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Vectra Genisys®/Intelect Legend XT®/ Intelect® Vet Therapy Systems
2.2 PRECAUTIONARY INSTRUCTIONS (CONTINUED)
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.
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.
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 Vectra Genisys Therapy System optional modules and
associated accessories are designed for use only with the
Chattanooga Group Vectra Genisys Electrotherapy and
Combination Therapy Systems.
Remove the Ultrasound or Laser Applicator by pulling the
cable connector only. DO NOT remove by pulling the cable.
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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.
When the unit is on, not all wavelengths are visible
to the naked eye. Therefore, when performing any
operational or functional check, make certain all persons
in the vicinity of the laser wear Chattanooga Group laser
protective eyewear.
DO NOT point the laser beam directly into human or
animal eyes. The lens of the eye does not detect the
invisible, coherent laser beams, potentially resulting in
permanent retinal damage.
Class 3B Lasers are considered an acute hazard to the
skin and eyes from direct radiation. Eye injury will occur
is laser is viewed directly or from specular frelection. Eye
protection is required for all persons in the treatment
area.
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.
Never, under any circumstances, open the battery
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 Vectra Genisys
Therapy Systems.
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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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,
therapeutic ultrasound diathermy or laser diathermy
anywhere on their body. Energy from diathermy
(shortwave, microwave, ultrasound and laser) 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.
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2 SAFETY PRECAUTIONS
