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OMNISTIM

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 FX

2

 CYCLE / WALK PROFESSIONAL USER MANUAL 

  7 

 

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

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not permitted exercise, NMES therapy should be avoided.  Generally, NMES over a DVT of six weeks or less 
should be avoided altogether. 
 

Precautions 

 

 

The safety of electrical stimulation during pregnancy has not been established; 

 

Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical 
conductive medium. The irritation can usually be reduced by using an alternate conductive medium, or alternate 
electrode placement. 

 

Application site and settings should be based on the guidance of the prescribing practitioner. 

 

All equipment and accessories should be kept out of the reach of children or unqualified persons. 

 

Do not connect  this device to any  wall outlet  that  has  not  been properly grounded, or to any electrically  non-
isolated  medical  device 

Powered  muscle  stimulators  should  be  used  only  with  the  leads  and  electrodes 

recommended  for  use  by  the  manufacturer.  Use  this  device  only  with  the  leads,  electrodes,  and  accessories 
recommended by the manufacturer.

 Use only ACP specified accessories and/or supplies with ACP devices. Do 

not use any power cords, or power supplies, other than the ones provided or specified for this device. Use of any 
other power supply could seriously damage the device and will void the warranty. 

 

The use of conductive mediums other than specifically approved pre-gelled or self-adhering electrodes such as 
ultrasound  gel  or  lotion,  hand  or  body  lotion,  electrolyte  spray  mist,  paper  towels,  non-approved  reusable  or 
disposable pre-gelled or self-adhering electrodes—are not advised for use with Omnistim Cycle/Walk Systems. 

 

When cleaning the device, never immerse them or wash them with water. See the infection control section in this 
manual for cleaning instructions. Devices should not be submerged in water or other liquids. 

 

Failure  to  follow  the  manufacturer’s  prescribed  maintenance  for  this  device  may  lead  to  device  failure  and 
transient or unreliable performance.  State and federal survey and JCAHO require all equipment to be maintained 
and calibrated according to the manufacturer recommended 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 be voided if the outer casing has 
been removed or tampered with. 

 

Use caution when the patient has a tendency to bleed internally, such as following an injury or fracture. 

Do not 

apply over areas of hemorrhage or active bleeding.  

 

Inspect and cleanse the skin prior to application.  Following treatment check the skin for evidence of irritation or 
burns, and if present, treat as appropriate.  If the patient has, or complains of, skin irritation following treatment; 
shorten  the  treatment  time  on  the  next  treatment  session,  or  use  an  alternative  type  of  therapy  or  electrode 
placement. 

 

Gradually increase the output intensity/power to required dose or patient tolerance while monitoring the device 
display. 

 

Caution  should  be  taken  with  patient  exhibiting  psychological  or  physical  hypersensitivity  to  the  therapeutic 
treatment. Several attempts should be made to place them at ease so that their confidence and cooperation can be 
gained during the treatment. 

 

The treatment area should be checked from time to time, and if there is evidence of, or if the patient complains 
of, pain during treatment, adjust the output downward until it is tolerated by the patient.  If the patient continues 
to complain of pain, discontinue the treatment and shorten the treatment time on the next treatment session, or 
use an alternative type of therapy or electrode placement. 

 

Do not apply treatment directly over/under hot or cold packs.  Caution is recommended when treatment follows 
the application of hot or cold therapy, which may alter the patient’s sensation.  Application of thermal agents over 
areas of impaired circulation should be performed with caution as the circulation may be insufficient to heat or 
cool the tissue, altering the patient’s perception of warmth and pain, and burns or tissue necrosis may result from 
subsequent treatment. 

 

Caution is recommended when treatment follows the application of medicated patches, salves, or creams which 
may alter the patient’s sensation.  If there is a medical necessity to perform such treatments, these patients should 
be monitored diligently during application.  The effect of electrical stimulation may be altered by the presence of 
these materials on the patient’s skin. 

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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