6
Senior Solutions™ Therapy System
2 SAFETY PRECAUTIONS
2.2 PRECAUTIONARY INSTRUCTIONS (CONTINUED)
DO NOT connect the unit to an electrical supply
without first verifying that the power supply is
the correct voltage. Incorrect voltage may cause
unit damage, malfunction, electrical shock, fire, or
personal injury. Your unit was constructed to operate
only on the electrical voltage specified on the
Voltage Rating and Serial Number Plate. Contact your
dealer if the unit is not properly rated.
Power Supplies retain High Voltage!
NiMH batteries contain Class E corrosive materials. In
the event of battery cell rupture or leakage, handle
battery module wearing neoprene or natural rubber
gloves. Contents of a ruptured or leaking battery can
cause respiratory irritation. Hypersensitivity to nickel
can cause allergic pulmonary asthma. Contents
of cell coming in contact with skin can cause skin
irritation and chemical burns.
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Electronic monitoring equipment (such as ECG monitors and
ECG alarms) may not operate properly when TENS stimulation
is in use. Powered muscle stimulators should be used only
with the leads and electrodes recommended for use by the
manufacturer.
In the event that an Error message or Warning appears
beginning with a 2 or 3, immediately STOP all use of the unit
and contact the dealer or Chattanooga Group for service.
Errors and Warnings in these categories indicate an internal
problem with the unit that must be tested by Chattanooga
Group or a Field Service Technician certified by Chattanooga
Group before any further operation or use of the unit. Use of a
unit that indicates an Error or Warning in these categories may
pose a risk of injury to the patient, user, or cause extensive
internal damage to the unit.
Use of controls or adjustments or performance of procedures
other than those specified herein may result in hazardous
exposure to ultrasonic energy.
Before administering any treatment to a patient you should
become acquainted with the operating procedures for
each mode of treatment available, as well as the indications,
contraindications, warnings and precautions. Consult other
resources for additional information regarding the application
of Electrotherapy and Ultrasound.
To prevent electrical shock, disconnect the unit from
the power source before attempting any maintenance
procedures.
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Keep electrodes separated during treatment. Electrodes in
contact with each other could result in improper stimulation
or skin burns.
Long term effects of chronic electrical stimulation are
unknown. Stimulation should not be applied over the anterior
neck or mouth. Severe spasm of the laryngeal and pharyngeal
muscles may occur and the contractions may be strong
enough to close the airway or cause difficulty in breathing.
Stimulation should not be applied transthoracically in that
the introduction of electrical current into the heart may cause
cardiac arrhythmia.
Stimulation should not be applied over swollen, infected,
and inflamed areas or skin eruptions, e.g., phlebitis,
thrombophlebitis, varicose veins, etc.
Stimulation should not be applied over, or in proximity to,
cancerous lesions.
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Output current density is related to electrode size. Improper
application may result in patient injury. If any question arises
as to the proper electrode size, consult a licensed practitioner
prior to therapy session.
The Senior Solutions optional modules and associated accessories
are designed for use only with the Chattanooga Group
Electrotherapy and Combination unit.
Use only accessories that are specially designed for this device.
Do not use accessories manufactured by other companies
on this device. Chattanooga Group is not responsible for any
consequence resulting from using products manufactured by
other companies. The use of other accessories or cables may
result in increased emissions or decreased immunity of this
device and can degrade minimum safety.
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Stimulus delivered by the TENS waveforms of this
device, in certain configurations, will deliver a charge
of 25 microcoulombs (μC) or greater per pulse and
may be sufficient to cause electrocution. Electrical
current of this magnitude must not flow through the
thorax because it may cause a cardiac arrhythmia.
Patients with an implanted neurostimulation device
must not be treated with or be in close proximity to
any shortwave diathermy, microwave diathermy, or
therapeutic ultrasound diathermy anywhere on their
body. Energy from diathermy (shortwave, microwave,
ultrasound) can be transferred through the implanted
neurostimulation system, can cause tissue damage,
and can result in severe injury or death. Injury,
damage or death can occur during diathermy therapy
even if the implanted neurostimulation system is
turned “off.”
Handle, clean and dispose of components and
accessories that have come in contact with bodily
fluids according to National, Local and Facility rules,
regulations and procedures.
Equipment not suitable for use in the presence of
a flammable anesthetic mixture with air, oxygen or
nitrous oxide.
Never, under any circumstances, open the Battery
Module housing or cells. Should an individual cell
from a battery become disassembled, spontaneous
combustion of the negative electrode is possible.
There can be a delay between exposure to air and
spontaneous combustion.
Charge the Battery Module according to the
instructions found in this manual. Never attempt to
charge the Battery Module on any other charging
mechanism.
Use the Battery Module only with the Senior
Solutions unit.
Do not reverse the polarity of the Battery Module.
Doing so can increase the individual cell temperature
and cause cell rupture or leakage.
Never dispose of Battery Module in fire. Never short
circuit the battery. The battery may explode, ignite,
leak or get hot causing serious personal injury.
Dispose of NiMH batteries according to national,
state and local codes and regulations.
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