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  10 

OMNISTIM

®

 FX

2

 CYCLE / WALK PROFESSIONAL USER MANUAL 

 

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

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Controls and Functions 

 

 

(1)

 

Main Power Switch – is used to turn the device 
on and/or off. 

(2)

 

Program  Button  A  –  is  used  to  select  the  first 
program prescribed. 

(3)

 

Program Button B – is used to select the second 
program prescribed. 

(4)

 

Output Adjustment Channel A – 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 channel which corresponds to 
the Program Button “A” being used. 

(7)

 

Channel  B  Connection  –  plug  the  blue  marked 
lead  into  the  blue  channel  which  corresponds  to 
the Program Button “B” being used.  

(8)

 

Display  –  displays  program  information  and 
intensity readings. The A and B at the top of the 
display mark the channels. 

(9)

 

Battery  Compartment  –  this  is  where  the  9-volt 
battery is located. 

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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