Manual

Mobile Stim & Combo Therapy Systems
SERVICE MANUAL
Model- 2778
Mobile Combo
Therapy System
Applies to Serial numbers 1000 and above
Model- 2777
Mobile Stim
Therapy System
Applies to Serial numbers 1000 and above
© 2005 Encore Medical, L.P.

TABLE OF CONTENTS Intelect® Mobile Stim and Combo Therapy Systems
FOREWORD . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 1 6 REMOVAL & REPLACEMENT .. .. .. .. .. .. .. .. .. .. .. 32

1 SAFETY PRECAUTIONS .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2 6.1 SEPARATING TOP & BOTTOM .. .. .. .. .. .. .. .. 32
1.1 PRECAUTIONARY SYMBOL DEFINITIONS . .. 2 6.2 THERAPY SYSTEM FAN .. .. .. .. .. .. .. .. .. .. .. .. 33
1.2 SAFETY PRECAUTIONS.. .. .. .. .. .. .. .. .. .. .. .. .. 2 6.3 POWER SUPPLY .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 34
2 THEORY OF OPERATION .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5 6.4 CHANNEL 1 STIM BOARD .. .. .. .. .. .. .. .. .. .. . 36
2.1 OVERVIEW . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5 6.5 CHANNEL 2 STIM BOARD .. .. .. .. .. .. .. .. .. .. .. 37
2.2 POWER SUPPLY CIRCUIT.. .. .. .. .. .. .. .. .. .. .. .. 5 6.6 ULTRASOUND BOARD
2.3 CONTROL BOARD .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5 COMBO SYSTEMS ONLY . .. .. .. .. .. .. .. .. .. .. .. 38
2.4 STIM BOARDS . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5 6.7 CONTROL BOARD ASSEMBLY .. .. .. .. .. .. .. .. 39
2.5 ULTRASOUND BOARD AND APPLICATOR 6.8 KEYMAT ASSEMBLY AND ON/OFF
COMBINATION SYSTEMS ONLY . .. .. .. .. .. .. 5 BUTTON KEYMAT .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 40
2.6 USER INTERFACE AND ACCESSORIES .. .. .. .. 5 7 GENERAL MAINTENANCE .. .. .. .. .. .. .. .. .. .. .. .. 41
2.7 NIMH BATTERY . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 5 7.1 CLEANING THE SYSTEM .. .. .. .. .. .. .. .. .. .. .. 41
3 NOMENCLATURE . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 6 7.2 CALIBRATION REQUIREMENTS .. .. .. .. .. .. .. 41
3.1 COMPONENT AND CONTROLS .. .. .. .. .. .. .. .. 6 7.3 FIELD SERVICE .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 41
3.2 HARDWARE AND SOFTWARE 7.4 FACTORY SERVICE.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 41
SYMBOL DEFINITIONS .. .. .. .. .. .. .. .. .. .. .. .. .. 8 8 ULTRASOUND APPLICATOR CALIBRATION . .. 42
4 SPECIFICATIONS .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 9 8.1 GENERAL PROCEDURES .. .. .. .. .. .. .. .. .. .. .. 42
4.1 INTELECT MOBILE COMBO SYSTEM.. .. .. .. .. 9 9 PARTS . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 43
4.2 INTELECT MOBILE STIM SYSTEM . .. .. .. .. .. 10 10 SCHEMATICS . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 51
4.3 INTELECT ELECTROTHERAPY 11 WARRANTY. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 68
WAVEFORM SPECIFICATIONS . .. .. .. .. .. .. .. 11
4.4 INTELECT MOBILE COMBO
ULTRASOUND SPECIFICATIONS .. .. .. .. .. .. 17
5 TROUBLESHOOTING . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 18
5.1 INTELECT MOBILE STIM AND
COMBO ERROR MESSAGES . .. .. .. .. .. .. .. .. 18
5.2 INTELECT MOBILE STIM AND
COMBO SYSTEM TESTING .. .. .. .. .. .. .. .. .. 21
5.3 VISUAL INSPECTION . .. .. .. .. .. .. .. .. .. .. .. .. 22
5.4 LEAKAGE TESTS . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 22
5.5 UNIT STARTUP AND FAN TESTING .. .. .. .. 22
5.6 ELECTRICAL STIMULATOR TEST
SYSTEM SETUP .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 23
5.7 VMS™ MODE TEST .. .. .. .. .. .. .. .. .. .. .. .. .. .. 23
5.8 INTERFERENTIAL MODE TEST.. .. .. .. .. .. .. 24
5.9 PREMODULATED MODE TEST.. .. .. .. .. .. .. 24
5.10 RUSSIAN MODE TEST .. .. .. .. .. .. .. .. .. .. .. .. 25
5.11 MICROCURRENT MODE TEST .. .. .. .. .. .. .. 26
5.12 HIGH VOLTAGE PULSED CURRENT
HVPC MODE TEST .. .. .. .. .. .. .. .. .. .. .. .. .. 27
5.13 ULTRASOUND TESTS. .. .. .. .. .. .. .. .. .. .. .. .. 28
5.14 ULTRASOUND APPLICATOR
IDENTIFICATION TEST . .. .. .. .. .. .. .. .. .. .. .. 28
5.15 ULTRASOUND APPLICATOR
OUTPUT TEST.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 29
5.16 ULTRASOUND DUTY CYCLE TEST . .. .. .. .. 30
5.17 COMBO OPERATION TEST .. .. .. .. .. .. .. .. .. 31
FOREWORD Intelect® Mobile Stim and Combo Therapy Systems
Read, understand, and follow the Safety Precautions and all other information contained in this
manual.
This manual contains the necessary safety and field service information for those field service
technicians, certified by Chattanooga Group, to perform field service on the Intelect Mobile Stim or
Combo Therapy Systems.
At the time of publication, the information contained herein was current and up-to-date. However,
due to continual technological improvements and increased clinical knowledge in the field of
electrotherapy, as well as Chattanooga Group’s policy of continual improvement, Chattanooga
Group reserves the right to make periodic changes and improvements to their equipment and
documentation without any obligation on the part of Chattanooga Group.
©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 the Chattanooga Group of Encore
Medical, L.P. is strictly prohibited. This publication was written, illustrated and prepared for print by the Chattanooga Group of Encore Medical, L.P.
1
1 SAFETY PRECAUTIONS Intelect® Mobile Stim and Combo Therapy Systems
1.1 PRECAUTIONARY SYMBOL DEFINITIONS 1.2 SAFETY PRECAUTIONS

The precautionary instructions found in this manual are indicated by specific Read, understand, and follow all safety precautions found in this manual.
symbols. Understand these symbols and their definitions before operating or Below are general safety precautions that must be read and understood before
servicing this equipment. The definitions of these symbols are as follows: attempting any service techniques on these systems.
A. CAUTION
Text with a “CAUTION” indicator will explain possible safety infractions
that have the potential to cause minor to moderate injury or damage
to equipment. • 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 Stim or Combo System when connected to any
B. WARNING unit other than Chattanooga Group devices. Do not operate the unit in an
Text with a “WARNING” indicator will explain possible safety environment of short-waveform diathermy use.
infractions that will potentially cause serious injury and equipment • The Ultrasound modality should be routinely checked before each use to
damage. determine that all controls function normally; especially that the intensity
control properly adjusts the intensity of the ultrasonic power output in a
stable manner. Also, determine that the treatment time control actually
terminates ultrasonic power output when the timer reaches zero.
• Use of controls or adjustments or performance of procedures other than
C. DANGER
those specified herein may result in hazardous exposure to ultrasonic energy.
Text with a “DANGER” indicator will explain possible safety infractions
• DO NOT use sharp objects such as a pencil point or ballpoint pen to operate
that are imminently hazardous situations that would result in death
the buttons on the control panel as damage may result.
or serious injury.
• Operate, transport, and store this unit in temperatures between 59 °F and
104 °F (15 °C and 40 °C), with Relative Humidity ranging from 30%-60%.
• Inappropriate handling of, and subjecting the ultrasound applicator to
physical abuse, may adversely affect its characteristics.
D. DANGEROUS VOLTAGE • Inspect Sound Head and Applicator handle for cracks, which may allow the
Text with a “Dangerous Voltage” indicator serves to inform the user ingress of conductive fluid before each use.
of possible hazards resulting in the electrical charge delivered to the • Inspect all cables, leads, and associated connectors before each use.
patient in certain treatment configurations of TENS waveforms.
• Never disconnect Applicator Cable, Lead Wires, Patient Switches, and Mains
Power Cord from the system by pulling the cable or wire. Pulling cable or
wire may cause system or accessory damage and result in injury to patient
and personnel.
E. CORROSIVE HAZARD NIMH BATTERY

Text with a “Corrosive Hazard” indicator will explain possible safety
infractions if the chemical components of this product are exposed to
air, skin, or other materials.
F. NOTE:
Throughout this manual “NOTE” may be found. These Notes
are helpful information to aid in the particular area or function being
described.
2
1.2 SAFETY PRECAUTIONS (continued)
• These devices are restricted to sale by, or on the order of, a • Stimulation should not be applied transthoracically in that
physician or licensed practitioner. This device should be used the introduction of electrical current into the heart may cause
only under the continued supervision of a physician or licensed cardiac arrhythmia.
practitioner. • Stimulation should not be applied over swollen, infected,
• For continued protection against fire hazard, replace fuses and inflamed areas or skin eruptions, (e.g., phlebitis,
only with ones of the same type and rating.
thrombophlebitis, varicose veins, etc.).
• Make certain the unit is electrically grounded by connecting • Stimulation should not be applied over, or in proximity to,
only to a grounded electrical service receptacle conforming to
the applicable national and local electrical codes. cancerous lesions.
• Care must be taken when operating this equipment around • Output current density is related to electrode size. Improper
other equipment. Potential electromagnetic or other application may result in patient injury. If any question arises
interference could occur to this or to the other equipment. Try as to the proper electrode size, consult a licensed practitioner
to minimize this interference by not using other equipment in prior to therapy.
conjunction with it. • Unplug the unit from the power source before attempting
• The safety of TENS waveforms for use during pregnancy or removal or replacement procedures to prevent electrical
birth has not been established. shock.
• TENS is not effective for pain of central origin. This includes • Use only Degassed Water in Power Meter for testing Ultrasound
headache. Applicators. Use of other types of water will cause false test
• TENS should be used only under the continued supervision of results. Refer to page 21 for Degassed Water Recipes.
a physician or licensed practitioner. • Do not aerate water when filling Power Meter.
• TENS waveforms have no curative value. • Unit failing Dielectric Withstand Test or Leakage Test could
• TENS is a symptomatic treatment, and as such, suppresses the indicate serious internal problems! Do not place unit back into
sensation of pain which would otherwise serve as a protective service! Send unit to factory for repair! Do not attempt to repair.
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.
• 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.
3
1.2 SAFETY PRECAUTIONS (continued)
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.”
4
2 THEORY OF OPERATION Intelect® Mobile Stim and Combo Therapy Systems
2.1 OVERVIEW
The Intelect Mobile Therapy Systems are comprised of several PC board assemblies housed within a common
enclosure. These assemblies each support a distinct function in the product. The basic elements are User
Interface, Control Board, Stim Boards, Ultrasound Board (Combo only), Ultrasound Applicator (Combo only),
and Power Supply Circuits.
2.2 POWER SUPPLY CIRCUIT
A universal 75 Watt input power supply provides each system with the required 24 volts DC. The supply is
connected to the mains at all times when the Mains Power Cord is attached and plugged into an outlet
supplying 100 - 240 VAC. The 24 V supply is regulated locally at each PC board as required.
2.3 CONTROL BOARD
The Control Board serves just as its name implies. It controls the operation of the Stim Boards, Ultrasound
Board, User Interface, and Accessories. The Control Board communicates to the Stim Boards and Ultrasound
Board through a proprietary bus. The Control Board drives the display. The Control Board reads the menu
buttons. The Control Board also reads the amplitude and the Contrast Control on the systems. Sound output
is generated by the Control Board and routed to an internal speaker.
2.4 STIM BOARDS
The Stim Boards create all muscle stimulation output. Communication to the Stim Boards is via a
proprietary bus. A Processor on each Stim Board acts on messages passed to it by the Control Board
to set up waveforms and adjust output amplitude. Information can likewise be passed from each
Stim Board back to the Control Board for monitoring current, etc. If a Stim Board does not respond as
expected to a command from the Control Board, output is stopped and an Error Message is generated.
2.5 ULTRASOUND BOARD AND APPLICATOR COMBINATION SYSTEMS ONLY
The Ultrasound Board generates the 1 or 3.3 MHz output to drive the Sound Head of the Applicator. The
Ultrasound Board is accessed through the proprietary bus by the Control Board. It can provide current
and voltage information about the ultrasound output of the board. The calibration data for the Sound Head
is passed through the Ultrasound Board from the Applicator to the Control Board. By storing the calibration
data in the Applicator, there is no calibration necessary for the Ultrasound Board and any
calibrated Chattanooga Group Intelect Advanced or Intelect Mobile Ultrasound Applicator can be connected
and operated to provide accurate coupling and output.
2.6 USER INTERFACE AND ACCESSORIES
The LCD display panel provides the operator visible feedback in the way of menu choices. Pressing the
User Interface buttons makes selections from the menus. The Control Board interprets these user inputs and
responds accordingly. Audible feedback is given for such events as key presses and end of treatment.
2.7 NIMH BATTERY
The NiMH Battery Module incorporates a Nickel Metal Hydride (NiMH) Battery Pack and a PC Board. The
PC Board monitors the Battery Charge Level. The Battery Pack supplies the required 24 VDC to the system
which is then distributed to the respective PCB’s through the Universal Power Supply. The Battery
Pack is interfaced with the system via a Wire Harness that facilitates communication with the Control
Board and delivery of power to an Electrotherapy or Combination Therapy System. When the Therapy
System is connected to a Mains Power Supply via the Mains Power Cord, the NiMH Battery Pack will charge.
Once the Battery Pack is fully charged, the software will stop the charging process, eliminating the possibility
of overcharging. Battery power is used only when the Therapy System is not connected to a Mains Power
Supply.
5
3 NOMENCLATURE Intelect® Mobile Stim and Combo Therapy Systems
3.1 COMPONENT AND CONTROLS

A. Intelect Mobile Combo System
The nomenclature graphics below, Figure 3.1, indicate the general Know the components and their functions before performing any
locations of the exterior components of the Two Channel Intelect operation of or service to the Intelect Mobile Combo System.
Mobile Combo System.
CONTRAST
CONTROL
FAN VENT
ON/OFF
POWER
SWITCH
LCD
USER INTERFACE
ULTRASOUND
APPLICATOR
PLYNTH
ELECTROTHERAPY
LEAD WIRE
RECEPTACLES
ULTRASOUND
RECEPTACLE
FIGURE 3.1
6
3.1 COMPONENT AND CONTROLS LOCATION (continued)

B. Intelect Mobile Stim System
The nomenclature graphics below, Figure 3.2, indicate the general Know the components and their functions before performing any
locations of the exterior components of the Two Channel Intelect operation of or service to the Intelect Mobile Stim system.
Mobile Electrotherapy System.
CONTRAST
CONTROL
FAN VENT
ON/OFF LCD
POWER
SWITCH
USER INTERFACE
PLYNTH
ELECTROTHERAPY
LEAD WIRE
RECEPTACLES
FIGURE 3.2
7
3.2 HARDWARE AND SOFTWARE SYMBOL DEFINITIONS

The symbols below are found on the system as well as within the Know the symbols and their definitions before performing
software. These symbols are defined for the purpose of recognition and any operation of or service to the Intelect Mobile Combo or Stim
functionality when operating or performing service on the Intelect Systems.
Mobile Combo or Stim Systems.
A. Intelect Mobile Combo and Stim Therapy System Hardware Symbols
CONTRAST CONTROL TREATMENT TIME
ON/OFF PARAMETER DISPLAY/ENTER

SWITCH
DATA INTENSITY
PORT
STOP UP ARROW
TREATMENT
DOWN ARROW
PAUSE
TREATMENT
START
TREATMENT
INCREASE
DECREASE
CLINICAL
RESOURCES
BACK
CHANNEL 1
LEAD WIRES
CHANNEL 2
LEAD WIRES
ULTRASOUND
APPLICATOR
CHARGE LEVEL
BATTERY
CHARGING
8
4 SPECIFICATIONS Intelect® Mobile Stim and Combo Therapy Systems
4.1 INTELECT MOBILE COMBO SYSTEM

Figure 4.1 below provides physical details of the Intelect Mobile Combo. Refer to this section when performing troubleshooting,
This section also provides waveform specifications to aid in replacement, and repair of the Intelect Mobile Combo System.
troubleshooting.
A. Intelect Mobile Combination Therapy System Physical Specifications
DEPTH
HEIGHT
WIDTH
FIGURE 4.1
Dimensions Operating Environment

Width.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. ..25.7 cm (10.125 in) Temperature .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. Between 15° C and 40° C
Height . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 18.4 cm (7.250 in) (59° F and 104° F)
Depth.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 29.2 cm (11.5 in) Relative Humidity .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 30%-60%
Atmospheric Pressure .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 950-1,050 h Pa
Weight
Complies with:
Standard Weight (with base) .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.3 kg (5.07 lb)
UL/IEC/EN 60601-1
Battery Pack. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 0.85 kg (1.87 lb) IEC/EN 60601-1-2
Power IEC 60601-2-10
Input. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 100 - 240 VAC, 1.0 A, 50/60 Hz 100 W Max IEC 60601-2-5
Output. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. +24 V, 3.125 A
Fuses .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 3.15 A Time Lag (not user serviceable) 0413
Electrical Class .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. CLASS I
Electrical Type
Ultrasound TYPE B.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .
Electrotherapy TYPE BF. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .
Battery Type . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. Nickel Metal Hydride (NiMH)
(1.2 V x 20 size AA)
9
4.2 INTELECT MOBILE STIM SYSTEM

Figure 4.2 below provides the physical details of the Intelect Refer to this section when performing troubleshooting,
Mobile Stim. This section also provides waveform specifications to aid in replacement, and repair of the Intelect Mobile Stim .
troubleshooting.
A. Intelect Mobile Stim Therapy System Physical Specifications
DEPTH
HEIGHT
WIDTH
FIGURE 4.2
Dimensions Operating Environment

Width.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. ..25.7 cm (10.125 in) Temperature .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. Between 15° C and 40° C
Height . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 16.8 cm (6.625 in) (59° F and 104° F)
Depth.. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 29.2 cm (11.5 in) Relative Humidity .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 30%-60%
Atmospheric Pressure .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 950-1,050 h Pa
Weight
Complies with:
Standard Weight (with base) .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 2.3 kg (5.07 lb)
UL/IEC/EN 60601-1
Battery Pack. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 0.85 kg (1.87 lb) IEC/EN 60601-1-2
Power IEC 60601-2-10
Input. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. . 100 - 240 VAC, 1.0 A, 50/60 Hz 100 W Max IEC 60601-2-5
Output. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. +24 V, 3.125 A
Fuses .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 3.15 A Time Lag (not user serviceable) 0413
Electrical Class .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. CLASS I
Electrical Type
Electrotherapy TYPE BF. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .
Battery Type . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. Nickel Metal Hydride (NiMH)
(1.2 V x 20 size AA)
10
4.3 INTELECT ELECTROTHERAPY WAVEFORM SPECIFICATIONS
The specifications found in this section provide the necessary waveform NOTE:
specifications to aid in troubleshooting. A waveform graphic from an All waveforms except High Voltage Pulsed Current (HVPC) of the Intelect
oscilloscope is also provided for clarification. Mobile Therapy System have been designed with a 200 mA current limit.
Refer to this section when performing troubleshooting, replacement, and VMS™, and all TENS waveform output intensities are measured, specified, and
repair of the Intelect Mobile Stim and Combo Systems. listed to peak, not peak to peak.
All Waveforms are available on all channels.
A. IFC (Interferential) Traditional (4 Pole)- Figure 4.3
Interferential Current is a medium frequency waveform. Current is
distributed from two channels (four electrodes). The currents cross
in the body within the area being treated. 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
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA
Carrier Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2,000-10,000 Hz
Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-200 Hz
Sweep Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 seconds
Sweep Low Beat Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . .1-200 Hz
Sweep High Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . .1-200 Hz
Scan Percentage . . . . . . . . . . . . . . . . . . . . . . . . .Static, 40%, and 100%
Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Minutes FIGURE 4.3
B. TENS- Asymmetrical Biphasic- Figure 4.4

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.
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20-1,000 μsec
Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-250 Hz
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Burst Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-25 bps
Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-250 Hz
Amplitude Modulation. . . . . . . . . . . Off, 40%, 60%, 80%, and 100%
FIGURE 4.4
Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Minutes
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 *CC= Constant Current
electrocution. Electrical current of this magnitude must not flow CV= Constant Voltage
through the thorax because it may cause a cardiac arrhythmia.
11
4.3 INTELECT ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)

C. TENS- Symmetrical Biphasic- Figure 4.5
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.
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20-1,000 μsec
Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-250 Hz
Burst Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-25 bps
Frequency Modulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-250 Hz
Amplitude Modulation. . . . . . . . . . . Off, 40%, 60%, 80%, and 100% FIGURE 4.5
D. High Voltage Pulsed Current (HVPC)- Figure 4.6
The High Voltage Pulsed Current (HVPC) has a very brief pulse
duration characterized by 2 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 seconds, 1 seconds, 2 seconds, 5 seconds
Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Peak Current or Volts
Sweep . . . . . . . . . . . . . . Continuous, 80/120 pps, 1/120 pps, 1/10 pps
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-120 Hz
Cycle Time . . . . . . . . . . . . . . . . . . . . . . . 5/5, 4/12, 10/10, 10/20, 10/30,
10/50, and Continuous FIGURE 4.6
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-99 Minutes
E. VMS™- Figure 4.7
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.
Channel Mode . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, Co-Contract
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20-1000 μsec
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 FIGURE 4.7
Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 pps
Ramp . . . . . . . . . . . . . . .0.5 seconds, 1 seconds, 2 seconds, 5 seconds *CC= Constant Current
Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Minutes CV= Constant Voltage
12

F. Diadynamic Waveforms- Figures 4.8 - 4.12
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 Minutes
MF: (Monophasé Fixe)- Figure 4.8
Frequency of 50 Hz: phase duration of 10 ms followed by a pause of
10 ms.
DF: (Diphasé Fixe)- Figure 4.9
Frequency of 100 Hz: phase duration of 10 ms followed immediately FIGURE 4.9
by another identical phase of 10 ms.
CP: Modulé en Courtes Périodes- Figure 4.10
1 second of MF followed abruptly by 1 second of DF.
LP: (Modulé en Longues Périodes)- Figure 4.11
Rhythmical fluctuation between 2 MF currents.
CP-iso: (Courtes Periodes Isodynamic)- Figure 4.12
A combination of MF and DF waveforms.
FIGURE 4.10
FIGURE 4.8
FIGURE 4.11
*CC= Constant Current

CV= Constant Voltage FIGURE 4.12
13

G. IFC (Interferential) Premodulated (2p)-
Figure 4.13
Premodulated Current is a medium frequency waveform. Current is
distributed from one channel (two electrodes). The current intensity
is modulated: it increases and decreases at a regular frequency (the
Amplitude Modulation Frequency).
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA
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, 5/5, 4/12, 10/10,
10/20, 10/30, and 10/50 FIGURE 4.13
H. Russian- Figure 4.14
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 Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 mA
Channel Mode . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, Co-Contract
Duty Cycle . . . . . . . . . . . . . . . . . . . . . .10%, 20%, 30%, 40%, and 50%
Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Off or On
Cycle Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5/5, 4/12, 10/10, 10/20,
10/30, 10/50, and Continuous
Burst Frequency (Anti-Fatigue Off) . . . . . . . . . . . . . . . . . . . .20-100 pps FIGURE 4.14
Ramp . . . . . . . . . . . . . . . .0.5 seconds, 1 seconds, 2 seconds, 5 seconds
I. Microcurrent- Figure 4.15
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 promote tissue healing by
stimulating the "current of injury": a current which naturally occurs
in healing tissue.
Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Electrodes or Probe
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-1,000.0 μA
Polarity . . . . . . . . . . . . . . . . . . . . . . . . .Positive, Negative, or Alternating

CV= Constant Voltage FIGURE 4.15
14

J. MONOPHASIC: Monophasic Rectangular Pulsed
Figure 4.16
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 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-5,000 ms
Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Minutes
FIGURE 4.16
K. MONOPHASIC: Monophasic Triangular Pulsed

Figure 4.17
The Monophasic Triangular Pulsed waveform is an interrupted
unidirectional current with a triangular pulse shape.
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-80 mA
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.1-500.0 ms
Phase Interval . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-5,000 ms
FIGURE 4.17
L. GALVANIC: Continuous- Figure 4.18

Continuous Galvanic Current is a direct current flowing in one
direction only.
Output Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Polarity Reversal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .On or Off
With Polarity Reversal On, Polarity will change after
50% of treatment time.
Cycle Time . . . . . . . . . . . . . . . . . . . . . . . . . Continuous, 5/60, and 10/60
Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-60 Minutes
FIGURE 4.18

CV= Constant Voltage
15

M. GALVANIC: Interrupted- Figure 4.19
Interrupted Galvanic Current is a direct current flowing in one
direction only. The current is delivered in pulses.
Output Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-80 mA
Polarity Reversal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .On or Off
50% of treatment time
Cycle Time. . . . . . . . . . . . . . . . . . . . . . . . . Continuous, 5/60, and 10/60
Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8,000 Hz
Duty Cycle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95%
Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-60 Minutes
FIGURE 4.19
N. Träbert (Ultrareiz)- Figure 4.20

Träbert 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
50% of treatment time.
Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-60 Minutes
FIGURE 4.20
16
4.4 INTELECT MOBILE COMBO ULTRASOUND SPECIFICATIONS

This section provides the necessary Ultrasound
Specifications to aid in troubleshooting.
Refer to these specifications as necessary when
troubleshooting the Ultrasound PC Board and Applicators.
A. Ultrasound
Frequency. . . . . . . . . . . . . . . . . . . . . . . . 1 MHz, ± 5%; 3.3 MHz, ±5%
Duty Cycles . . . . . . . . . . . . . . . . . . . . 10%, 20%, 50%, and Continuous
Pulse Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . .16 Hz, 48 Hz, 100 Hz
Pulse Duration . . . . . . . . . . . . . . . . . . . 1 mSec, ±20%; 2 mSec, ±20%
5 mSec, ±20%
Output Power
10 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-20 Watts at 1 MHz,
0-10 Watts at 3.3 MHz
2
5 cm Crystal . . . . . . . . . . . . . . . . . . . . . . . . 0-10 Watts, 1 and 3.3 MHz
2 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . .0-4 Watts, 1 and 3.3 MHz
1 cm2 Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-2 Watts 3.3 MHz Only
Amplitude . . . . . . . . . . . . . . . . . . . 0 - 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 Ratios:
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
Effective Radiating Areas . . . . . . . . . . .10 cm2 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
B. Head Warming Feature Specifications
The Head Warming feature of an Intelect 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 "Warming".
Output .. .. .. .. .. .. .. .. .. .. .. .. .. ..0 - 50% Cycling of maximum power
Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.3 Mhz
Do not apply the Ultrasound Applicator to the patient during the Head
Warming period. Applicator must remain in Applicator Hook during the
Head Warming period.
17
5 TROUBLESHOOTING Intelect® Mobile Stim and Combo Therapy Systems
5.1 INTELECT MOBILE STIM AND COMBO ERROR MESSAGES

A. The following information is provided as an aid in defining the All Troubleshooting and tests will be to validate a “Bad Board”
Software Error Messages of the Intelect Mobile Therapy System. Once only. No component level troubleshooting information is or will be
a particular Error Message is defined, the information will also list provided by Chattanooga Group for field troubleshooting of board
probable causes and possible remedies. Once the problem area is components.
determined, subsequent tests for verification will be necessary to B. Once a particular PC Board has been determined as bad, refer to the
determine a “Bad Board”. appropriate Removal and Replacement Section for the board affected
and follow the instructions for replacement of the board.
ERROR ERROR DEFINITION PROBABLE CAUSES POSSIBLE REMEDY

CODE TYPE
USER CORRECTABLE WARNING MESSAGES
100 WARNING Ultrasound Applicator became unplugged. Ultrasound Applicator was unplugged while an Ultrasound Plug Ultrasound Applicator into proper receptacle on unit
treatment was running. making certain it is completely seated.
101 WARNING Ultrasound Applicator unplugged. User attempted to start an Ultrasound treatment, but no Plug Ultrasound Applicator into proper receptacle on unit
Ultrasound Applicator was plugged into unit. making certain it is completely seated.
102 WARNING Ultrasound Applicator not calibrated. The Ultrasound Applicator plugged into the unit needs to Contact dealer or Chattanooga Group for service.
be calibrated.
103 WARNING Ultrasound Channel not available. User attempted to select Combo treatment, but the Wait until Ultrasound treatment is completed or stop
Ultrasound Channel was already in use. Ultrasound treatment and try again.
104 WARNING Stim Channel not available. User attempted to select an Electrotherapy or Combo Wait until Electrotherapy treatment is completed or stop
treatment, but all Stim Channels are in use. Electrotherapy treatment and try again.
105 WARNING Stim Channels not available. User attempted to select a two channel Electrotherapy Wait until Electrotherapy treatment is completed or stop
treatment, but at least one of the two stim channels were Electrotherapy treatment and try again.
already in use.
106 WARNING Overcurrent Stim channel has exceeded allowed current level and the Reset treatement parameters and attempt session again.
treatment has been stopped.
107 WARNING Bad Contact Quality. Electrode contact is poor. Apply new electrodes to the treatment area.
108 WARNING Shorted Lead Wires Lead Wires are bad. Replace with new lead wires.
109 WARNING Power Supply current limit. User attempted to start two channels of Electrotherapy Wait until Ultrasound treatment is completed or stop
while running an Ultrasound treatment with a 10 cm2 Ultrasound treatment and try again or decrease ultrasound
Ultrasound Applicator and Ultrasound Output is currently output to less than 15 Watts.
set to greater than 15 Watts..
18

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Mobile Stim & Combo Therapy Systems

© 2005 Encore Medical, L.P.

FOREWORD . .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 1 6 REMOVAL & REPLACEMENT .. .. .. .. .. .. .. .. .. .. .. 32

1.1 PRECAUTIONARY SYMBOL DEFINITIONS 1.2 SAFETY PRECAUTIONS

E. CORROSIVE HAZARD NIMH BATTERY

1.2 SAFETY PRECAUTIONS (continued)

1.2 SAFETY PRECAUTIONS (continued)

Stimulus delivered by the TENS waveforms of this

3.1 COMPONENT AND CONTROLS

3.1 COMPONENT AND CONTROLS LOCATION (continued)

3.2 HARDWARE AND SOFTWARE SYMBOL DEFINITIONS

A. Intelect Mobile Combo and Stim Therapy System Hardware Symbols

CONTRAST CONTROL TREATMENT TIME

ON/OFF PARAMETER DISPLAY/ENTER

4.1 INTELECT MOBILE COMBO SYSTEM

A. Intelect Mobile Combination Therapy System Physical Specifications

Dimensions Operating Environment

4.2 INTELECT MOBILE STIM SYSTEM

A. Intelect Mobile Stim Therapy System Physical Specifications

Dimensions Operating Environment

4.3 INTELECT ELECTROTHERAPY WAVEFORM SPECIFICATIONS

B. TENS- Asymmetrical Biphasic- Figure 4.4

Stimulus delivered by the TENS waveforms of this device, in

4.3 INTELECT ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)

4.3 INTELECT ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)

*CC= Constant Current

4.3 INTELECT ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)

*CC= Constant Current

4.3 INTELECT ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)

K. MONOPHASIC: Monophasic Triangular Pulsed

L. GALVANIC: Continuous- Figure 4.18

*CC= Constant Current

4.3 INTELECT ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)

N. Träbert (Ultrareiz)- Figure 4.20

4.4 INTELECT MOBILE COMBO ULTRASOUND SPECIFICATIONS

5.1 INTELECT MOBILE STIM AND COMBO ERROR MESSAGES

ERROR ERROR DEFINITION PROBABLE CAUSES POSSIBLE REMEDY

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