighted RMS Output Level (dB SPL) | 87 | 87 | 87 | 87 |
Max 1/3 Octave Output (dB SPL) | 87 | 87 | 87 | 87 |
Matrices: L, M, P, UP
Battery Size: 10, 312
IIC NW | L- | L | M |
---|---|---|---|
Measurement | ANSI/IEC 2cc Coupler | ANSI/IEC **2cc | |
Coupler** | ANSI/IEC 2cc Coupler | ||
Peak OSPL90 (dB SPL) | 110 | 110 | 115 |
HFA OSPL90 (dB SPL) | 104 | 105 | 110 |
Peak Gain (dB) | 36 | 41 | 49 |
HFA Full-On Gain (dB) | 30 | 36 | 46 |
Frequency Range (Hz) | <100-9400 | <100-9400 | <100-8660 |
HFA Frequencies (kHz) | 1.0,1.6,2.5 | 1.0,1.6,2.5 | 1.0,1.6,2.5 |
Reference Test Gain (dB) | 27 | 28 | 33 |
Equivalent Input Noise (dB)1 | 25 | 25 | 25 |
Equivalent Input Noise (dB)2 | 14 | 14 | 14 |
Harmonic Distortion | |||
500 Hz (%) | <3 | <3 | <3 |
800 Hz (%) | <3 | <3 | <3 |
1600 Hz (%) | <3 | <3 | <3 |
Estimated Battery Life for 16-Hour Day | |||
10 Zinc Air (days) | Up to 7 | Up to 7 | Up to 7 |
Battery Current (mA) | 1.1 | 1.1 | 1.2 |
Tinnitus Therapy Stimulus | |||
Max RMS Output (dB SPL) | 87 | 87 | 87 |
Weighted RMS Output Level (dB SPL) | 87 | 87 | 87 |
Max 1/3 Octave Output (dB SPL) | 87 | 87 | 87 |
Customer Support
StarLink and Starkey are trademarks of Starkey Laboratories, Inc
©2023 Starkey Laboratories, Inc. All Rights Reserved.
P00003720 11/23 BKLT3208-00-EN-XX
Patent: www.starkey.com/patents
References
- Find the Best Hearing Aids for You | Starkey
- Find the Best Hearing Aids for You | Starkey
- MedWatch: The FDA Safety Information and Adverse Event Reporting Program | FDA