Chattanooga Intelect Mobile 2 Ultrasound User manual

| Intelect®Mobile 2 - Service Manual 1
Intelect® Mobile 2
Service Manual
Repair and Maintenance Instructions
13-12088 - R ev B

EN
| Intelect®Mobile 2 - Service Manual 2
INTRODUCTION
1. INTRODUCTION
1.1.HISTORY P4
1.2. FOREWORD P4
1.3. INTENDED USER PROFILE P4
1.4. INTENDED ENVIRONMENT FOR USE P4
1.5. INTENDED USE P4
1.6. PRECAUTIONARY INSTRUCTIONS P4
2. GENERAL WARNINGS AND
PRECAUTIONS
2.1. CAUTION P6
2.2. WARNING P7
2.3. DANGER P8
3. DEVICE DESCRIPTION
3.1. GENERAL TERMINOLOGY P10
3.2. SYSTEM SOFTWARE SYMBOLS P10
3.3. DESCRIPTION OF DEVICE MARKINGS P11
3.4. PRODUCT DESCRIPTION P12
3.5. OPERATOR INTERFACE P12
3.6. COMPONENTS P13
3.7. SYSTEM DIMENSIONS & P14
SPECIFICATIONS
3.8. THERAPIES SPECIFICATIONS P15
4. USER INTERFACE
4.1. SOFTWARE VERSION & SERIAL NUMBER P23
4.2. SCREEN DESCRIPTION P23
4.3. SETTINGS MENU P23
4.4. ADVANCED SETTINGS P24
4.5. SERVICE MENU P24
4.6. SOFTWARE UPDATE P25
4.7. PRINTSCREEN P25
5. MAINTENANCE OPERATION
5.1. GENERAL P27
5.2. SPECIAL TOOLS, FIXTURES & P27
MATERIALS REQUIRED
5.3. EQUIPMENT REQUIRED P27
5.4. RECIPE FOR DEGASSED WATER P27
5.5. FULL FUNCTIONAL TESTS P27
5.6. US CALIBRATION REQUIREMENTS P27
5.7. US CALIBRATION PROCEDURE P28
5.8. CLEANING INSTRUCTION P30
6. TROUBLESHOOTING
6.1. NO POWER P32
6.2. SCREEN DEFAULT P33
6.3. FAN DEFAULT P33
6.4. BATTERIE TEST P34
6.5. FAILURE DURING TREATMENT P34
6.6. ERRORS CODES P34
7. REPAIR OPERATION
7.1. TOOLS & EQUIPMENTS TO REPAIR P36
7.2. BOTTOM OF THE DEVICE P37
7.3. SEPARATING TOP & LOWER ASSEMBLYP38
7.4. TOP SUB ASSEMBLY P39
7.5. LOWER SUB ASSEMBLY P42
7.6. REASSEMBLY P46
7.7. US APPLICATOR P47
8. FINAL TEST
8.1. INTELECT MOBILE 2 ULTRASOUND P49
8.2. INTELECT MOBILE 2 STIM P53
8.3. INTELECT MOBILE 2 COMBO P59
8.4. ULTRASOUND APPLICATOR P67
9. EXPLODED VIEWS and
SERVICE PART LISTS
9.1. INTELECT MOBILE 2 P71
9.2. DEVICE TOP SUB ASSEMBLY P72
9.3. LOWER SUB ASSEMBLY P74
9.3.1.ULTRASOUND LOWER SUB ASSEMBLY P76
9.3.2.STIM LOWER SUB ASSEMBLY P76
9.3.3.COMBO LOWER SUB ASSEMBLY P77
9.4. US APPLICATOR P78
9.5. CART 6 BINS P79

EN
| Intelect®Mobile 2 - Service Manual 3
INTRODUCTION
1.INTRODUCTION
1.1. HISTORY P4
1.2. FOREWORD P4
1.3. INTENDED USER PROFILE P4
1.4. INTENDED ENVIRONMENT FOR USE P4
1.5. INTENDED USE P4
1.6. PRECAUTIONARY INSTRUCTIONS P4

EN
| Intelect®Mobile 2 - Service Manual 4
INTRODUCTION
1.1 HISTORY
Revision
Date
Name
Change
A
01/10/2019
J-R Castelnau
Service Manual created
B
31/07/2020
J-R Castelnau
Phase 2: Advanced settings / Service menu / US
calibration / US applicators parts
1.2 FOREWORD
This manual is exclusively intended for the service
centers with the DJO agreement to repair the Intelect®
Mobile 2. It contains general information on operation,
precautionary practices, and maintenance.
In order to maximize use, efficiency, and the life of the
system, please read the User and the service manual
thoroughly and become familiar with the controls, as
well as the accessories before operating the system.
In addition to the above information, this manual
contains care and installation instructions for the
optional Cart 6 bins and Ultrasound applicators.
Specifications put forth in this manual were in effect at
the time of publication. However, owing to DJO’s policy
of continual improvement, changes to these
specifications may be made at any time without
notification on the part of DJO.
Before administering any treatment, the users of this
equipment should read, understand, and follow the
information contained in the User 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.
1.3 INTENDED USER PROFILE
The intended user of this device is a licensed
medical professional. The user should be able to:
• Read and understand the operator’s manual,
warnings, cautions and dangers.
• Sense auditory and visual signals.
• Readandunderstand cautionsandcontraindications
of thedevice
1.4 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 patient’s home will also be a frequent
use setting where the clinician treats the patient in
his/her own home environment.
1.5 INTENDED USE
The Intelect Mobile 2 device will be used
to deliver a variety of modalities to the
patient. These modalities are Ultrasound or
electrical stimulation delivered either as
stand-alone therapies or in combination.
1.6 PRECAUTIONARY INSTRUCTIONS
The precautionary instructions found in
this section and throughout this manual
are indicated byspecific symbols.
Understand these symbols and their
definitions before operating this
equipment. The definition of these symbols
are asfollows:
Text with a “CAUTION” indicator explains
possible safety infractions that have
potential to cause minor or moderate injury
or damage to the equipment.
Textwitha“WARNING”indicatorexplains
possiblesafety infractions that will
potentially cause serious injury and
equipmentdamage.
Textwith 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
CAUTION
WARNING
DANGER

GENERAL WARNINGS AND PRECAUTIONS
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2.GENERAL WARNINGS AND PRECAUTIONS
2.1. CAUTION P6
2.2. WARNING P7
2.3. DANGER P8

GENERAL WARNINGS AND PRECAUTIONS
EN
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| Intelect®Mobile 2 - Service Manual 6
• This unit should be operated at +5°C to +40°C and 30% to 75% Relative Humidity. The unit should be
transported and stored at -20°C to +60°C and 10% to 90% Relative Humidity.
• Use ofparts or materials other than DJO’s candegrade 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 beenspecifiedasbeingcompatiblewiththeMESYSTEM.
• DO NOT disassemble, modify, or remodel the unit or accessories. This may cause unit damage, malfunction,
electrical shock,fire,orpersonalinjury.
• 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 ofconductive 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:
• Donotshave 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
CAUTION

GENERAL WARNINGS AND PRECAUTIONS
EN
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| Intelect®Mobile 2 - Service Manual 7
• This device should beusedonlyunder thecontinued supervision ofaphysicianorlicensed practitioner.
• Contaminatedsponges,electrodes,leadwires,andgelcanleadtoinfection.
• 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 inanunshielded 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 couldresult.
• Use ofaccessories, transducers and cables other than those specified or provided bythemanufacturer
of this equipment could result in increased electromagnetic emissions or decreased electromagnetic
immunity of this equipment and result in improper operation.
• Device isdesigned tocomply with electromagnetic safety standards. This equipment generates,
uses, andcanradiate 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 orrelocate thereceiving 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 yourauthorized DJOdealer forhelp.
• Disconnect the system from the power source before attempting any maintenance, installation,
removal, or replacement proceduresto prevent electricalshockandpossible damagetosystem.
• The Intelect® Mobile 2 may be susceptible to Electro-Static Discharge (ESD) at greater than ±4 kV
when first grasping either the Ultrasound or Laser applicator. In the event of such a discharge,
the Intelect® Mobile 2 may experience communication loss. The Intelect® Mobile 2 will
terminate all active outputs (stim, ultrasound,), automatically place the unit in a safe state. TBC,
keep it for the moment. It will depend on formal EMC results
• To prevent Electro-Static Discharge (ESD) at greaterthan ±4 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 theholder.
• Maintain humidity in the use environment to at least 50% relative humidity.
• Floors should be wood, concrete, orceramic tile. If floors are covered with synthetic
material, DJO recommends implementing additional controls to maintain relative
humidity to at least 50%.
• Communicate theseESD-precautionary proceduresto healthcarestaff,contractors,visitors,
andpatients.TBC, keepitfor the moment. It will depend on formal EMC results
WARNING

GENERAL WARNINGS AND PRECAUTIONS
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| Intelect®Mobile 2 - Service Manual 8
• Stimulus delivered by the TENS waveforms of this device, incertain 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. TBC
• 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
DANGER

DEVICE DESCRIPTION
EN
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| Intelect®Mobile 2 - Service Manual 9
3.DEVICE DESCRIPTION
3.1. GENERAL TERMINOLOGY P10
3.2. SYSTEM SOFTWARE SYMBOLS P10
3.3. DESCRIPTION OF DEVICE MARKINGS P11
3.4. PRODUCT DESCRIPTION P12
3.5. OPERATOR INTERFACE P12
3.6. COMPONENTS P13
3.7. SYSTEM DIMENSIONS & SPECIFICATIONS P14
3.8. THERAPIES SPECIFICATIONS P15
3.8.1. ULTRASOUND THERAPY P15
3.8.2. ELECTRO-STIMULATION THERAPY P15

DEVICE DESCRIPTION
EN
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| Intelect®Mobile 2 - Service Manual 10
3.1. 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.
3.2. SYSTEM SOFTWARE SYMBOLS

DEVICE DESCRIPTION
EN
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| Intelect®Mobile 2 - Service Manual 11
3.3. 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 Oneor more of the following
markings may appear onthe device:

DEVICE DESCRIPTION
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3.4. PRODUCT DESCRIPTION
The Intelect® Mobile 2 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.
3.5. OPERATOR INTERFACE
The Intelect® Mobile 2 Operator Interface contains
all the functionsandcontrols necessary foroperator
access to all operator utilities, modalities, and
parameters for modification and system set up.
1.
Color Display and touch screen
2. Adjustment dial
3. Play/pauseCTRL BUTTON
4. “On/Off“ CTRL BUTTON.
Press and hold (2 sec) the CTRL BUTTON to switchOFF
thedevice.
5. ON/OFF switch (only active when connected to the
mains)
6. Ultrasound Applicator holder, left and right sides
7. MainsPowerCord
8. Batterycover
9. Serial Number Label
10. USB Flash DrivePort
11. Magnetic fixation to the cart
12. Vacuum cover
13. Device handle
Handle
ON/OFF Button
Ultrasound
Applicator support
Rotary knob
Color Touch Screen
PLAY/PAUSE Button
Batterycover Vacuum connector cover
Ultrasound
Applicator
connectors
Lead wire connectors
for electro-stimulation
ON/ OFFswitch only
active on mains power
Mains power
connector
USB port for
software
upgrade

DEVICE DESCRIPTION
EN
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| Intelect®Mobile 2 - Service Manual 13
3.6. COMPONENTS
Throughout these instructions the terms “left” and “right” 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 are shown below.
INTELECT MOBILE 2:
US SET INCLUDES:
15-0131 INTELECT MOBILE 2 ULTRASOUND
15-0144 Power cord EU
13-1604 Printed Quick Start Guide
15-0142 5 CM2 Ultrasound Applicator
4248 Ultrasound Gel Bottle
15-1140 INTELECT MOBILE 2 USB KEY
STIM SET INCLUDES:
15-0132 INTELECT MOBILE 2 STIM
79967 Carbon electrodes
70010 STIM lead wires
6522055 Nylatex wraps
42198 Electrodes gel
15-0144 Power cord EU
13-1604 Printed Quick Start Guide
15-1140 Intelect Mobile 2 USB Key
COMBO SET INCLUDES:
15-0133 INTELECT MOBILE 2 COMBO
79967 Carbon electrodes
70010 STIM lead wires
6522055 Nylatex wraps
42198 Electrodes gel
15-0144 Power cord
13-1604 Printed Quick Start Guide
15-0142 5 CM2 Ultrasound Applicator
4248 Ultrasound Gel Bottle
15-1140 Intelect Mobile 2 USB Key
POWERCORD
15-0144 Wall Power Cable 2m Black EU
15-0145 Wall Power Cable 2m Black US
15-0146 Wall Power Cable 2m Black UK
15-0147 Wall Power Cable 2m Black AUS
15-0148 Wall Power Cable 2m Black ARG
ULTRASOUND APPLICATORS
10 cm² : 15-0143
5 cm² : 15-0142
2 cm² : 15-0141
1 cm² : 15-0140
CART 6 BINS (15-1136)
OPTIONAL BATTERY MODULE (14-1086)
Battery is an 18V / 3350 mAh Li-ion rechargeable battery
LEADWIRES (PN 70010)
The available leadwires are shown below. If the user
orders a Mobile 2 Stim or Mobile 2 Combo, the box will
include the blueand greenleadwires
15-1200
Intelect Mobile 2 Ultrasound INTL Set EU
Plug
15-1201
Intelect Mobile 2 Ultrasound INTL Set All
Plug
15-1202
Intelect Mobile 2 Stim INTL Set EU Plug
15-1203
Intelect Mobile 2 Stim INTL Set All Plug
15-1204
Intelect Mobile 2 Combo INTL Set EU Plug
15-1205
Intelect Mobile 2 Combo INTL Set All Plug

DEVICE DESCRIPTION
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| Intelect®Mobile 2 - Service Manual 14
3.7. SYSTEM DIMENSIONS AND SPECIFICATIONS
Width
Depth
Height
Weight (no battery)
Intelect Mobile 2 Head Unit
COMBO
34cm
35.5cm
15cm
3.1kg
ULTRASOUND
34cm
35.5cm
15cm
TBD
STIM
25.5cm
35.5cm
15cm
TBD
Cart configurations
Cart
48cm (MAX)
52cm (MAX)
96cm
10.1Kg
Cart with vacuum
48cm (MAX)
52cm (MAX)
96cm
11.5 Kg
Device on cart
-
-
111 cm
-
POWER
Input 100 - 240 V AC, 1.0 to 0.42 A, 50/60 Hz
Electrical Class CLASS II
Mode of Operation Continuous
ELECTRICAL TYPE (DEGREE OF PROTECTION)
Ultrasound TYPE BF
Electrotherapy TYPE BF
Electrotherapy Vacuum TYPE BF
Ultrasound & Electrotherapy TYPE BF
GENERAL SYSTEM OPERATING AND STORAGE
TEMPERATURE
Operating Conditions
The device will meet its requirement under the following
conditions:
Temperature: 5°C to 40°C
Relative Humidity: 15 % to 90 %
Atmospheric Pressure: 70 kPa to 106 kPa
Transport and Storage Conditions
The device will remain in proper condition under the
following conditions:
Temperature: -20°C to 60°C
Relative Humidity: 10 % to 100 %
Atmospheric Pressure: 50 kPa to 106 kPa
Time required for the ME EQUIPMENT to warm from
the minimum storage temperature between uses until
the ME EQUIPMENT is ready for its INTENDED USE
when the ambient temperature is 20 °C: 5h
Time required for the ME EQUIPMENT to cool from the
maximum storage temperature between uses until the
ME EQUIPMENT is ready for its INTENDED USE when
the ambient temperature is 20 °C : 5h
IPXX RATING FOR UNIT
Rated to IP21
IP2* Protection against fingers or other object not greater
than 80mm in length and 12mm in diameter
IP*1 Protection from vertically dripping water
IPXX RATING FOR US APPLICATOR
Rated to IPX7
IPX7 Protection from immersed in water (up to 1m depth)
RED
RF transmitter/receiver characteristics:
Frequency Band transmission: 2400–2483.5 MHz
Modulation type: GFSK
Data rate: up to 2Mbps 500kHz deviation at 2Mbps
Effective radiated power: +6dBm

DEVICE DESCRIPTION
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| Intelect®Mobile 2 - Service Manual 15
3.8. THERAPIES SPECIFICATIONS
3.8.1. Ultrasound Therapy
Frequency 1 MHz; 3 MHz
Duty Cycles 10%, 20%, 50%, Continuous
Pulse Repetition Rate 16, 48, or 100 Hz
Pulse duration: 1-31.25 ms
Max (ON): 31.25 ms
Min (OFF): 5 ms
Unless otherwise specified, ultrasound
controls accuracy is: ± 20 %
Peak to Average Ratio: 1:1, at 50% Duty Cycle
4:1, at 20% Duty Cycle
9:1, at 10% Duty Cycle
Beam Nonuniformity Ratio <5:1
Beam Type Collimating
Treatment Time 1 to 30 min
Output Power
(*) An error of + 0.25 W can be measured with 1cm2 US applicator,
pulse mode 100Hz at 10% or 20% Duty Cycle.
3.8.2 Electro-Stimulation Therapy
Unless otherwise specified, electrotherapy controls accuracy is: ± 20 %.
WAVEFORMS
Advice on size and type of electrodes to be used is given in device GUI treatment guidelines.
CC:ConstantCurent CV: ConstantVoltage
IFC (Interferential) Traditional (4 Pole)
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
InterferentialCurrentisamediumfrequencywaveform.Currentisdistributed
through two channels (four electrodes). The currents cross each other in the body
atthearearequiring treatment. Thetwo currents interfere witheach otherat
thiscrossingpoint,resultinginamodulationoftheintensity(thecurrentintensity
increasesanddecreasesataregularfrequency).
OutputMode Electrodes
Carrier Frequency 2000-10,000 Hz
Beat Frequency 1-200 Hz
Sweep Time 14 sec
Sweep Low Beat Frequency 1-199 Hz
Sweep High Beat Frequency 2-200 Hz
Cycle Time Continuous or User Defined
Scan Percentage Static, 40%, 100%, Manual
Amplitude 0-100 mA (CC)
Treatment Time 1-60 Minutes
Available on Channel 1&2,
IRMS [mA] 0-100 mA
DC component : No
TENS- Asymmetrical Biphasic
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
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 0-140 mA (CC) 0-140 V (CV)
Phase Duration 30-400 µsec
Frequency 1 - 200 Hz
Mode Selection (Stim) CC or CV
Mode Selection (Combo) CV
Burst Frequency 0-10 Hz
Frequency Sweep On/Off
Sweep Low Frequency 1-199 Hz
Sweep High Frequency 2-200 Hz
Cycle Time Continuous or User Defined
Amplitude Modulation 0% (off) to 100% on 10% steps
Treatment Time (Stim) 1-60 minutes
Treatment Time (Combo) 1-30 minutes
Ramp -5 sec
Available on Channel 1,2
IRMS [mA] 0-53.61 mA
DC component No

DEVICE DESCRIPTION
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| Intelect®Mobile 2 - Service Manual 16
WAVEFORMS (CONTINUED)
TENS- Symmetrical Biphasic
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
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.
Output Mode Electrodes
Output Intensity 0-140 mA (CC) 0-140 V (CV)
Phase Duration 30-400 µsec
Frequency 1-200 Hz
Mode Selection (Stim) CC or CV
Mode Selection (Combo) CV
Burst Frequency 0-10 bps
Frequency Sweep On/Off
Sweep Low Frequency 1-199 Hz
Sweep High Frequency 2-200 Hz
Cycle Time Continuous or User Defined
Amplitude Modulation 0% (off) to 100% on 10% steps
Treatment Time (Stim) 1-60 min
Treatment Time (Combo) 1-30 minutes
Ramp 0-5 sec
Available on Channel 1,2
IRMS [mA] 0-49.32 mA
DC component : No
TENS - HAN
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
The HAN Waveform provides optimal parameters with a precisely controlled
sequence of Dense-and-Disperse (DD) modes of stimulation where a burst of
8 pulses at 80Hz is alternating with continuous stimulation (no burst), each
lasting for 3 seconds. This produces a synergistic analgesic effect.
Output Mode Electrodes
Output Intensity 0-100 mA (CC)
Phase Duration 180 μsec
Mode Selection CC
Burst Frequency 2 Hz
Frequency 80 Hz
Treatment Time 1-60 min
Available on Channels 1, 2
IRMS [mA] 0-20.36 mA
DC component No
VMS™
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
VMS is a symmetrical biphasic waveform with a 100 µsec interphase interval.
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- 140 mA (CC) 0-140 V (CV)
Channel Mode Single, Reciprocal, Co-Contract
Phase Duration 30-1,000 µsec
Mode Selection CC or CV
Anti-Fatigue Off or On
Set Intensity Individual/both Channel
Intensity Setting in Reciprocal
and Co-Contract modes
Cycle Time Continuous or User Defined
Frequency 1-200 pps
Ramp 0-5 sec
Treatment Time (Stim) 1-60 min
Treatment time (Combo) 1-30 min
Available on Channels 1, 2
IRMS [mA] 0-80 mA
DC component No

DEVICE DESCRIPTION
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| Intelect®Mobile 2 - Service Manual 17
WAVEFORMS (CONTINUED)
Microcurrent
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
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 thoughtto stimulate tissue healing by stimulating the ‘current
of injury’, a current which naturally occurs in healing tissue.
Output Mode Electrodes
Output Intensity 0-1,000 µA
Polarity Positive, Negative, or Alternating
Treatment Time 1-60 Min
Available on channels 1, 2
Duty Cycle 50%
Frequency 0.1-1,000 Hz
Mode Selection CC
IRMS [mA} 0-0.71 mA
DC component No
IFC Premodulated (Traditional 2 Pole)
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
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 Electrodes
Output Intensity 0-100 mA (CC) 0-100 V (CV))
Carrier Frequency 2,000-10,000 Hz
Beat Fixed (Sweep Off) 1-200 Hz
Sweep Low Beat Frequency 1- 199 Hz
Sweep High Beat Frequency 2-200 Hz
Cycle Time Continuous or User Defined
Mode Selection CC or CV
Treatment Time (STIM) 1-60 Min
Treatment Time (COMBO) 1-30 Min
Available on Channel 1, 2
DC component No
Diadynamic Waveforms
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
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- 60 mA
Treatment Time 1-60 min
Available on channels 1, 2
Mode Selection CC
MF (Monophasé Fixe)Frequency of 50 Hz :phase duration of 10 ms followed by a
pause of 10 ms.
IRMS [mA] 0-40 mA
DF (Diphasé Fixe) Frequency of 100 Hz:phase duration 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.
IRMS [mA] 0-56.57 mA
DC component Yes
Russian
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
Russian Current is a sinusoidal waveform, delivered in bursts or series of
pulses. This method was claimed by its author (Kotz) to produce maximal
muscle strengthening effects without significant discomfort to the patient.
Output Mode Electrodes
Output Intensity 0-100 mA (CC) 0-100 V (CV)
Channel Mode Single, Reciprocal, Co-Contract
Duty Cycle 10%, 20%, 30%, 40%, 50%
Mode Selection CC or CV
Anti-Fatigue Not available
Cycle Time Continuous or User Defined
Carrier Frequency 2,500 Hz
Burst Frequency (Anti-Fatigue Off) 1-100 bps
Ramp 0-5 sec
Treatment Time 1-60 min
Available on Channels 1, 2
IRMS [mA] 0-50 mA
DC component No

| Intelect®Mobile 2 - Service Manual 18
DEVICE DESCRIPTION
EN
WAVEFORMS (CONTINUED)
VMS™ Burst
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
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 muscle
strengthening protocols.
Output Mode Electrodes
Output Intensity 0-140 mA (CC) 0-140 V (CV)
Channel Mode Single, Reciprocal, Co-Contract Phase
Duration 30-400 µsec
Mode Selection CC or CV
Anti-Fatigue Off or On
Set Intensity Individual/both Channel Intensity
Setting in Reciprocal and Co-Contract modes
Cycle Time Continuous or User Defined
Burst Frequency 1-200 bps
Ramp 0-5 sec
Treatment Time 1-60 min
Available on Channels 1, 2
IRMS [mA] 0-138.56 mA
DC component No
MONOPHASIC: Monophasic Rectangular Pulsed
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
The Monophasic Rectangular Pulsed waveform is an interrupted
unidirectional current with a rectangular pulse shape.
Output Mode Electrodes
Output Intensity 0-60 mA
Phase Duration 0.1-1,000 ms
Phase Interval 5-5,000 ms
Treatment Time 1-60 min
Available on Channels 1, 2
Mode Selection CC
IRMS [mA] 0-79.60 mA
DC component Yes
MONOPHASIC: Monophasic Triangular Pulsed
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
The Monophasic Triangular Pulsed waveform is an interrupted unidirectional
current with a triangular pulse shape.
Output Mode Electrodes
Output Intensity 0-60 mA
Phase Duration 0.1-1,000 ms
Phase Interval 5-5,000 ms
Treatment Time 1-60 min
Available on Channels 1, 2
Mode Selection CC
IRMS [mA] 0-45.96 mA
DC component Yes
GALVANIC: Continuous
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
Galvanic Current is a direct current flowing in one direction only. The current
can be continuous or interrupted.
Output Mode Electrodes
Output Intensity 0-40 mA
Polarity Reversal On or Off
With Polarity Reversal On, Polarity will
change in the middle of the treatment time
Cycle Time Continuous, or User Defined
Treatment Time 1-60 min
Available on Channels 1, 2
Mode Selection CC
IRMS [mA] 0-80 mA
DC component Yes

| Intelect®Mobile 2 - Service Manual 19
DEVICE DESCRIPTION
EN
WAVEFORMS (CONTINUED)
GALVANIC: Interrupted
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
Galvanic Current is a direct current flowing in one direction only. The current
can be continuous or interrupted.
Pulse Duration 136 µsec
Output Mode Electrodes
Output Intensity 0-40 mA
Polarity Reversal On or Off
With Polarity Reversal On, Polarity will change in the middle of the
treatment time.
Polarity Reversal Ramp 1 sec
Cycle Time Continuous, or User Defined
Treatment Time 1-60 min
Available on Channels 1, 2
Mode Selection CC
IRMS [mA] 0-73.40 mA
DC component Yes
Low Level Galvanic
Advice on size and type of electrodes to be used is given in device GUI "treatment guidelines" feature
Low Level Galvanic Current is a direct current flowing in one direction
only. The intensity is limited to 4.0mA
Output mode Electrodes
Output Intensity 0-4 mA
Dosage 40-80 mA-min
Mode selection CC
Polarity Fixed at positive
DC component Yes
Träbert (Ultrareiz)
The Träbert Current is a monophasic waveform with a phase duration of 2 ms
and a pause of 5 ms resulting in a frequency of approximately 143Hz.
Output Mode Electrodes
Output Intensity 0-80 mA
Polarity Reversal On or Off
With Polarity Reversal On, Polarity will change in the middle of the
treatment time.
Treatment Time 1-60 min
Available on Channels 1, 2
Frequency 143 Hz
Phase Duration 2 ms
Mode Selection CC
IRMS [mA] 0-42.76 mA
DC component Yes
SURGED: monophasic triangular missing
The SURGED: Monophasic Rectangular Current is 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- 60 MA
Phase Duration 0.2-5.0 ms
Frequency 5-60 Hz
Surges per minute 1-20
Pause 0-57 sec
Treatment Time 1-60 min
Available on Channels 1, 2
Mode Selection CC
IRMS [mA] 0-43.82 mA
DC component Yes

DEVICE DESCRIPTION
EN
| Intelect®Mobile 2 - Service Manual 20
WAVEFORMS (CONTINUED)
VMS™ FR
The VMS-FR version of the VMS waveform is a physiologically based channel
interaction in which one channel stimulates the agonist and the other the
antagonist of the muscle group that is being exercised. The agonistic channel
initiates the movement with a brief burst of power, followed by a period of
sustained activity to complete the movement. The antagonistic channel has a
brief burst of power to slow down the initial acceleration of the agonist,
followed by a low output to regulate the movement of the agonist. The
movement is completed by a final burst of activity in both channels. VMS is a
symmetrical biphasic waveform with a 100 μsec interphase interval.
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 0-140 mA (CC)
Burst Duration 200 - 5000 ms
Phase Duration 30-400 μsec
Mode Selection CC
Cycle Time TBD
Frequency 20-80 pps
Treatment Time 1-60 min
Available on Channels 1&2
IRMS [mA] 0-20.57 mA
DC component No
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
Output Intensity 0-500 V
Polarity Positive or Negative
Ramp 0.5-5 sec
Display Volts
Sweep High Frequency 2-200 pps
Sweep Low Frequency 1-199 pps
Frequency 1-200 pps
Cycle Time Continuous or User Defined
Treatment Time (Stim) 1-60 Min
Treatment Time (Combo) 1-30 Min
Available on Channels 1, 2
Mode Selection CV
DC component Yes*