Intelect Legend XT Therapy System User Manual

TABLE OF CONTENTS

Intelect® Legend XT Therapy System

FOREWORD... 1 PRODUCT DESCRIPTION... 1 ABOUT INTELECT LEGEND XT... 2 STANDARD PRECAUTIONARY INSTRUCTIONS... 2 Caution... 2 Warning... 2 Danger... 2 Dangerous Voltage... 2 Corrosive... 2 Spontaneous Combustion... 2 Biohazardous Materials... 2 CAUTIONS... 3 WARNINGS... 4 DANGERS... 6 ELECTROTHERAPY INDICATIONS, CONTRAINDICATIONS, AND ADVERSE EFFECTS... 7 Indications for Russian, TENS, High Voltage Pulsed Current (HVPC), Interferential and Premodulated waveforms... 7 Additional Indications for Microcurrent, Interferential, Premodulated, and TENS waveforms... 7 Contraindications... 7 Additional Precautions... 8 Adverse Effects... 8 ULTRASOUND INDICATIONS AND CONTRAINDICATIONS... 9 Indications for Ultrasound... 9 Contraindications... 9 Additional Precautions... 9 NOMENCLATURE... 10

INTELECT LEGEND XT ELECTROTHERAPY AND COMBINATION THERAPY SYSTEMS... 10 Two Channel Electrotherapy System...10 Two Channel Combination System...10 Front Access Panel...11 Rear Access Panel...11 USER INTERFACE... 12 SYMBOL DEFINITIONS... 13 System Hardware Symbols...13 System Software Symbols...13 Optional Module and Accessory Symbols...13 Operator Remote...13 Battery Module...13 Channel 3/4 Electrotherapy Module...13 GENERAL TERMINOLOGY... 14 ULTRASOUND... 14 SPECIFICATIONS... 15 SYSTEM SPECIFICATIONS... 15 DIMENSIONS... 15 Width...15 Standard Weight...15 Power (Combination and Electrotherapy Units)...15 Electrical Type...15 Regulatory Compliance...15 WAVEFORM SPECIFICATIONS... 16 IFC- Interferential (Traditional 4 Pole)...16 Russian...16 TENS- Symmetrical Biphasic...17 Microcurrent...17

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TABLE OF CONTENTS

Intelect® Legend XT Therapy System

Premodulated (Traditional 2 Pole IFC)...18 High Voltage Pulsed Current (HVPC)...18 ULTRASOUND SPECIFICATIONS... 19 Ultrasound...19 SETUP... 20 INTELECT LEGEND XT THERAPY SYSTEMS... 20 THERAPY SYSTEM SETUP... 21 Clinic Name...21 Restoring Default Protocols...22 Restoring Default Unit Settings...22 Erasing Patient Data Card...23 Setting Date and Time...23 Setting System Volume...24 Displaying Unit Version Information...24 Pad Contact Quality...25 Selecting Language...25 Connecting Accessories to the Therapy System...26 PATIENT PREPARATION... 27 ELECTROTHERAPY PATIENT PREPARATION... 27 Electrode Placement...27 DURA-STICK™ Electrodes...28 Reusable Carbon Electrodes...28 DURA-STICK™ Electrode Instructions...29 Connecting Lead Wires...29 Securing Electrodes...29 Reusable Carbon Electrodes...30 Connecting Lead Wires...30 Conductive Medium...30 Securing Electrodes...30

ULTRASOUND PATIENT PREPARATION... 31 Preparing Treatment Area...31 Size of Applicator...31 Applicator Preparation...31 Conductive Medium...31 Treatment Area...31 Applicator LED...31 OPERATION... 32 OPERATOR INTERFACE... 32 HOME SCREEN... 33 ELECTROTHERAPY SCREEN... 34 GENERAL ELECTROTHERAPY WAVEFORM SETUP... 35 Prepare Patient...35 Select Modality...35 Select Waveform...35 Edit Waveform Parameters...35 Installing Patient Interrupt Switch...36 Patient Interrupt Switch...36 Setting Waveform Intensity...36 Intensity Knob Rotation...36 Start Treatment...37 Pause Treatment...37 Stop Treatment...37 Save to Patient Data Card...37 ADJUSTING ELECTROTHERAPY CHANNEL PARAMETERS DURING TREATMENT... 38 Selecting Channel...38 Editing Channel Parameters...38 ULTRASOUND... 39

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TABLE OF CONTENTS

Intelect® Legend XT Therapy System

Preparing Patient...39 Selecting Modality...39 Editing Ultrasound Parameters...39 Head Warming...39 Setting Ultrasound Intensity...40 Intensity Knob Rotation...40 Starting Treatment...40 Pausing Treatment...40 Stopping Treatment...41 Saving to Patient Data Card...41 Editing Ultrasound from Home Screen...42 Editing Ultrasound from Treatment Review Screen...42 COMBINATION... 43 Preparing Patient...43 Selecting Modality...43 Accessing Combination Parameters...43 Editing Ultrasound Parameters...44 Selecting Waveform...44 Using the Patient Interrupt Switch...44 Editing Waveform Parameters...45 Setting Waveform Intensity...45 Intensity Knob Rotation...45 Setting Ultrasound Intensity...45 Intensity Knob Rotation...45 Starting Treatment...46 Pausing Treatment...46 Stopping Treatment...46 Saving to Patient Data Card...46

ADJUSTING COMBINATION PARAMETERS DURING TREATMENT... 47 Editing Waveform Parameters...47 Editing Ultrasound Parameters...47 PATIENT DATA CARD SETTING UP A NEW CARD... 48 General Information...48 Inserting New Patient Data Card...48 Setting up Treatment...48 Setting up a New Patient Data Card...48 Entering Patient ID...49 Accessing Electrode Placement...50 Setting up Electrodes...50 Electrode Placement...50 Accessing Pain Map...51 Selecting Pain Type...51 Adding Pain Locations...51 Selecting Location of Pain...52 Editing Pain Locations...52 Deleting Pain Locations...53 Pain Scales...53 Selecting Pain Scale...53 Adjusting Pain Scale...53 Saving to Patient Data Card...54 EXISTING PATIENT DATA CARD USE... 55 Inserting Existing Patient Data Card...55 Accessing Patient Data Card...55 Viewing Patient Data Card...55 Starting a New Treatment from Patient Data Card...56 Using the Patient Interrupt Switch...56

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TABLE OF CONTENTS

Intelect® Legend XT Therapy System Saving to Patient Data Card...63 INSTALLATION/REMOVAL... 64 INSTALLING THE CHANNEL 3/4 ELECTROTHERAPY AND NiMH BATTERY MODULE... 64 Nomenclature- Channel 3/4 Electrotherapy Module...65 Specifications...66 Waveform & Current Specifications...66 Disconnecting Mains Power...67 Removing Lead Wires and Accessories...67 Removing Therapy System from Cart...67 Releasing Ribbon Cable...68 Positioning Therapy System and Module...68 Connecting Ribbon Cable...68 Setting Therapy System onto Module...69 Securing Therapy System to Module...69 Attaching the Lanyard...69 Installing Lead Wires and Accessories...70 Installing Front Access Panel...70 Mounting to Therapy System Cart...70 Connecting Mains Power...70 Turning Therapy System On...71 REMOVING THE CHANNEL 3/4 ELECTROTHERAPY AND NiMH BATTERY MODULE... 72 Disconnecting Mains Power...72 Removing Lead Wires and Accessories...72 Removing Therapy System from Cart...72 Removing Screws Securing Module...73 Disconnecting Ribbon Cable at Module...73 Storing and Securing Ribbon Cable...73

Setting Intensity...56 Intensity Knob Rotation...56 Starting Treatment...57 Pausing Treatment...57 Erasing Patient Data Card...57 Stopping Treatment...57 CREATING USER PROTOCOLS... 58 General Information...58 Selecting Modality...58 Editing Modality Parameters...58 Selecting Clinical Resources Library...58 Entering User Protocol Name...59 DELETING USER PROTOCOLS... 60 General Information...60 Selecting Clinical Resources Library...60 Selecting User Protocol to Delete...60 Deleting User Protocol...60 USING USER PROTOCOLS... 61 Accessing User Protocols...61 Selecting User Protocol...61 Preparing Patient...61 Editing Modality Parameters...61 Using the Patient Interrupt Switch...62 Setting Modality Intensity...62 Intensity Knob Rotation...62 Starting Treatment...63 Pausing Treatment...63 Stopping Treatment...63

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TABLE OF CONTENTS

Intelect® Legend XT Therapy System Charging Temperature...84 BATTERY MODULE SERVICE LIFE... 85 STORING THE BATTERY MODULE... 85 Short Term Storage...85 Long Term Storage...85 TROUBLESHOOTING... 86 ERROR CODES... 86 General Information...86 REPLACEMENT ACCESSORIES... 90 GENERAL INFORMATION... 90 MAINTENANCE... 91 CARING FOR THE THERAPY SYSTEM... 91 Cleaning the Therapy System...91 Cleaning the Lens...91 CALIBRATION REQUIREMENTS... 91 Calibrating Ultrasound Applicators...91 FACTORY SERVICE... 91 WARRANTY... 92

Attaching the Lanyard...74 Installing Lead Wires and Accessories...74 Connecting Mains Power...74 Turning Therapy System On...75 GENERAL INFORMATION OPERATOR REMOTE... 76 Installing the Operator Remote...76 GENERAL INFORMATION THERAPY SYSTEM CART... 77 Nomenclature...77 Specifications...77 MOUNTING THERAPY SYSTEM TO THERAPY SYSTEM CART 78 Assembling the Therapy System Cart...78 Preparing the Therapy System Cart...78 Mounting Therapy System to Cart...78 Connecting Mains Power...79 Installing Storage Bins...79 Removing System from Therapy System Cart...79 OPTION OPERATION... 80 USING THE OPERATOR REMOTE... 80 Nomenclature...80 Operation...80 Storing the Operator Remote...81 USING THE THERAPY SYSTEM CART... 82 Nomenclature...82 Operation...82 USING THE NiMH BATTERY MODULE... 83 Nomenclature...83 CHARGING BATTERY MODULE... 84 When to Recharge...84

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FOREWORD

Intelect® Legend XT Therapy System

This manual has been written for the users of the Intelect Legend XT Therapy Systems. It contains general information on the operation, precautionary practices, and maintenance information. In order to maximize use, efficiency, and the life of the system, please read this manual thoroughly and become familiar with the controls, as well as the accessories before operating the system. This manual contains general safety, operating, maintenance, and care instructions as well as installation instructions for the optional Therapy System Cart, Channel 3/4 Electrotherapy and NiMH Battery for the users of the Intelect Legend XT Therapy two channel electrotherapy and combination systems. Specifications put forth in this manual were in effect at the time of publication. However, owing to Chattanooga Group's policy of continual improvement, changes to these specifications may be made at any time without obligation on the part of Chattanooga Group. Before administering any treatment to a patient, the users of this equipment should read, understand and follow the information contained in this manual for each mode of treatment available, as well as the indications, contraindications, warnings and precautions. Consult other resources for additional information regarding the application of electrotherapy and ultrasound. PRODUCT DESCRIPTION The Intelect Legend XT Therapy Systems are two channel electrotherapy and combination systems with the option of adding additional channels of electrotherapy by installation of the optional Channel 3/4 Electrotherapy Module. Other optional modality modules are available for separate purchase and may be installed by the end user. Stay current with the latest clinical developments in the field of electrotherapy and ultrasound. Observe all applicable precautionary measures for treatment. Keep informed of appropriate indications and contraindications for the use of electrotherapy and ultrasound. This equipment is to be used only under the prescription and supervision of a licensed practitioner.

©2005 Encore Medical Corporation or its affiliates, Austin, Texas, USA. Any use of editorial, pictorial, or layout composition of this publication without express written consent from Chattanooga Group of Encore Medical, L.P. is strictly prohibited. This publication was written, illustrated, and prepared for distribution by Chattanooga Group of Encore Medical, L.P.

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ABOUT INTELECT LEGEND XT

Intelect® Legend XT Therapy System

STANDARD PRECAUTIONARY INSTRUCTIONS The precautionary instructions found in this section and throughout this manual are indicated by specific symbols. Understand these symbols and their definitions before operating this equipment. The definition of these symbols are as follows: Dangerous Voltage Text with a “Dangerous Voltage” indicator serves to inform the user of possible hazards resulting in the electrical charge delivered to the patient in certain treatment configurations of TENS waveforms.

Caution Text with a “CAUTION” indicator will explain possible safety infractions that could have the potential to cause minor to moderate injury or damage to equipment.

Corrosive Text with a “CORROSIVE" indicator will explain possible safety infractions if the chemical components of the battery are exposed to air, skin, or other materials. Spontaneous Combustion Text with a “SPONTANEOUS COMBUSTION" indicator will explain possible safety infractions that could create conditions for a Spontaneous Combustion if the material is mishandled and not disposed of properly. Biohazardous Materials Text with a “BIOHAZARD” indicator serves to inform the user of possible hazards resulting in improper handling of components and accessories that have come in contact with bodily fluids. NOTE: Throughout this manual, “NOTE” may be found. These Notes are helpful information to aid in the particular area or function being described.

Warning Text with a “WARNING” indicator will explain possible safety infractions that will potentially cause serious injury and equipment damage.

Danger Text with a “DANGER” indicator will explain possible safety infractions that are imminently hazardous situations that would result in death or serious injury.

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ABOUT INTELECT LEGEND XT

Intelect® Legend XT Therapy System

CAUTIONS

• Inspect Applicator cables and associated connectors before

• Read, understand, and practice the precautionary and operating

each use.

instructions. Know the limitations and hazards associated with using any electrical stimulation or ultrasound device. Observe the precautionary and operational decals placed on the unit. • DO NOT operate the Intelect Legend XT Therapy System when connected to any unit other than Chattanooga Group devices. • DO NOT operate this unit in an environment where other devices are being used that intentionally radiate electromagnetic energy in an unshielded manner. • Ultrasound should be routinely checked before each use to determine that all controls function normally, especially that the intensity control does properly adjust the intensity of the ultrasonic power output in a stable manner. Also, determine that the treatment time control does actually terminate ultrasonic power output when the timer reaches zero. • DO NOT use sharp objects such as a pencil point or ballpoint pen to operate the buttons on the control panel. • This unit should be operated, transported and stored in temperatures between 59° F and 104° F (15° C and 40° C), with Relative Humidity ranging from 30%-60%. • Handle Ultrasound Applicator with care. Inappropriate handling of the Ultrasound Applicator may adversely affect its characteristics. • Before each use, inspect Ultrasound Applicator for cracks, which may allow the ingress of conductive fluid.

• The Intelect Legend XT Therapy System is not designed to prevent the ingress of water or liquids. Ingress of water or liquids could cause malfunction of internal components of the system and therefore create a risk of injury to the patient. • This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to other devices in the vicinity. However, there is no guarantee that interference will not occur in a particular installation. Harmful interference to other devices can be determined by turning this equipment on and off. Try to correct the interference using one or more of the following: reorient or relocate the receiving device, increase the separation between the equipment, connect the equipment to an outlet on a different circuit from that to which the other device(s) are connected and consult the factory field service technician for help. • The Nylatex® Wraps shipped with this unit contain dry natural rubber and may cause allergic reactions in patients with allergies to latex.

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ABOUT INTELECT LEGEND XT

Intelect® Legend XT Therapy System

WARNINGS

• U.S.A. Federal Law restricts these devices to sale by, or on the order

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

of, a physician or licensed practitioner. This device should be used only under the continued supervision of a physician or licensed practitioner. • For continued protection against fire hazard, replace fuses only with ones of the same type and rating. • Make certain the unit is electrically grounded by connecting only to a grounded electrical service receptacle conforming to the applicable national and local electrical codes. • Care must be taken when operating this equipment around other equipment. Potential electromagnetic or other interference could occur to this or to the other equipment. Try to minimize this interference by not using other equipment in conjunction with it. • The safety of TENS waveforms for use during pregnancy or birth has not been established. • TENS is not effective for pain of central origin. (This includes headache.) • TENS should be used only under the continued supervision of a physician or licensed practitioner. • TENS waveforms have no curative value. • TENS is a symptomatic treatment, and as such, suppresses the sensation of pain which would otherwise serve as a protective mechanism. • The user must keep the device out of the reach of children. • Electronic monitoring equipment (such as ECG monitors and ECG alarms) may not operate properly when TENS stimulation is in use.

electrodes recommended for use by the manufacturer.

• In the event that an Error message or Warning appears beginning with a 2 or 3, immediately stop all use of the system and contact the dealer or Chattanooga Group for service. Errors and Warnings in these categories indicate an internal problem with the system that must be tested by Chattanooga Group or a Field Service Technician certified by Chattanooga Group before any further operation or use of the system. Use of a system that indicates an Error or Warning in these categories may pose a risk of injury to the patient, user or cause extensive internal damage to the system. • Use of controls or adjustments or performance of procedures other than those specified herein may result in hazardous exposure to ultrasonic energy. • Before administering any treatment to a patient you should become acquainted with the operating procedures for each mode of treatment available, as well as the indications, contraindications, warnings, and precautions. Consult other resources for additional information regarding the application of Electrotherapy and Ultrasound. • To prevent electrical shock, disconnect the unit from the power source before attempting any maintenance procedures. • Keep electrodes separated during treatment. Electrodes in contact with each other could result in improper stimulation or skin burns. • Long term effects of chronic electrical stimulation are unknown.

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ABOUT INTELECT LEGEND XT

Intelect® Legend XT Therapy System

WARNINGS (continued)

• Stimulation should not be applied over the anterior neck or mouth. Severe spasm of the laryngeal and pharyngeal muscles may occur and the contractions may be strong enough to close the airway or cause difficulty in breathing. • Stimulation should not be applied transthoracically in that the introduction of electrical current into the heart may cause cardiac arrhythmia. • Stimulation should not be applied over swollen, infected, and inflamed areas or skin eruptions, e.g., phlebitis, thrombophlebitis, varicose veins, etc. • Stimulation should not be applied over, or in proximity to, cancerous lesions. • Output current density is related to electrode size. Improper application may result in patient injury. If any question arises as to the proper electrode size, consult a licensed practitioner prior to therapy session. • The Intelect Legend XT Therapy System optional modules and associated accessories are designed for use only with the Chattanooga Group Intelect Legend XT Electrotherapy and Combination Therapy Systems.

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ABOUT INTELECT LEGEND XT

Intelect® Legend XT Therapy System

DANGERS

• Stimulus delivered by the TENS waveforms of this

• NiMH Batteries contain Class E Corrosive materials. In the event of battery cell rupture or leakage, handle Battery Module wearing neoprene or natural rubber gloves. Contents of a ruptured or leaking battery can cause respiratory irritation. Hypersensitivity to nickel can cause allergic pulmonary asthma. Contents of cell coming in contact with skin can cause skin irritation and/or chemical burns. • Never, under any circumstances, open the Battery Module housing or cells. Should an individual cell from a battery become disassembled, spontaneous combustion of the negative electrode is possible. There can be a delay between exposure to air and spontaneous combustion. • Charge the Battery Module according to the instructions found in this manual. Never attempt to charge the Battery Module on any other charging mechanism. • Use the Battery Module only with the Intelect Legend XT Therapy Systems. • Do not reverse the polarity of the Battery Module. Doing so can increase the individual cell temperature and cause cell rupture or leakage. • Never dispose of Battery Module in fire. Never short circuit the battery. The battery may explode, ignite, leak or get hot causing serious personal injury. • Dispose of NiMH batteries according to national, state and local codes and regulations.

device, in certain configurations, will deliver a charge of 25 microcoulombs (μC) or greater per pulse and may be sufficient to cause electrocution. Electrical current of this magnitude must not flow through the thorax because it may cause a cardiac arrhythmia. • Patients with an implanted neurostimulation device must not be treated with or be in close proximity to any shortwave diathermy, microwave diathermy, therapeutic ultrasound diathermy, or laser diathermy anywhere on their body. Energy from diathermy (shortwave, microwave, ultrasound, and laser) can be transferred through the implanted neurostimulation system, can cause tissue damage, and can result in severe injury or death. Injury, damage, or death can occur during diathermy therapy even if the implanted neurostimulation system is turned “off.” • Handle, clean, and dispose of components and accessories that have come in contact with bodily fluids according to National, Local and Facility rules, regulations and procedures.

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ABOUT INTELECT LEGEND XT

Intelect® Legend XT Therapy System

ELECTROTHERAPY INDICATIONS, CONTRAINDICATIONS, AND ADVERSE EFFECTS Indications for Russian, TENS, High Voltage Pulsed Current Contraindications (HVPC), Interferential and Premodulated waveforms • This device should not be used for symptomatic local pain relief unless etiology is established or unless a pain syndrome has • Relaxation of muscle spasms been diagnosed. • Prevention or retardation of disuse atrophy • This device should not be used when cancerous lesions are • Increase local blood circulation present in the treatment area. • Muscle re-education • Stimulation should not be applied over swollen, • Maintaining or increasing range of motion infected, inflamed areas or skin eruptions (e.g. phlebitis, Additional Indications for Microcurrent, Interferential, thrombophlebitis, varicose veins, etc.). Premodulated, and TENS waveforms • Other contraindications are patients suspected of carrying • Symptomatic relief and management of chronic, serious infectious disease and or disease where it is advisable, intractable pain for general medical purposes, to suppress heat or fevers. • Post-traumatic acute pain • Electrode placements must be avoided that apply current to the carotid sinus region (anterior neck) or transcerebrally • Post-surgical acute pain (through the head). • Safety has not been established for the use of therapeutic electrical stimulation during pregnancy. • Powered muscle stimulators should not be used on patients with cardiac demand pacemakers. • There should not be any use of TENS waveforms on patients with cardiac demand pacemakers.

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ABOUT INTELECT LEGEND XT

Intelect® Legend XT Therapy System

ELECTROTHERAPY INDICATIONS, CONTRAINDICATIONS, AND ADVERSE EFFECTS (continued)

• With TENS waveforms, isolated cases of skin irritation may

Additional Precautions • Caution should be used for patients with suspected or diagnosed heart problems. • Caution should be used for patients with suspected or diagnosed epilepsy. • Caution should be used in the presence of the following: • When there is a tendency to hemorrhage following acute trauma or fracture. • Following recent surgical procedures when muscle contraction may disrupt the healing process. • Over a menstruating or pregnant uterus. • Over areas of the skin which lack normal sensation. • 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 alternative conductive medium or an alternative electrode placement. • Electrode placement and stimulation settings should be based on the guidance of the prescribing practitioner. • Powered muscle stimulators should be used only with the lead wires and electrodes recommended for use by the manufacturer.

occur at the site of electrode placement following long-term application. • The effectiveness of TENS waveforms is highly dependent upon patient selection by a person qualified in pain management. Adverse Effects • Skin irritation and burns beneath the electrodes have been reported with the use of powered muscle stimulators. • Potential adverse effects with TENS are skin irritation and electrode burns.

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ABOUT INTELECT LEGEND XT

Intelect® Legend XT Therapy System

ULTRASOUND INDICATIONS AND CONTRAINDICATIONS Indications for Ultrasound Application of therapeutic deep heat for the treatment of selected sub-chronic and chronic medical conditions such as: • Relief of pain, muscle spasms, and joint contractures • Relief of pain, muscle spasms, and joint contractures that may be associated with: • Adhesive capsulitis • Bursitis with slight calcification • Myositis • Soft tissue injuries • Shortened tendons due to past injuries and scar tissues • Relief of sub-chronic, chronic pain, and joint contractures resulting from: • Capsular tightness • Capsular scarring Contraindications • This device should not be used for symptomatic local pain relief unless etiology is established or unless a pain syndrome has been diagnosed. • This device should not be used when cancerous lesions are present in the treatment area. • Other contraindications are patients suspected of carrying serious infectious disease and disease where it is advisable for general medical purposes to suppress heat or fevers.

• This device should not be used over or near bone growth centers until bone growth is complete.

• This device should not be used over the thoracic area if the patient is using a cardiac pacemaker. • This device should not be used over a healing fracture. • This device should not be used over or applied to the eye. • This device should not be used over a pregnant uterus. • This device should not be used on ischemic tissues in individuals with vascular disease where the blood supply would be unable to follow the increase in metabolic demand and tissue necrosis might result. Additional Precautions Additional precautions should be used when ultrasound is used on patients with the following conditions: • Over an area of the spinal cord following a Laminectomy, i.e., when major covering tissues have been removed • Over anesthetic areas • On patients with hemorrhagic diatheses

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NOMENCLATURE

Intelect® Legend XT Therapy System

INTELECT LEGEND XT ELECTROTHERAPY AND COMBINATION THERAPY SYSTEMS Two Channel Electrotherapy System

Two Channel Combination System 4

4

1

1 6

6 2

7 2 3

3 5

5

1. Two Channel Electrotherapy System 2. User Interface (See Page 12) 3. Front Access Panel 4. Rear Access Panel 5. Patient Data Card access port 6. Multimedia Card (MMC) access port (Unused)

1. Two Channel Combination System 2. User Interface (See Page 12) 3. Front Access Panel 4. Rear Access Panel 5. Patient Data Card access port 6. Multimedia Card (MMC) access port (Unused) Ultrasound Applicator (5cm2 shown) 10

NOMENCLATURE

Intelect® Legend XT Therapy System

INTELECT LEGEND XT ELECTROTHERAPY AND COMBINATION THERAPY SYSTEMS (continued) Front Access Panel Rear Access Panel 1 7

2

5 3 4 1

3 2

5 4

7 6 6

1. Front Access Panel Lanyard When reinstalling the Front Access Panel, make certain the Lanyard does not become kinked. 2. Operator Remote Control Connector 3. Patient Interrupt Switch Connector 4. Channel 1 Lead Wire Connector 5. Channel 2 Lead Wire Connector 6. Microcurrent Probe Connector 7. Ultrasound Applicator Connector

1. Screen Contrast Control 2. Power On/Off Switch 3. Technical Maintenance Port 4. Fuses 5. Mains Power Cord 6. Rear Access Panel 7. Serial Decal 11

NOMENCLATURE

Intelect® Legend XT Therapy System

USER INTERFACE 1 15 2 14

13 3 12 11 4

10 9

5

8 7

6 5 12

1. Rear Access Panel (See Page 11) 2. Ultrasound Applicator LED Indicator (Combination only) 3. Ultrasound Applicator- 5 cm2 Standard (Optional 1 cm2, 2 cm2, and 10 cm2 applicators available, Combination only) 4. Intensity knob 5. Cable and Lead Wire Hook 6. Front Access Panel (See Page 11) 7. Start button 8. Pause button 9. Stop button 10. Clinical Resources Library button 11. Home Screen button 12. Back button 13. Patient Data Card Port 14. Multimedia Card (MMC) Port (Unused) 15. User Setup and Parameter Control buttons

NOMENCLATURE

Intelect® Legend XT Therapy System

SYMBOL DEFINITIONS Below are the definitions for all of the symbols used in the Intelect Legend XT hardware and software. Study and learn these symbols before any operation of the system. System Software Symbols

System Hardware Symbols PATIENT INTERRUPT SWITCH

CONTRAST CONTROL

ON/OFF SWITCH

THERAPY INTENSITY CONTROL

MOVE UP

MULTIMEDIA CARD* PATIENT DATA CARD

PAUSE TREATMENT

MOVE RIGHT CHANNEL 2 LEAD WIRES MOVE LEFT CLINICAL RESOURCES LIBRARY

START TREATMENT * Used for System Software Upgrades

DECREASE INTENSITY PAUSE TREATMENT

PATIENT INTERRUPT SWITCH

CHANNEL 3 LEAD WIRES

MANUAL

ACCEPT AND RETURN

BACK

CHANNEL 1/2 OPERATOR REMOTE CONTROL OPTIONAL

Channel 3/4 Electrotherapy Module

MOVE DOWN

CHANNEL 1 LEAD WIRES

MICROCURRENT PROBE STOP TREATMENT

Operator Remote INCREASE INTENSITY

DATA PORT HOME

Optional Module and Accessory Symbols

DO NOT ACCEPT AND RETURN

ULTRASOUND APPLICATOR

PAD CONTACT QUALITY SINGLE CHANNEL GRAPH

M STIMULATION Battery Module

CHARGE LEVEL BATTERY CHARGING

PAD CONTACT QUALITY DUAL CHANNEL GRAPH

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CHANNEL 4 LEAD WIRES

MICROCURRENT PROBE

CHANNEL 3/4 OPERATOR REMOTE CONTROL OPTIONAL

NOMENCLATURE

Intelect® Legend XT Therapy System

GENERAL TERMINOLOGY Below are the definitions for all of the unique terminology used throughout this manual. Study these and become familiar with these terms for ease of system operation and familiarization with the components and control functionality of the Intelect Legend XT Therapy System. Some of these terms and definitions refer to a specific button or control on the system. Refer to page 13 for Symbol Definitions. ULTRASOUND Back button 1 3 The dedicated button on the Main unit, below the display, that each time pressed takes the user back one screen at a time. Previous Page button The button used in some modalities and functions that will take the user back one page when reading 2 multiple pages of text. UP and DOWN Arrows 1. Sound Head Controls used in various modality parameter screens to navigate That component of the Applicator that makes contact with or change a value up or down within the parameter. the patient during Ultrasound or Combination therapy. Electrotherapy 2. Applicator Refers to the Electrical muscle or nerve Stimulation modalities of The assembly that connects to the System and incorporates the system. the Sound Head. System 3. Applicator LED The primary system with all controls and functions. The component of the Applicator which, when illuminated, Module indicates if the Sound Head is emitting Ultrasound. Any optional modular modality component designed for installation onto the System.

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