Chattanooga Intelect Advanced Therapy System Manual

TABLE OF CONTENTS

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

FOREWORD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

PRODUCT DESCRIPTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

SAFETY PRECAUTIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

PRECAUTIONARY DEFINITIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2

CAUTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3

WARNINGS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

DANGERS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

ELECTROTHERAPY INDICATIONS, CONTRAINDICATIONS, AND

ADVERSE EFFECTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Indications for VMS, VMS Burst, Russian, TENS, High Voltage Pulsed . . . . .

Current (HVPC), Interferential, and Premodulated waveforms. . . . . . . . . . . 7

Additional Indications for Microcurrent, Interferential, Premodulated, . .

VMS™, VMS™ Burst, and TENS waveforms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Indications for Galvanic Continuous Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Additional Precautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

Adverse Eff ects. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

ULTRASOUND INDICATIONS AND CONTRAINDICATIONS . . . . . . . . . . . 9

Indications for Ultrasound . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

Additional Precautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

NOMENCLATURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1014

INTELECT ADVANCED ELECTROTHERAPY AND COMBINATION

THERAPY SYSTEMS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

Two (2) Channel Electrotherapy System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

Two (2) Channel Combination System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10

Front Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

Rear Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

USER INTERFACE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12

SYMBOL DEFINITIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

System Hardware Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

SystemSoftware Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

Operator Remote . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13

Battery Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

Channel 3/4ElectrothrapyModule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

GENERAL TERMINOLOGY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14

SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1526

SYSTEM SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

DIMENSIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

Width. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

Standard Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

Power (Combination and Electrotherapy Units) . . . . . . . . . . . . . . . . . . . . . . . . . 15

Electrical Type. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

WAVEFORM SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

IFC (Interferential) Traditional (4 Pole). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

TENS- Asymmetrical Biphasic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

TENS- Symmetrical Biphasic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

TENS- Alternating Rectangular . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

TENS- Monophasic Rectangular . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18

High Voltage Pulsed Current (HVPC). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18

VMSTM. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

Diadynamic Waveforms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

IFC Premodulated (2p) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20

Russian . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20

Microcurrent . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

VMSTM Burst . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

MONOPHASIC: Monophasic Rectangular Pulsed . . . . . . . . . . . . . . . . . . . . . . . .22

MONOPHASIC: Monophasic Triangular Pulsed . . . . . . . . . . . . . . . . . . . . . . . . . . 22

GALVANIC: Continuous . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

GALVANIC: Interrupted . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

Träbert (Ultrareiz) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24

SURGED: Monophasic Rectangular . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24

SURGED: Monophasic Triangular . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

ULTRASOUND SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26

Ultrasound . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26

SETUP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2734

INTELECT ADVANCED COLOR SERIES THERAPY SYSTEMS. . . . . . . . . . 27

Color Series Standard Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27

Color Series Optional Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27

Mains Power Cords. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27

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TABLE OF CONTENTS

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

INTELECT ADVANCED MONOCHROMATIC SERIES

THERAPY SYSTEMS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28

Monochromatic Series Standard Features. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28

Monochromatic Series Optional Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . .28

Mains Power Cords. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28

THERAPY SYSTEM SET UP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

Clinic Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .29

Restore Default Protocols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30

Restore Default Unit Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30

Erase Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31

Set Date and Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31

Setting System Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32

Ultrasound Coupling. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32

Display Unit Version Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33

Pad Contact Quality. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33

Select Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34

Connecting Accessories to the Therapy System . . . . . . . . . . . . . . . . . . . . . . . . . 34

PATIENT PREPARATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3539

ELECTROTHERAPY PATIENT PREPARATION. . . . . . . . . . . . . . . . . . . . . . . . . 35

Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35

Dura-Stick™ Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36

Reusable Carbon Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36

Dura-Stick™ Electrode Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37

Connecting Lead Wires. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .37

Securing Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37

Reusable Carbon Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38

Connecting Lead Wires. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .38

Conductive Medium . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38

Securing Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38

ULTRASOUND PATIENT PREPARATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

Preparing Treatment Area . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

Size of Applicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

Applicator Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

Conductive Medium . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

Treatment Area. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

Applicator Coupling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .39

OPERATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4094

OPERATOR INTERFACE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40

HOME SCREEN. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41

ELECTROTHERAPY SCREEN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42

GENERAL ELECTROTHERAPY WAVEFORM SET UP . . . . . . . . . . . . . . . . . . 43

Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43

Select Modality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43

Select Waveform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43

View Waveform Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43

View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44

Edit Waveform Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44

Install Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44

Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

Set Waveform Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

Save to Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

ADJUSTING ELECTROTHERAPY CHANNEL PARAMETERS

DURING TREATMENT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47

Select Channel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47

Edit Channel Paramenters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47

ULTRASOUND . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48

Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48

Select Modality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48

View Parameter Rationale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48

Sound Head Recommendation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48

Edit Ultrasound Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49

Head Warming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49

Set Ultrasound Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50

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TABLE OF CONTENTS

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

Save to Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50

Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50

Editing Ultrasound from Home Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51

Editing Ultrasound from Treatment Review Screen . . . . . . . . . . . . . . . . . . . . . 51

QUICK LINK INDICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52

Available Quick Link Indications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52

Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52

Select Quick Link Indication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52

View Waveform Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53

View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53

Edit Waveform Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53

Install Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54

Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54

Setting Waveform Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .55

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55

Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56

Editing Parameters during Treatment Session . . . . . . . . . . . . . . . . . . . . . . . . . . 56

Save to Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56

COMBINATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

Select Modality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

View Application Description. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

Access Combination Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

Edit Ultrasound Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

Select Waveform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59

Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59

Edit Waveform Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59

Set Waveform Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Set Ultrasound Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61

Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61

Save to Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61

ADJUSTING COMBINATION PARAMETERS DURING TREATMENT . . . 62

Edit Waveform Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62

Edit Ultrasound Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62

PATIENT DATA CARD SET UP OF NEW CARD. . . . . . . . . . . . . . . . . . . . . . . . 63

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63

Insert New Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63

Setup Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63

Set Up of New Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63

Enter Patient ID . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64

Access Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65

Electrode Placement Set Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65

Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65

Access Pain Map. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66

Select Pain Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66

Add Pain Locations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66

Select Location of Pain. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67

Editing Pain Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67

Deleting Pain Locations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68

Pain Scales . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68

Select Pain Scale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68

Adjust Pain Scale. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68

Save to Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69

EXISTING PATIENT DATA CARD USE. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70

Insert Existing Patient Data Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70

Access Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70

View Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70

Starting a New Treatment from Patient Data Card . . . . . . . . . . . . . . . . . . . . . . 71

Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71

Set Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72

iii

TABLE OF CONTENTS

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

Erasing Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72

Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72

CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS™ . . . . . . . . . . 73

Clinical Protocols™ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73

Access Clinical Resources . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73

Access Clinical Protocols™ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73

Select Body Area . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73

Select Clinical Indication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74

Select Pathological Condition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74

Select Pathological Severity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74

View Waveform Rationale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75

View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75

Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75

Edit Modality Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75

Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76

Set Modality Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77

Save to Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77

Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77

CLINICAL RESOURCES LIBRARY CREATING USER PROTOCOLS . . . . 78

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78

Select Modality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78

Edit Modality Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78

Select Clinical Resources Library. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78

Enter User Protocol Name. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79

CLINICAL RESOURCES LIBRARY DELETING USER PROTOCOLS . . . . 80

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80

Select Clinical Resources Library. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80

Select User Protocol to Delete . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80

Delete User Protocol . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80

CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS . . . . . . . . 81

Access User Protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81

Select User Protocol. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81

View Waveform Rationale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81

View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82

Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82

Edit Modality Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82

Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82

Set Modality Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84

Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84

Save to Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84

CLINICAL RESOURCES LIBRARY CREATING NEW SEQUENCES . . . . . 85

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85

Access Sequencing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85

Select Sequence. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85

Select First Waveform or Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85

Edit First Waveform or Current. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86

Select Second Waveform or Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86

Saving New Sequence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86

Enter Sequence Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87

CLINICAL RESOURCES LIBRARY DELETING SEQUENCES. . . . . . . . . . . 88

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88

Access Sequencing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88

Select Sequence. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88

Delete Sequence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88

CLINICAL RESOURCES LIBRARY USING SEQUENCES. . . . . . . . . . . . . . . 89

Access Sequencing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89

Select Sequence. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89

Select Waveform/Current . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89

View Waveform Rationale . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90

View Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90

Prepare Patient. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90

Patient Interrupt Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90

Set Sequence Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91

Intensity Knob Rotation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91

iv

TABLE OF CONTENTS

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

Start Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92

Pause Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92

Save to Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92

Stop Treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92

CLINICAL RESOURCES LIBRARY MMC GRAPHICAL LIBRARY . . . . . . 93

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93

Select Clinincal Resources Library . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93

Select MMC Graphical Library . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .93

Select Body Area . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93

Select Library Type. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 94

INSTALLATION/REMOVAL . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95106

INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE . . . . . . . . 95

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95

Nomenclature. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96

Specifi cations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97

Waveform & Current Specifi cations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97

Disconnect Mains Power. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98

Remove Lead Wires and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98

Remove Therapy System from Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98

Release Ribbon Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99

Position Therapy System and Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99

Connect Ribbon Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99

Set Therapy System onto Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100

Secure Therapy System to Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .100

Front Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .100

Install Lead Wires and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .101

Install Front Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .101

Mount to Therapy System Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .101

Connect Mains Power. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .101

Turn Therapy System On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .102

REMOVAL CHANNEL 3/4 ELECTROTHERAPY MODULE . . . . . . . . . . . . 103

Disconnect Mains Power. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .103

Remove Therapy System from Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .103

Remove Lead Wires and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 103

Remove Screws Securing Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .104

Disconnect Ribbon Cable at Module. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .104

Store and Secure Ribbon Cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .104

Front Access Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .105

Install Lead Wires and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .105

Connect Mains Power. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .105

Turn Therapy System On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .106

TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 107112

ERROR CODES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .107-112

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 107

MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113

CARING FOR THE THERAPY SYSTEM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113

Cleaning the Therapy System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113

Cleaning the Lens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113

CALIBRATION REQUIREMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113

Calibrating Ultrasound Applicators. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113

FACTORY SERVICE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .113

WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 114

v

FOREWORD

Supplied by EME Services Ltd

This manual has been written for the users of the Intelect Advanced 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
Channel 3/4 Electrotherapy Module for the users of the Intelect Advanced Therapy two channel electrotherapy and combination systems.
Instructions for additional options such as sEMG, sEMG + Stim, Laser, Battery, and Vacuum are found in their respective User Manuals which
contain operation and installation instructions.

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 Advanced 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, ultrasound, laser therapy, sEMG, and sEMG + Stim. Observe
all applicable precautionary measures for treatment.

Keep informed of appropriate indications and contraindications for the use of electrotherapy, ultrasound, laser therapy, sEMG, and
sEMG+Stim.

This equipment is to be used only under the prescription and supervision of a licensed practitioner.

Intelect® Advanced Therapy System

©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.

1

SAFETY PRECAUTIONS

Supplied by EME Services Ltd

PRECAUTIONARY DEFINITIONS

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;

Intelect® Advanced Therapy System

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.

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.

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.

NOTE:

Throughout this manual, “NOTE” may be found. These Notes are
helpful information to aid in the particular area or function being
described.

2

SAFETY PRECAUTIONS

Supplied by EME Services Ltd

CAUTIONS

Read, understand, and practice the precautionary and operating
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 Advanced 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 15° C and 40° C (59° F and 104° F), 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.

Intelect® Advanced Therapy System

Inspect Applicator cables and associated connectors before

•

each use.
The Intelect Advanced 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.

3

SAFETY PRECAUTIONS

Supplied by EME Services Ltd

WARNINGS

Intelect® Advanced Therapy System

These devices are restricted to sale by, or on the order 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.

Powered muscle stimulators should be used only with the leads and

•

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.

4

SAFETY PRECAUTIONS

Supplied by EME Services Ltd

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.

Intelect® Advanced Therapy System

5

SAFETY PRECAUTIONS

Supplied by EME Services Ltd

DANGERS

Stimulus delivered by the TENS waveforms of this
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.”

Intelect® Advanced Therapy System

6

SAFETY PRECAUTIONS

Supplied by EME Services Ltd

ELECTROTHERAPY INDICATIONS, CONTRAINDICATIONS, AND ADVERSE EFFECTS

INDICATIONS FOR VMS, VMS BURST, RUSSIAN, TENS, HIGH
VOLTAGE
PREMODULATED WAVEFORMS

Relaxation of muscle spasms

•

•

Prevention or retardation of disuse atrophy

•

Increase local blood circulation

•

Muscle re-education

•

Maintaining or increasing range of motion

Additional Indications for Microcurrent, Interferential,
Premodulated, VMS™, VMS™ Burst and TENS waveforms

•

Symptomatic relief and management of chronic,
intractable pain

•

Post-traumatic acute pain

•

Post-surgical acute pain

Indications for Galvanic Continuous Mode

•

Relaxation of muscle spasm

PULSED CURRENT HVPC, INTERFERENTIAL AND

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.

•

Stimulation should not be applied over swollen,
infected, inflamed areas, or skin erruptions, e.g. phlebitis,
thrombophlebitis, varicose veins, etc.

•

Other contraindications are patients suspected of carrying
serious infectious disease and or disease, where it is advisable,
for general medical purposes, to suppress heat or fevers.

•

Electrode placements must be avoided that apply current
to the carotid sinus region (anterior neck) or transcerebrally
(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.

Intelect® Advanced Therapy System

7

SAFETY PRECAUTIONS

Supplied by EME Services Ltd

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

nosed heart problems.

diag

•

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.

Intelect® Advanced Therapy System

8

SAFETY PRECAUTIONS

Supplied by EME Services Ltd

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.

•

Stimulation should not be applied over swollen,
infected, inflamed areas, or skin erruptions, e.g. phlebitis,
thrombophlebitis, varicose veins, etc.

Intelect® Advanced Therapy System

•

Other contraindications are patients suspected of carrying
serious infectious disease and disease wher
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;

•

Laminectomy, i.e., when major covering tissues have been
removed.

•

Over anesthetic areas.

On patients with hemorrhagic diatheses.

e it is advisable for

9

NOMENCLATURE

Supplied by EME Services Ltd

INTELECT ADVANCED ELECTROTHERAPY AND COMBINATION THERAPY SYSTEMS

Two (2) Channel Electrotherapy System

4

1

6

2

Two (2) Channel Combination System

4

6

Intelect® Advanced Therapy System

1

7

2

5

1.

Two (2) Channel Electrotherapy System

2.

User Inter
Front Access Panel

3.
Rear Access Panel

4.
Patient Data Card and sEMG Data Card access port.

5.
Multimedia Card (MMC) access port.

6.

face (See Page 12)

3

10

5

Two Channel Combination System

1.
User Interface (See Page 12)

2.
Front Access Panel

3.
Rear Access Panel

4.
Patient Data Card and sEMG Data Card access port.

5.
Multimedia Card (MMC) access port.

6.

Ultrasound Applicator (5cm2 shown) Combination Systems Only

3

NOMENCLATURE

Supplied by EME Services Ltd

INTELECT ADVANCED ELECTROTHERAPY AND COMBINATION THERAPY SYSTEMS (continued)

Rear Access PanelFront Access Panel

7

5

4

Intelect® Advanced Therapy System

1

2

3

1

Front Access Panel Lanyard

1.

When reinstalling the Front Access Panel, make certain the
Lanyard does not become kinked.

Operator Remote Control Connector

2.
Patient Interrupt Switch Connector

3.
Channel 1 Lead Wire Connector

4.
Channel 2 Lead Wire Connector

5.
Microcurrent Probe Connector

6.
Ultrasound Applicator Connector

7.

3

2

4

5

6

7

6

Screen Contrast Control (Not functional on Color Systems)

1.
Power On/Off Switch

2.
Technical Maintenance Port

3.
Fuses

4.
Mains Power Cord

5.
Rear Access Panel

6.
Serial Decal

7.

11

NOMENCLATURE

Supplied by EME Services Ltd

USER INTERFACE

15

16

14

13

12

11

10

9

8

6

Intelect® Advanced Therapy System

1

2

1.

3

4

5

6

7

Rear Access Panel (See Page 11)

2.

User Interface (Color Shown)

3.

Ultrasound LED Coupling Indicator

(Combination only)

2

4.

Ultrasound Applicator- 5 cm

(Optional 1 cm2, 2 cm2 and 10 cm2 )
applicators available (Combination only)

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 and sEMG Data Card Port

14.
User Set Up and Parameter Control buttons

15.
Multimedia Card (MMC) Port

16.

Standard.

12

NOMENCLATURE

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

SYMBOL DEFINITIONS

Below are the definitions for all of the symbols used in the Intelect Advanced hardware and software. Study and learn these symbols before
any operation of the system.

System Hardware Symbols

CONTRAST CONTROL
NOT FUNCTIONAL ON
COLOR SYSTEMS

ON/OFF SWITCH

DATA PORT

MULTIMEDIA CARD,
PATIENT DATA CARD,
AND SEMG DATA CARD

STOP TREATMENT

THERAPY
INTENSITY
CONTROL

HOME

CLINICAL
RESOURCES
LIBRARY

BACK

PATIENT INTERRUPT
SWITCH

CHANNEL 1
LEAD WIRES

CHANNEL 2
LEAD WIRES

MICROCURRENT PROBE

System

Software Symbols

MOVE UP

MOVE DOWN

MOVE RIGHT

MOVE LEFT

ACCEPT AND
RETURN

DO NOT ACCEPT

AND RETURN

Optional Module and Accessory Symbols

Operator Remote

Channel 3/4

Electrothrapy

INCREASE
INTENSITY

DECREASE
INTENSITY

PAUSE
TREATMENT

MANUAL

M

STIMULATION

Battery Module

Module

PATIENT INTERRUPT SWITCH

CHANNEL 3 LEAD WIRES

CHANNEL 4 LEAD WIRES

MICROCURRENT PROBE

PAUSE TREATMENT

START TREATMENT

CHANNEL 1/2
OPERATOR
REMOTE
CONTROL
OPTIONAL

ULTRASOUND
APPLICATOR

PAD CONTACT QUALITY

SINGLE CHANNEL GRAPH

PAD CONTACT QUALITY

DUAL CHANNEL GRAPH

13

CHARGE LEVEL

BATTERY CHARGING

CHANNEL 3/4 OPERATOR
REMOTE CONTROL
OPTIONAL

NOMENCLATURE

Supplied by EME Services Ltd

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 Adavnced 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.

Intelect® Advanced Therapy System

GENERAL TERMINOLOGY

Back button

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 multiple pages of text.

UP and DOWN Arrows

Controls used in various modality parameter screens to navigate or
change a value up or down within the parameter.

Electrotherapy

Refers to the Electrical muscle or nerve Stimulation modalities of
the system.

System

The primary system with all controls and functions.

Module

Any optional modular modality component designed for
installation onto the System.

ULTRASOUND

1

2

1. Sound Head

That component of the Applicator that makes contact with the
patient during Ultrasound or Combination therapy.

2. Applicator

The assembly that connects to the System and incorporates the
Sound Head.

3. Coupling LED

The component of the Applicator which indicates if the
Sound Head is Coupled or Uncoupled on the the treatment
area.

14

3

SPECIFICATIONS

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

SYSTEM SPECIFICATIONS

HEIGHT

DEPTH

WIDTH

NOTE:

All waveforms except High Voltage Pulsed Current (HVPC) have been
designed with a 200mA current limit.

VMS™, VMS™ Burst and all TENS waveform output intensities are
measured, specified and listed to peak, not peak to peak.

DIMENSIONS

Width

Combination System . . . . . . . . . . . . . . . . . . . . . . . . . . 28.9 cm (11.375”)

Electrotherapy System . . . . . . . . . . . . . . . . . . . . . . . . . . . 24.8 cm (9.750”)

Depth (Combination and Electrotherapy System) 32.4 cm (12.750”)
Height (Combination and Electrotherapy System) . 22.2 cm (8.750”)
Standard Weight

Two Channel Combination System . . . . . . . . . . . . . . . . . 3.2 kg (7 lbs)

Two Channel Electrotherapy System . . . . . . . . . . . . . . . . 2.7 kg (6 lbs)

Power (Combination and Electrotherapy Units)

Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .100 - 240 V - 1.0 A, 50/60 Hz

Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . +12 V, 8.3 A

Fuses . . . . . . . . . . . . . . . . . . . . . Two 6.3A Time Lag (Part Number 71772)

Electrical Class . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .CLASS I

Electrical Type

Ultrasound . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TYPE B

Electrotherapy and sEMG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .TYPE BF

Regulatory Compliance

UL/IEC/EN 60601-1

IEC/EN 60601-1-2
IEC 60601-2-5
IEC 60601-2-10

0413

15

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS

Intelect® Advanced Therapy System

IFC (Interferential) Traditional (4 Pole)

Interferential Current is a medium frequency waveform. Current
is distributed through of t
currents cross each other in the body at the area requiring
treatment. The two currents interfere with each other at this
crossing point, resulting in a modulation of the intensity (the
current intensity increases and decreases at a regular frequency).

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Carrier Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2000-10,000 Hz

Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-200 Hz

Sweep Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 sec

Sweep Low Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz

Sweep High Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz

Scan Percentage . . . . . . . . . . . . . . . . . . . . . . . . . . Static, 10%, 40%, 100%

Amplitude . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA RMS into 500 ohm

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Minutes

Available on Channel . . . . . . . . . . . . . . . . . . . . . . . . . . . .1&2, 3&4 Option

*CC= Constant Current
CV= Constant Voltage

wo channels (four electrodes). The

TENS- Asymmetrical Biphasic

The Asymmetrical Biphasic waveform has a short pulse duration.
It is capable of strong stimulation of the nerve fibers in the skin
as well as of muscle tissue. This waveform is often used in TENS
devices. Because of its short pulse, the patient typically tolerates
the current well, even at relatively high intensities.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-110 mA

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . Adjustable 20-1,000 µsec

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-250 Hz

Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*

Burst Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-10 bps

Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-250 Hz

Amplitude Modulation . . . . . . . . . . . . Off, 40%, 60%, 80% and 100%

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Stimulus delivered by the TENS waveforms of this 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.

16

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

TENS- Symmetrical Biphasic

The Symmetrical Biphasic waveform has a short pulse duration
and is capable of strong stimulation of nerve fibers in the skin
and in muscle. This waveform is often used in portable muscle
stimulation units, and some TENS devices. Because of its short
pulse duration, the patient typically tolerates the current well,
even at relatively high intensities.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . Adjustable 20-1,000 µsec

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-250 Hz

Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*

Burst Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-4 bps

Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-250 Hz

Amplitude Modulation . . . . . . . . . . . . Off, 40%, 60%, 80% and 100%

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

*CC= Constant Current
CV= Constant Voltage

Intelect® Advanced Therapy System

TENS- Alternating Rectangular

The Alternating Rectangular waveform is an interrupted biphasic
current with a rectangular pulse shape. This waveform is
commonly used as a pain management application.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . Adjustable 20-1,000 µsec

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz

Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*

Burst Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-10 bps

Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-250 Hz

Amplitude Modulation . . . . . . . . . . . . Off, 40%, 60%, 80% and 100%

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Stimulus delivered by the TENS waveforms of this 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.

17

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

Intelect® Advanced Therapy System

TENS- Monophasic Rectangular

The Monophasic Rectangular waveform is an interrupted
unidirectional current with a rectangular pulse shape. This
waveform is commonly used with electrodiagnostic testing and
clinically to stimulate denervated muscle.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-110 mA

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . Adjustable 20-1,000 µsec

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz

Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*

Burst Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-10 bps

Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-250 Hz

Amplitude Modulation . . . . . . . . . . . . . Off, 40%, 60%, 80%and 100%

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Stimulus delivered by the TENS waveforms of this 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.

High Voltage Pulsed Current (HVPC)

The High Voltage Pulsed Current (HVPC) has a very brief pulse
duration characterized by two distinct peaks delivered at
high voltage. The waveform is monophasic (current flows in
one direction only). The high voltage causes a decreased skin
resistance making the current comfortable and easy to tolerate.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Electrodes or Probe

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-500 V

Polarity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Positive or Negative

Ramp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0.5 sec, 1 sec, 2 sec, 5 sec

Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Peak Current or Volts

Sweep . . . . . . . . . . . . . .Continuous, 80/120 pps, 1/120 pps, 1/10 pps

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-120 pps

Cycle Time . . . . . .5/5, 4/12, 10/10, 10/20, 10/30, 10/50, Continuous

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

*CC= Constant Current
CV= Constant Voltage

18

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

TM

VMS

VMS is a symmetrical biphasic waveform with a 100 µsec interphase
interval. Because the pulse is r
skin load, making it suitable for applications requiring high intensities,
such as in muscle strengthening protocols.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-255 mA

Channel Mode . . . . . . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, Co-Contract

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20-1000µsec

Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*

Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Off or On

Set Intensity . . . . . . . . . . . . . . . . . . . . . Individual Channel Intensity Setting in

Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 pps

Ramp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0.5 sec, 1 sec, 2 sec, 5 sec

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

*CC= Constant Current
CV= Constant Voltage

elatively short, the waveform has a low

Reciprocal and Co-Contract modes

Intelect® Advanced Therapy System

Diadynamic Waveforms

The Diadynamic waveforms are rectified alternating currents. The
alternating current is modified (rectified) to allow the current to
flow in one direction only.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on channels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1, 2, 3, 4

MF: (Monophasé Fixe) - Frequency of 50 Hz: phase duration of
10 ms followed by a pause of 10 ms.

DF: (Diphasé Fixe) - Frequency of 100 Hz: phase duration of 10 ms
followed immediately by another identical phase of 10 ms.

CP: (Modulé en Courtes Périodes) - 1 second of MF followed
abruptly by 1 second of DF.

LP: (Modulé en Longues Périodes) - Rhythmical fluctuation
between 2 MF currents.

CP-iso: (Courtes Periodes Isodynamic) - A combination of MF and
DF waveforms.

CP-id: Same as CP-iso.
MF+CP: A period of MF followed by a period of CP.
MF+CP-id: A period of MF followed by a period of CP-ID.
DF+LP: A period of DF followed by a period of LP.
DF+CP: A period of DF followed by a period of CP.

19

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

Intelect® Advanced Therapy System

IFC Premodulated (2p)

Premodulated Current is a medium frequency waveform. Current
comes out of one channel (two electrodes). The current intensity
is modulated: it increases and decreases at a regular frequency
(the Amplitude Modulation Frequency).

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Pads

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA

Carrier Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2000-10,000 Hz

Beat Fixed (Sweep Off ) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz

Sweep Low Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-149 Hz

Sweep High Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . 81-200 Hz

Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50

Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*

Carrier Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2,000-10,000 Hz

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Min

Available on Channel . . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

*CC= Constant Current
CV= Constant Voltage

Russian

Russian Current is a sinusoidal waveform, delivered in bursts or
series of pulses. This method was claimed by its author (Kots)
to produce maximal muscle strengthening effects without
significant discomfort to the patient.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Pads

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA

Channel Mode . . . . . . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, Co-Contract

Duty Cycle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10%, 20%, 30%, 40%, 50%

Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*

Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Off or On

Cycle Time . . . . . .5/5, 4/12, 10/10, 10/20, 10/30, 10/50, Continuous

Burst Frequency (Anti-Fatigue Off ) . . . . . . . . . . . . . . . . . . . . 20-100 pps

Ramp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.5, 1, 2 and 5 sec

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

20

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

Intelect® Advanced Therapy System

Microcurrent

Microcurrent is a monophasic waveform of very low intensity.
The literature reports beneficial effects of this waveform in the
treatment of wounds. The physiological working mechanism of
this effect is as yet not clearly understood. It is thought to
stimulate tissue healing by stimulating the 'current of injury', a
current which naturally occurs in healing tissue.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Electrodes or Probe

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-1000.0 µA

Polarity . . . . . . . . . . . . . . . . . . . . . . . . . .Positive, Negative or Alternating

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Min

Available on channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

*CC= Constant Current
CV= Constant Voltage

VMSTM Burst

VMS Burst is a symmetrical biphasic waveform delivered in a burst
format. Because the pulse is relatively short, the waveform has a
low skin load, making it suitable for applications requiring high
intensities, such as in muscle strengthening protocols.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-255 mA

Channel Mode . . . . . . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, Co-Contract

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20-1000 µsec

Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*

Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Off or On

Set Intensity . . . . . . . . . . . . . . . . . . . . . .Individual Channel Intensity Setting in

Reciprocal and Co-Contract modes

Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 pps

Ramp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0.5 sec, 1 sec, 2 sec, 5 sec

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

21

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

MONOPHASIC: Monophasic Rectangular Pulsed MONOPHASIC: Monophasic Triangular Pulsed

The Monophasic Rectangular Pulsed waveform is an interrupted
unidirectional current with a rectangular pulse shape.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.1-500.0 ms

Phase Interval . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5000 ms

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Stimulus delivered by the TENS waveforms of this 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.

Intelect® Advanced Therapy System

The Monophasic Triangular Pulsed waveform is an interrupted
unidirectional current with a triangular pulse shape.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-80 mA

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.1-500.0 ms

Phase Interval . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5000 ms

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

22

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

GALVANIC: Continuous GALVANIC: Interrupted

Intelect® Advanced Therapy System

Galvanic Current is a direct current flowing in one direction only.
The current can be continuous or interrupted.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA

Polarity Reversal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . On or Off

With Polarity Reversal On, Polarity will change every five minutes.

Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Galvanic Current is a direct current flowing in one direction only.
The current can be continuous or interrupted.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA

Polarity Reversal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . On or Off

With Polarity Reversal On, Polarity will change every five minutes.

Cycle Time . . . . . . . . . . .Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

23

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

Intelect® Advanced Therapy System

Träbert (Ultrareiz)

It is a monophasic waveform with a phase duration of 2 ms and a
pause of 5 ms resulting in a frequency of approximately 143 Hz.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA

Polarity Reversal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . On or Off

With Polarity Reversal On, Polarity will change every 7.5 minutes.

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Stimulus delivered by the TENS waveforms of this 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.

SURGED: Monophasic Rectangular

A series of rectangular, monophasic pulses. The pulses surge to
maximum power, hold and then decrease before the pause. This
waveform is well suited for muscle strengthening.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.2-5.0 ms

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-60 Hz

Surges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1/min - 20/min

Pause . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-57 sec

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

24

SPECIFICATIONS

Supplied by EME Services Ltd

WAVEFORM SPECIFICATIONS (continued)

SURGED: Monophasic Triangular

A series of triangular, monophasic pulses. The pulses surge to
maximum power, hold and then decrease before the pause. This
waveform is well suited for muscle strengthening.

Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes

Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA

Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.2-5.0 ms

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-60 Hz

Surges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1/min - 20/min

Pause . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-57 sec

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min

Available on Channels . . . . . . . . . . . . . . . . . . . . . . . . 1 & 2, 3 & 4 Option

Stimulus delivered by the TENS waveforms of this 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.

Intelect® Advanced Therapy System

25