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OMNISTIM

®

FX

2

PORTABLE PENS PATIENT USER MANUAL

COPYRIGHT © 2008 - 2021, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED

TABLE OF CONTENTS

ELECTROTHERAPY INDICATIONS & CONTRAINDICATIONS .................... 3

Indications ........................................................................................................................................... 3
Contraindications ................................................................................................................................ 3
Adverse Reactions .............................................................................................................................. 3
Warnings ............................................................................................................................................. 4
Precautions .......................................................................................................................................... 5

THE OMNISTIM® FX2 PORTABLE PENS ...................................................... 7

Delivery of the Omnistim® FX2 Portable PENS ............................................................................... 7
Introduction ......................................................................................................................................... 7
Controls and Functions ....................................................................................................................... 8
Patient Operational Sequence ............................................................................................................. 9

TREATMENT PREPARATION ......................................................... 13

Treatment Site / Skin Inspection ....................................................................................................... 13
ACP Reusable Pre-gelled Surface Electrodes .................................................................................. 13
Lead Wires ........................................................................................................................................ 13

CLEANING ..................................................................................................... 14
TROUBLESHOOTING .................................................................................... 14
TECHNICAL SPECIFICATIONS .................................................................... 15
STANDARD AND OPTIONAL ACCESSORIES ............................................ 16
TREATMENT CHART .................................................................................... 17
STANDARD LIMITED PRODUCT WARRANTY ............................................ 17

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Summary of Contents for OMNISTIM FX2

Page 1: ... 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 review and written authorization from ACP No authorization is given to market sell disclose or exploit this Manual except as for purposes of using the Equipment as contemplated by the Lease Agreement ACCELERATED CARE PLUS MAKES NO WARRANTY ...

Page 2: ......

Page 3: ...utic Ultrasound Pulsed Shortwave Diathermy devices and advanced Therapeutic Exercise Systems Our OMNISTIM OMNICYCLE OMNIVR OMNISTAND OMNIVERSA OMNISWD and SYNCHRONY represent the most recent worldwide advances available for therapeutic application of electromedical devices and other rehabilitation technology ACP is internationally recognized for its contribution to research in the development of m...

Page 4: ...nings 4 Precautions 5 THE OMNISTIM FX2 PORTABLE PENS 7 Delivery of the Omnistim FX2 Portable PENS 7 Introduction 7 Controls and Functions 8 Patient Operational Sequence 9 TREATMENT PREPARATION 13 Treatment Site Skin Inspection 13 ACP Reusable Pre gelled Surface Electrodes 13 Lead Wires 13 CLEANING 14 TROUBLESHOOTING 14 TECHNICAL SPECIFICATIONS 15 STANDARD AND OPTIONAL ACCESSORIES 16 TREATMENT CHAR...

Page 5: ...ive treatment in the management of acute pain post surgical pain and pain associated with post traumatic injury Electrical muscle stimulator devices should be used under medical supervision for adjunctive therapy for the treatment of medical diseases and conditions Contraindications 1 Do not use this device on patients who have a cardiac pacemaker implanted defibrillator or other implanted metalli...

Page 6: ...oximity 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...

Page 7: ...es 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 to...

Page 8: ...lter 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 Caution should be used over areas of body where circulation is impaired or which lack normal sensation Absent or diminished sensation shou...

Page 9: ...as to be delivered Retain the original shipping container and inserts for validation of damage claim or use at a later date Introduction The Omnistim FX2 Portable PENS provides Patterned Electrical Neuromuscular Stimulation PENS which is a form of stimulation that replicates the correct firing patterns of muscles agonist and antagonist or reciprocal muscle pairs in Upper and Lower Extremity Tripha...

Page 10: ...s 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 Connections plug the blue marked lead into the blue channel which corresponds to the Program Button B being used 8 Display displays...

Page 11: ... Program Button A 2 7 Apply electrodes to treatment area prescribed by your physician or therapist 8 Adjust stimulation intensity to level prescribed by your physician or therapist a Increase decrease 4 Output A Press button to increase intensity in channel A Press the button to decrease intensity in channel A NOTE If the channel indicator flashes or you see this symbol you must reset the output l...

Page 12: ...il pouch electrodes and follow the directions on the label for electrode care and storage NOTE If you are using single use electrodes discard after each use 12 Clean unit with ACP Germicidal Wipes 13 Store unit in carrying case 14 Record treatment activity and setting on form provided 1 Install battery in compartment located on the back of the unit 2 Connect lead wires to corresponding bar code un...

Page 13: ...A or Program Button B as directed by your physician or therapist 7 Apply electrodes to treatment area prescribed by your physician or therapist 8 Adjust stimulation intensity to level prescribed by your physician or therapist NOTE To readjust 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 ...

Page 14: ...useable electrodes into their foil pouch electrodes and follow the directions on the label for electrode care and storage NOTE If you are using single use electrodes discard after each use 11 Turn the unit off by pressing the Power Button 12 Clean unit with ACP Germicidal Wipes 13 Store the device in carry case 14 Record treatment activity and setting on form provided ...

Page 15: ...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 decrease the treatment times and lower the intensities if necessary discontinue treatment If an allergic reaction is suspected attempt to identify and change the allergic substance s If skin irritation pers...

Page 16: ...ed measures do not correct the machine malfunction call your physician for assistance PROBLEM CAUSE REMEDY Unit will not power on No batteries Low batteries Install batteries Replace batteries Verify type of batteries Inspect battery contacts Display shows low battery symbol Battery voltage is too low Replace batteries for future use Channel indicator flashing and caution symbol is displayed Batte...

Page 17: ...nstruction set STIMULATION SYSTEM Output Constant current up to maximum preset current limit of 60mA into a 500 ohm load PENS PATTERNED ELECTRICAL NEUROMUSCULAR STIMULATION PROGRAMS Waveform Asymmetric Biphasic Pulsed Current 0 60mA average single pulsecurrentintoa 500 ohm load Phase Duration Set at 70µs Variable from 50µs to 120µs Pulse Rate Set at 50 Hz burst pattern TENS MEDIUM FREQUENCY CURREN...

Page 18: ...4747 9V Alkaline battery 38155 2x2 Reusable E stim Electrodes 4 ea pkg 10 pkg bx 61227 2x4 Reusable E stim Electrodes 4 ea pkg 10 pkg bx https acplus com acp technology user manuals OMNISTIM FX2 PORTABLE PENS Professional User Manual https acplus com acp technology user manuals OMNISTIM FX2 PORTABLE PENS Patient User Manual Infection Control Supplies ITEM ITEM NO DESCRIPTION 55536 Super Sani Cloth...

Page 19: ...NS 1 2 3 TENS 1 2 3 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 electrode placement for each treatment prescribed Mark each electrode location with or sign to indicate the polarity of the electrodes or use red and black marker to identify the color code for each wire Red represents...

Page 20: ... be void if any of the following have occurred 1 The product contains repairs orreplacement parts not furnished by ACP 2 Theproduct isdamaged resulting frommisuse ornegligence 3 The product has been tampered with and or altered includingserial number alteration Note UseoftheEquipmentwithaccessoriesand orsuppliesnotapprovedbyACPLforusewith the Equipment may void the warranty if such accessory or su...

Page 21: ...ipping charges and related costs to return the unit to the customer provided repair is deemed to be under warranty ACP is not responsible 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 original packing or equivalent so as not to be damaged while in tra...

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