Miracle-Ear ENERGY 5 ITC R EV Manual Del Usuario página 24

Regulatory Information
We are required by regulations to provide the following warnings:
WARNING:
Use of wireless hearing aids directly next to other electronic
equipment should be avoided because it could result in improper performance. If
such use is necessary, note as to whether your hearing aids and the other equipment
are operating normally.
WARNING:
Use of accessories, components or replacement parts other than
those provided by the manufacturer of your hearing aids could result in increased
electromagnetic emissions and decreased electromagnetic immunity and could
result in degradation of performance.
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.
DO NOT OPEN HEARING AID OR CHARGER,
NO USER-SERVICEABLE PARTS INSIDE
The Miracle-Ear Charger has a rating of IP 21 per IEC 60529. This means the unit is
protected against solid objects over 12 mm, such as fingers and falling water drops,
such as condensation.
Do not connect the Miracle-EarENERGY
described in this manual.
The service life of the Miracle-Ear Charger is 3 years.
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™ 5/4/3/2 ITC R EV to any devices not
Regulatory Information
Required Hearing Aid Information
The following additional information is provided in compliance with U.S. Food and
Drug Administration (FDA) regulations:
WARNING TO HEARING AID DISPENSERS
A hearing aid dispenser should advise a prospective hearing aid user to consult
promptly with a licensed physician (preferably an ear specialist) before dispensing
a hearing aid if the hearing aid dispenser determines 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:
i. Visible congenital or traumatic deformity of the ear.
ii. History of active drainage from the ear within the previous 90 days.
iii. History of sudden or rapidly progressive hearing loss within the previous
90 days.
iv. Acute or chronic dizziness.
v. Unilateral hearing loss of sudden or recent onset within the previous 90 days.
vi. Audiometric air-bone gap equal to or greater than 15 decibels at 500 Hertz
(Hz), 1,000 Hz and 2,000 Hz.
vii. Visible evidence of significant cerumen accumulation or a foreign body in the
ear canal.
viii. Pain or discomfort in the ear.
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