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OMNISTIM

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 FX

2

 CYCLE / WALK PROFESSIONAL USER MANUAL 

 

COPYRIGHT © 2011 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED 

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ELECTROTHERAPY WARNINGS & PRECAUTIONS 

 

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 note that Accelerated Care Plus cannot provide medical advice. If you have specific medical 
questions, please contact your healthcare professional. 

 

Warnings 

 

 

The long-term effects of electrical stimulation are unknown; 

 

Do not apply stimulation over the patient’s neck because this could cause severe muscle spasms resulting in 
closure of the airway, difficulty in breathing, or adverse effects on heart rhythm or blood pressure 

 

Do not apply stimulation across the patient’s chest because the introduction of electrical current into the chest 
may cause rhythm disturbances to the patient’s heart, which could be lethal.  Stimulation should not be applied 
transthoracically in the vicinity of the heart, as introduction of electrical current into the heart may cause cardiac 
arrhythmias. 

 

Do not apply stimulation when the patient is in the bath or shower 

 

Do not apply stimulation while the patient is sleeping; and 

 

Do not apply stimulation while the patient is driving, operating machinery, or during any activity in which 
electrical stimulation can put the patient at risk of injury. 

 

Consult with the patient’s physician before using this device because the device may cause lethal rhythm 
disturbances to the heart in susceptible individuals 

 

Apply stimulation only to normal, intact, clean, healthy skin. 

 

Do not operate this device until the User Manual, including all Indications for Use, Contraindications, Warnings 
and Precautions, have been carefully read and understood. 

 

Operation of this device or placement of lead wires, probes, pads and electrodes in close proximity (less than 5 
feet) to an operating shortwave or microwave diathermy unit may produce instability in the device output or 
burns at the treatment site.   Lead wires and device can pick up the magnetic field output of the diathermy and 
through induction convert it into an electrical field, transmit the energy into the patient increasing the current 
density at the electrodes of applicators.  Since the patient may not feel the 27 MHz frequency, they lack the 
protective sensation and tissue burns could result.  Short-wave field could potentially damage or reset medical 
devices in close proximity to the drum applicator. 

 

Treatment should not be applied over the carotid sinus nerves, (located in the anterior neck triangle), including, 
stellate ganglion, vagus nerve, or laryngeal or pharyngeal muscle.   Particular care should be taken for patients 
with a known sensitivity to the carotid sinus reflex, as carotid sinus stimulation may alter blood pressure and 
cardiac contractility. 

 

Do not apply treatment over testes, heart or eyes.  Electrical stimulation may affect organ function. 

 

Do not apply over or in close proximity to active cancer (except in terminal / palliative / hospice care), as 
therapy may increase blood flow to the tumor. 

 

Treatment should not be applied when high fever is present over swollen, severe infection (osteomyelitis, 
sepsis, tuberculosis, etc.) or inflamed areas/skin eruptions (phlebitis, thrombophlebitis, varicose veins, etc.). 

 

Do not apply over the lumbar or abdominal region, or over the uterus during pregnancy (to prevent uterine 
contraction), or during menstruation as therapy may temporarily increase menstrual flow. 

 

Treatment  should  not  be  applied  transcranially.

  Since  the  effects  of  stimulation  of  the  brain  are  unknown, 

stimulation should not be applied across the head, and electrodes should not be placed on opposite sides of the 
head; 

 

Stimulation should not be applied to patients connected to patient monitoring equipment, as the stimulation may 
have an effect on the proper operation of the monitoring equipment. 

 

Stimulation should not be applied directly over external stimulator systems with lead wires 

 

Neuromuscular electrical stimulation (NMES) should not be applied directly over or in close proximity to Deep 
Vein Thrombosis (DVT), as it activates the muscle and causes muscle contractions.  This should be avoided in 
tissue following an acute DVT when the thrombosis is not completely resolved.  Therapists should follow the 
guidelines provided by the referring physician on recommended activity level and modality use.  If the patient is 

Summary of Contents for OMNISTIM FX2 CYCLE/WALK

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Page 3: ...ed lease agreement This manual may not be used for any other purpose Any additional copies of the Manual shall be ordered from ACP No changes or modifications shall be made to the Manual without prior...

Page 4: ...py Therapeutic Ultrasound Pulsed Shortwave Diathermy devices and advanced Therapeutic Exercise Systems Our MEGAPULSE NEUROPROBE OMNISTIM OMNISOUND OMNICYCLE OMNIVR OMNISTAND OMNIVERSA OMNISWD and SYNC...

Page 5: ...anying documents Caution electrical precautions Remote Control connection CE mark of confidence compliant to MDD 93 42 EEC Connection Electrode Cable IP2X Classification against intrusion of water dus...

Page 6: ...ttings 11 Professional Programming Sequence 11 Program Counters 11 Operational Sequence 12 Electrode Application Techniques 16 Treatment Preparation 17 INFECTION CONTROL EQUIPMENT AND PRINCIPLES OF US...

Page 7: ...ectrical 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...

Page 8: ...he diathermy and through induction convert it into an electrical field transmit the energy into the patient increasing the current density at the electrodes of applicators Since the patient may not fe...

Page 9: ...ed schedules A potential electric shock hazard exists once the device outer casing has been in part or fully removed Only qualified service personnel should perform Service and repairs Warranty will b...

Page 10: ...ontraction may disrupt the healing process Caution should be used for patients with suspected or diagnosed epilepsy Patients with suspected or diagnosed epilepsy should follow precautions recommended...

Page 11: ...e was to be delivered Retain the original shipping container and inserts for validation of damage claim or use at a later date Unpack and check all accessories A list of enclosed accessories is provid...

Page 12: ...is used to adjust the intensity level of channel A 5 Output Adjustment Channel B is used to adjust the intensity level of channel B 6 Channel A Connection plug the green marked lead into the green cha...

Page 13: ...ress the Program Button B 3 once to select WALK then press and hold for 5 seconds to enter the programming mode In the programming mode the program setting for RPM will flash Use the buttons 5 to incr...

Page 14: ...ling or walking The stimulation is intended to provide sensory input and comfortable motor activation to re educate muscle movement or treat disuse atrophy of the muscles a Increase decrease 4 Output...

Page 15: ...n the back of the unit 2 Connect lead wires to corresponding bar code under the display window green lead wire in the left input blue lead in the right input 3 Wash the skin with water use soap if dir...

Page 16: ...E To re adjust stimulation intensity remove the lock by pressing Button and then Button to preferred level 9 Treatment is completed when bars appear in the Display Window 10 Remove the stimulation ele...

Page 17: ...ROFESSIONAL USER MANUAL 15 COPYRIGHT 2011 2017 ACCELERATED CARE PLUS CORP ALL RIGHTS RESERVED 12 Clean unit with ACP Germicidal Wipes 13 Store the device in carry case 14 Record treatment activity and...

Page 18: ...t etc If sitting balance is poor have the patient supported during cycling If joint pathology is present establish the correct joint range of motion by altering the seat to pedal L E or shoulder to pe...

Page 19: ...ons Therefore use additional electrode stimulation sites to decrease or eliminate skin irritation on electrically sensitive patients If skin irritation persists with alternate site applications decrea...

Page 20: ...ed per facility infection control policy ACP recommends the following guidelines Cleaning and Low Level Disinfection This is a recommended daily housekeeping practice to keep the equipment clean and f...

Page 21: ...ds 2 Apply Intermediate Level Disinfection prior to barrier application 3 Select tear or cut with clean scissors a length of barrier film to fit over the operator surfaces of the OMNISTIM FX2 CYCLE WA...

Page 22: ...e medium Remove electrode s and replace if necessary Patient cannot detect output Failure of lead wire s electrode s You may not be using enough gel or the gel is dried out Device failure Replace with...

Page 23: ...ment to treatment in non volatile memory System Architecture CMOS integrated micro controller with on board memory and instruction set PENS PATTERNED ELECTRICAL NEUROMUSCULAR STIMULATION PROGRAMS Wave...

Page 24: ...mmable stimulation with CYCLE and WALK programs 28126 OMNISTIM FX2 CYCLE WALK Hard Carry Case 59762 9V Alkaline battery 38155 2x2 Reusable E stim Electrodes 4ea pkg 61227 2x4 Reusable E stim Electrode...

Page 25: ...TIME PROGRAM Cycle or Walk and RPM BUTTON A B INTENSITY 1 to 100 COMMENTS TWITCH OR TINGLE ELECTRODE PLACEMENT GUIDE Provide the patient with the Patient Electrode Placement Guide and indicate the el...

Page 26: ...cluding serial number alteration Note Use of the Equipment with accessories and or supplies not approved by ACPL for use with the Equipment may void the warranty if such accessory or supply item cause...

Page 27: ...e for any loss or damage to the Equipment prior to receipt at the ACP Service Center Equipment returned for warranty service must be shipped complete with all accessories except for manuals in its ori...

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