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

SPECIFICATIONS

Supplied by EME Services Ltd

ULTRASOUND SPECIFICATIONS

Ultrasound

Intelect® Advanced Therapy System

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 MHz, ± 5%; 3.3 Mhz, ±5%

Duty Cycles . . . . . . . . . . . . . . . . . . . . . . . . . . . 10%, 20%, 50%, Continuous

Pulse Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100Hz

Pulse Duration . . . . . . . 1 mSec, ±20%; 2 mSec, ±20%; 5 mSec, ±20%

Output Power

10 cm2 Crystal . . . . . . . . . . . . . . . . .0-20 W at 1MHz, 0-10 W at 3.3 MHz

5 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-10 W, 1 and 3.3 MHz

2 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-4 W, 1 and 3.3 MHz

1 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-2 W 3.3 MHz Only

Amplitude . . . . . . . . . . . . . . . . . . . . 0 to 2.5 w/cm2 in continuous mode,

0-3 w/cm2 in pulsed modes

Output accuracy . . . . . . . . . . . . . . . . . . . ±20% above 10% of maximum

Temporal Peak to Average Ratio: . . . . 2:1, ± 20%, at 50% Duty Cycle

5:1, ± 20%, at 20% Duty Cycle

9:1, ± 20%, at 10% Duty Cycle

Beam Nonuniformity Ratio . . . . . . . . . . . . . . . . . . . . . . 5.0 : 1 maximum

Beam Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Collimating

2

Effective Radiating Areas. . . . . . . . . . . . 10 cm

Crystal: 8.5 cm2, ±1.5

5 cm2 Crystal: 4.0 cm2, ±1.0

2 cm2 Crystal: 1.8 cm2, +0.2/- 0.4

1 cm2 Crystal: 0.8 cm2, +0.2/-0.4

Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-30 min

Head Warming Feature

The Head Warming feature of an Intelect Advanced Combination
Therapy System utilizes Ultrasound output resulting in warming
of the Sound Head to increase patient comfort.

With Head Warming enabled, ultrasound is emitted without
pressing the Start button. The Applicator LED will not illuminate
during the Head Warming period. US Channel will indicate "Head
Warming".

Output . . . . . . . . . . . . . . . . . . . . . . . 0 - 50% Cycling of maximum power

Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.3 Mhz

Sound Head Temperature . . . . . . . . . 29.4 °C - 43.3 °C (85 °F - 110 °F)

Do not apply the Ultrasound Applicator to the patient during the Head
Warming period. Applicator must remain in Applicator Hook duing the
Head Warming period.

26

SET UP

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

INTELECT ADVANCED COLOR SERIES THERAPY SYSTEMS

Remove the Therapy System and all accessories from shipping cartons. Visually inspect for damage. Report any damage to the carrier.

Color Series Standard Features

Order No. Description Qty

2765CS Two Channel Electrotherapy System (or) 1

2762CC Two Channel Combination System 1

27378 Electrotherapy Accessory Kit- Includes the following: 1

27312 Channel 1 Lead Wire 1

27313 Channel 2 Lead Wire 1

10648 Nylatex® Wrap 2

79967 6 x 8 cm Carbon Electrodes 4

79970 6 x 8 cm Electrode Sponges 4

42044 7 cm (2.75") Round Disposable Electrodes (4 per pack) 1

27469 Patient Interrupt Switch for Channels 1/2 1

27335 5 cm

4248 Conductor

27085 Anatomical/Pathological Library (MMC Card) 1

27465 Patient Data Card 5

2771 sEMG Module (Factory Installed) 1

27567 sEMG Accessory Kit- Includes the Following 1

27321 sEMG Channel 1 (A) Lead Wire 1

27322 sEMG Channel 2 (B) Lead Wire 1

77725 Intravaginal Probe 1

42061 3.2 cm (1.25") Round Disposable Electrode Pack (4 per pack) 3

27455 User Manual (CD-ROM) 1

2

Ultrasound Applicator (Combination Systems Only) 1

TM

Transmission Gel- 9 oz Bottle (Combination Systems Only) 1

Order No. Description

2770 Two Channel Electrotherapy Module

2767 NiMH Battery Module

2766 Laser Therapy Module

2771 sEMG Module

27567 sEMG Accessory Kit

2785 Vacuum Electrode Module

2774 Vacuum Electrode Module w/Cart

2775 Therapy System Cart

2768 Patient Data Management System- Includes

27779 Version 1.0 PC Software (Windows)

27176 Card Reader

27300 USB Cable

27167 sEMG Data Card

27516 sEMG Data Card Sleeve

27780 User Manual (on Software CD)

27508 Operator Remote (Ch 1/2)

27079 Operator Remote (Ch 3/4)

27333 1 cm

27334 2 cm

27336 10 cm

Color Series

Optional Accessories

the following:

2

US Applicator (Combination Only)

2

US Applicator (Combination Only)

2

US Applicator (Combination Only)

Mains Power Cords

Order No.

21284 Euro 1

78121 US 1

20971 Austr

20972 Swiss 1

20973 UK 1

20974 Danish 1

20975 Japanese 1

20976 Indian 1

20977 Israeli 1

Type Qty

alian 1

NOTE:

The Power Cord shipped with
the System will accommodate
the electrical requirements for
the country of use.

27

SET UP

Supplied by EME Services Ltd

Intelect® Advanced Therapy System

INTELECT ADVANCED MONOCHROMATIC SERIES THERAPY SYSTEMS

Remove the Therapy System and all accessories from shipping cartons. Visually inspect for damage. Report any damage to the carrier.

Monochromatic Series

Monochromatic Series Standard Features

Order No. Description Qty

2773MS Two Channel Electrotherapy System (or) 1

2772MC Two Channel Combination System 1

27378 Electrotherapy Accessory Kit- Includes the following: 1

27312 Channel 1 Lead Wire 1

27313 Channel 2 Lead Wire 1

10648 Nylatex® Wrap 2

79967 6 x 8 cm Carbon Electrodes 4

79970 6 x 8 Electrode Sponges 4

42044 7 cm (2.75") Round Disposable Electrodes (4 per Pack) 1

27469 Channel 1/2 Patient Interrupt Switch 1

27335 5 cm2 Ultrasound Applicator (Combination Systems Only) 1

4248 Conductor

27085 Anatomical/Pathological Library (MMC Card) 1

27465 Patient Data Card 5

27455 User Manual (CD-ROM) 1

TM

Transmission Gel- 9 oz Bottle (Combination Systems Only) 1

Optional Accessories

Order No. Description

2770 Two Channel Electrotherapy Module

2767 NiMH Battery Module

2766 Laser Therapy Module

2771 sEMG Module

27567 sEMG Accessory Kit

2785 Vacuum Electrode Module

2774 Vacuum Electrode Module w/Cart

2775 Therapy System Cart

2768 Patient Data Management System- Includes

the following:

27779 Version 1.0 PC Software (Windows)

27176 Card Reader

27300 USB Cable

27167 sEMG Data Card

27516 sEMG Data Card Sleeve

27780 User Manual (on Software CD)

27508 Operator Remote (Ch 1/2)

27079 Operator Remote (Ch 3/4)

27333 1 cm

27334 2 cm

27336 10 cm

2

US Applicator (Combination Only)

2

US Applicator (Combination Only)

2

US Applicator (Combination Only)

Mains Power Cords

Order No.

21284 Euro 1

78121 US 1

20971 Austr

20972 Swiss 1

20973 UK 1

20974 Danish 1

20975 Japanese 1

20976 Indian 1

20977 Israeli 1

Type Qty

alian 1

NOTE:

The Power Cord shipped with
the System will accommodate
the electrical requirements for
the country of use.

28

SET UP

Supplied by EME Services Ltd

THERAPY SYSTEM SET UP

Accessing Operator Utilities

Plug unit into wall outlet.

Turn system On.

Press the Home and Back buttons
simultaneously.

To return to the System Home
screen, press the Home button.

Clinic Name

Press Clinic Name button.

POWER SWITCH

CLINIC NAME BUTTON

Select the row of alpha or numeric
characters desired by pushing the

on beside the corresponding

butt
row. Select the desired character in
the row by pressing the row button
until the desired letter is framed.

Once selection is framed, press the
Accept and Return Arrow button.
The character just chosen will
display in the top of the screen and
the cursor will advance to the next
character.

To go back a character press the
Move Left Arrow button. To delete
the character, press the Delete
button.

Once Clinic Name is completed,
press the Save button.

To discard entry, press the Back
button.

Intelect® Advanced Therapy System

SELECT ROW AND CHARACTER BUTTONS

MOVE
LEFT

DELETE SAVE

BACK

ACCEPT AND

RETURN

29

SET UP

Supplied by EME Services Ltd

THERAPY SYSTEM SET UP (continued)

Restore Default Protocols

Press Restore Default Protocols
button.

RESTORE DEFAULT
PROTOCOLS BUTTON

Restore Default Unit Settings

Press the Restore Default Unit
Settings button to restore the
system defaults. This control will
neither change the Date and
Time nor affect any of the Clinical
Protocols stored in the system.

Intelect® Advanced Therapy System

RESTORE DEFAULT UNIT
SETTINGS BUTTON

Press Yes button to restore the
Protocols to Factory Settings. This
will permanently remove all User
Protocols and Sequences.

If it is not desired to permanently
remove all of the User Protocols
and User Sequences from the
System, press the No button.

PRESS YES BUTTON TO
RESTOREPROTOCOLS

PRESS NO BUTTON TO
KEEP PROTOCOLS
AS THEY ARE

After the settings have been
restored, a message will appear
stating that the Default Unit
Settings are restored. Press any
button to return to Utilities
screen.

30

SET U

Supplied by EME Services Ltd

T RAPY SYSTEM ET UP (conti ed)

Erase Patie Data Card

n ll ati at a to b

rase n tie t D ta Ca

e s o t n he s te .

Pre E ase ti nt C d utto

I SERT

A NT

C R

ERASE PAT NT

CARD BUTT

t l ct A ance h py em

Se Dat i

ess Set Date a Tim ton

E DAT

ND TIM

U

Pr ss t Y s bu on to a

data r Pati t D t Ca d.

Pre th No b t n to kee all

at on a ie t D a C d.

f e P ti nt ta rd i

a ed a rif at o s ag
wi ap ar r s an bu on
r t r t the ilities scr n.

YES

TT

YES

U T

BUT ON

BUT O

Pre s th or Down Arrow
button for th respec e r a
un il d s e cha e play

A t r d s r d ch g re

ade, r s t k b tt t

r t the U i ie c ee

1

P ESS THE S UP N

AR W B T ON CH NGE

BACK

TO

SET UP

Supplied by EME Services Ltd

THERAPY SYSTEM SET UP (continued)

Setting System Volume

Press Volume button until
the desired system volume is
achieved. There are six settings:
Off, X-Low, Low, Med, High, and
X-High.

Each time the Volume button is
pressed the setting displayed will
emit three beep tones at that
level.

VOLUME
BUTTON

Intelect® Advanced Therapy System

Ultrasound Coupling

This warning system works in conjunction with the Applicator
LED to alert the user should the Sound Head become uncoupled
from the patient. Press the US Coupling button until the desired
setting is displayed. There are four different alarm settings and an
Off setting.

Pause and Beep
Pauses Treatment Time and
emits an audible beep. When

US COUPLING

BUTTON

the Applicator Sound Head is
re-coupled to the patient, the
Treatment Timer will automatically
restart.

Pause and No Beep
Pauses Treatment Timer. When
the Applicator Sound Head is
re-coupled to the patient, the
Treatment Timer will automatically
restart.

Beep
Emits an audible beep.

No Beep
No beep is emitted.

Off
Turns the Ultrasound
Coupling feature.

32

SET UP

Supplied by EME Services Ltd

THERAPY SYSTEM SET UP (continued)

Display Unit Version Information

Press the Display Unit Version
Information button to show
the system software versions
installed.

Press the Back button to return
the Operator Utilities screen.

PRESS DISPLAY UNIT

VERSION BUTTON TO VIEW

SOFTWARE VERSIONS

BACK
BUTTON

Intelect® Advanced Therapy System

Pad Contact Quality

The Pad Contact Quality feature indicates to the user the contact
quality of the electrodes on the patient. This function, if On,
displays a bar graph at the bottom of Treatment Review screen for
the following waveforms only:

IFC Traditional (4p):

•

Dual Channel Graph

IFC Premod (2p):

•

PAD CONTACT QUALITY
BUTTON

Single Channel Graph

Russian:

•

Single Channel Graph

To turn on, press Pad Contact
Quality button until On is
displayed.

Single Channel Waveforms will

SINGLE CHANNEL GRAPH

display a single bar graph. Dual
Channel waveforms will display a
double bar graph.

Contact quality is measured by
the amount of the graph filled
with black.

DUAL CHANNEL GRAPH

GOOD CONTACT
QUALITY

CHANNEL 1:
GOOD CONTACT QUALITY

An ideal contact quality is 75% or
more of the graph filled.

CHANNEL 2:
NO CONTACT QUALITY

33

SET UP

Supplied by EME Services Ltd

THERAPY SYSTEM SET UP (continued)

Select Language

To change the language
displayed on the system, press
the Language button until the
desired language is displayed.

Press Home button to set the
language and return to Home
screen.

If Unit Default Settings are
restored, the language will revert
back to English.

LANGUAGE
BUTTON

PRESS HOME BUTTON
TO SET LANGUAGE

Intelect® Advanced Therapy System

Connecting Accessories to the Therapy System

Install Lead Wires, Ultrasound Applicator, Patient Interrupt Switch,
and any other accessories according to the Front Access Panel as
illustrated below. Refer to page 13 for Symbol Definitions.

OPERATOR REMOTE

OPTIONAL

CHANNEL 1/2

PATIENT INTERRUPT SWITCH

CHANNEL 1
LEAD WIRE

BLACK

CHANNEL 2
LEAD WIRE

MICROCURRENT PROBE

OPTIONAL

ULTRASOUND APPLICATOR
COMBO SYSTEMS ONLY

GREY

34

PATIENT PREPARATION

Supplied by EME Services Ltd

ELECTROTHERAPY PATIENT PREPARATION

Electrode Placement

Examine the skin for any wounds and clean the skin.

•

Apply the electrodes to the treatment area.

•

Ensure the electrodes are applied securely to the skin.

•

Ensure good contact between each electrode and the skin.

•

Check the electrode contact regularly during the treatment.

•

Examine the skin again after the treatment.

•

Choose electrodes that fit the anatomy.

•

View the Electrode Placement recommendations in the

•

Treatment Review screen for the particular modality being used
for treatment as a reference point only prior to administering
treatment.

Refer to the respective electrode type instructions on pages 37

•

through 38.
Follow electrode manufacturer instructions.

•

Intelect® Advanced Therapy System

•

Keep electrodes separated during treatment. Electrodes in contact with
each other could result in improper stimulation or skin burns.

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.

Powered muscle stimulators should be used only with the leads and

•

electrodes recommended for use by the manufacturer.

35

PATIENT PREPARATION

Supplied by EME Services Ltd

ELECTROTHERAPY PATIENT PREPARATION (continued)

Dura-Stick™ Electrodes

Chattanooga Group Dura-Stick Electrodes are a self adhesive, single
patient, one time use disposable product designed specifically for
use with Chattanooga Group Electrotherapy systems.

It is recommended that Chattanooga Group Dura-Stick Electrodes
be used whenever possible to ensure the highest level of contact
with the treatment area and most uniform delivery of the
prescribed electrotherapy treatment.

Properly dispose of used Dura-Stick Electrodes upon completion of
the therapy session.

Intelect® Advanced Therapy System

Reusable Carbon Electrodes

If used for delivery of electrotherapy, the Carbon Electrodes must
be inserted into the sponges moistened with distilled water prior to
placement on the patient.

These Carbon Electrodes should be secured to the treatment area
using the Nylatex® Wraps shipped with the Therapy System.

36

PATIENT PREPARATION

Supplied by EME Services Ltd

ELECTROTHERAPY PATIENT PREPARATION (continued)

Dura-Stick™ Electrode Instructions
Connecting Lead Wires

Insert the lead with the Red (+) electrode
connector into one Dura-Stick Elec

trode.
Insert the lead with the Black (-) electrode
connector into the other electrode.

Make certain the lead wires are
seated completely into the electrodes.

NOTE:

Use of conductive medium or sponges is

not required or recommended. Dura-Stick

Electrodes are manufactured to ensure

the optimum conductivity during therapy

when properly applied.

LEAD WIRE SEATED

RED +

LEAD WIRE

Securing Electrodes

Remove the Dura-Stick Electrodes from
the protective backing and apply to the
treatment area as prescribed. Ensure the
entire electrode surface is in contact with
patient skin by pressing into place.

Intelect® Advanced Therapy System

BLACK 
LEAD WIRE

37

PATIENT PREPARATION

Supplied by EME Services Ltd

ELECTROTHERAPY PATIENT PREPARATION (continued)

Reusable Carbon Electrodes

Connecting Lead Wires

Insert the lead with the Red (+) electrode
connector into electrode. Insert the lead
with the black (-) electrode connector into
the other electrode.

Make certain the lead wires are seated
completely into the electrodes.

LEAD WIRE SEATED

RED +

LEAD WIRE

BLACK 
LEAD WIRE

Conductive Medium

Use wet sponges or liberally apply
Conductor™ Transmission Gel to electrode
prior to placement on patient.

Intelect® Advanced Therapy System

Securing Electrodes

®

Use the Nylatex

Wrap to secure each

electrode in position on the patient.

SECURE WITH
NYLATEX

The Nylatex® Wraps contain dry natural rubber and
may cause allergic reactions in patients with allergies
to latex.

38

PATIENT PREPARATION

Supplied by EME Services Ltd

ULTRASOUND PATIENT PREPARATION

Preparing Treatment Area

Examine the skin for any wounds and clean the skin. Liberally apply Conductor™

Size of Applicator

View the Sound Head Recommendation in the Treatment
Review screen for Ultrasound (as a reference point only) prior to
administering treatment.

Sound Heads are available in the sizes shown below.

2

1 CM

5 CM

STANDARD

2

2 CM

2

10 CM

2

Applicator Preparation

Clean applicator before each therapy session with warm soapy
water.

Conductive Medium

Transmission Gel or equivalent to
the treatment area on the patient.

Treatment Area

Move the Sound Head during
therapy session in a circular
motion. The area treated should
be two times the diameter of the
Sound Head.

Applicator Coupling

If US Coupling is On, the Sound
Head is properly coupled to
the patient and administering
ultrasound when the LED is
constantly illuminated

NOTE:

Refer to page 29 for US Coupling
settings.

Intelect® Advanced Therapy System

APPLY

CONDUCTIVE GEL

COUPLING
INDICATOR
LED

39

OPERATION

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Intelect® Advanced Therapy System

OPERATOR INTERFACE

The Intelect Advanced Therapy System user Operator Interface houses all of the functions and controls necessary for the operator to
access all operator utilities, modalities, and parameters for modification and system set up.

Clinical Resources Library button

6.

Used to access Clinical Protocols, User
Protocols, Sequencing, and the Clinical
(Anatomical/Pathological) Libraries
screen.

Home button

7.

Used to go back to the System Home
screen. Used in conjunction with the
Back button to access the Operator
Utilities screen.

Modality and Parameter buttons

8.

Used to select modality and edit
treatment parameters.

Intensity Knob

9.

Rotate clockwise to increase Modality
intensity. Rotate counterclockwise to
decrease Modality intensity.

Start button

10.

Press to start therapy session after all
initial parameters have been set.

Pause button

11.

Press to pause a therapy session. Press
again to restart session.

Stop button

12.

Press to completely stop the therapy
session.

8

7

12

11

Top of Screen

1

8

10

1.

The Title Bar indicates the Screen Title
for the modality being used. When at

2

3

4

5

6

9

the System Home screen, the Clinic
Name is displayed.

Center of Screen

2.

Contains available Modality options.
Select Modality by pressing the desired
Modality button and then make
parameter modifications.

Bottom of Screen

3.

Displays available channels and their
respective status. Displays Treatment
Time and status. After starting therapy
session, Modality and Parameter buttons
are used to select and modify channel
parameters.

Unit On Indicator

4.

Illuminates green when System is
connected to an AC mains power source.
When the System is On, the indicator
will illuminate blue. With System On,
and if the system sits unused, the Screen
Saver initiates (blank screen) and the Blue
Indicator will flash.

Back button

5.

Used to return back one screen. Used in
conjunction with the Home button to
access the Operator Utilities screen.

40

OPERATION

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Intelect® Advanced Therapy System

HOME SCREEN

The Intelect Advanced Home screen affords access to all of the system modalities and functions. The area surrounding the screen has 10
modalit

y and parameter modification buttons

.

Electrotherapy

1.

Accesses all the available waveforms and parameter editing controls.

Quick Link Indications

2.

Accesses specific pre-programmed indications, for general reference only, which
aid in selecting the proper waveform and electrode placement for particular

1

3

5

7

9

2

4

6

8

10

indicated patient syndrome diagnoses.

Ultrasound

3.

Accesses the Ultrasound set up screen and parameter editing controls.

Combination

4.

Accesses combination therapy set up screens and parameter editing controls.

sEMG*

5.

Accesses the Surface EMG (sEMG) modality and parameter editing controls.

sEMG + Stim*

6.

Accesses the Surface EMG (sEMG) + Electrical Stimulation modality and
parameter editing controls.

View/Edit Channel

7.

Accesses the selected channel and allows editing of the channel's parameters
during therapy. Also used in the saving of information to the Patient Data Card.

Patient Card

8.

Accesses Patient Data Card data.

Select Channel

*NOTE:

The sEMG Module is standard on the Intelect
Advanced Therapy System Color Series and
optional for the Monochromatic Series.

9.

Use to select desired channel for viewing and editing of channel parameters.

Unused

10.

Reserved for optional expansion Modules.

41

OPERATION

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ELECTROTHERAPY SCREEN

Intelect® Advanced Therapy System

The screen allows the operator to access, set up, and modify
parameters of each of the available wav
Intelect Advanced Therapy System. The following pages give a
general explanation of a treatment setup.
Refer to the Specifications section, beginning on page 15,
for detailed specifications of the system and each available
waveform.

NOTE:

Give patient the appropriate Patient Interrupt Switch for the
channels being used. Prior to starting a therapy session, explain
to the patient how to use the Patient Interrupt Switch.

eforms within the

42

OPERATION

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Intelect® Advanced Therapy System

GENERAL ELECTROTHERAPY WAVEFORM SET UP

The following information is an example of step by step set up for the Electrotherapy waveforms. All waveforms in the Intelect Advanced
Therapy System are set up and edit

ed in the same basic fashion. The following set up instructions use IFC Traditional (4p) Waveform.

Prepare Patient

Refer to pages 35 through 38 for electrode
selection, preparing patient, and securing
electrodes.

Select Modality

Press the Electrotherapy button on the
Home screen.

ELECTROTHERAPY
BUTTON

Select Waveform

Press button beside the desired waveform

from the listing on the screen.

PRESS DESIRED WAVEFORM BUTTON

Refer to Specifications section of this
manual for all available waveforms on the
Intelect Advanced Therapy System.

43

View Waveform Description

Press the Waveform Description button
to view text explaining the waveform
rationale.

WAVEFORM DESCRIPTION

BUTTON

NEXT
PAGE

BUTTON

BACK
BUTTON

Press the Next Page button to view
additional text. Press the Back button to
return to the Treatment Review screen.

OPERATION

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GENERAL ELECTROTHERAPY WAVEFORM SET UP (continued)

View Electrode Placement

Press the Electrode Placement button to
view the most commonly used electrode
placement for the wa

ELECTRODE PLACEMENT

BUTTON

veform selected.

Edit Waveform Parameters

Press Edit button to access waveform
parameters.

Press the corresponding button to edit
each parameter as prescribed.

Intelect® Advanced Therapy System

Install Patient Interrupt Switch

Make certain the Patient Interrupt Switch is
connected to the Therapy System. Refer to
page 13 for Symbol Definitions.

LANYARD

Press the Next button to read Electrode
Placement Text. Press the Back button to
return to the Treatment Review screen.

NEXT
PAGE

BUTTON

BACK

BUTTON

EDIT

BUTTON

PARAMETER

BUTTONS

BACK
BUTTON

Press the Back button to return to the
Treatment Review screen.

44

PATIENT
INTERRUPT
SWITCH

NOTE:

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

OPERATION

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GENERAL ELECTROTHERAPY WAVEFORM SET UP (continued)

Patient Interrupt Switch

Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

PRESSING BUTTON ONCE PAUSES SESSION

If Patient Interrupt Switch is depressed, the
treatment will be paused and a message
will appear on the System screen.

Press any button to clear the message.

NOTE:

If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

Set Waveform Intensity

Set intensity by rotating the Intensity Control
Knob to the prescribed level.

INTENSITY
DISPLAYED

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

Intelect® Advanced Therapy System

Start Treatment

Press the Start button to begin therapy
session.

START
BUTTON

ROTATE
INTENSITY
KNOB

45

OPERATION

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GENERAL ELECTROTHERAPY WAVEFORM SET UP (continued)

Pause Treatment

Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

PAUSE
BUTTON

Stop Treatment

To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.

STOP BUTTON

Intelect® Advanced Therapy System

Save to Patient Data Card

After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

46

OPERATION

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Intelect® Advanced Therapy System

ADJUSTING ELECTROTHERAPY CHANNEL PARAMETERS DURING TREATMENT

The Electrotherapy channel parameters may be changed during a treatment session without pausing or stopping the treatment. The
waveform Intensity may be increased or decreased at any time during the session without utilizing this process.

Select Channel

Press the Home button.

Press the Select Channel button until the
channel desired is framed.

VIEW/EDIT

BUTTON

SELECT CHANNEL

BUTTON

DESIRED

CHANNEL

FRAMED

Edit Channel Paramenters

Press the Edit button. Edit parameters as
desired.

EDIT

BUTTON

PARAMETER

BUTTONS

When finished editing the selected
channel, press the Home button to select
another channel if desired.

Press the View/Edit Channel button. The
Treatment Review screen will display.

To view the Treatment Review screen, if
the Home screen is displayed, press the
View/Edit Channel button. If the Edit
screen is displayed, press the Back button.

47

OPERATION

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Intelect® Advanced Therapy System

ULTRASOUND

The Intelect Advanced Therapy System Ultrasound modality allows the user to select specific Sound Head recommendations and edit
treatment parameters for var

ious syndromes requiring the use of ultrasound therapy. The following information gives general instructions
for the setup of ultrasound therapy when selecting Ultrasound from the Home screen. Clinical Protocol and Quick Link Indication Ultrasound
treatment parameters are edited in the same basic fashion.

Prepare Patient View Parameter Rationale

Refer to page 39 for Applicator sizes,
patient preparation, and use of conductive
medium.

NOTE:

Use only Intelect Advanced Ultrasound

Press the Parameter Rationale button for
text. Press the Next Page button to continue
viewing text.

PARAMETER RATIONALE
BUTTON

Applicators. Previous models of
Chattanooga Group Ultrasound Applicators
will not work with the Intelect Advanced
Therapy System.

NEXT
PAGE
BUTTON

Sound Head Recommendation

Press Sound Head Recommendation
button to view text explaining how to select
an Ultrasound Applicator size based on
treatment area.

SOUND HEAD
RECOMMENDATION
BUTTON

Select Modality

Press the Ultrasound button on the Home
screen.

ULTRASOUND
BUTTON

Press the Back button to the return to
Treatment Review screen.

48

BACK
BUTTON

BACK
BUTTON

Press the Back button to the return to
Treatment Review screen.

OPERATION

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ULTRASOUND (continued)

Edit Ultrasound Parameters

Press Edit button to access ultrasound
parameters.

ess the corresponding button to edit as

Pr
prescribed.

EDIT

BUTTON

Head Warming

The Intelect Advanced Therapy System
incorporates a Head Warming feature that
pre-heats the Sound Head of the Applicator
for increasing patient comfort. The control
for the Head Warming feature is in the Edit
screen of the Ultrasound modality.

Press the Head Warming button until On is
displayed.

HEAD WARMING
BUTTON

Intelect® Advanced Therapy System

Set Ultrasound Intensity

Set intensity by rotating the Intensity Control
Knob to the prescribed level.

INTENSITY
DISPLAYED

ROTATE
INTENSITY
KNOB

PARAMETER
BUTTONS

Press the Back button to return to
Treatment Review screen.

BACK
BUTTON

To set the default of the Head Warming
feature to On, press the Home button after
On is displayed in the Head Warming icon.
Head Warming will then start when the
Therapy System is turned On.

NOTE:

Head Warming time is approximately 2
minutes.

49

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

OPERATION

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ULTRASOUND (continued)

Intelect® Advanced Therapy System

Start Treatment

Press the Start button to begin therapy
session.

Move the Applicator in a circular motion
over the treatment area.

START

BUTTON

NOTE:

If US Coupling is On and the Sound Head
looses coupling with the treatment area
the session will pause. When coupling is
reestablished the session will automatically
restart. See page 32 for US Coupling
settings.

Pause Treatment

Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

or

If US Coupling is On, and the Sound
Head looses coupling with the treatment
area, the session will pause. When
coupling is reestablished, the session will
automatically restart. Refer to page 32 for
US Coupling settings.

PAUSE
BUTTON

Stop Treatment

To Stop treatment, press the Stop button
once. Treatment will stop and the
Treatment Review screen will display.

STOP BUTTON

Save to Patient Data Card

After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

50

OPERATION

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Intelect® Advanced Therapy System

ADJUSTING ULTRASOUND PARAMETERS DURING TREATMENT

The ultrasound parameters may be changed during a treatment session without pausing or stopping the treatment. The following
information provides instructions for changing ultrasound treatment parameters during a treatment session. The ultrasound intensity may be
increased or decreased at any time during the session without utilizing this process.

Editing Ultrasound from Home Screen

Press Select Channel button until US:
Running is framed.

Press View/Edit Channel button.

Press the Edit button on the Treatment
Review screen.

Press the cooresponding parameter
button and edit as prescribed.

Editing Ultrasound from Treatment
Review Screen

Press the Edit button on the Treatment
Review screen.

Press the cooresponding parameter
button and edit as prescribed.

VIEW/EDIT

CHANNEL

BUTTON

SELECT

CHANNEL

BUTTON

US: RUNNING

FRAMED

EDIT
BUTTON

PARAMETER
BUTTONS

BACK
BUTTON

When editing is complete, press the Back
button to return to Treatment Review
screen

51

EDIT

BUTTON

PARAMETER
BUTTONS

BACK
BUTTON

When editing is complete, press the Back
button to return to Treatment Review
screen.

OPERATION

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Intelect® Advanced Therapy System

QUICK LINK INDICATIONS

The Intelect Advanced Therapy System incorporates a unique Quick Link Indications section which allows the user to select specific Clinical
Indications and apply the most common therapy for the Indication selec

ted. All modalities are editable, in their normal editing fashion, in

order to customize the treatment for each patient’s prescribed therapy.

Available Quick Link Indications

Pain- (Acute, Subacute and Chronic)
Increase Local Circulation
Neuromuscular Re-education- (Spasticity,

Muscle Re-education and Stroke Muscle
Re-education)

Select Quick Link Indication

Press the Quick Link Indications button on
the Home screen.

Press the corresponding button beside the
desired Quick Link Indication.

QUICK LINK INDICATIONS BUTTON

If prompted by the Therapy System, press
the corresponding button for the desired
Pathological Severity.

SELECT PATHOLOGICAL SEVERITY

Wound Healing- (Stage III and Stage IV)
Iontophoresis
Muscle Spasm
Edema- (Acute and Chronic)

PRESS
DESIRED
BUTTON

Denervated Muscle- (Muscle Re-education
and S/D Curve)

Muscle Strengthening- (Phasic Muscle
Strengthening and Tonic Muscle Strengthening)

Waveforms- Link to Waveform and Current
Library. (Same as under Electrotherapy on Home
screen)

Prepare Patient

Refer to pages 35 through 38 for electrode
selection, preparing patient, and securing
electrodes.

52

OPERATION

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QUICK LINK INDICATIONS (continued)

View Waveform Description

Press the Waveform Description button
to view text explaining the waveform
rationale.

WAVEFORM DESCRIPTION

BUTTON

View Electrode Placement

Press the Electrode Placement button to
view the most commonly used electrode
placement for the waveform selected.

ELECTRODE PLACEMENT

BUTTON

Intelect® Advanced Therapy System

Edit Waveform Parameters

Press Edit button to access waveform
parameters.

Press the corresponding button to edit
each parameter as prescribed.

Press the Next Page button to view
additional text. Press the Back button to
return to the Treatment Review screen.

NEXT
PAGE

BUTTON

BACK

BUTTON

NEXT
PAGE

BUTTON

BACK

BUTTON

Press the Next button to read Electrode
Placement Text. Press the Back button to
return to the Treatment Review screen.

53

EDIT

BUTTON

PARAMETER

BUTTONS

Press the Back button to return to the
Treatment Review screen

OPERATION

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QUICK LINK INDICATIONS (continued)

Install Patient Interrupt Switch

Make certain the Patient Interrupt Switch is
connected to the unit. Ref
Symbol Definitions.

LANYARD

PATIENT
INTERRUPT
SWITCH

NOTE:

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

er to page 13 for

Patient Interrupt Switch

Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

PRESSING BUTTON ONCE PAUSES SESSION

If Patient Interrupt Switch is depressed, the
treatment will be paused and a message
will appear on the System screen.

Press any button to clear the message.

NOTE:

If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

Intelect® Advanced Therapy System

Reset intensity and press the Start button
to resume session.

START
BUTTON

54

OPERATION

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QUICK LINK INDICATIONS (continued

Setting Waveform Intensity

Set intensity by rotating the Intensity Control
Knob to the prescr

INTENSITY
DISPLAYED

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

ibed level.

ROTATE
INTENSITY
KNOB

Start Treatment

Press the Start button to begin therapy
session.

START
BUTTON

Intelect® Advanced Therapy System

Pause Treatment

Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

PAUSE
BUTTON

55

OPERATION

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QUICK LINK INDICATIONS (continued)

Stop Treatment

To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.

STOP BUTTON

Editing Parameters during Treatment
Session

The parameters may be edited during
a treatment session without pausing or
stopping the treatment.

Refer to page 47 for parameter changes
to electrotherapy waveforms and currents
and page 51 for editing Ultrasound.

NOTE:

The intensity can be increased or decreased
by rotating the Intensity Knob as desired
without pressing the Edit button.

Intelect® Advanced Therapy System

Save to Patient Data Card

After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

56

OPERATION

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Intelect® Advanced Therapy System

COMBINATION

The Intelect Advanced Therapy System Combination modality allows the user to select and use ultrasound therapy in combination with
electr

ical muscle stimulation.
Combination therapy utilizes the Ultrasound modality in conjuction with High Voltage Pulsed Current (HVPC), IFC (4p), IFC (2p), Asymmetrical
Biphasic, Symmetrical Biphasic, or VMS

TM

to generate a therapeutic effect. In this mode of therapy, the Sound Head of the Ultrasound

Applicator becomes one half of the electrical circuit. An electrode attached to the Red (+) Lead Wire completes the circuit.

Refer to pages 35 through 38 to prepare
patient, select electrode, and securing
electrodes. Refer to page 39 for Ultrasound
patient preparation.

Connect the Black (-) Lead Wire from
Channel 2 to the electrode. Make certain
the Lead Wire is completely seated in the
electrode.

The Red (+) Lead Wire is not used. The
Ultrasound Applicator completes the
circuit for Combination Therapy.

Select ModalityPrepare Patient

Press the Combination button on the Home
screen.

COMBINATION
BUTTON

57

View Application Description

Press the Waveform Description button
to view text explaining the waveform
rationale.

APPLICATION
DESCRIPTION

BUTTON

BACK

BUTTON

Press the Back button to return to the
Treatment Review screen.

OPERATION

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COMBINATION (continued)

View Electrode Placement

Press the Electrode Placement button to
view the most commonly used electrode
placement for Combination therapy.

ELECTRODE PLACEMENT

BUTTON

NEXT
PAGE

BUTTON

BACK

BUTTON

Press the Next button to read Electrode
Placement Text. Press the Back button to
return to the Treatment Review screen.

Access Combination Parameters

Press Edit button to access Combination
parameters.

EDIT
BUTTON

Press the Back button to return to the
Treatment Review screen.

Intelect® Advanced Therapy System

Edit Ultrasound Parameters

Press the corresponding button to edit
the desired Ultrasound parameter as
prescribed.

PARAMETER

BUTTONS

NOTE:

See page 49 for Head Warming feature
instructions.

58

OPERATION

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COMBINATION (continued)

Select Waveform

Press the Select Waveform button.

SELECT WAVEFORM

BUTTON

UP ARROW

BUTTON

Patient Interrupt Switch

Connect Patient Interrupt Switch to the
Therapy System. Give Patient Interrupt
Switch to patient and explain that pressing
the Red button once pauses the therapy
session.

CONNECT PATIENT
INTERRUPT SWITCH

Intelect® Advanced Therapy System

Edit Waveform Parameters

Press the Edit Stim button to edit the
parameters of the waveform selected.

Press the corresponding button to edit
each parameter as prescribed.

EDIT STIM

BUTTON

DOWN ARROW

BUTTON

Press the Up or Down Arrow buttons until
the prescribed waveform is highlighted.

Press the Accept and Return Arrow button.

ACCEPT AND

RETUN ARROW

BUTTON

PATIENT INTERRUPT
SWITCH

If Patient Interrupt Switch is depressed, the
treatment will be paused and a message
will appear on the System screen.

Press any button to clear the message.

NOTE:

If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

59

PARAMETER

BUTTONS

OPERATION

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COMBINATION (continued)

Set Waveform Intensity

Set intensity by rotating the Intensity Control
Knob to the prescribed level.

INTENSITY
DISPLAYED

ROTATE
INTENSITY
KNOB

Set Ultrasound Intensity

Press the Edit Ultrasound button.
Set Ultrasound intensity by rotating the

Intensity Control Knob to the prescribed level.

EDIT
ULTRASOUND
BUTTON

ROTATE
INTENSITY
KNOB

Intelect® Advanced Therapy System

Start Treatment

Press the Start button to begin therapy
session.

Move the Applicator in a circular motion
on the treatment area.

START

BUTTON

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

60

NOTE:

If US Coupling is On and the Sound
Head looses coupling with the treatment
area the session will pause. When
coupling is reestablished, the session will
automatically restart. See page 32 for US
Coupling settings.

OPERATION

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COMBINATION (continued)

Pause Treatment

Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

PAUSE

BUTTON

Stop Treatment

To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.

STOP BUTTON

Intelect® Advanced Therapy System

Save to Patient Data Card

After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

61

A S

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OPERATION

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Intelect® Advanced Therapy System

PATIENT DATA CARD SET UP OF NEW CARD

General Information

The Intelect Advanced Therapy System incorporates a Patient Data Card reading and recording device that allows transfer of patient therapy
data from the system to the car

d for reviewing patient modality and pain profile information. Information may be transferred to a PC via the
optional Patient Data Management System. The PC software is designed to allow easy access to patient data and printing of reports as well as
adding session notes to the Patient Data Card.

The reading and recording device allows storage and recall of the following patient session data onto the Patient Data Card: therapy session
parameters, Electrode Placement, Pain Map, Numeric Pain Scale or Visual Pain Scale, and Session Notes (stored on card via PC only). Each
Patient Data Card can store multiple sessions and each session can be recalled on the Intelect Advanced Therapy System.

Insert New Patient Data Card

Insert a new Patient Data Card into the
system access port as shown below. The
Therapy System will automatically format
the new Patient Data Card and a verification
message will appear.

Press any button to continue.

INSERT NEW

PATIENT DATA CARD

PRESS ANY BUTTON
TO CONTINUE

Setup Treatment

Set up the patient's prescribed treatment.
Refer to the appropriate area of this manual
for modality set up.

Administer treatment as prescribed. When
treatment is complete, the Treatment
Review screen will be visible.

Set Up of New Patient Data Card

With new Patient Data Card inserted in
the system, press the Save to Patient Card
button.

SAVE TO
PATIENT CARD
BUTTON

63

OPERATION

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PATIENT DATA CARD SET UP OF NEW CARD (continued)

Enter Patient ID

Select the row of alpha or numeric
characters desired by pushing the butt

on
beside the corresponding row. Select the
desired character in the row by pressing
the row button until the desired letter is
framed.

SELECT ROW AND CHARACTERS

When the desired character is framed, press
the Accept and Return Arrow button. The
character selected will display in the top of
the screen and the cursor will advance to
the next position.

To move back a character, press the Left
Arrow button.

CHARACTER

DISPLAYED

Intelect® Advanced Therapy System

To discard entire entry, press the Back
button.

Repeat this procedure until the desired
Patient ID is entered.

After Patient ID is entered, press the Save
button.

SAVE
BUTTON

LEFT
ARROW
BUTTON

ACCEPT AND RETURN

ARROW BUTTON

To delete a character, press the Left Arrow
button until the character to be deleted is
framed. Press the Delete button.

64

OPERATION

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PATIENT DATA CARD SET UP OF NEW CARD (continued)

Access Electrode Placement

The following information uses the IFC
Traditional (4p) as an example. Electr

ode
Placement procedures for all modalities are
performed in the same basic fashion.

Press the Electrode Placement button.

ELECTRODE PLACEMENT BUTTON

Electrode Placement Set Up

Press the Pad button to select the Red (+) or
Black (-) electrode.

Press the Chan button to select (1) or
Channel B (2).

Press the Side button to select Front, Back,
Left, or Right of the body graphic.

Press the Size button until desired electrode
size is displayed. If electrode desired is not
listed, select Other.

PAD
BUTTON

CHAN
BUTTON

SIDE
BUTTON

SIZE
BUTTON

Intelect® Advanced Therapy System

Electrode Placement

Press the Up, Down, Left and Right Arrow
buttons to position the selected electrode
as close to the actual treatment location as
possible.

Press the Pad button to select the other
electrode. Repeat above procedure for
electrode positioning.

If applicable, press the Chan button, to
select another channel and repeat above
procedures.

After positioning the electrodes, press the
Accept and Return Arrow button.

ELECTRODES
POSITIONED

NOTE:

When Ultrasound is the modality, only the
Side button is available.

65

ACCEPT AND RETURN
ARROW BUTTON

OPERATION

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PATIENT DATA CARD SET UP OF NEW CARD (continued)

Access Pain Map

Press the Pain Map button to select
the body area of the associated pain as
described by the patient.

PAIN MAP BUTTON

Select Pain Type

Press the Pain Type button until the
desired description is displayed in the Pain
Type icon.

Intelect® Advanced Therapy System

Add Pain Locations

Press the Add button. The Add Pain Map
window will display.

ADD
BUTTON

PAIN TYPE

BUTTON

66

OPERATION

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PATIENT DATA CARD SET UP OF NEW CARD (continued)

Select Location of Pain

Press the Up and Down Arrow buttons to
move the Pain Locator to the area of the
body where the pain originates.

Press the Accept and Return Arrow button.
The Pain Map window will display.

PAIN

LOCATO R

UP AND DOWN

ARROW BUTTONS

ACCEPT AND RETURN

ARROW BUTTON

Press the Add button to continue selecting,
in sequence, the radiating path of the pain
using the above procedure.

Up to eight pain locations may be selected.

ADD

BUTTON

After all desired Pain Locations have been
made, press the Back button.

BACK
BUTTON

Intelect® Advanced Therapy System

Editing Pain Locations

Press the Edit button on the Pain Map
window.

EDIT

BUTTON

UP AND DOWN

ARROW BUTTONS

EDIT NEXT

BUTTON

ACCEPT AND RETURN

ARROW BUTTON

Press the Edit Next button to highlight the
Pain Location to be edited.

Use the Up and Down Arrow buttons to
relocate the selected Pain Location.

Press the Accept and Return Arrow button.
Repeat until all editing is complete, then

press the Back button.

67

OPERATION

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PATIENT DATA CARD SET UP OF NEW CARD (continued)

Deleting Pain Locations

Press the Delete button on the Pain Map
window

DELETE

BUTTON

UP AND DOWN

ARROW BUTTONS

DELETE

BUTTON

ACCEPT AND RETURN

ARROW BUTTON

Use the Up and Down Arrow buttons to
highlight the Pain Location to be deleted.

Press the Delete button.
Press the Accept and Return Arrow button.
Repeat until all editing is complete, then

press the Back button.

Pain Scales

The Intelect Advanced Therapy System incorporates two internationally recognized Pain
Scales; VAS Visual Analog Scale, Scale has no indicator marks or Numeric (indicated 1
through 10) for use in describing the amount of pain the patient is experiencing. Once one
of the pain scales is set, the other will automatically set to the corresponding level.

Select Pain Scale

Select the desired Pain Scale by pressing the
corresponding button.

NUMERIC PAIN
SCALE BUTTON

VISUAL PAIN
SCALE BUTTON

Intelect® Advanced Therapy System

Adjust Pain Scale

Press the Left and Right Arrow buttons to
adjust the Pain Scale to the level the patient
is experiencing.

LEFT
ARROW
BUTTON

ACCEPT AND RETURN
ARROW BUTTON

RIGHT

ARROW

BUTTON

After the desired level is achieved, press the
Accept and Return Arrow button.

NOTE:

Numeric Pain Scale illustrated.

68

OPERATION

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PATIENT DATA CARD SET UP OF NEW CARD (continued)

Save to Patient Data Card

After all desired session data has been
entered in the Patient Data Card screens,
press the Save to Patient Card button. A
message will appear stating the data has
been saved to the Patient Data Card.

Press any button.

SAVE TO PATIENT
CARD BUTTON

After pressing any button, the Completed
Treatment Review screen will display. Press

the Home button.
Remove the Patient Data Card for filing with

patient records.
The Patient Data Card can also be used with

the optional Patient Data Management
System.

Intelect® Advanced Therapy System

69

OPERATION

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EXISTING PATIENT DATA CARD USE

Insert Existing Patient Data Card

Insert the Patient Data Card assigned to the
patient receiving treatment into the system
access port as shown below.

INSERT EXISTING
PATIENT DATA CARD

Access Patient Data Card

Press the Patient Card button to access
Patient Data Card.

Select the date of the treatment session

desired using the Up and Down Arrow

buttons until date desired is highlighted.

PATIENT CARD

BUTTON

UP ARROW

BUTTON

DOWN ARROW
BUTTON

Intelect® Advanced Therapy System

View Patient Data Card

Press the corresponding button beside the
Patient Data to be viewed.

NOTE:

No Session Notes will be available unless
the optional Patient Data Management
System was utilized to enter Session Notes
onto the Patient Data Card.

70

OPERATION

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EXISTING PATIENT DATA CARD USE (continued)

Starting a New Treatment from Patient
Data Card

Refer to pages 35-38 for Electrotherapy
patient preparation, select electrodes, and
secure electrodes. Refer to page 39 for
Ultrasound patient preparation.

Press the Up and Down Arrow buttons to
highlight the desired treatment date and
time.

Press the View Treat. button.
Press Start New Treatment button.

VIEW TREAT.

BUTTON

START NEW
TREATMENT
BUTTON

Patient Interrupt Switch

Connect Patient Interrupt Switch to the
Therapy System. Give Patient Interrupt
Switch to patient and explain that pressing
the Red button once pauses the therapy
session.

CONNECT PATIENT
INTERRUPT SWITCH

If Patient Interrupt Switch is depressed, the
treatment will be paused and a message
will appear on the System screen.

Press any button to clear the message.

NOTE:

If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

PATIENT
INTERRUPT
SWITCH

Intelect® Advanced Therapy System

Set Intensity

Set intensity by rotating the Intensity Control
Knob to the prescribed level.

INTENSITY
DISPLAYED

ROTATE
INTENSITY
KNOB

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

71

OPERATION

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EXISTING PATIENT DATA CARD USE (continued)

Intelect® Advanced Therapy System

Start Treatment

Press the Start button to begin therapy
session.

START
BUTTON

Pause Treatment

Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

PAUSE
BUTTON

Stop Treatment

To Stop treatment, press the Stop button

once. Treatment will stop and the Home

screen will display.

STOP BUTTON

Erasing Patient Data Card

Refer to page 31 for proper Patient Data
Card Erasing instructions.

72

OPERATION

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Intelect® Advanced Therapy System

CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS™

The Intelect Advanced Clinical Resources Library contains Clinical Protocols™, User Protocols, Sequencing functions and access to the
Multimedia Card (MMC) which contains the Anatomical and Pathological Libraries.

Clinical Protocols™

This library is a series of protocol presets where the Body Area, Clinical Indication, Pathological Condition, and Pathological Severity are
selected by the user,

and the Clinical Protocols algorithm will select the parameter

settings. These Clinical Protocols are to be used only as
guidelines. Each patient should be individually assessed to determine the appropriateness of the protocol parameters prior to use. All
Clinical Protocols can be edited to suit appropriate patient treatment prescription and patient comfort.

The following information gives general instructions to access, selection and setup of Clinical Protocols. Each Clinical Protocol is set up and
edited in the same basic manner.

Access Clinical Resources Access Clinical Protocols™

Select Body Area

Press the Clinical Resources Library button. Press the Clinical Protocols button. Press the button corresponding to the

CLINICAL RESOURCES
LIBRARY BUTTON

CLINICAL
PROTOCOLS
BUTTON

body area desired.

BODY AREA BUTTONS

73

OPERATION

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CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS™ (continued)

Select Clinical Indication

ress the button beside the Clinical

P
Indication desired in either the
Electrotherapy or Ultrasound screen
section.

CLINICAL INDICATION BUTTONS

Select Pathological Condition

Press the button beside the desired
Pathological Condition.

PATHOLOGICAL CONDITION BUTTONS

Intelect® Advanced Therapy System

Select Pathological Severity

Press the button beside the desired
Pathological Condition.

PATHOLOGICAL SEVERITY BUTTONS

NOTE:

Not all Pathological Conditions have
corresponding Pathological Severity
windows. Some go directly to the
associated modality Treatment Review
screen.

74

OPERATION

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CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS™ (continued)

View Waveform Rationale

Press the Waveform Rationale button
(Electrotherapy Modalities) or the Parameter
Rationale (Ultrasound Modality) to view
the text explaining the rationale for the
modality associated with the specific
Clinical Protocol selected.

WAVEFORM RATIONALE
BUTTON

BACK
BUTTON

Press the Back button to return to the
Treatment Review screen.

View Electrode Placement

Press the Electrode Placement button to
view the specific electrode placement for
the Clinical Protocol selected.

ELECTRODE PLACEMENT

BUTTON

Press the Next Page button to view text
relating to the electrode placement.

Press the Back button to return to the
Treatment Review screen.

NEXT PAGE

BUTTON

BACK

BUTTON

Intelect® Advanced Therapy System

Prepare Patient

Refer to pages 35 through 38 for
Electrotherapy and page 39 Ultrasound
patient preparation instructions. For sEMG
and sEMG+Stim patient Preparation, refer
to the sEMG and sEMG+Stim Module User
Manual.

Edit Modality Parameters

Press the Edit button.
Edit modality parameters as prescribed.

Refer to page 44 for Electrotherapy
modalities and page 49 for Ultrasound.

Refer to the sEMG and sEMG+Stim Module
User Manual for sEMG and sEMG+Stim
modalities.

EDIT
BUTTON

75

OPERATION

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CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS™ (continued)

Patient Interrupt Switch

Make certain the Patient Interrupt Switch,
for the channel(s) being used, is connected
to the Therapy System. Refer to page 13 for
Symbol Definitions.

LANYARD

PATIENT
INTERRUPT
SWITCH

Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

PRESSING BUTTON ONCE PAUSES SESSION

Intelect® Advanced Therapy System

Set Modality Intensity

Set intensity by rotating the Intensity Control
Knob to the prescribed level.

INTENSITY
DISPLAYED

ROTATE
INTENSITY
KNOB

NOTE:

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

If Patient Interrupt Switch is depressed, the
treatment will be paused and a message
will appear on the System screen.

Press any button to clear the message.

NOTE:

If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

76

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

OPERATION

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CLINICAL RESOURCES LIBRARY CLINICAL PROTOCOLS™ (continued)

Intelect® Advanced Therapy System

Start Treatment

Press the Start button to begin therapy
session.

START

BUTTON

NOTE:

Modality parameters ma

y be editied at any
time during the therapy session. Refer to
page 47 for Electrotherapy and page 51 for
Ultrasound.

Pause Treatment

Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

PAUSE
BUTTON

Stop Treatment

To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.

STOP BUTTON

Save to Patient Data Card

After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

77

OPERATION

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Intelect® Advanced Therapy System

CLINICAL RESOURCES LIBRARY CREATING USER PROTOCOLS

General Information

This library is a series of protocols created by the user and stored in the system memory. The following information gives general instructions
as to setting up, saving and accessing User Protocols. Should the Default Protocols be restored, through the User Utilities, all User Protocols will
be permanently removed from the system.

The Therapy System memory will accommodate up to 200 user defined protocols. This is inclusive of all User Protocols, User Sequences and
System Default Protocols. It does not include the Clinical Protocols.

Select Modality

Press the button beside the desired
modality on the Home screen or select
a Clinical Protocol using the Clinical
Resources Library button.

MODALITY BUTTONS

Edit Modality Parameters

Press the modality Edit button (usually
in the lower right corner of the modality
Treatment Review screen) and edit as
prescribed.

Refer to respective sections of this manual

Select Clinical Resources Library

Press the Clinical Resources Library button
to begin the save process of the new User
Protocol.

for Electrotherapy, Quick Link Indications
Ultrasound, and Combination modalities.
For sEMG and sEMG+Stim modalities, refer
to the sEMG and sEMG+Stim Module User
Manual.

CLINICAL RESOURCES
LIBRARY BUTTON

EDIT

BUTTON

78

OPERATION

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CLINICAL RESOURCES LIBRARY CREATING USER PROTOCOLS (continued)

Enter User Protocol Name

Select the row of alpha or numeric
characters desired by pushing the button
beside the corresponding row. Select the
desired character in the row by pressing
the row button until the desired letter is
framed.

SELECT ROW AND CHARACTERS

When the desired character is framed, press
the Accept and Return Arrow button. The
character selected will display in the top of
the screen and the cursor will advance to
the next position.

To move back a character, press the Left
Arrow button.

CHARACTER
DISPLAYED

Intelect® Advanced Therapy System

To discard entire entry, press the Back
button.

Repeat this procedure until the desired User
Protocol Name is entered.

After User Protocol Name is entered, press
the Save button.

SAVE
BUTTON

LEFT
ARROW
BUTTON

ACCEPT AND RETURN

ARROW BUTTON

To delete a character, press the Left Arrow
button until the character to be deleted is
framed. Press the Delete button.

79

OPERATION

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Intelect® Advanced Therapy System

CLINICAL RESOURCES LIBRARY DELETING USER PROTOCOLS

General Information

The following information provides instructions for the deletion of one User Protocol at a time. Once any single User Protocol is deleted, it
cannot be recovered. Should the Default Protocols be restored, through the User Utilities, all User Protocols will be permanently removed from
the system.

There is no method for recovery of the User Protocols nor can they be saved to any other medium.

Select Clinical Resources Library

Press the Clinical Resources Library button.
Then press the User Protocols button.

USER
PROTOCOLS
BUTTON

Select User Protocol to Delete

Press the UP and Down Arrow buttons until the
desired User Protocol to delete is highlighted.

UP AND DOWN
ARROW BUTTONS

80

Delete User Protocol

Press the Delete button to delete highlighted
User Protocol.

A verification screen will appear. Press Yes
button to delete protocol or No button to keep
protocol.

DELETE

BUTTON

NO

BUTTON

YES

BUTTON

Repeat this process until all desired User
Protocols are deleted.

Press the Home button to return to the Home
screen.

OPERATION

Supplied by EME Services Ltd

CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS

Access User Protocols

Press the Clinical Resources Library button.
Press the User Protocols button.

Select User Protocol

Press the UP and Down Arrow buttons until the
prescribed User Protocol is highlighted.

Press the Accept and Return Arrow button.

UP ARROW

BUTTON

Intelect® Advanced Therapy System

View Waveform Rationale

Press the Waveform Rationale button
(Electrotherapy Modalities) or the Parameter
Rationale (Ultrasound Modality) button
to view the text explaining the rationale
for the modality associated with the User
Protocol selected.

WAVEFORM RATIONALE
BUTTON

USER

PROTOCOLS

BUTTON

ACCEPT AND

RETURN ARROW

BUTTON

81

DOWN ARROW

BUTTON

BACK
BUTTON

Press the Back button to return to the
Treatment Review screen.

OPERATION

Supplied by EME Services Ltd

CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS (continued)

View Electrode Placement

Press the Electrode Placement button to
view the electrode placement for the User
P

rotocol selected.

ELECTRODE PLACEMENT

BUTTON

NEXT PAGE

BUTTON

BACK

BUTTON

Prepare Patient

Refer to pages 35 through 38 for
Electrotherapy and page 39 for Ultrasound
patient preparation instructions. For sEMG
and sEMG+Stim patient preparation, refer
to the sEMG and sEMG+Stim Module User
Manual.

Edit Modality Parameters

Press the Edit button.
Edit modality parameters as prescribed.

Refer to page 44 for Electrotherapy
modalities and page 49 for Ultrasound.
Refer to the sEMG and sEMG+Stim Module
User Manual for sEMG and sEMG+Stim
modalities.

Intelect® Advanced Therapy System

Patient Interrupt Switch

Make certain the Patient Interrupt Switch,
for the channel(s) being used, is connected
to the Therapy System. Refer to page 13 for
Symbol Definitions.

LANYARD

PATIENT
INTERRUPT
SWITCH

EDIT

BUTTON

Press the Next Page button to view text
relating to the electrode placement.

Press the Back button to return to the
Treatment Review screen.

NOTE:

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

82

OPERATION

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CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS (continued)

Set Modality Intensity

Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

PRESSING BUTTON ONCE PAUSES SESSION

Set intensity by rotating the Intensity Control
Knob to the prescribed level.

INTENSITY
DISPLAYED

Intelect® Advanced Therapy System

Start Treatment

Press the Start button to begin therapy
session.

START

BUTTON

ROTATE
INTENSITY
KNOB

If Patient Interrupt Switch is depressed, the
treatment will be paused and a message
will appear on the System screen.

Press any button to clear the message.

NOTE:

If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

83

NOTE:

Modality parameters may be edited at any
time during the therapy session. Refer to
page 47 for Electrotherapy and page 51 for
Ultrasound.

OPERATION

Supplied by EME Services Ltd

CLINICAL RESOURCES LIBRARY USING USER PROTOCOLS (continued)

Pause Treatment

Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

PAUSE
BUTTON

Stop Treatment

To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.

STOP BUTTON

Intelect® Advanced Therapy System

Save to Patient Data Card

After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

84

OPERATION

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Intelect® Advanced Therapy System

CLINICAL RESOURCES LIBRARY CREATING NEW SEQUENCES

General Information

This Library is a series of Electrotherapy Waveform/Current Sequences created by the user for special electrotherapy treatment purposes and
stored in the system memory for recall and use. The following information gives general instructions for setting up, saving and accessing of
sequences. Should the Default Protocols be restored, through the User Utilities, all user saved Sequences will be permanently removed from
the system.

The Therapy System memory will accommodate up to 200 user defined protocols. This is inclusive of all User Protocols, Sequences, and
System Default Protocols. It does not include the Clinical Protocols.

Access Sequencing

Press the Clinical Resources Library button.
Press the Sequencing button.

SEQUENCING
BUTTON

Select Sequence

Press the Up and Down Arrow buttons until
the desired sequence is highlighted.

Press the Accept and Return Arrow button.

UP ARROW

BUTTON

ACCEPT AND

RETURN ARROW

BUTTON

DOWN ARROW

BUTTON

85

Select First Waveform or Current

Press the New button. Press the Up and
Down Arrow buttons to highlight the
desired waveform/current.

NEW

BUTTON

UP ARROW

BUTTON

DOWN

ACCEPT AND RETURN
ARROW BUTTON

ARROW

BUTTON

Press the Accept and Return Arrow button.

OPERATION

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CLINICAL RESOURCES LIBRARY CREATING NEW SEQUENCES (continued)

Edit First Waveform or Current

Press the Edit button on the Sequence
screen.

Press the Edit button on the waveform/
current Treatment Review screen.

Select Second Waveform or Current

Press the Down Arrow button on the
Sequence screen to highlight the next
waveform in the Sequence.

Intelect® Advanced Therapy System

Saving New Sequence

After all waveforms/currents have been

selected and edited as prescribed, press the

Save button on the Sequence screen.

Edit waveform or current as prescribed.
Press the Back button twice to go back to

the Sequence screen.

EDIT

BUTTON

BUTTON

EDIT

DOWN
ARROW
BUTTON

Repeat steps used in selecting and editing
first waveform/current for second and third
waveform/current.

86

SAVE

BUTTON

OPERATION

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CLINICAL RESOURCES LIBRARY CREATING NEW SEQUENCES (continued)

Enter Sequence Name

Select the row of alpha or numeric
characters desired b

y pushing the button
beside the corresponding row. Select the
desired character in the row by pressing
the row button until the desired letter is
framed.

SELECT ROW AND CHARACTERS

When the desired character is framed, press
the Accept and Return Arrow button. The
character selected will display in the top of
the screen and the cursor will advance to
the next position.

To move back a character, press the Left
Arrow button.

CHARACTER
DISPLAYED

Intelect® Advanced Therapy System

To discard entire entry, press the Back
button.

Repeat this procedure until the desired
sequence name is entered.

After sequence name is entered, press the
Save button.

SAVE
BUTTON

LEFT

ARROW

BUTTON

ACCEPT AND RETURN

ARROW BUTTON

To delete a character, press the Left Arrow
button until the character to be deleted is
framed. Press the Delete button.

87

OPERATION

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Intelect® Advanced Therapy System

CLINICAL RESOURCES LIBRARY DELETING SEQUENCES

General Information

The following information provides instructions for the deletion of one user defined sequence at a time. Once any single sequence is deleted,
it cannot be recovered. Should the Default Protocols be restored, through the User Utilities, all user defined sequences will be permanently
removed from the system.

There is no method for recovery of the user defined Sequences nor can they be saved to any other medium. There are nine Default
Sequences, indicated by an asterisk(*), that cannot be deleted.

Access Sequencing

Press the Clinical Resources Library button.
Press the Sequencing button.

Select Sequence

Press the Up and Down Arrow buttons until
the desired Sequence is highlighted.

UP AND DOWN

ARROW BUTTONS

Delete Sequence

Press the Delete button to delete highlighted
Sequence.

A verification screen will appear. Press Yes button
to delete Sequence or No button to keep
Sequence.

SEQUENCING
BUTTON

DELETE

BUTTON

NO

BUTTON

YES

BUTTON

Repeat this process until all desired user defined
Sequences are deleted.

Press the Home button to return to the Home
screen.

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OPERATION

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CLINICAL RESOURCES LIBRARY USING SEQUENCES

Access Sequencing

Press the Clinical Resources Library button.
Press the Sequencing button.

SEQUENCING
BUTTON

Select Sequence

Press the UP and Down Arrow buttons until the
prescribed Sequence is highlighted.

Press the Accept and Return Arrow button.

ACCEPT AND

RETURN ARROW

BUTTON

UP ARROW

BUTTON

DOWN ARROW

BUTTON

Intelect® Advanced Therapy System

Select Waveform/Current

Press the Down Arrow button, on the
Sequence screen, to highlight the
prescribed waveform/current in the
Sequence.

Press the Edit button.

DOWN

ARROW

BUTTON

EDIT
BUTTON

89

OPERATION

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CLINICAL RESOURCES LIBRARY USING SEQUENCES (continued)

View Waveform Rationale

Press the Waveform Description button to
view the text explaining the rationale for
the modalit

y associated with the Sequence

selected.

WAVEFORM RATIONALE
BUTTON

BACK
BUTTON

Press the Back button twice to return to the
Sequence screen.

View Electrode Placement

Press the Electrode Placement button
to view the electrode placement for the
Sequence selected.

ELECTRODE PLACEMENT

BUTTON

Press the Next Page button to view text
relating to the electrode placement.

Press the Back button twice to return to the
Sequence screen.

NEXT PAGE

BUTTON

BACK

BUTTON

Intelect® Advanced Therapy System

Prepare Patient

Refer to pages 35 through 38 for
Electrotherapy patient preparation
instructions.

Patient Interrupt Switch

Make certain the Patient Interrupt Switch,
for the channel(s) being used, is connected
to the Therapy System. Refer to page 13 for
Symbol Definitions.

LANYARD

PATIENT
INTERRUPT
SWITCH

NOTE:

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

90

OPERATION

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CLINICAL RESOURCES LIBRARY USING SEQUENCES (continued)

Set Sequence Intensity

Give Patient Interrupt Switch to patient
and explain that pressing the Red button
once pauses the therapy session.

PRESSING BUTTON ONCE PAUSES SESSION

If Patient Interrupt Switch is depressed, the
treatment will be paused and a message
will appear on the System screen.

Press any button to clear the message.

NOTE:

If the Patient Interrupt Switch is depressed
a second time, the message will clear from
the screen and the treatment will remain
paused.

The first waveform/current in the Sequence
should be highlighted. Set intensity by
rotating the Intensity Control Knob to the
prescribed level.

INTENSITY DISPLAYED

Intensity Knob Rotation
Clockwise- Increases Intensity

Counterclockwise- Decreases Intensity

Intelect® Advanced Therapy System

Press the Down Arrow button until the
second waveform/current in the sequence is
Highlighted.

Set intensity by rotating the Intensity Control
Knob to the prescribed level.

DOWN

ARROW

BUTTON

Repeat for the third waveform/current in the
Sequence.

91

OPERATION

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CLINICAL RESOURCES LIBRARY USING SEQUENCES (continued)

Intelect® Advanced Therapy System

Start Treatment

Press the Start button to begin therapy
session.

START
BUTTON

Pause Treatment

Press the Pause button to pause therapy
session and maintain remaining time. To
resume treatment, press the Pause button
again.

PAUS E
BUTTON

Stop Treatment

To Stop treatment, press the Stop button
once. Treatment will stop and the Home
screen will display.

STOP BUTTON

Save to Patient Data Card

After session is complete, press the Save
to Patient Card button. Refer to pages 63
through 72 for Patient Data Card Setup
and use.

92

OPERATION

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OPERATION

Intelect® Advanced Therapy System

CLINICAL RESOURCES LIBRARY MMC GRAPHICAL LIBRARY

General Information

The Clinical Resources Library contains the unique Anatomical and Pathological Graphic Libraries* from Chattanooga Group. These Graphic
Libraries are contained on a single Multimedia Card (MMC) and are designed to aid the operator in visually understanding and locating
specific muscle groups and commonly found problems associated with Pathological Conditions as well as providing an educational tool for
the clinician to use with the patient.

Select Clinincal Resources Library

Make certain the Multimedia Card (MMC) is
inserted into the system MMC Access Port.

Press the Clinical Resources Library button.

Select MMC Graphical Library

Press the MMC Graphical Library button.

Select Body Area

The default setting displays Upper Body
Selections. To view Lower Body Selections,
press the Lower Body button.

Press the button beside the desired Body
Area.

BODY AREA SELECTION BUTTONS

MMC
CARD

LOWER BODY

BUTTON

*Copyright ©2003 Nucleus Medical Art. All rights reserved.
www.nucleusinc.com

NOTE:

For representation purposes the Shoulder
has been selected for this section.

93

OPERATION

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OPERATION

CLINICAL RESOURCES LIBRARY MMC GRAPHICAL LIBRARY (continued)

Select Library Type

Select the desired graphic by pressing the
corresponding button.

Left Side buttons- Anatomical Selections
Right Side buttons- Pathological

Selections

Anatomical Example- Muscles
Superficial

Intelect® Advanced Therapy System

Pathological Example- Rotator Cuff Tear

ANATOMICAL

SELECTIONS

PATHOLOGICAL
SELECTIONS

Press the Back button to return to the
selection screen.

Press the Home button to return to the
Home screen.

94

Press the Back button to return to the
selection screen.

Press the Home button to return to the
Home screen.

INSTALLATION/REMOVAL

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INSTALLATION CHANNEL 3/4 ELECTROTHERAPY MODULE

General Information

The Intelect Advanced Therapy System Channel 3/4 Electrotherapy Module is a two channel electrotherapy module intended to upgrade
the Intelect Advanced Therapy System Two Channel Electrotherapy and Two Channel Combination Therapy Systems to Four Channel
Electrotherapy or Combination Therapy Systems. This module is designed for use with the Intelect Advanced Therapy Systems only.

Read, understand, and follow all precautionary instructions found on pages 2 through 6, and throughout this manual as indicated,

•

before performing any installation or removal of optional modules and accessories.
Perform all optional module and accessory installation and removal procedures as described in this manual. Failure to follow these

•

explicit instructions could cause permanent damage to internal components of the equipment and render the system unsafe for
patient therapy.

Understand all symbols and their definitions before operating or performing any installation or removal of optional modules and

•

accessories. The Symbol Definitions are on pages 2 and 13 of this manual.
Follow all safety precautions before, during, and after any treatment.

•

Read, understand and follow the indications, contraindications, and adverse effects of the modalities associated with this system found

•

on pages 7 through 9 of this manual before administering any treatment.
Keep informed of appropriate indications and contraindications for the use of all modalities utilized with this Therapy System.

•

This system, optional modules, and accessories are to be used and sold only under the prescription and supervision of a physician or

•

licensed practitioner.

Intelect® Advanced Therapy System

DISCONNECT THE SYSTEM FROM THE POWER SOURCE (OUTLET OR
REMOVE BATTERY MODULE IF INSTALLED) BEFORE ATTEMPTING
ANY MAINTENANCE, INSTALLATION, REMOVAL, OR REPLACEMENT
PROCEDURES TO PREVENT ELECTRICAL SHOCK AND POSSIBLE
DAMAGE TO SYSTEM.

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