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Vectra Genisys®/Intelect Legend XT®/ Intelect® Vet Therapy Systems
2 SAFETY PRECAUTIONS
2.2 PRECAUTIONARY INSTRUCTIONS
Read, understand, and practice the precautionary and
operating instructions. Know the limitations and hazards
associated with using any laser device. Observe the
precautionary and operational decals placed on the unit.
Do not operate this unit when connected to any unit other
than Chattanooga Group devices.
Do not operate this unit in an environment where
other devices are being used that intentionally radiate
electromagnetic energy in an unshielded manner. Portable
and mobile RF communications equipment can affect
Medical Electrical Equipment.
The Laser System should be routinely checked before
each use to determine that all controls function normally;
especially that the dosage control properly adjusts the
intensity of the laser output in a stable manner. Also,
determine that the treatment time control actually terminates
the laser output when the timer reaches zero.
Ultrasound should be routinely checked before each use to
determine that all controls function normally, especially that
the intensity control does properly adjust the intensity of the
ultrasonic power output in a stable manner. Also, determine
that the treatment time control does actually terminate
ultrasonic power output when the timer reaches zero.
DO NOT use sharp objects such as a pencil point or ballpoint
pen to operate the buttons on the control panel as damage
may result.
Use of controls or adjustments or performance of procedures
other than those specified herein may result in hazardous
exposure to laser energy.
Handle all Applicators with care. Inappropriate handling of
the Laser Applicator may adversely affect its characteristics.
Inspect Laser Applicator, Lenses, Cables, and associated
connectors before each use. Do not use a damaged or
otherwise compromised Laser Applicator.
This unit should be operated, transported and stored in
temperatures between 59° F and 104° F (15° C and 40° C),
with Relative Humidity ranging from 30%-60%.
Where the integrity of the external protective earth conductor
arrangement is in doubt, equipment shall be operated from
its internal electrical power source.
DO NOT permit any foreign materials or liquids to enter the
unit. Take care to prevent any foreign materials including, but
not limited to, inflammables, water, and metallic objects from
entering the unit. These may cause unit damage, malfunction,
electrical shock, fire, or personal injury.
Before each use, inspect Ultrasound Applicator for cracks,
which may allow the ingress of conductive fluid.
Inspect all cables and associated connectors before
each use.
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 other devices in the vicinity. However,
there is no guarantee that interference will not occur in
a particular installation. Harmful interference to other
devices can be determined by turning this equipment on
and off. Try to correct the interference using one or more
of the following: reorient or relocate the receiving device,
increase the separation between the equipment, connect
the equipment to an outlet on a different circuit from that
to which the other device(s) are connected and consult the
factory field service technician for help.
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The Vectra Genisys Therapy System, the Intelect Legend XT
Therapy System and the Intelect Vet Therapy System are not
designed to prevent the ingress of water or liquids. Ingress
of water or liquids could cause malfunction of internal
components of the system and therefore create a risk of
injury to the patient.
Nylatex® Wraps contain dry natural rubber and may cause
allergic reactions in patients with allergies to latex.
Use of parts or materials other than Chattanooga Group's
can degrade minimum safety.
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U.S.A. Federal Law restricts these devices to sale by, or on
the order of, a physician or licensed practitioner. This device
should be used only under the continued supervision of a
physician or licensed practitioner.
Make certain the unit is electrically grounded by connecting
only to a grounded electrical service receptacle conforming
to the applicable national and local electrical codes.
This device should be kept away from children.
Care must be taken when operating this equipment around
other equipment. Potential electromagnetic or other
interference could occur to this or to the other equipment.
Try to minimize this interference by not using other
equipment in conjunction with it.
This equipment is not designed to prevent the ingress of water
or liquids. Ingress of water or liquids could cause malfunction
of internal components of the system and therefore create a
risk of injury to the patient.
Do not drop the applicator or unit on hard surfaces. Do not
cool an overheated applicator with ice water or ice packs. Do
not allow the applicator to reach maximum temperatures
repeatedly. Do not submerge the applicator or unit in water.
All of these conditions will damage the applicator and unit.
Damage resulting from these conditions is not covered under
the warranty.
The safety of TENS waveforms for use during pregnancy or
birth has not been established.
TENS is not effective for pain of central origin. (This includes
headache.)
TENS should be used only under the continued supervision
of a physician or licensed practitioner.
TENS waveforms have no curative value.
TENS is a symptomatic treatment, and as such, suppresses
the sensation of pain which would otherwise serve as a
protective mechanism.
Electronic monitoring equipment (such as ECG monitors
and ECG alarms) may not operate properly when TENS
stimulation is in use.
In the event that an Error message or Warning appears
beginning with a 2 or 3, immediately stop all use of the
system and contact the dealer or Chattanooga Group for
service. Errors and Warnings in these categories indicate an
internal problem with the system that must be tested by
Chattanooga Group or a Field Service Technician certified
by Chattanooga Group before any further operation or
use of the system. Use of a system 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
system.
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