Chattanooga Vectra Genisys, Intelect Legend XT, Intelect VET Service manual
Therapy Systems:
Genisys Therapy System
(Serial Numbers- 1000 and above)
Intelect Legend XT Therapy System
(Serial Numbers- 1000 and above)
Intelect Vet Therapy System
(Serial Numbers- 1000 and above)
Optional Accessories:
Channel 3/4 Electrotherapy Module
(Serial Numbers- 1000 and above)
NiMH Battery Module
(Serial Numbers- 1000 and above)
sEMG Module (Genisys Only)
(Serial Numbers- 1000 and above)
Laser Module
(Genisys and Intelect Vet)
(Serial Numbers- 1000 and above)
Therapy System Cart
Operator Remote Control
Therapy Systems
SERVICE MANUAL
ISO 13485 CERTIFIED
TABLE of CONTENTS
Intelect®/Genisys® Therapy Systems
FOREWORD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
1 THEORY OF OPERATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.1 OVERVIEW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.2 POWER SUPPLY CIRCUITS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.3 CONTROL BOARD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.4 STIM BOARD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.5 ULTRASOUND BOARD AND APPLICATOR COMBINATION
SYSTEMS ONLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.6 USER INTERFACE AND ACCESSORIES . . . . . . . . . . . . . . . . . . . . . . . 2
2 SAFETY PRECAUTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
2.1 PRECAUTIONARY DEFINITIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
A. Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
B. Warning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
C. Danger . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
D. Dangerous Voltage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
E. Laser . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
F. Corrosive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
G. Laser Eye Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
H. Biohazard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
I. Spontaneous Combustion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
J. Note . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
2.2 PRECAUTIONARY INSTRUCTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . 5
A. Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
B. Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
C. Dangers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
3 NOMENCLATURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
3.1 INTELECT/GENISYS THERAPY SYSTEMS . . . . . . . . . . . . . . . . . . . . 7
A. Intelect XT, Intelect Vet and Vectra Genisys
Therapy Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
B. Intelect XT, Intelect Vet and Vectra Genisys
Combination Therapy Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
C. Intelect XT, Intelect Vet and Vectra Genisys
Electrotherapy Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
D. Intelect XT, Intelect Vet and Vectra Genisys
Channel 3/4 Electrotherapy Module . . . . . . . . . . . . . . . . . . . . . . 10
E. Intelect XT, Intelect Vet and Vectra Genisys
NiMH Battery Module. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
F. Intelect Vet and Vectra Genisys Laser Module . . . . . . . . . . . . . . 12
G. Intelect Vet and Vectra Genisys Laser Applicators . . . . . . . . . . . 13
H. Vectra Genisys Dual Channel sEMG Module . . . . . . . . . . . . . . . . 14
I. Intelect/Genisys Therapy System Cart . . . . . . . . . . . . . . . . . . . . . 15
J. Intelect/Genisys Operator Remote Control . . . . . . . . . . . . . . . . . 16
3.2 INTELECT/GENISYS THERAPY SYSTEM HARDWARE AND
SOFTWARE SYMBOL DEFINITIONS . . . . . . . . . . . . . . . . . . . . . . . . 17
A. Hardware Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
B. Software Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
C. Optional Accessory Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
4 SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
4.1 VECTRA GENISYS, INTELECT XT,
AND INTELECT VET THERAPY SYSTEMS . . . . . . . . . . . . . . . . . . . . 18
A. Therapy Systems Physical Specifications . . . . . . . . . . . . . . . . . . . 18
4.2 ELECTROTHERAPY WAVEFORM SPECIFICATIONS . . . . . . . . . . . 19
A. IFC (Interferential) Traditional (4 Pole)- Figure 4.2 . . . . . . . . . . 19
B. TENS- Asymmetrical Biphasic- Figure 4.3 . . . . . . . . . . . . . . . . . . 19
C. TENS- Symmetrical Biphasic- Figure 4.4 . . . . . . . . . . . . . . . . . . . 20
D. High Voltage Pulsed Current (HVPC)- Figure 4.5 . . . . . . . . . . . . 20
E. VMS™- Figure 4.6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
F. IFC (Interferential) Premodulated (2p)- Figure 4.7 . . . . . . . . . . 21
G. Russian- Figure 4.8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
H. Microcurrent- Figure 4.9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
I. VMS™ Burst- Figure 4.10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
J. DC (Direct Current)- Figure 4.11 . . . . . . . . . . . . . . . . . . . . . . . . . . 23
4.3 ULTRASOUND SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
4.4 LASER MODULE SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . 25
4.5 LASER APPLICATOR SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . 26
A. Single Diode Applicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
B. 9, 13, and 19 Diode Applicators . . . . . . . . . . . . . . . . . . . . . . . . . . 27
C. 33 Diode Applicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
5 TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
5.1 THERAPY SYSTEM ERROR MESSAGES . . . . . . . . . . . . . . . . . . . . . 29
5.2 THERAPY SYSTEM TESTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
5.3 VISUAL INSPECTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
5.4 LEAKAGE TESTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
5.5 UNIT STARTUP AND FAN TESTING . . . . . . . . . . . . . . . . . . . . . . . . 38
5.6 STIMULATOR TEST SYSTEM SETUP . . . . . . . . . . . . . . . . . . . . . . . . 39
5.7 VMS™ MODE TEST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
5.8 INTERFERENTIAL MODE TEST . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
5.9 PREMODULATED MODE TEST . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
5.10 RUSSIAN MODE TEST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
5.11 MICROCURRENT MODE TEST . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
5.12 HIGH VOLTAGE PULSED CURRENT HVPC MODE TEST . . . . . . 45
5.13 MICROCURRENT PROBE MODE TEST . . . . . . . . . . . . . . . . . . . . . 46
5.14 ULTRASOUND TESTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
5.15 ULTRASOUND APPLICATOR IDENTIFICATION TEST . . . . . . . . . 48
5.16 ULTRASOUND APPLICATOR OUTPUT TEST . . . . . . . . . . . . . . . . 49
5.17 ULTRASOUND DUTY CYCLE TEST . . . . . . . . . . . . . . . . . . . . . . . . 50
5.18 COMBO OPERATION TEST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
5.19 sEMG AND sEMG + ELECTRICAL STIMULATION TESTS . . . . . . 52
5.19 NiMH BATTERY MODULE CHECKS . . . . . . . . . . . . . . . . . . . . . . . . 56
6 REMOVAL/REPLACEMENT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
6.1 CHANNEL 3/4 ELECTROTHERAPY, NIMH BATTERY,
AND LASER MODULE INSTALLATION AND REMOVAL.. . . . . . . . 58
6.2. MODULE INSTALLATION AND REMOVAL . . . . . . . . . . . . . . . . . . 58
SEMG MODULE INSTALLATION AND REMOVAL
6.3
GENISYS ONLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
6.4. THERAPY SYSTEM FUSE REPLACEMENT . . . . . . . . . . . . . . . . . . . 65
6.5 THERAPY SYSTEM SEPARATING TOP & BOTTOM . . . . . . . . . . . 66
6.6 THERAPY SYSTEM FAN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
6.7 THERAPY SYSTEM CONTROL BOARD ASSEMBLY . . . . . . . . . . . 69
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TABLE of CONTENTS
6.8 THERAPY SYSTEM KEYMAT ASSEMBLY . . . . . . . . . . . . . . . . . . 70
6.9 THERAPY SYSTEM CONNECTOR BOARD . . . . . . . . . . . . . . . . . 71
6.10 THERAPY SYSTEM ULTRASOUND BOARD
COMBINATION SYSTEMS ONLY . . . . . . . . . . . . . . . . . . . . . . . . 72
6.11 THERAPY SYSTEM STIM BOARD CHANNELS 1/2 . . . . . . . . 73
6.12 THERAPY SYSTEM POWER SUPPLIES . . . . . . . . . . . . . . . . . . . 74
6.13 CHANNEL 3/4 ELECTROTHERAPY MODULE
CONNECTOR BOARD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
6.14 CHANNEL 3/4 ELECTROTHERAPY MODULE STIM BOARD . . . 77
6.15 MOUNTING AND DISMOUNTING THERAPY SYSTEM AND
THERAPY SYSTEM CART . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
7 GENERAL MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
7.1 CLEANING THE SYSTEM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
7.2 CALIBRATION REQUIREMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . 79
7.3 FIELD SERVICE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
7.4 FACTORY SERVICE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
8 ULTRASOUND CALIBRATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80
8.1 GENERAL . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80
9 PARTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
TOP TO BOTTOM ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
COMBINATION SYSTEM BASE ASSEMBLY . . . . . . . . . . . . . . . . . . . . 82
COMBINATION STIM & ULTRASOUND PC BOARD ASSEMBLY . . . . 83
TOP HOUSING ASSEMBLY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
VECTRA GENISYS CONTROL BOARD ASSEMBLY . . . . . . . . . . . . . . . 85
INTELECT XT CONTROL BOARD ASSEMBLY . . . . . . . . . . . . . . . . . . . 86
CHANNEL 3/4 ELECTROTHERAPY MODULE ASSEMBLY . . . . . . . . . 87
10 SCHEMATICS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
INTELECT/GENISYS THERAPY SYSTEM- CONTROL BOARD . . . . . 88-90
INTELECT/GENISYS THERAPY SYSTEM-
ULTRASOUND PC BOARD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91-93
INTELECT/GENISYS THERAPY SYSTEM- STIM BOARD . . . . . . . . 94-103
INTELECT/GENISYS THERAPY SYSTEM- CONNECTOR BOARD . . . . . 104
INTELECT/GENISYS THERAPY SYSTEM- CHANNEL 3/4
ELECTROTHERAPY MODULE CONNECTOR BOARD . . . . . . . . . . . . . . 105
INTELECT/GENISYS THERAPY SYSTEM- POWER SUPPLIES . . . . . . . 106
VECTRA GENISYS THERAPY SYSTEM- LASER MODULE BOARD . . . . 107
11 WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 108109
Intelect®/Genisys® Therapy Systems
ii
FOREWORD
Intelect®/Genisys® 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 Vectra Genisys, Intelect
XT, and Intelect Vet Therapy Systems, modules, and accessories.
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, ultrasound, Iontophoresis, and Laser therapy. 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.
It is the sole responsibility for certified field service technicians to stay informed and trained in
the latest technology utilized in the Vectra Genisys, Intelect XT, and Intelect Vet Therapy Systems
by Chattanooga Group. From time to time, as significant improvements are incorporated, service
bulletins will be produced and made available on our web site (chattgroup.com) in lieu of reprinting
a complete manual prematurely. These service bulletins will provide updated service information and
technological improvements to the Vectra Genisys, Intelect XT, and Intelect Vet Therapy Systems for
use by certified service technicians.
Due to the complex nature of the technology utilized by Chattanooga Group, the recommended
troubleshooting techniques are to determine “Bad Board” and board replacement only. No board
component level troubleshooting is recommended, nor will information or parts be supplied by
Chattanooga Group.
Any board component level troubleshooting performed will be at the sole risk and liability of the
certified field service technician performing such troubleshooting techniques. Performance of such
techniques may render the warranty null and void.
The Vectra Genisys and Intelect XT equipment is to be used only under the prescription and
supervision of a licensed medical practitioner.
The Intelect Vet is to be used only under the prescription and supervision of a licensed veterinarian.
©2006 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 THEORY OF OPERATION
1.1 OVERVIEW
The Vectra Genisys, Intelect XT, and Intelect Vet 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 Board, Ultrasound Board, Ultrasound
Applicator, and Power Supply Circuits.
When a Module (Channel 3/4 Electrotherapy, NiMH Battery, Laser, or sEMG) is installed, the Control Board
software automatically recognizes that a Module has been installed and prompts the installer to perform
certain tasks, for verification of Module installed, to make the respective Module fully functional. No additional
software installation is required as the Therapy System contains all necessary software to accommodate any
Module installation.
1.2 POWER SUPPLY CIRCUITS
A universal input 100 Watt power supply provides the Control Board and Stim Board of the system with 24
volts DC. The supply is connected to the mains at all times when the cord is attached. The 24 VDC supply is
regulated locally at each PC board as required. On Combination Systems, a separate universal 75 Watt Power
Supply provides 24 volts DC to the Ultrasound PC Board. The 24 volt DC power is regulated at the board, as
required.
1.3 CONTROL BOARD
The Control Board serves just as its name implies. It controls the operation of the stim board, ultrasound
board, user interface, optional modules, 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 (Intelect
XT Only) systems. The control board reads and manages the Multimedia (MMC) Card, Patient Data Card,
and sEMG Data Card. Sound output is generated by the control board and routed to an internal speaker.
The control board reads the Patient Interrupt Switch (Intelect XT and Vectra Genisys only) and the Operator
Remote Control (used to administer Manual Stimulation Therapy).
1.4 STIM BOARD
The Stim Board creates all muscle stimulation output. Communications to the Stim Board is via a
proprietary bus. A Processor on the 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 the Stim
Board back to the Control Board for monitoring Current, Microcurrent Probe (Intelect XT and Vectra
Genisys only) Contact Quality indication, etc. If the Stim Board does not respond as expected to a
command from the Control Board, output is stopped and an Error Message is generated.
1.5 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 XT, Intelect Vet, Vectra Genisys or Intelect TranSport Ultrasound Applicator can be
connected and operated to provide accurate coupling and output.
1.6 USER INTERFACE AND ACCESSORIES
The LCD display panel provides the operator visible feedback in the way of menu choices. Pressing of the
menu buttons makes selections from the menus. The control board interprets these user inputs and responds
accordingly. Audible feedback is given as well for events such as key presses and end of treatment.
The control board accesses the Patient Data Card, sEMG Data Card and MMC Card via an on board Reader/
Writer Interface. The voltage necessary to operate the reader is provided by the 100 Watt Power Supply and is
regulated by the Control Board.
A. Channel 3/4 Electrotherapy Module
The Channel 3/4 Electrotherapy Module creates all muscle stimulation output for Channels 3 and 4.
The Channel 3/4 Electrotherapy Module is interfaced with the System via a ribbon cable which
supplies power and facilitates communication between the stim board and control board of the
system. All waveforms available to channels 1 and 2 are available to channels 3 and 4 via the system
software. No additional software is required for full functionality of the module.
Intelect®/Genisys® Therapy Systems
2
1 THEORY OF OPERATION
1.6 USER INTERFACE AND ACCESSORIES (continued)
B. NiMH Battery Module
The NiMH Battery Module incorporates two Nickel Metal Hydride (NiMH) Battery packs and
a PC Board. The PC Board monitors the Charge Level of the Batteries. The Batteries supply 24 VDC to
the system which is then distributed to the respective pcb’s through the system power supply.
The Battery Module is interfaced with the system via a ribbon cable that facilitates communication
with the Control Board and delivery of power to a Two Channel Electrotherapy or Combination
Therapy System. When the Therapy System is connected to a Mains Power Supply via the Power
Cord, the NiMH Battery Module will charge. Once the Module 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.
C. Laser Module and Applicators (Genisys and Intelect Vet Therapy Systems ONLY)
The Laser Module utilizes a PC Board to communicate with the Control Board via a ribbon cable. The
Laser Module supplies the power required for each Laser Applicator through the Laser Applicator
Cable to PC Boards mounted within the Applicator housing. All Calibration Data for the Applicators
is stored on board the respective Applicator. Each Applicator incorporates a lens that is instrumental
in delivery of the laser radiation to the patient. The Laser applicators are classified as Class 3B
Laser products and are capable of up to 1440 nm of laser radiation in the infrared spectrum.
Approved eye protection must be worn by all persons in the vicinity when the Laser is on. The
Therapy System incorporates and demands entry of a unique PIN before operation of the Laser
Applicators is allowed by the Therapy System. The Module also incorporates a Therapy Room Door
Lockout Jack to accommodate a lockout switch that would prevent operation of the Laser
Applicators should the lockout safety device be breached by persons entering or exiting the therapy
room. Purchase and installation of the Lockout Device is the responsibility of the facility or clinic.
D. sEMG Module (Genisys Therapy Systems ONLY)
The Surface Electromyography (sEMG) Module utilizes a PC board to communicate to the Stim and
Control Boards via direct PC Board Contacts. The sEMG module reads and transmits muscle activity
through lead wires and electrodes. The sEMG Module communicates muscle activity data to the Control
Board which can store the data on an sEMG Data Card via the on board Card Reader/Writer for viewing on
a PC in graph form via the optional Chattanooga Group Patient Data Management System (PDMS)
Software and Card Reader.
E. Operator Remote Control
The Operator Remote Control is just as its name indicates and incorporates a PC Board. The Channel 1/2
Operator Remote Control is interfaced with the Therapy System through its unique connector on the
front of the Therapy System and the Channel 3/4 Electrotherapy Module. The Operator Remote Control
communicates with the Stim Board(s) to the Control Board for the administration of Manual Stim Therapy
only.
F. Therapy System Cart
The Therapy System Cart is designed for use with the Chattanooga Group Therapy Systems only. The
cart alone provides mobility to the Therapy System and storage of necessary accessories and supplies
used in conjunction with the Therapy System.
Intelect®/Genisys® Therapy Systems
3
2 SAFETY PRECAUTIONS
2.1 PRECAUTIONARY DEFINITIONS
The precautionary instructions found in this
section and throughout this manual are indicated
by specific symbols. Understand these symbols
and their definitions before operating this
equipment. The definition of these symbols are as
follows;
A. Caution
Intelect®/Genisys® Therapy Systems
F. Corrosive
Text with a “CORROSIVE" indicator will explain
possible safety infractions if the chemical
components of the battery are exposed to air,
skin, or other materials.
Text with a “CAUTION” indicator will explain
possible safety infractions that could have the
potential to cause minor to moderate injury or
damage to equipment.
B. Warning
Text with a “WARNING” indicator will explain
possible safety infractions that will potentially
cause serious injury and equipment damage.
C. Danger
Text with a “DANGER” indicator will explain
possible safety infractions that are imminently
hazardous situations that would result in death
or serious injury.
D. Dangerous Voltage
G. Laser Eye Protection
Text with a “LASER EYE PROTECTION" indicator
will explain possible safety infractions that could
cause serious eye injury or blindness if the eyes
are directly or reflectively exposed to Laser
Radiation.
H. Spontaneous Combustion
Text with a “SPONTANEOUS COMBUSTION"
indicator will explain possible safety infractions
that could create conditions for a Spontaneous
Combustion if the material is mishandled and
not disposed of properly.
Text with a “Dangerous Voltage” indicator serves
to inform the technician of possible hazards
resulting in the electrical charge disbursement
from certain components if handled or serviced
improperly.
E. Laser
Text with a “LASER" indicator will explain
possible safety infractions that are imminently
hazardous situations that would result serious
injury to eyes or blindness..
I. Note
Throughout this manual “NOTE” may be found.
These Notes are helpful information to aid in
the particular area or function being described.
4
2 SAFETY PRECAUTIONS
2.2 PRECAUTIONARY INSTRUCTIONS
A. Cautions
Read, understand, and practice the precautionary
•
and operating instructions. Know the limitations and
hazards associated with using any laser device. Observe
the precautionary and operational decals placed on the
unit.
Do not operate this unit when connected to any unit
•
other than Chattanooga Group devices.
Do not operate this unit in an environment where
•
other devices are being used that intentionally radiate
electromagnetic energy in an unshielded manner.
Portable and mobile RF communications equipment
can affect Medical Electrical Equipment.
The Laser System should be routinely checked before
•
each use to determine that all controls function
normally; especially that the dosage control properly
adjusts the intensity of the laser output in a stable
manner. Also, determine that the treatment time
control actually terminates the laser output when the
timer reaches zero.
DO NOT use sharp objects such as a pencil point or
•
ballpoint pen to operate the buttons on the control
panel as damage may result.
Use of controls or adjustments or performance of
•
procedures other than those specified herein may
result in hazardous exposure to laser energy.
Handle the Laser Applicator with care. Inappropriate
•
handling of the Laser Applicator may adversely affect its
characteristics.
Inspect Laser Applicator, Lenses, Cables, and associated
•
connectors before each use. Do not use a damaged or
otherwise compromised Laser Applicator.
This unit should be transported and stored in
•
temperatures between 0°F and 140°F (-18°C and 60°C)
to prevent damage to the unit or its components.
Where the integrity of the external protective earth
•
conductor arrangement is in doubt, equipment shall be
operated from its internal electrical power source.
DO NOT remove the cover. This may cause unit
•
damage, malfunction, electrical shock, fire, or personal
injury. There are no serviceable components inside
the unit. If a malfunction occurs, discontinue use, and
immediately send to the factory for service.
DO NOT permit any foreign materials or liquids to enter
•
the unit. Take care to prevent any foreign materials
including, but not limited to, inflammables, water, and
metallic objects from entering the unit. These may
cause unit damage, malfunction, electrical shock, fire, or
personal injury.
Intelect®/Genisys® Therapy Systems
This equipment generates, uses, and can radiate radio
•
frequency energy and, if not installed and used in
accordance with the instructions, may cause harmful
interference to other devices in the vicinity. However,
there is no guarantee that interference will not occur in
a particular installation. Harmful interference to other
devices can be determined by turning this equipment
on and off, try to correct the interference using one
or more of the following: Reorient or relocate the
receiving device, increase the separation between the
equipment, connect the equipment to an outlet on a
different circuit from that to which the other device(s)
are connected and/or consult the factory field service
technician for help.
B. Warnings
Federal law restricts this device to sale by, or on the
•
order of, a physician or licensed practitioner. This device
should be used only under the continued supervision
of a physician or licensed practitioner.
For continued protection against fire hazard, replace
•
fuses only with ones of the same type and rating.
Make certain the unit is electrically grounded by
•
connecting only to a grounded electrical service
receptacle conforming to the applicable national and
local electrical codes.
This device should be kept away from children.
•
Care must be taken when operating this equipment
•
around other equipment. Potential electromagnetic or
other interference could occur to this or to the other
equipment. Try to minimize this interference by not
using other equipment in conjunction with it.
This equipment is not designed to prevent the ingress
•
of water or liquids. Ingress of water or liquids could
cause malfunction of internal components of the system
and therefore create a risk of injury to the patient.
Do not drop the applicator or unit on hard surfaces. Do
•
not cool an overheated applicator with ice water or ice
packs. Do not allow the applicator to reach maximum
temperatures repeatedly. Do not submerge the
applicator or unit in water. All of these conditions will
damage the applicator and unit. Damage resulting from
these conditions is not covered under the warranty.
5
2 SAFETY PRECAUTIONS
2.2 PRECAUTIONARY INSTRUCTIONS (continued)
C. Dangers
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
dealer if the unit is not properly rated.
When the unit is on, not all wavelengths are
•
visible to the naked eye. Therefore, when
performing any operational or functional
check, make certain all persons in the vicinity
of the laser wear Chattanooga Group laser
protective eyewear.
DO NOT point the laser beam directly into
•
human or animal eyes. The lens of the eye
does not detect the invisible, coherent laser
beams, potentially resulting in permanent
retinal damage.
Class 3B Lasers are considered an acute hazard
•
to the skin and eyes from direct radiation.
Eye injury will occur if laser is viewed directly
or from specular reflection. Eye protection is
required for all persons in the treatment area.
Intelect®/Genisys® Therapy Systems
Power Supplies retain High Voltage!
•
NiMH batteries contain Class E corrosive
•
materials. In the event of battery cell rupture
or leakage, handle battery module wearing
neoprene or natural rubber gloves. Contents
of a ruptured or leaking battery can cause
respiratory irritation. Hypersensitivity to
nickel can cause allergic pulmonary asthma.
Contents of cell coming in contact with skin
can cause skin irritation and chemical burns.
Never, under any circumstances, open the
•
battery cells. Should an individual cell from a
battery become disassembled, spontaneous
combustion of the negative electrode is
possible. There can be a delay between
exposure to air and spontaneous combustion.
6
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS
A. Intelect XT and Vectra Genisys Therapy Systems
The nomenclature graphic below, Figure 3.1,
locates the major components of an Intelect
or Genisys two channel combination therapy
system equipped with the following: Channel
3/4 Electrotherapy Module, *sEMG Module, and
Therapy System Cart.
TWO CHANNEL COMBINATION THERAPY SYSTEM
REFER TO PAGE 8
TWO CHANNEL ELECTROTHERAPY SYSTEM
REFER TO PAGE 9
DUAL CHANNEL SEMG MODULE*
REFER TO PAGE 14
INSTALLED TO BOTTOM OF THERAPY SYSTEM
Intelect®/Genisys® Therapy Systems
Refer to the respective pages of this section
for specific nomenclature of the optional
modules.
* Genisys Therapy Systems ONLY
ULTRASOUND APPLICATOR
CHANNEL 3/4 ELECTROTHERAPY MODULE
REFER TO PAGE 10
OR
NIMH BATTERY MODULE
REFER TO PAGE 11
OR
LASER MODULE & APPLICATORS*
REFER TO PAGES 12 AND 13
CHANNELS 1/2 AND 3/4 OPERATOR REMOTE
REFER TO PAGE 16
THERAPY SYSTEM CART
REFER TO PAGE 15
FIGURE 3.1
7
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
B. Vectra Genisys, Intelect XT, and Intelect Vet
Combination Therapy Systems
The nomenclature graphics below, Figure
3.2, indicate the general locations of the exterior
components of the Two Channel Intelect and
Genisys Combination Therapy Systems.
1
12
Intelect®/Genisys® Therapy Systems
Know the components and their functions
before performing any operation of or service
to the Intelect or Genisys Two Channel
Combination Therapy Systems.
7
9
2
3
4
5
6
11
20
8
10
Screen Contrast Control (Not functional on color
1.
Systems)
System Power On/Off Switch
2.
Technical Maintenance Port
3.
Fuses
4.
Main Power Cord
5.
Rear Access Panel
6.
Two Channel Combo System
7.
Ultrasound Applicator (5cm
8.
2
shown) Combo
Systems Only
User Interface (Screen and Buttons)
9.
Front Access Panel
10.
Patient Data Card and sEMG Data Card access port
11.
FIGURE 3.2
12.
13.
14.
15.
16.
17.
18.
19.
20.
8
13
14
16
15
18
17
19
Multimedia Card (MMC) access port
Front Access Panel Lanyard- When reinstalling the
Front Access Panel, make certain the Lanyard does
not become kinked
Optional Channel 1/2 Operator Remote Control
Connector
Patient Interrupt Switch Connector
Channel 1 Lead Wire Connector
Channel 2 Lead Wire Connector
Microcurrent Probe Connector
Ultrasound Applicator Connector
Therapy System to Module Ribbon Cable
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
C. Vectra Genisys, Intelect XT, and Intelect Vet
Electrotherapy Systems
The nomenclature graphics below, Figure
3.3, indicate the general locations of the exterior
components of the Two Channel Intelect and
Genisys Two Channel Electrotherapy Systems.
1
2
3
4
5
6
11
Intelect®/Genisys® Therapy Systems
Know the components and their functions
before performing any operation of or service
to the Intelect or Genisys Two Channel
Electrotherapy Systems.
7
8
10
18
Screen Contrast Control (Not functional on Color
1.
Systems)
System Power On/Off Switch
2.
Technical Maintenance Port
3.
Fuses
4.
Main Power Cord
5.
Rear Access Panel
6.
Two Channel Electrotherapy System
7.
User Interface (Screen and Buttons)
8.
Front Access Panel
9.
Patient Data Card and sEMG Data Card access
10.
port
FIGURE 3.3
11.
12.
13.
14.
15.
16.
17.
18.
9
12
13
15
14
17
16
Multimedia Card (MMC) access port
Front Access Panel Lanyard- When reinstalling
the Front Access Panel, make certain the Lanyard
does not become kinked
Optional Channel 1/2 Operator Remote Control
Connector
Patient Interrupt Switch Connector
Channel 1 Lead Wire Connector
Channel 2 Lead Wire Connector
Microcurrent Probe Connector
Therapy System to Module Ribbon Cable
9
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
D. Vectra Genisys, Intelect XT, and Intelect Vet
Channel 3/4 Electrotherapy Module
The nomenclature graphics below, Figure 3.4,
indicate the general locations of the exterior
components of the Vectra Genisys, Intelect XT,
and Intelect Vet Therapy Systems Channel 3/4
Electrotherapy Module.
6
Intelect®/Genisys® Therapy Systems
Know the components and their functions
before performing any operation of or
service to the Vectra Genisys, Intelect XT, and
Intelect Vet Therapy Systems Channel 3/4
Electrotherapy Module.
5
4
3
1
2
1. Two (2) Channel Electrotherapy Module
2. Extended Front Access Panel
3. Module to System Mounting Holes
4. Module to System Feet Alignment Indents
5. Power Cord Routing Port
6. Module to System Connector
7. Operator Remote Control Connector
8. Patient Interrupt Switch Connector
9. Channel 3 Lead Wire Connector
10. Channel 4 Lead Wire Connector
11. Microcurrent Probe Connector
FIGURE 3.4
Also Included:
•
Four 4mm X 20mm mounting screws
•
Channel 3 and 4 Lead Wires
•
Patient Interrupt Switch (Ch 3/4)
•
Carbon Electrodes
•
Electrode Sponges
•
Sample of Dura-Stick™ II electrodes
•
Nylatex® Wraps
NOTE:
The Channel 3/4 Electrotherapy Module is not
operable unless it is properly connected to an Intelect
XT or Vectra Genisys Therapy System.
10
7
8
9
10
11
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
E. Vectra Genisys, Intelect XT, and Intelect Vet
NiMH Battery Module
Intelect®/Genisys® Therapy Systems
The nomenclature graphic below, Figure 3.5,
indicates the general locations of the exterior
components of the Intelect XT, Intelect Vet, and
Vectra Genisys Therapy Systems NiMH Battery
Module.
5
4
Know the components and their functions
before performing any operation of or service to
the Vectra Genisys, Intelect XT, and Intelect Vet
Therapy Systems NiMH Battery Module.
6
1
2
3
1. NiMH Battery Module
2. Extended Front Access Panel
3. Module to System Mounting Holes
4. Module to System Feet Alignment Indents
5. Power Cord Routing Port
6. Module to System Connector
FIGURE 3.5
NOTE:
The NiMH Battery Module is not operable unless it is
properly connected to an Intelect XT, Intelect Vet or
Vectra Genisys Therapy System.
11
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
F. Vectra Genisys and Intelect Vet Laser Module
The nomenclature graphic below, Figure 3.6,
indicates the general locations of the exterior
components of the Vectra Genisys and Intelect
Vet Therapy System Laser Module.
6
Intelect®/Genisys® Therapy Systems
Know the components and their functions
before performing any operation of or service to
the Therapy System Laser Module.
5
4
3
1
2
7
8
9
10
FIGURE 3.6
1. Laser Module
2. Extended Front Access Panel
3. Module to System Mounting Holes
4. Module to System Feet Alignment Indents
5. Power Cord Routing Port
6. Module to System Header
7. Patient Interrupt Switch
8. Therapy Room Door Lockout Jack
9. Point Locator (for use with Single Applicator Laser
Applicators)
10. Laser Applicator
NOTE:
The Vectra Genisys Laser Module is not operable
unless it is properly connected only to the Genisys
Therapy System.
NOTE:
No Field Service is applicable to the Laser Module or
Laser Applicators. All Laser Modules and Applicators
suspected to require service or calibration must be
sent to the factory.
DO NOT point the laser beam directly into
•
human or animal eyes. The lens of the eye
does not detect the invisible, coherent laser
beams, potentially resulting in permanent
retinal damage.
Class 3B Lasers are considered an acute hazard
•
to the skin and eyes from direct radiation.
Eye injury will occur if laser is viewed directly
or from specular reflection. Laser protective
eyewear is required for all persons in the
treatment area.
Approved Laser protective eyewear must be
•
worn at all times by all persons in the vicinity
when the Laser is On.
12
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
G. Vectra Genisys Laser Applicators
The nomenclature graphics below, Figure 3.7,
indicate the general locations of the exterior
components of the Vectra Genisys and Intelect
Vet Therapy System Laser Applicators.
1
Intelect®/Genisys® Therapy Systems
Know the components and their functions
before performing any operation of or service
to theVectra Genisys and Intelect Vet Therapy
System Laser Therapy System Laser Applicators.
7
6
2
3
1
2
4
1
2
5
7
6
6
NOTE:
No Field Service is applicable to the Laser Module or Laser Applicators. All Laser
Modules and Applicators suspected to require service or calibration must be sent
to the factory.
FIGURE 3.7
Laser On LED
1.
Laser Applicator On/Off Button
2.
Single Diode Applicator Housing
3.
LED Cluster Applicator Housing
4.
Laser Cluster Applicator Housing
5.
Laser Aperture Lens
6.
Laser Aperture
7.
NOTE:
The Genisys Laser Applicators are not operable unless
they are connected to the Genisys Therapy Systems
only via the Laser Module.
No Field Service is applicable to the Laser Module or
Laser Applicators. All Laser Modules and Applicators
suspected to require service or calibration must be
sent to the factory.
DO NOT point the laser beam directly into
•
human or animal eyes. The lens of the eye
does not detect the invisible, coherent laser
beams, potentially resulting in permanent
retinal damage.
Class 3B Lasers are considered an acute hazard
•
to the skin and eyes from direct radiation.
Eye injury will occur if laser is viewed directly
or from specular reflection. Laser protective
eyewear is required for all persons in the
treatment area.
Approved Laser protective eyewear must be
•
worn at all times by all persons in the vicinity
when the Laser is On.
7
13
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
H. Vectra Genisys Dual Channel sEMG Module
The nomenclature graphics below, Figure 3.8,
indicate the general locations of the exterior
components of the Genisys Therapy System
Dual Channel sEMG Module.
Intelect®/Genisys® Therapy Systems
Know the components and their functions
before performing any operation of or service to
the Genisys Therapy System Dual Channel sEMG
Module.
1
4
3
2
1. sEMG Module Top Housing
2. Module Removal Slot
3. Module to System Mounting Tabs
4. Module to System PC Board Contacts
5. Module to System Retaining Tab
6. sEMG Module Bottom Housing
6
FIGURE 3.8
NOTE:
The Genisys Dual Channel sEMG Module is not
operable unless it is connected to the Genisys Therapy
System.
5
14
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
I. Intelect/Genisys Therapy System Cart
The nomenclature graphics below, Figure 3.9,
indicate the general locations of the exterior
components of the Vectra Genisys, Intelect XT,
and Intelect Vet Therapy Systems Cart.
1
Intelect®/Genisys® Therapy Systems
Know the components and their functions
before performing any operation of or service to
the Vectra Genisys, Intelect XT, and Intelect Vet
Therapy Systems Cart.
3
4
5
6
1. Cart Top
2. System to Cart Retaining Screw (4)
3. Storage Bins (6)
4. Cart Rear Swivel Casters
5. Cart Base
6. Cart Front Swivel, Locking Casters
7. Cart Bottom Access Plate
8. Front and Rear Cart Extrusions
2
8
7
FIGURE 3.9
15
3 NOMENCLATURE
3.1 INTELECT/GENISYS THERAPY SYSTEMS (continued)
J. Intelect/Genisys Operator Remote Control
The nomenclature graphics below, Figure 3.10,
indicate the general locations of the exterior
components of the Intelect/Genisys Therapy
Systems Operator Remote Control.
Intelect®/Genisys® Therapy Systems
Know the components and their functions
before performing any operation of or service to
the Intelect or Genisys Therapy Systems Operator
Remote Control.
7
6
5
4
1
2*
3
* Blue button for Channels 1/2 Operator Remote Control
Orange button for Channels 3/4 Operator Remote Control
1. Operator Remote Storage Hook
2. Treatment Pause Button
3. Channel 2 Increase Intensity Button
4. Channel 2 Decrease Intensity Button
5. Manual Stimulation Button
6. Channel 1 Decrease Intensity Button
7. Channel 1 Increase Intensity Button
NOTE:
The Intelect/Genisys Operator Remote Control is
not operable unless it is properly connected to the
Intelect XT, Intelect Vet or Vectra Genisys Therapy
System.
FIGURE 3.10
Operator Remote Control Symbol Definitions
INCREASE
INTENSITY
DECREASE
INTENSITY
M
PAUSE
TREATMENT
MANUAL
STIMULATION
16
3 NOMENCLATURE
Intelect®/Genisys® Therapy Systems
3.2 INTELECT/GENISYS THERAPY SYSTEM HARDWARE AND SOFTWARE SYMBOL DEFINITIONS
The symbol graphics below are found on the
system as well as within the software. These
symbols are defined below for the purpose of
recognition and functionality when operating
or performing service on an Intelect or Genisys
Therapy System, Modules, and Accessories.
Know the symbols and their definitions before
performing any operation of or service to the
Intelect or Genisys Therapy Systems, Modules, or
Accessories.
A. Hardware Symbols
CONTRAST CONTROL
NOT FUNCTIONAL ON
GENISYS SYSTEMS
ON/OFF
SWITCH
DATA
PORT
MULTIMEDIA AND
PATIENT CARD
STOP
TREATMENT
PAUSE
TREATMENT
START
TREATMENT
CLINICAL
RESOURCES
BACK
CHANNEL 1/2
OPERATOR
REMOTE
CONTROL
OPTIONAL
PATIENT
INTERRUPT
SWITCH
CHANNEL 1
LEAD WIRES
CHANNEL 2
LEAD WIRES
C. Optional Accessory Symbols
1. Operator Remote Control Symbols
INCREASE
INTENSITY
DECREASE
INTENSITY
2. NiMH Battery Module Symbols
CHARGE LEVEL
3. Channel 3/4 Electrotherapy Module Symbols
PATIENT
INTERRUPT
SWITCH
CHANNEL 3
LEAD WIRES
CHANNEL 4
LEAD WIRES
PAUSE
TREATMENT
MANUAL
M
STIMULATION
MICROCURRENT
PROBE
INACTIVE ON
INTELECT VET
CHANNEL 3/4
OPERATOR
REMOTE|
CONTROL
OPTIONAL
BATTERY
CHARGING
THERAPY
INTENSITY
CONTROL
HOME
B. Software Symbols
MOVE UP
MOVE DOWN
MOVE RIGHT
MICROCURRENT
PROBE
INACTIVE ON
INTELECT VET
ULTRASOUND
APPLICATOR
MOVE LEFT
ACCEPT AND
RETURN
DO NOT ACCEPT
AND RETURN
4. Laser Module Symbols (Genisys Only)
PATIENT
INTERRUPT
SWITCH
TREATMENT
ROOM INTERLOCK
CONNECTOR
POINT
LOC ATOR
INACTIVE
LASER
APPLICATOR
5. Laser Applicator Symbols (Genisys Only)
PAUSE
TREATMENT
17
4 SPECIFICATIONS
4.1 VECTRA GENISYS, INTELECT XT, AND INTELECT VET THERAPY SYSTEMS
The specifications found in this section provide
physical details of the Intelect XT, Intelect Vet,
and Vectra Genisys Therapy Systems. This section
also provides waveform specifications to aid in
troubleshooting.
A. Therapy Systems Physical Specifications
Refer to this section when performing
troubleshooting, replacement, and repair of an
Intelect or Genisys Therapy System, Modules, and
Accessories.
Intelect®/Genisys® Therapy Systems
HEIGHT
HEIGHT
CART ONLY
WITH SYSTEM & SYSTEM WITH MODULE
DEPTH
WIDTH
FIGURE 4.1
Dimensions
Height
Cart Only . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33.75 in (85.7 cm)
With System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42.50 in (108 cm)
With System and Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44.25 in (112.4 cm)
Width . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17 in (43.2 cm)
Depth . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16.25 in (41.3 cm)
Power (Combination and Electrotherapy Systems)
Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100 - 240 V - 175 VA, 50/60 Hz
Output (Internal Power Supply) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .+24, 7.3 A
Fuses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Two 6.3 A Time Lag (Part Number 71772)
Electrical Class . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CLASS I
Electrical Type
Ultrasound (Combination Systems Only) and Laser Module (Intelect Vet and Vectra Genisys Only) . . . . TYPE B
Electrotherapy, sEMG and Channel 3/4 Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TYPE BF
18
4 SPECIFICATIONS
4.2 ELECTROTHERAPY WAVEFORM SPECIFICATIONS
The specifications found in this section provide
the necessary waveform specifications to aid in
troubleshooting. A waveform graphic from an
oscilloscope is also provided for clarification.
Refer to this section when performing
troubleshooting, replacement, and repair of the
Therapy System, Modules, and Accessories.
A. IFC (Interferential) Traditional (4 Pole)-
Figure 4.2
Output Mode . . . . . . . . . . . . . . . . . . . . . . . Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . .0-100 mA
Carrier Frequency . . . . . . . . . . . . . . .2,500-5,000 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
Intelect®/Genisys® Therapy Systems
NOTE:
All waveforms, except High Voltage Pulsed Current
(HVPC), of the Vectra Genisys, Intelect XT, and
Intelect Vet Therapy Systems have a 200 mA current
limit.
VMS™, VMS™ Burst, and all TENS waveform output
intensities are measured, specified, and listed to
peak, not peak to peak.
All waveforms are available on all channels.
B. TENS- Asymmetrical Biphasic- Figure 4.3
Output Mode . . . . . . . . . . . . . . . . . . . . . . . Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . .0-110 mA
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%
Treatment Time . . . . . . . . . . . . . . . . . . 1-60 minutes
FIGURE 4.2
FIGURE 4.3
*CC= Constant Current
CV= Constant Voltage
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.
19
4 SPECIFICATIONS
4.2 ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)
C. TENS- Symmetrical Biphasic- Figure 4.4
Output Mode . . . . . . . . . . . . . . . . . . . . . . . Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . 0-80 mA
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%
Treatment Time . . . . . . . . . . . . . . . . . . 1-60 minutes
Intelect®/Genisys® Therapy Systems
FIGURE 4.4
D. High Voltage Pulsed Current (HVPC) Figure 4.5
Output Mode . . . . . . . . . . . . . . Electrodes or Probe
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . 0-500 V
Polarity . . . . . . . . . . . . . . . . . . . Positive or Negative
Ramp . . . . . . . . . . . . . . . . 0.5 sec, 1 sec, 2 sec, 5 sec
Display . . . . . . . . . . . . . . . . . . .Peak Current or Volts
Sweep . . . . . . . . . . . . . . . . Continuous, 80/120 pps,
1/120 pps, 1/10 pps
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . 10-120 Hz
Cycle Time . . . . . . .5/5, 4/12, 10/10, 10/20, 10/30,
10/50, and Continuous
Treatment Time . . . . . . . . . . . . . . . . . . 1-60 Minutes
FIGURE 4.5
*CC= Constant Current
CV= Constant Voltage
20
4 SPECIFICATIONS
4.2 ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)
E. VMS™- Figure 4.6
Output Mode . . . . . . . . . . . . . . . . . . . . . . . Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . .0-200 mA
Channel Mode . . . . Single, Reciprocal, Co-Contract
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . 20-400 μsec
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Off or On
(Not available on Intelect Vet)
Set Intensity . .Individual Channel Intensity Setting
in Reciprocal and Co-Contract modes
Cycle Time . . . . . . . . . . . . . . . . . .Continuous, 5/5, 4/12,
10/10, 10/20, 10/30, 10/50
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-200 pps
Ramp . . . . . . . . . . . . . 0.5 sec, 1 sec, 2 sec, and 5 sec
Treatment Time . . . . . . . . . . . . . . . . . . 1-60 minutes
Intelect®/Genisys® Therapy Systems
FIGURE 4.6
F. IFC (Interferential) Premodulated (2p)-
Figure 4.7
Output Mode . . . . . . . . . . . . . . . . . . . . . . Electrodes
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . .0-100 mA
Carrier Frequency . . . . . . . . . . . . . . . . . . . . 2,500 Hz
Beat Fixed (Sweep Off ) . . . . . . . . . . . . . .1-200 Hz
Sweep Low Beat Frequency . . . . . . . . . .1-199 Hz
Intelect Vet . . . . . . . . . . . . . . . . . . . . . . . .1-200 Hz
Sweep High Beat Frequency . . . . . . . 81-200 Hz
Intelect Vet . . . . . . . . . . . . . . . . . . . . . . . .2-200 Hz
Cycle Time . . . . . . . . . Continuous, 5/5, 4/12, 10/10,
10/20, 10/30, and 10/50
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Treatment Time . . . . . . . . . . . . . . . . . 1-60 Minutes
FIGURE 4.7
*CC= Constant Current
CV= Constant Voltage
21
4 SPECIFICATIONS
4.2 ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)
G. Russian- Figure 4.8
Output Mode . . . . . . . . . . . . . . . . . . . . . . Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . .0-100 mA
Channel Mode . . . Single, Reciprocal, Co-Contract
Duty Cycle . . . . . 10%, 20%, 30%, 40%, and 50%
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Off or On
Cycle Time . . . . . . . . . . . . .5/5, 4/12, 10/10, 10/20,
10/30, 10/50, and Continuous
Burst Frequency (Anti-Fatigue Off) 20-100 bps
(Not available on Intelect Vet)
Ramp . . . . . . . . . . . . . . . . . 0.5, 1, 2, and 5 seconds
Treatment Time . . . . . . . . . . . . . . . . . 1-60 minutes
Intelect®/Genisys® Therapy Systems
FIGURE 4.8
H. Microcurrent- Figure 4.9
Not
Output Mode . . . . . . . . . . . . . Electrodes or Probe
Output Intensity. . . . . . . . . . . . . . . . . . . . . . 0-1000.0 μA
Polarity . . . . . .Positive, Negative, or Alternating
Treatment Time . . . . . . . . . . . . . . . . . 1-60 Minutes
FIGURE 4.9
*CC= Constant Current
CV= Constant Voltage
22
4 SPECIFICATIONS
4.2 ELECTROTHERAPY WAVEFORM SPECIFICATIONS (continued)
I. VMS™ Burst- Figure 4.10
Output Mode . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . . . 0-200 mA
Channel Mode . . . . . . . . . . . . . . . . . . . Single, Reciprocal,
and Co-Contract
Phase Duration . . . . . . . . . . . . . . . . . . . . . . . . .20-400 μsec
Mode Selection . . . . . . . . . . . . . . . . . . . . . . . . . . CC or CV*
Anti-Fatigue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Off or On
Set Intensity . . . . . . . . . . . Individual Channel Intensity
Setting in Reciprocal
and Co-Contract modes
Cycle Time . . . . . . . . . . . . Continuous, 5/5, 4/12, 10/10,
10/20, 10/30, and 10/50
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-200 Hz
Ramp . . . . . . . . . . . . . .0.5 sec, 1 sec, 2 sec, and 5 sec
Treatment Time . . . . . . . . . . . . . . . . . . 1-60 minutes
Intelect®/Genisys® Therapy Systems
FIGURE 4.10
J. DC (Direct Current)- Figure 4.11
Output Mode . . . . . . . . . . . . . . . . . . . . . . .Electrodes
Output Intensity . . . . . . . . . . . . . . . . . . . . . . . 0-4 mA
Polarity Reversal . . . . . . . . . . . . . . . . . . . . .On or Off
With Polarity Reversal On, Polarity will
change after 50% of treatment time.
Cycle Time . . . . . . . . . . . . . .5/5, 4/12, 10/10, 10/20,
10/30, 10/50, and Continuous
Treatment Time . . . . . . . . . . . . . . . . . . 1-10 minutes
FIGURE 4.11
*CC= Constant Current
CV= Constant Voltage
23
4 SPECIFICATIONS
4.3 ULTRASOUND SPECIFICATIONS
Intelect®/Genisys® Therapy Systems
This section provides the necessary Ultrasound
Specifications to aid in troubleshooting the Intelect
or Genisys Ultrasound PC Board and Applicators.
2
1 cm
2
2 cm
Refer to these specifications as necessary when
troubleshooting the Ultrasound PC Board and
Applicators.
2
5 cm
STANDARD
10 cm
2
Ultrasound
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 MHz, ± 5%; 3.3 MHz, ±5%
Duty Cycles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10%, 20%, 50%, and Continuous
Pulse Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 mSec, ±20%; 2 mSec, ±20%, and 5 mSec, ±20%
Output Power
2
10 cm
5 cm
2 cm
1 cm
Amplitude . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 to 2.5 w/cm
Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-20 Watts at 1 MHz and 0-10 Watts at 3.3 MHz
2
Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0-10 Watts, 1 and 3.3 MHz
2
Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-4 Watts, 1 and 3.3 MHz
2
Crystal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-2 Watts 3.3 MHz Only
2
in continuous mode,
0-3 w/cm
2
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
2
Effective Radiating Areas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 cm
5 cm
2 cm
1 cm
Crystal - 8.5 cm2, ±1.5
2
Crystal - 4.0 cm2, ±1.0
2
Crystal - 1.8 cm2, +0.2/-0.4
2
Crystal - 0.8 cm2, +0.2/-0.4
Treatment Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-30 Minutes
Head Warming Feature
The Head Warming feature of an Intelect/Genisys Combination Therapy System utilizes Ultrasound output
resulting in warming of the Sound Head to increase patient comfort.
With Head Warming enabled, ultrasound is emitted without pressing the Start button. The Applicator LED will not
illuminate during the Head Warming period. US Channel will indicate "Head Warming".
Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .0 - 50% Cycling of maximum power
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.3 Mhz
Sound Head Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85 °F - 110 °F (29.4 °C - 43.3 °C)
24
4 SPECIFICATIONS
4.4 LASER MODULE SPECIFICATIONS VECTRA GENISYS ONLY
Intelect®/Genisys® Therapy Systems
This section provides the necessary Laser
Module and Applicator Specifications to aid in
troubleshooting.
Refer to these specifications as necessary when
troubleshooting the Laser Module and Applicators.
Power Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Therapy System Dependent
Output to Laser Applicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Per Applicator Requirement
NOTE:
No Field Service is applicable to the Laser Module or
Laser Applicators. All Laser Modules and Applicators
suspected to require service or calibration must be
sent to the factory.
DO NOT point the laser beam directly into
•
human or animal eyes. The lens of the eye
does not detect the invisible, coherent laser
beams, potentially resulting in permanent
retinal damage.
Class 3B Lasers are considered an acute hazard
•
to the skin and eyes from direct radiation.
Eye injury will occur if laser is viewed directly
or from specular reflection. Laser protective
eyewear is required for all persons in the
treatment area.
Approved Laser protective eyewear must be
•
worn at all times by all persons in the vicinity
when the Laser is On.
25
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