OMNISTIM® FX2 PRO USER MANUAL 5COPYRIGHT © 2004 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVEDELECTROTHERAPY INDICATIONS & CONTRAINDICATIONSCAUTION: Federal law restricts this device for sale or use by or on the order of a Practitionerlicensed 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 specificmedical questions, please contact your healthcare professional.IndicationsThe Omnistim FX2 Pro 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 themanagement 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 forthe treatment of medical diseases and conditions.Contraindications Do not use this device on patients who have a cardiac pacemaker, implanted defibrillator, or otherimplanted 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 MuscleStimulation over metal implants. Never connect lead wires to the power line or electro-surgery equipment. Use only the lead wiresrecommended or approved by the manufacturerAdverse Reactions Skin irritation and burns, beneath the electrodes; have been reported with the use of powered musclestimulators. Patients may experience skin irritation and burns beneath the stimulation electrodes applied tothe skin. Patients may experience headache and other painful sensations during or following the application ofelectrical 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 adversereactions from the device.