Accelerated Care Plus OMNISTIM FX2 CYCLE/WALK, Руководство пользователя

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OMNISTIM
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FX
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CYCLE / WALK PROFESSIONAL USER MANUAL 5
COPYRIGHT © 2011 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
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ELECTROTHERAPY INDICATIONS & CONTRAINDICATIONS
CAUTION: Federal law restricts this device for sale or use by or on the order of a Practitioner
licensed by the laws of the state in which he/she practices to use or order the use of the device.
Please notice that Accelerated Care Plus cannot provide medical advice. If you have specific
medical questions, please contact your healthcare professional.
Indications
The Omnistim Cycle/Walk is indicated for:

Relaxation of muscle spasms

Re-Education of muscle

Prevention or retardation of disuse atrophy

Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis

Increase local circulation

Maintaining or increasing range of motion

Symptomatic relief and management of chronic intractable pain and as an adjunctive treatment in the
management of acute pain, post-surgical pain and pain associated with post-traumatic injury.
Electrical muscle stimulator devices should only be used under medical supervision for adjunctive therapy for the
treatment of medical diseases and conditions.
Contraindications

Do not use this device on patients who have a cardiac pacemaker, implanted defibrillator, or other implanted
metallic or electronic device because this may cause electric shock, burns, electrical interference, or death.
Note:
There is no contraindication to the application of Transcutaneous Electrical Stimulation or Powered Muscle
Stimulation over metal implants.

Never connect lead wires to the power line or electro-surgery equipment. Use only the lead wires
recommended or approved by the manufacturer
Adverse Reactions

Skin irritation and burns, beneath the electrodes, have been reported with the use of powered muscle
stimulators.
Patients may experience skin irritation and burns beneath the stimulation electrodes applied to
the skin.

Patients may experience headache and other painful sensations during or following the application of
electrical stimulation near the eyes and to the head and face.

Patients should stop using the device and should consult with their physicians if they experience adverse
reactions from the device.