Intelect Mobile 2 Combo Ultrasound and Electrotherapy Unit User Manual Rev A Sept 2019

2

CONTENTS

EN

FOREWORD5

INDICATIONS10

INTENDED USER PROFILE

5

CONTRAINDICATIONS10

INTENDED ENVIRONMENT FOR USE

5

ADDITIONAL PRECAUTIONS

10

INTENDED USE

5

PRODUCT DESCRIPTION

11

PRECAUTIONARY INSTRUCTIONS

5

COMPONENTS11

GENERAL TERMINOLOGY

6

HEAD11

SYSTEM SOFTWARE SYMBOLS

6

CART11

DESCRIPTION OF DEVICE MARKINGS

7

BATTERY MODULE (optional)

11

VACUUM MODULE MARKINGS

7

ULTRASOUND APPLICATORS

11

VACUUM MODULE (OPTIONAL)

11

OPERATOR INTERFACE

12

VACUUM MODULE OPERATOR INTERFACE

13

INTELECT MOBILE 2 SET COMPONENTS

17

ELECTROTHERAPY INDICATIONS

8

INDICATIONS8 CONTRAINDICATIONS8

ELECTROTHERAPY INDICATIONS (CONTINUED)9

HEAD17 LEADWIRES17

ADDITIONAL PRECAUTIONS

9

POWERCORD17

ADVERSE EFFECTS

9

COMBO SET INCLUDES

17

STIM SET INCLUDES

17

US SET INCLUDES

17

ULTRASOUND APPLICATOR

18

HEAD TO CART FIXATION

19

CONNECTING CABLES AND INSERTING PLUGS 

20

INITIAL RECEIPT

20

ULTRASOUND INDICATIONS

INTELECT® MOBILE 2 COMBO USER MANUAL

10

3

CONTENTS

EN

IFU DOWNLOAD

20

PRINT SCREEN FUNCTION

36

DEVICE CONNECTED TO THE MAINS

21

HOME SCREEN

36

DEVICE WORKING ON BATTERY

21

TREATMENT REVIEW SCREEN

37

GUIDELINES SCREEN

39

ELECTROTHERAPY OPERATION

40

START TREATMENT 

42

VACUUM OPERATION

45

ULTRASOUND OPERATION

50

COMBINATION OPERATION

54

SPS (SUGGESTED PARAMETER SETUP)

59

TREATMENT DATA

63

CUSTOM PROTOCOLS

68

SHORT CUTS

72

UNASSIGN SHORT CUT

74

CLINICAL RESOURCES

75

MODALITY/WAVEFORM DESCRIPTIONS

78

DEVICE LIGHT INDICATORS

22

FRONT PANEL INDICATORS

22

ON/OFF BUTTON BLUE INDICATOR

22

PLAY/PAUSE BUTTON BLUE INDICATOR

22

SYSTEM SPECIFICATIONS AND DIMENSIONS

23

POWER 

23

ELECTRO STIMULATION SPECIFICATIONS

23

VACUUM SPECIFICATIONS

23

ULTRASOUND SPECIFICATIONS

24

OUTPUT POWER

24

GENERAL SYSTEM OPERATING AND STORAGE TEMPERATURE24 WAVEFORMS25

TROUBLESHOOTING80

ELECTROTHERAPY PATIENT PREPARATION AND ELECTRODE PLACEMENT

28

VACUUM ELECTRODE PREPARATION (OPTIONAL) 

29

REPLACEMENT ACCESSORIES

ULTRASOUND PATIENT PREPARATION

31

ELECTRODES81

DEVICE USER INTERFACE

32

SCREEN DESCRIPTION

32

SETTINGS

INTELECT® MOBILE 2 COMBO USER MANUAL

35

81

ELECTROTHERAPY ACCESSORIES

82

GENERAL ACCESSORIES

82

4

CONTENTS

EN

BATTERY82 VACUUM ACCESSORIES

83

ULTRASOUND APPLICATORS AND GEL

83

CLEANING THE INTELECT® MOBILE 2

84

VACUUM MODULE CLEANING

84

CALIBRATION REQUIREMENTS

85

DEVICE DISPOSAL

85

INSTRUCTION FOR SOFTWARE UPGRADE

85

IFU DOWNLOAD

85

INSTALLATION OF BATTERY

85

REPLACEMENT BATTERY

85

WARRANTY REPAIR/OUT OF WARRANTY REPAIR

86

WARRANTY87 ELECTROMAGNETIC COMPATIBILITY (EMC)

INTELECT® MOBILE 2 COMBO USER MANUAL

88

5

INTRODUCTION

EN

FOREWORD

INTENDED USE

This manual is intended for users of Intelect® Mobile 2 . It

The Intelect Mobile 2 device will be used to deliver a variety

contains general information on operation, precautionary

of modalities to the patient, Ultrasound and electrical

practices, and maintenance.

stimulation delivered either as stand alone therapies or in

In order to maximize use, efficiency, and the life of the

combination.

system, please read this manual thoroughly and become familiar with the controls, as well as the accessories before operating the system.

PRECAUTIONARY INSTRUCTIONS

In addition to the above information, this manual contains

The precautionary instructions found in this section and

care and installation instructions for the optional Cart and

throughout this manual are indicated by specific symbols.

Vacuum module for the users of the Intelect Mobile 2.

Understand these symbols and their definitions before

®

operating this equipment. The definition of these symbols Before administering any treatment to a patient, the

are as follows:

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, cautions, warnings, and dangers. Consult other resources for additional information regarding the application of electrotherapy and ultrasound.

INTENDED USER PROFILE

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

WARNING Text with a “WARNING” indicator explains possible safety

The intended user of this device is a licensed medical

infractions that will potentially cause serious injury and

professional. The user should be able to:

equipment damage.

• Read and understand the operator’s manual, warnings, cautions and dangers. • Sense auditory and visual signals. • Read and understand indications and contraindications of the device

INTENDED ENVIRONMENT FOR USE The device is intended to be operated in the clinic and remote treatment locations. The intended clinical conditions for use are a typical clinic setting including chiropractic clinics, physical therapist clinics, athletic training rooms or other rehabilitation settings. The patients home will also be a frequent use setting where the clinician treats the patient in his/her own home environment.

INTELECT® MOBILE 2 COMBO USER MANUAL

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

NOTE: Throughout this manual, “NOTE” indicators provide helpful information regarding the particular area of function being described.

6

INTRODUCTION

EN

GENERAL TERMINOLOGY The following are definitions for the terminology used throughout this manual . Study these terms to become familiar with them for ease of system operation and control functionality of the Intelect® Mobile 2 .

SYSTEM SOFTWARE SYMBOLS Home

Run again

Back to previous screen

Exit

Settings

Export

Indicates a USB Flash Drive is Inserted

Import

Indicates Battery Level

Delete

Indicates more content can be viewed by swiping vertically Indicates more content can be viewed by swiping horizontally

Delete all Stop treatment

Indicates more content can be viewed by scrolling

Stim

Close window / exit full screen

Ultrasound

Confirm

Combo

Save Data

Shortcut

Edit

SPS (Suggested Parameter Setup)

Guidelines / Assign to

Custom Protocols

Pain information

Treatment Data Clinical Resources

INTELECT® MOBILE 2 COMBO USER MANUAL

7

INTRODUCTION

EN

DESCRIPTION OF DEVICE MARKINGS The markings on the unit are assurance of its conformity to the highest applicable standards of medical equipment safety and electromagnetic compatibility and conform to ISO 7010 and ISO15-223-1 One or more of the following markings may appear on the device:

Refer to Instructional Manual Booklet

Atmospheric Pressure Range

Warning, Caution, or Danger

Test agency

Electrical Type BF Equipment

CE Mark of Conformity with notified body number

Ultrasound

Alternating current

Stim

Class II equipment

Combo

IP21

Play

Radio frequency equipment

Pause

WEEE Directive conformity

ON/OFF

Shelf life

Manufacturer

Batch number

Date of manufacture

US amplitude modulated

Catalogue number Serial number Fragile, handle with care This end up Keep dry Temperature Range Relative Humidity Range

INTELECT® MOBILE 2 COMBO USER MANUAL

VACUUM MODULE MARKINGS 1

Channel 1 device connection to vacuum Channel 2 device connection to vacuum +/- Channel 1 polarity +/- Channel 2 Polarity

1

2

2

1 1

8

INDICATIONS FOR USE

EN

ELECTROTHERAPY INDICATIONS INDICATIONS

CONTRAINDICATIONS

TENS

The Intelect® Mobile 2 should NOT be used under the

• Symptomatic relief of chronic pain • Management of post-operative pain

following conditions: • Do not use for symptomatic local pain relief unless etiology is established or unless a pain syndrome has

NMES • Muscle re-education • Increasing local blood supply • Relaxation of muscle spasms • Maintaining/Increasing range of motion

been diagnosed. • Do not use when cancerous lesions are present in the treatment area. • Do not apply stimulation over swollen, infected, inflamed areas or skin eruptions (e.g., phlebitis, thrombophlebitis, varicose veins, etc.). • Do not use when patient is suspected or known to have infectious disease and/or disease where it is advisable, for general medical purposes, to suppress heat or fevers. • Do not place electrode placements to the carotid sinus region (anterior neck) or transcerebrally (through the head). • Do not use on pregnant women. Safety has not been established for the use of therapeutic electrical stimulation during pregnancy. • Do not use Intelect® Mobile 2 on patients who have or have had implantable neurostimulating cardiac demand pacemakers, ICD, or other implantable electronic devices. • Do not use Intelect® Mobile 2 on patients with body worn electro mechanical medical devices, i.e. insulin pump. • Do not use this system in an MRI or CT environment. The Intelect® Mobile 2, its components, and accessories are not to be present in an MRI or CT environment. • Do not apply stimulation transthoratically or on the chest, the introduction of electrical current into the heart may cause cardiac arrhythmia • Do not apply stimulation 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.

INTELECT® MOBILE 2 COMBO USER MANUAL

9

INDICATIONS FOR USE

EN

ELECTROTHERAPY INDICATIONS (CONTINUED) ADDITIONAL PRECAUTIONS • Use caution for patients with suspected or diagnosed heart problems. • Use caution for patients with suspected or diagnosed epilepsy. • Use caution in the presence of the following: »»When there is a tendency to hemorrhage following acute trauma or fracture

ADVERSE EFFECTS • Skin irritation and burns beneath the electrodes have been reported with the use of powered muscle stimulators. The irritation can usually be reduced by using an alternative conductive medium or an alternative electrode placement • Potential adverse effects with TENS are skin irritation and electrode burns

»»Following recent surgical procedures when muscle contraction may disrupt the healing process »»Over a menstruating or pregnant uterus »»Over areas of the skin that lack normal sensation • Powered muscle stimulators should be used only with the lead wires and electrodes recommended for use by the manufacturer. • With TENS waveforms, isolated cases of skin irritation may occur at the site of electrode placement following long-term application. • The effective management of pain by TENS waveforms is highly dependent upon patient selection by a person qualified in pain management.

INTELECT® MOBILE 2 COMBO USER MANUAL

Note: 1. Skin irritation and burns beneath the electrodes can be reduced or avoided by using appropriate electrode size and ensuring optimal contact quality. If any question arises as to the proper electrode size, consult a licensed practitioner prior to therapy session. 2.Some people, with very sensitive skin, may experience redness under the electrodes after a session. Generally, this redness is totally harmless and usually disappears after 10 to 20 minutes. However, do not start another stimulation session on the same area if the redness is still visible

10

INDICATIONS FOR USE

EN

ULTRASOUND INDICATIONS INDICATIONS

ADDITIONAL PRECAUTIONS

• Relief of pain from muscle spasm

Additional precautions should be used when ultrasound is

• Relief of pain from joint contracture

used on patients with the following conditions:

• Relief of pain associated with ligament sprains, tendinitis and muscle sprain

• Over an area of the spinal cord following a laminectomy, i.e., when major covering tissues have been removed

CONTRAINDICATIONS • Do not use for symptomatic local pain relief unless etiology is established or unless a pain syndrome has been diagnosed. • Do not use when cancerous lesions are present in the treatment area. • Do not use when patient is suspected or known to have infectious disease and/or disease where it is advisable, for general medical purposes, to suppress heat or fevers. • Do not use over or near bone growth centers until bone growth is complete. • Do not use over the thoracic area if the patient is using a cardiac pacemaker. • Do not use over a healing fracture. • Do not use over or applied to the eye. • Do not use over a pregnant uterus. • Tissue necrosis might result if the device is used on ischemic tissues in individuals with vascular disease, where the blood supply would not keep up with the metabolic demand. • Do not use Intelect® Mobile 2 on patients who have or have had implantable neurostimulating cardiac demand pacemakers, ICD, or other implantable electronic devices. • Do not use Intelect® Mobile 2 on patients with body worn electro mechanical medical devices, i.e. insulin pump. • Do not use this system in an MRI or CT environment. The Intelect® Mobile 2, its components, and accessories are not to be present in an MRI or CT environment.

INTELECT® MOBILE 2 COMBO USER MANUAL

• Over anesthetic areas • On patients with hemorrhagic diatheses

11

DEVICE DESCRIPTION

PRODUCT DESCRIPTION

EN

BATTERY MODULE (optional)

The Intelect® Mobile 2 COMBO is a two-channel electrotherapy, ultrasound therapy and Combo system used with or without an optional Cart, allowing for the inclusion of a Vacuum module. This equipment is to be used only under the prescription and supervision of a licensed medical practitioner.

COMPONENTS Throughout these instructions the terms “left” and“right”

Battery is an 18V 3350mAh LiIon rechargeable battery

referring to the machine sides are from the perspective of a user standing in front of the unit. The components of the Intelect® Mobile 2 COMBO are

ULTRASOUND APPLICATORS

shown below.

HEAD

VACUUM MODULE (OPTIONAL)

CART

INTELECT® MOBILE 2 COMBO USER MANUAL

12

DEVICE DESCRIPTION

EN

OPERATOR INTERFACE The Intelect® Mobile 2 COMBO Operator Interface contains

4.

ON/OFF switch (only active when connected to the mains)

all the functions and controls necessary for operator access to all operator utilities, modalities, and parameters for

5.

Ultrasound Applicator holder, left and right sides

modification and system set up. Color Display and touch

6.

Mains power connector

screen

7.

Battery cover

8.

USB Flash Drive Port Magnetic fixation to the cart

1.

Adjustment dial

9.

2.

Play/pause button

10. Vacuum cover

3.

“On/Off“ button. Press and hold (2 sec) the button to

11.

Device handle

switch OFF the device.

Handle

Colour Touch Screen “On/Off“ button Play / pause button

Ultrasound applicator support Adjustment dial

Battery cover

Vacuum cover

Ultrasound applicator connectors

Lead wire connectors for electro stimulation

ON / OFF switch only active on mains power

USB port for software upgrade Mains power connector

INTELECT® MOBILE 2 COMBO USER MANUAL

13

DEVICE DESCRIPTION

EN

VACUUM MODULE OPERATOR INTERFACE

Resevoir

Channel 1 device connection to vacuum

+/- Channel 1 polarity

Channel 2 device connection to vacuum

1

INTELECT® MOBILE 2 COMBO USER MANUAL

2

+/- Channel 2 Polarity

14

GENERAL WARNINGS AND PRECAUTIONS

EN

CAUTION • This unit should be operated at +5°C to +40°C and 15% to 90% Relative Humidity. The unit should be transported and stored at -20°C to +60°C and 10% to 90% Relative Humidity. • Use of parts or materials other than DJO’s can degrade minimum safety. • Connect to this unit only items and equipment that have been specified in this IFU as part of the ME SYSTEM or that have been specified as being compatible with the ME SYSTEM. • DO NOT disassemble, modify, or remodel the unit or accessories. This may cause unit damage, malfunction, electrical shock, fire, or personal injury. • DO NOT permit foreign materials, liquids or cleaning agents to enter the unit, including, but not limited to, inflammables, water, and metallic objects, to prevent unit damage, malfunction, electrical shock, fire, or personal injury. • Before each use, inspect Ultrasound Applicator for cracks, which may allow the ingress of conductive fluid. • Before each use, inspect Applicator cables, STIM cables and associated connectors. • Before each use, inspect Vacuum Electrode Cups and Lead Hoses for cracks and damage which may not allow the vacuum to properly secure the electrodes. • Handle Ultrasound Applicator with care. Inappropriate handling may adversely affect its characteristics. • Caution should always be exercised with current densities more than 2mA/cm². • There are no user-serviceable parts inside the unit. If a malfunction occurs, discontinue use immediately and consult dealer for repair service. • In case of device unused with battery embedded, it is recommended to connect the device at least once every 4 months to allow battery recharge. • For waveforms with a DC component: »»Do not shave electrodes application area »»Warn the patient that tingling sensation under electrodes is normal and it is not linked to burn risk. »»Rinse thoroughly treatment area with tap water immediately after the treatment

INTELECT® MOBILE 2 COMBO USER MANUAL

15

GENERAL WARNINGS AND PRECAUTIONS

EN

WARNING • This device should be used only under the continued supervision of a physician or licensed practitioner. • Contaminated sponges, electrodes, leadwires, and gel can lead to infection. • Use of electrode on multiple patients can lead to infection. • Do not apply electro stimulation treatment during bath, shower, sauna,.. • DO NOT operate the Intelect® Mobile 2 within the vicinity or environment of an ultrasonic diathermy system. • DO NOT operate the Intelect® Mobile 2 within the vicinity or environment of any microware and RF shortwave diathermy system. • DO NOT operate this unit in an environment where other devices are being used that intentionally radiate electromagnetic energy in an unshielded manner. • Electronic monitoring equipment (such as ECG monitors and ECG alarms) may not operate properly when electrical stimulation is in use. • Simultaneous connection of a PATIENT to a high frequency surgical ME EQUIPMENT may result in burns at the site of the STIMULATOR electrodes and possible damage to the STIMULATOR. • Portable RF communications equipment should be used no closer than 30 cm (12 inches) to any part of the Intelect Mobile 2, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result. • Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation. • Battery replacement by inadequately trained personnel could result in fire or explosion. Please read carefully the battery replacement instructions in the Mobile 2 IFU before attempting to replace the battery. • Device is designed to comply with electromagnetic safety standards. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with instructions for use, may cause harmful interference to other devices in the vicinity. 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 »»Consult your authorized DJO dealer for help. • Disconnect the system from the power source before attempting any maintenance, installation, removal, or replacement procedures to prevent electrical shock and possible damage to system. • The Intelect® Mobile 2 may be susceptible to Electro-Static Discharge (ESD) at greater than ±6 kV when first grasping the Ultrasound applicator. In the event of such a discharge, the Intelect® Mobile 2 may display a permanent error. The Intelect® Mobile 2 will terminate all active outputs (stim, ultrasound,), automatically place the unit in a safe state. • To prevent Electro-Static Discharge (ESD) at greater than ±6 kV: »»Grasp and hold the Ultrasound prior to starting treatment. If the applicator must be put down prior to completion of treatment, stop the current treatment first and then place the applicator in the holder. »»Maintain humidity in the use environment to at least 50% relative humidity. »»Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, DJO recommends implementing additional controls to maintain relative humidity to at least 50%. »»Communicate these ESD-precautionary procedures to healthcare staff, contractors, visitors, and patients.

INTELECT® MOBILE 2 COMBO USER MANUAL

16

GENERAL WARNINGS AND PRECAUTIONS

EN

DANGER • DO NOT connect the unit to an electrical supply without first verifying that the power supply is the correct voltage. Incorrect voltage may cause unit damage, malfunction, electrical shock, fire, or personal injury. Your unit was constructed to operate only on the electrical voltage specified on the Voltage Rating and Serial Number Plate. Contact your DJO dealer if the unit is not properly rated. • Device is not designed to be used in oxygen rich environment, Explosion hazard if the device is used in the presence of flammable anesthetic mixture with air, oxygen, or nitrous oxide.

INTELECT® MOBILE 2 COMBO USER MANUAL

17

DETAIL DEVICE DESCRIPTION

EN

INTELECT MOBILE 2 SET COMPONENTS

COMBO SET INCLUDES:

The components of the Intelect® Mobile 2 set are shown

15-0133

below.

79967

Carbon electrodes

70010

STIM lead wires

INTELECT MOBILE 2 COMBO

15-1200

Intelect Mobile 2 Ultrasound INTL Set EU Plug

6522055

Chattanooga straps

15-1201

Intelect Mobile 2 Ultrasound INTL Set All Plug

42198

Electrodes gel

15-1202

Intelect Mobile 2 Stim INTL Set EU Plug

15-0144/46/47

Power cord

15-1203

Intelect Mobile 2 Stim INTL Set All Plug

13-1604

Printed Quick Start Guide

15-1204

Intelect Mobile 2 Combo INTL Set EU Plug

15-0142

5 CM2 Ultrasound Applicator

15-1205

Intelect Mobile 2 Combo INTL Set All Plug

4248

Ultrasound Gel Bottle

15-1140

USB Drive

STIM SET INCLUDES:

HEAD

LEADWIRES The available leadwires are shown below. If the user orders a Mobile 2 Stim or Mobile 2 Combo, the box will include the blue and green leadwires

POWERCORD 15-0144

Wall Power Cable 2m Black EU

15-0146

Wall Power Cable 2m Black UK

15-0147

Power Cable 2m Black AUS

INTELECT® MOBILE 2 COMBO USER MANUAL

15-0132

INTELECT MOBILE 2 STIM

79967

Carbon electrodes

70010

STIM lead wires

6522055

Chattanooga straps

42198

Electrodes gel

15-0144/46/47

Power cord

13-1604

Printed Quick Start Guide

15-1140

USB Drive

US SET INCLUDES: 15-0131

INTELECT MOBILE 2 ULTRASOUND

15-0144/46/47

Power cord

13-1604

Printed Quick Start Guide

15-0142

5 CM2 Ultrasound Applicator

4248

Ultrasound Gel Bottle

15-1140

USB Drive

18

DETAIL DEVICE DESCRIPTION

ULTRASOUND APPLICATOR 1. Applicator Head The 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 Applicator head. 3. LED The component of the applicator that indicates if the Applicator is coupled or uncoupled on the treatment area.

INTELECT® MOBILE 2 COMBO USER MANUAL

EN

19

SETUP INSTRUCTIONS

HEAD TO CART FIXATION The optional Therapy System Cart, is designed for use with the Intelect® Mobile 2 only and allows the user to easily transport the System from patient to patient within the clinic as well as store all necessary accessories, supplies, and applicators used for the various modalities of the System. The fixation of the head to the cart is magnetic. Remove the Intelect® Mobile 2 device and cart from the shipping carton. Visually inspect for damage. Report any damage to the carrier immediately. To assemble the Mobile 2 Head to the Cart, follow these steps: 1. Insert device front bottom on the cart lip 2. Release device back gently on the cart. Magnets will help to position the device correctly on the cart top.

INTELECT® MOBILE 2 COMBO USER MANUAL

EN

20

SETUP INSTRUCTIONS

CONNECTING CABLES AND INSERTING PLUGS

EN

1. The Initialisation screen below will be shown for a few seconds whilst the device starts.

When inserting the plugs, be sure to align the flat side of the plug with the flat side of the slot and push in gently. This is to avoid bending the pins in the plug. Insert cable into the appropriate connector prior to starting therapy.

INITIAL RECEIPT Remove all packaging 2. The first setup screen will be dispalyed after this allowing

IF UNIT SUPPLIED WITH OPTIONAL BATTERY

the user to set language, device name and time.

After unpacking Intelect Mobile 2 to fit the battery follow the following steps 1. Unscrew the battery cover from the base of the device by removing the 2 screws see below 2. Remove the battery cover 3. Plug the battery into the battery connector on the device 4. Insert the battery into its location 5. Replace the 2 screws to close the battery cover

3. Click on "Continue" button to go to home screen

IFU DOWNLOAD 1. Go to the Chattanooga website www.chattanoogarehab.com 2. Go to Intelect Mobile 2 product tab 3. Complete the registration form to be informed about new product software version availability and IFU updates. 4. Go to documents tab 5. Click on the latest version of your Intelect Mobile 2 device

POWERING UP THE DEVICE First time use always use mains power even if battery connected. Insert the power cord into the back of the unit, insert the plug into a power outlet, do not position the Intelect Mobile 2 in such a way that makes it difficult to disconnect from the mains power. Switch device on with ON/OFF switch switch on the back of the unit

INTELECT® MOBILE 2 COMBO USER MANUAL

(COMBO, US or STIM) User manual to download Nota: a pdf viewer is required to display IFU