Chattanoga Triton Equipo de Traccion Manual

Moving
Rehabilitation
Forward™
User Manual
Model 4739 - Triton® Traction Unit
Model 4778 - Triton® Traction Unit with sEMG
Model 2841 - Triton® DTS Traction Unit with sEMG
ISO 13485 CERTIFIED

TABLE OF CONTENTS Triton® Traction
FOREWORD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Operating Controls - Home Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26-28

Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Operating Controls - Treatment Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29-32
sEMG Traction Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33-35
ABOUT TRACTION THERAPY. . . . . . . . . . . . . . . . . . . . . . . . 28 Starting, Pausing and Stopping Treatment. . . . . . . . . . . . . . . . . . . . . . . . . 36-37
Precautionary Instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Saving Treatment to a Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . 38-40
Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4 Retrieving Data from Existing Patient Data Card . . . . . . . . . . . . . . . . . . . . . . .41
Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5 Erasing Patient Data Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .42
Dangers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 User Protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43-44
Overview of Traction Therapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 Clinical Protocols™ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45-46
Common Terms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 Multimedia Card (MMC) Graphics Library . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .47
Indications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 DTS Pull Patterns (If Applicable) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .48
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
NOMENCLATURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 813 ACCESSORIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Base Unit - Front View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9 TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5053
Base Unit - Rear View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-11 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50-51
LCD Base. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12 Error Messages. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52-53
Symbol Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1416 Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .54
Traction Unit Dimensions and Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . .14 Preventative Maintenance Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .54
sEMG Module Dimensions and Specifications . . . . . . . . . . . . . . . . . . . . . . . . . .15 Calibration Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .54
Description of Device Markings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16 Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .54
SETUP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1723 WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Contents of Carton . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
Mounting Unit on Table . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18
Attaching the Patient Switch Hook . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19
Installing the sEMG Module. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .20
Removing the sEMG Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .21
Initial Unit Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22-23
OPERATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2448
Patient Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24-25
FOREWORD Triton® Traction
This manual has been written for the operators of the Triton traction unit. It contains general instructions for operation, precautionary
instructions, and maintenance recommendations. In order to obtain maximum life and efficiency from your Triton traction unit, and to
assist in the proper operation of the unit, read and understand this manual thoroughly.
The specifications put forth in this manual were in effect at the time of publication. However, owing to Chattanooga Group's policy of
continuous improvement, changes to these specifications may be made at any time without obligation on the part of Chattanooga Group.
Before administering any treatment to a patient, you should become acquainted with the operating procedures, as well as the indications,
contraindications, cautions, warnings, and dangers. Consult other resources for additional information regarding the application of traction
therapy.
Product Description
The Triton traction unit is a simple to use digital touch screen user interface traction unit that offers static, intermittent, and cyclic traction
with user definable hold, rest, and treatment times. An optional sEMG Module and DTS software upgrade are available for separate
purchase. Patient Pain Profiles are recorded before and after treatment with a Numeric Pain Scale, VAS (Visual Analog Scale), and Pain Map
for each patient. Once treatment parameters are customized for a patient, clinicians can store them as either the default user protocol or
as one of twenty user defined protocols. The Triton traction unit contains a Patient Data Card port, providing access to store the above
session parameters on Patient Data Cards. Information may be transferred to a PC via the optional Patient Data Management System. The
PC software is designed to allow easy access to patient data and printing of reports as well as adding session notes to the Patient Data
Card.
This equipment is to be used only under the prescription and supervision of a licensed practitioner.
©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
ABOUT TRACTION THERAPY Triton® Traction
PRECAUTIONARY INSTRUCTIONS
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 definitions of
these symbols are as follows:
NOTE:
Throughout this manual “NOTE” may be found. These Notes are helpful
information to aid in the particular area or function being described.
Caution-
Text with a “CAUTION” indicator will explain possible safety infractions
that could have the potential to cause minor to moderate injury or
damage to equipment.
Warning-
Text with a “WARNING” indicator will explain possible safety infractions
that will potentially cause serious injury and equipment damage.
Danger-
Text with a “DANGER” indicator will explain possible safety infractions that
are imminently hazardous situations that would result in death or serious
injury.
2
• Read, understand, and practice the precautionary and operating • Do not operate the unit when connected to any unit other than
instructions. Know the limitations and hazards associated with using Chattanooga Group devices. Do not use devices manufactured by
sEMG, DTS Pull Patterns and the Triton traction unit. Observe the other companies on Chattanooga Group equipment. Chattanooga
precautionary and operational decals placed on the unit. Group is not responsible for any consequence resulting from using
• DO NOT operate this unit in an environment where other devices products manufactured by other companies.
are being used that intentionally radiates electromagnetic energy • Handle the unit with care. Inappropriate handling of the unit may
in an unshielded manner. Portable and mobile RF communications adversely affect its characteristics.
equipment can affect Medical Electrical Equipment. • Before each use, inspect the Traction Cord for wear. Prolonged wear
• This equipment generates, uses, and can radiate radio frequency on the cord will cause it to break, which may cause sudden release
energy and, if not installed and used in accordance with the of traction pressure on a patient.
instructions, may cause harmful interference to other devices in • Inspect lead wires and associated connectors for signs of damage
the vicinity. However, there is no guarantee that interference will before each use. Replace damaged lead wires immediately before
not occur in a particular installation. Harmful interference to other any treatment is applied.
devices can be determined by turning this equipment on and off. • Always test the Patient Interrupt Switch cable before each use for
Try to correct the interference using one or more of the following: proper operation.
reorient or relocate the receiving device, increase the separation
between the equipment, connect the equipment to an outlet on a • Do not use sharp objects such as a pencil point or ballpoint pen
different circuit from that which the other device(s) are connected to operate the buttons on the Touch Screen base as damage may
and consult the Chattanooga Group Service Department for help. result.
• This unit should be operated, transported, and stored in • Do not remove the cover. This may cause unit damage, malfunction,
temperatures between 0° F and 140° F (-18° C and 60° C). electrical shock, fire, or personal injury. There are no user-serviceable
parts inside the unit. If a malfunction occurs, discontinue use
• The unit should be routinely checked before each use to determine immediately, disconnect the Mains Power Cord from the outlet, and
all controls function normally. consult the dealer for repair service.
• Do not use electrodes that have been previously used as the • Do not disassemble, modify, or remodel the unit or accessories.
electrodes used with this unit are designed for single use only. This may cause unit damage, malfunction, electrical shock, fire, or
personal injury.
• Do not use the traction unit near devices such as X-ray units or
diathermy units. These units may emit high frequency noise that
may affect the operation of the unit.
3
• Do not use the Clevis as a handle to pick up or carry the unit. • This device should only be used under the continued supervision of a
• Do not permit any foreign materials or liquids to enter the unit. Take licensed practitioner.
care to prevent any foreign materials including, but not limited to, • Care must be taken when operating this equipment adjacent to or
inflammables, water, and metallic objects from entering the unit. stacked with other equipment. Potential electromagnetic or other
These may cause unit damage, malfunction, electrical shock, fire, or interference could occur to this or other equipment. Try to minimize
personal injury. this interference by not using other equipment in conjunction with it.
• If you have difficulty operating the unit after carefully reviewing • Use of controls or adjustments or performance of procedures other
this operator’s guide, contact your Chattanooga Group dealer for than those specified herein may result in a hazardous traction related
assistance. injury.
• Failure to use and maintain the traction unit and its accessories • Before connecting the unit to an electrical outlet, make certain the
in accordance with the instructions outlined in this manual will unit is electronically grounded by connecting only to a grounded
invalidate your warranty. electrical service receptacle conforming to the applicable national
• The Patient Interrupt Switch is essential for the functioning of the and local electrical codes.
unit. If it is not connected, or if it is malfunctioning, the unit will not • Do not use a damaged Mains Power Cord. Using a damaged Mains
work. Power Cord may cause unit damage, malfunction, electrical shock,
• A licensed practitioner experienced with traction therapy must be fire, or personal injury. If the Mains Power Cord becomes damaged,
familiar with all instructions contained in this manual before discontinue use immediately and contact the dealer for replacement
administering traction therapy. Do not attempt to become familiar of the Mains Power Cord.
with the Triton traction unit while administering traction therapy on • To prevent electrical shock, disconnect the unit from the power
a patient. source before attempting any maintenance procedures.
• In the event of a loss of power to the unit or when quick release • This device should be kept out of the reach of children.
is needed, traction tension should only be released by having the • Always hand tighten the Lock Knob securely to avoid any slippage.
patient move towards the traction head to release the tension on • The Patient Interrupt Switch must be in the patient’s grasp
the rope. Once the tension on the rope has been released, loosen throughout the traction therapy.
the patient harness adjustment straps.
• Do not apply external pressure (heat or cold) to the electrode sites
during therapy.
• Dispose of all products in accordance with local and national
regulations and codes.
4
• Use only tables, stands, power cords and accessories that are • Disconnect the traction unit from the power source before attempting
specially designed for the Triton traction unit. Do not use accessories any maintenance, installation, removal, or replacement procedures to
manufactured by other companies on the Triton traction unit. prevent electrical shock and possible damage to the unit.
Chattanooga Group is not responsible for any consequence resulting • The traction unit should only be used by a qualified licensed
from using products manufactured by other companies. The use practitioner in a position of supervision during therapy. For that
of other accessories or cables may result in increased emissions or reason, do not attempt to put yourself in traction with this unit.
decreased immunity of the Triton traction unit.
• Do not use other accessories other than those supplied with the
system or recommended by Chattanooga Group. The safety of other
products has not been established, and their use could result in injury
to the patient.
• To prevent accidental disengagement, this unit must be securely
attached to the mounting surface of the pedestal or traction stand. It • Handle, clean, and dispose of components and accessories that
is the responsibility of the user to verify the adequacy of the have come in contact with bodily fluids according to National, Local
installation before use in therapy. and Facility rules, regulations and procedures.
• Do not apply electrodes over broken or compromised skin (e.g., • Do not connect the unit to an electrical supply without first
sunburn, cuts, acne) due to increased risk of skin reactions. verifying that the power supply is the correct voltage. Incorrect
• Do not plug lead wires into power outlets such as wall sockets and voltage may cause unit damage, malfunction, electrical shock, fire,
line cord receptacles. Doing so could result in severe shock or burns or personal injury. Your unit was constructed to operate only on the
whether or not the lead wires are attached to the unit. electrical voltage specified on the Voltage Rating and Serial Number
• In the event that an Error message or Warning appears beginning plate. Contact your Chattanooga Group dealer if the unit is not
with a 2 or 3, immediately stop all use of the system and contact properly rated.
the dealer or Chattanooga Group for service. Errors and Warnings
in these categories indicate an internal problem with the unit that • Should Traction Cord fray or damage to the Traction Cord or knot be
must be tested by Chattanooga Group or a Field Service Technician apparent from visual inspection, immediately stop use of the unit
certified by Chattanooga Group before any further operation or use and contact the Dealer or Chattanooga Group for service.
of the unit. Use of a unit that indicates an Error or Warning in these • Do not attempt to repair the Traction Cord.
categories may pose a risk of injury to the patient, user or extensive
internal damage to the unit. • An improperly tied knot may result in injury. Do not attempt to
re-tie the knot unless properly trained.
5
OVERVIEW OF TRACTION THERAPY

Effects of Traction Therapy Static Traction Therapy
The Triton traction device provides a treatment in static, intermittent, This term denotes that a steady amount of traction is applied for periods
and cyclic distraction forces to relieve pressures on structures that may from a few minutes up to 99 minutes. The shorter duration is usually
be causing pain of skeletal or muscular origin (cervical, thoracic, lumbar, coupled with more tension. Static lumbar traction is most effective if
hip, wrist, shoulder). Therapeutic distraction can be applied in a variety of a split table is utilized to reduce friction. It is important that it is the
programmable patterns, cycles and functions. type that maintains constant tension. This way, any slack developed as
the patient relaxes during the traction therapy is automatically taken
COMMON TERMS
up and the desired amount of traction is maintained. Static traction is
Progressive Traction sometimes referred to as sustained traction.
Progressive traction refers to a traction phase during the treatment when
the tension gradually increases. Intermittent Traction Therapy
This form of traction alternates traction tension between tension levels
Regressive Traction - Maximum and Minimum - every few seconds throughout the timed
Regressive traction refers to a traction phase during the treatment when treatment. It is also most effective if a split table is used to reduce friction
the tension gradually decreases. when giving lumbar traction. In the progressive and regressive phases,
TX (Traction) the traction unit pulls to the calculated tension, holds for the set hold time,
TX (Traction) refers to the type of traction used during a treatment. There then drops to 50% of this tension, holds the set rest time and then repeats
are three modes to choose from: Static, Intermittent or Cyclic Traction this step for the number of steps selected. However, once the minimum
Mode. level is reached, the traction unit uses the minimum level for the rest time.
Cyclic Traction
Steps Cyclic traction refers to progressive and regressive phases of the traction
The term “step” refers to the increment in which the traction tension is program being repeated continuously throughout the entire course of
either increased or decreased during therapy. the traction treatment.
6
INDICATIONS CONTRAINDICATIONS
The Triton traction device provides traction and mobilization of skeletal Traction is contraindicated for the following:
structures and skeletal muscles.
• Structural disease secondary to tumor or infection
The Triton traction device may be used to relieve peripheral radiation/
• Patients with vascular compromise
sciatica and pain associated with:
• Any condition for which movement is contraindicated
• Protruding discs • Spinal root impingement
• Bulging discs • Hypomobility • Patients with acute strains, sprains, and inflammation which would be
• Herniated discs • Degenerative joint disease aggravated by traction therapy
• Degenerative disc disease • Facet syndrome • Patients with joint instability of the spine
• Posterior facet syndrome • Compressions fracture • Pregnancy
• Acute facet problems • Joint pain
• Radicular pain • Discogenic pain • Osteoporosis
• Prolapsed discs • Hiatus hernia
• Claustrophobia
• Cardiac or pulmonary problems
7
NOMENCLATURE Triton® Traction
BASE UNIT FRONT VIEW

Touch Screen The Base Unit serves to house the mechanical and electrical components
User Interface that provide the actual traction tension for the Triton traction unit under
the electronic control and supervision of the Controller.
Traction Cord
To prevent wear and fraying, the unit
should be mounted facing toward the
desired direction of pull so that the
Traction Cord does not contact the
side of the slot from which it extends.
Traction Cord
Clevis
Attachment Slots
sEMG
Lead Wire
Receptacle
(Model 4778,
2841 or with
sEMG Module
Patient
Interrupt
P/N 4766) • Should Traction Cord fray or damage to the Traction Cord or knot be
Switch apparent from visual inspection, immediately stop use of the unit and
Receptacle contact the Dealer or Chattanooga Group for service.
• Do not attempt to repair the Traction Cord.
• An improperly tied knot may result in injury. Do not attempt to re-tie
the knot unless properly trained.
8
BASE UNIT FRONT VIEW CONTINUED
Accessory Clip Patient Interrupt Switch

The Accessory Clip allows you to Receptacle
attach the desired accessory (i.e., The Patient Interrupt Switch
Spreader Bar or traction harnesses) to Receptacle is located on the front of
the unit. the unit.
Clevis Attachment Slots

The Clevis Attachment Slots serve as
a connection point for other traction
• The Patient Interrupt Switch is essential for the functioning of the unit. If
apparatus (not included), such as
it is not connected, or if it is malfunctioning, the unit will not work.
cervical or wrist.
sEMG Lead Wire Receptacle

(Model 4778, 2841 or with sEMG
Module P/N 4766)
The sEMG lead wire connection is
located on the front of the unit.
• Do not use the Clevis as a handle to pick up or carry the unit.
9
BASE UNIT REAR VIEW
Screen The rear view of the base unit is the site of electric current control and
Contrast surge protection, and serves as a connection point for both the traction
Control
controls and safety features of the Triton traction unit.
Power On/Off Switch

Lock Power
The Power On/Off Switch is a toggle
Knob On/Off switch located on the back of the
Switch unit. This switch controls the flow of
electricity from the outlet to the unit.
Data Port
Mains (Factory
Power use Only)
Cord
Receptacle Mains Power Cord Receptacle
The Mains Power Cord Receptacle
accepts the Mains Power Cord
(female end).
Serial Number and
Electrical Rating
Plate
Screen Contrast Control
The Screen Contrast Control is
used to set a comfortable viewing
of brightness of the Touch Screen
User Interface. Functional On
Monochrome Units Only.
10
BASE UNIT REAR VIEW CONTINUED
Lock Knob
The Lock Knob is used to clamp the
Triton traction unit to the base
(i.e. pedestal, traction stand).
11
LCD BASE
(1) LED Indicator (Power On/Off)
The LCD Base serves as a programming terminal during the selection
This indicator will illuminate when the unit is powered on.
of the traction parameters, as well as a display showing all the factors NOTE: The LED indicator will blink when the unit goes in screen saver
affecting the traction during therapy. Traction parameters are selected mode (the screen will go blank after twenty minutes of inactivity).
with the buttons on the LCD Base and the Touch Screen User Interface. Simply touch the screen to reactivate.
The Touch Screen and beeper make various audio and visual indications, (2) Clinical Resources
and warn the operator when unsuitable parameters are chosen. This button allows you to access the following features of the traction
unit:
• Patient Card • Protocols
• Patient Card (Patient Name) • Retrieve Protocol
1 • Edit Current Pain Profile • Save Protocol
• Edit/Save Completed Pain Profile • Clinical Protocols™
• Erase Patient Card
2 4 • Utilities
• Unit Settings
(3) Stop
This button will stop the treatment program. Traction tension slowly
decreases to zero.
3 (4) Pause
5 This button will pause the treatment program. Traction tension slowly
decreases to zero. Press the pause button again to resume treatment
6 program and traction tension.
(5) Start
7 Touch this button to start the treatment program.
(6) Patient Data Card Port
Access port to insert a Patient Data Card to save and retrieve patient
treatments.
(7) Multimedia Card (MMC) Port
Access port to insert a MMC Card to display traction techniques and the
anatomical library.
12
SYMBOL DEFINITIONS
Below are the definitions for all of the Symbols used on the Triton traction unit hardware and software. Study and learn these symbols before any operation
of the unit.
System Hardware Symbols System Software Symbols
Contrast Stop Patient

Control Treatment Interrupt Move UP
Switch
On/Off Pause Move DOWN

Switch Treatment
Patient
Card/
Multi- Accept and
Data Start Media Return
Port Treatment Card
(Factory (MMC)/
Use Only) DTS Cancel
sEMG Software
Lead Wires Upgrade
Push Lock Card
Knob Back
Clinical Forward
Lock/ Resources
Unlock
Lock Knob Home
13
SPECIFICATIONS Triton® Traction
TRACTION UNIT DIMENSIONS AND SPECIFICATIONS
Width . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9.5 in (24 cm) Meets Directive 93 /42 /EEC
Depth . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17.5 in (45 cm) IEC/UL/EN: 60601-1
Height . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17.5 in (45 cm) 60601-1-2
Weight 9700675
CAN C22.2 No. 601.1-M90w/A2
Standard Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .30 lbs (14 kg)
Shipping Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .40 lbs (18 kg)
Power
Voltage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .100V-240V (50/60Hz)
Power Consumption . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .75 VA
Current Consumption . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3.2 Amps Max
Electrical Class . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Class I
Traction Electrical Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Type B Height
sEMG Electrical Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Type BF
For Continuous Operation
Traction Modes
Static, Intermittent, Cyclic, and their combinations.
Traction Type: Mechanical
LCD Display: High contrast color touch screen
Traction Tension
Parameters Minimum Maximum Increments
Traction Period 1 minute 99 minutes 1 minute
Hold Period 0 seconds 99 seconds 1 second
Rest Period 0 seconds 99 seconds 1 second Dep
Traction Tension 0 lb (0 kg/0 N) 200 lb (90 kg/890 N) 1 lb (1 kg/5 N) th
th
Progressive and Wid
Regressive Steps 1 step 9 steps 1 step
14
sEMG MODULE DIMENSIONS AND SPECIFICATIONS
Width . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6.63 in (16.83 cm)
Depth . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 in (7.62 cm)
Height . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1.63 in (4.13 cm)
Input Impedance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . > 1,000,000 ohm
Input Sensitivity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . < 1.0 μV RMS
Width
Frequency Range . . . . . . . 15Hz - 1000Hz with CMMR of > 120 dB CMMR
at 50/60 Hz > 180 dB
Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.2 oz (146 g)
Product Type
Internally Powered . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .Triton Traction Unit th
Dep
Electrical Class . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Class I
Electrical Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Type BF Height
For Continuous Operation
Regulatory Compliance
Meets Directive 93 /42 /EEC

IEC/UL/EN: 60601-1
60601-1-2
9700675
CAN C22.2 No. 601.1-M90w/A2
15
DESCRIPTION OF DEVICE MARKINGS
The markings on the Triton traction unit are your assurance of its conformity to the highest applicable standards of medical equipment safety and
electromagnetic compatibility. One or more of the following markings may appear on the device:
Meets Directive 93 /42 /EEC

IEC/UL/EN: 60601-1, 60601-1-2
9700675
CAN C22.2 No. 601.1-M90w/A2

Electromedical equipment, Canadian Electrical Code.
Part II: Safety standards for Electrical Equipment Risk Class 1.
Classified by Intertek Group, PLC with respect to electric shock, fire and
mechanical hazards only in accordance with UL 60601-1, and
CAN C22.2 No. 601.1-M90w/A2.
Refer to ACCOMPANYING DOCUMENTS !
Type B Equipment
Type BF Equipment
16
SETUP Triton® Traction
CONTENTS OF CARTON
Remove the Triton traction unit and all accessories from the shipping NOTE: When shipping the unit back to the dealer or factory, make
cartons. Visually inspect for damage. certain the original packaging is used. If the original packaging
Report any damage to the carrier immediately. is not available, contact Chattanooga Group to obtain the
following packaging materials for shipment:
Contents of Cartons:
48059 Inner Pack Box Top
Model 4739 - Triton Traction Unit
48093 Left Inner Pack
• Triton Traction Unit
48094 Right Inner Pack
• Patient Data Cards (5) 48092 Shipping Box
• Securing Bracket 48095 Shipping Bag
• Patient Interrupt Switch - 9 ft (2.75 m) in cable length, shielded, 26 AWG
• Patient Interrupt Switch Hook Kit Any damage sustained from improper packaging may render the
warranty null and void.
• Mains Power Cord - 80 in (203 cm) in cable length, shielded, 18 AWG
• User Manual (CD-ROM)
Model 4778 - Triton Traction Unit with sEMG
Model 2841 - Triton DTS Traction Unit with sEMG
• Triton Traction Unit
• Patient Data Cards (5)
• Securing Bracket
• sEMG lead wire - 8 ft (2.44 m) in cable length, unshielded, 16/18 AWG
• (4) Dura-Stick II Electrodes - 1.25 in (3 cm) Round
• (4) Dura-Stick II Electrodes - 2 in (5 cm) Round
• Patient Interrupt Switch - 9 ft (2.75 m) in cable length, shielded, 26 AWG
• Patient Interrupt Switch Hook Kit
• Mains Power Cord - 80 in (203 cm) in cable length, shielded, 18 AWG
• User Manual (CD-ROM)
17
MOUNTING UNIT ON TABLE
The Triton traction unit was designed to be utilized with Chattanooga 1. To secure the Triton traction unit
Group traction tables: to the mounting surface, press
the Lock Knob to raise the knob
and turn left to loosen the clamp.
Fit the unit to the mounting
surface and turn right to tighten
• Do not operate the unit when connected to any unit other than
the clamp down onto the
Chattanooga Group devices. Do not use devices manufactured by
other companies on Chattanooga Group equipment. Chattanooga mounting surface. Push the Lock
Group is not responsible for any consequence resulting from using Knob to secure the unit to the
products manufactured by other companies. mounting surface.
2. Remove the cover on the back
of the unit and connect the Mains
Power Cord (female end) to the
Mains Power Cord Receptacle.
3. Verify that there is a good
• To prevent accidental disengagement, this unit must be securely connection between the Mains
attached to the mounting surface of the pedestal or traction stand. It Power Cord and the Mains Power
is the responsibility of the user to verify the adequacy of the Cord Receptacle. Always make
installation before use in patient therapy. certain that the Mains Power Cord
is properly plugged into the unit.
NOTE: The Triton traction unit should be mounted facing the direction 4. Check the voltage rating on the
of pull so the Traction Cord does not contact the side of the slot serial plate located on the back of
from which it extends. the unit. Plug the Mains Power
Cord into a 100V-240V AC outlet,
as required. Replace the cover on
the back of the unit.
18
ATTACHING THE PATIENT INTERRUPT SWITCH HOOK

Insert the Patient Interrupt Switch
The Patient Interrupt Switch Hook may be placed on either the left or
Hook Cover to cover the hook screw
right side of the unit to hook the Patient Interrupt Switch.
hole.
A screw hole cap with the

Chattanooga Group logo is located
on both sides of the traction unit.
Using a screwdriver, pop the screw

hole cap off.
The Patient Interrupt Switch can now

be placed on the Patient Interrupt
Switch Hook.
Place the Patient Interrupt Switch

Hook over the screw hole and tighten
the Hook Screw in place.
19
INSTALLING THE sEMG MODULE

Patient
NOTE: Model 4739 can be upgraded to become a traction unit with FRONT VIEW sEMG
Interrupt Switch
sEMG by attaching a sEMG Module (P/N 4766) to the unit. Receptacle Lead Wire
Receptacle
BACK VIEW
Connector
• Disconnect the traction unit from the power source before attempting
any maintenance, installation, removal, or replacement procedures to
prevent electrical shock and possible damage to the unit.
Turn the unit off. Disconnect the Gently push the sEMG Module into
traction unit from its power source. the front of the traction unit. Once
Disconnect the Patient Interrupt the plastic of the unit and the module
Switch from its receptacle. are aligned, the connector should
be inserted properly, with the tabs
locked in place.
Plug the traction unit back into the

power source. Connect the Patient
Interrupt Switch and the sEMG lead
Gently press the tabs underneath the wire into the receptacles.Turn the
unit, pull and remove the front panel unit on.
from the traction unit
The traction unit should automatically
recognize the sEMG Module with
the sEMG Traction button now being
active on the Home Screen.
20
REMOVING OF THE sEMG MODULE

Gently push the front panel back into
the front of the traction unit. Once
the plastic of the unit and the front
panel are aligned, the connector
• Disconnect the traction unit from the power source before attempting
should be inserted properly, with the
any maintenance, installation, removal, or replacement procedures to
tabs locked in place.
prevent electrical shock and possible damage to the unit.
Plug the traction unit back into the
Turn the unit off. Disconnect the power source. Connect the Patient
traction unit from its power source. Interrupt Switch into its receptacle.
Disconnect the Patient Interrupt Turn the unit on.
Switch and the sEMG lead wire from
the receptacles. The traction unit should automatically
recognize that the sEMG Module
has been removed, with the sEMG
Traction button now being inactive
on the Home Screen.
Gently press the tabs underneath

the unit, pull and remove the sEMG
Module from the traction unit
21
INITIAL UNIT SETUP
Accessing User Utilities Clinic Name

Press the Clinic Name button. Enter the Clinic Name on the keyboard.
To save the Clinic Name as entered, press the Return Arrow button. To
Turn the unit On. discard the Clinic Name, press the Cancel (X) button.
NOTE: The default of the Clinic Name is set as Chattanooga Group.
Press the Clinical Resources button.
Volume
Press the Volume button until the desired unit volume is achieved.
There are six settings: Off, X-Low, Low, Med, High and X-High. Each time
the Volume button is pressed, the setting displayed will also give three
audible tones of that level.
NOTE: The default of the unit volume is set at Medium.
Units of Measure
There are three units of measure to choose from: pounds (lbs), kilograms
Press the Unit Settings button under
(kg), and newtons (N). Press the Unit of Measure button to toggle to the
the Utilities section.
desired unit of measure and the setting will automatically save.
NOTE: The default of the unit of measure is set in pounds (lbs).
Set Date and Time

Press the Set Date and Time button. Press the Move Up or Down Arrow
button for the respective area (Year, Month, Day, Hour and Minute) until
the desired change is displayed.
NOTE: The time is set in a 24-hour format.
22
INITIAL UNIT SETUP CONTINUED
Language Reset Default Protocols

To change the language displayed on the unit, press the Language Press the Reset Default Protocols to restore all protocols to factory
button until the desired language is displayed and the setting will settings.
automatically save. NOTE: All User Protocols will be removed.
The available languages are: To return to the unit Home Screen, press the Home button.
• English
• French
• Spanish
NOTE: The default of Language is set as English.
Reset Unit Settings

Press the Reset Unit Settings button to restore the unit defaults (Clinic
Name, Volume, Unit of Measure, and Language). This control will not
change the Date and Time nor will it affect any of the User Protocols
stored in the unit.
23
OPERATION Triton® Traction
PATIENT PREPARATION NOTE: The Patient Interrupt Switch must be plugged in for the unit to
operate. If the Patient Interrupt Switch is not inserted into the
Traction therapy may be given by or on order of a qualified licensed
traction unit, a continuous audible tone will sound and a
practitioner. The person administering the treatment must be familiar
with the principles of traction therapy and be able to choose the correct message will display saying, "Patient Switch is not plugged into
mode of traction, traction forces, and treatment times. Any settings the unit. Correct the problem." Touch the Screen anywhere to
or types of traction mentioned in this manual are for illustrative and continue.
expository purposes only. Each patient should be individually assessed 2. Turn the unit on from the Power On/Off Switch, located on the back of
by a licensed practitioner to determine the appropriateness of the the unit. Wait about five seconds for the unit to go through
parameter settings prior to use. initialization before attempting any further patient preparation
procedures.
3. Test the Patient Interrupt Switch by pressing the red button. A warning
• A licensed practitioner experienced with traction therapy must be message will be displayed saying The Patient Interrupt Switch has
familiar with all instructions contained in this manual before traction been pressed. Touch the screen to continue.
therapy. Do not attempt to become familiar with the Triton traction
unit while administering traction therapy on a patient.
To prepare the patient for traction therapy, do the following:

1. Attach the Patient Interrupt Switch by • Always test the Patient Interrupt Switch cable before each use for
inserting the male end of the cable proper operation.
into the Patient Interrupt Switch
4. Give the Patient Interrupt Switch to the patient, instructing that
Receptacle located on the front of the
pressing the red button will stop the treatment.
unit.
• The Patient Interrupt Switch must be in the patient’s grasp throughout

the traction therapy.
24
PATIENT PREPARATION CONTINUED

6. Position the patient on the appropriate type of table in accordance
with the instructions supplied with the table.
• In the event of a loss of power to the unit or when quick release is

needed, traction tension should only be released by having the
patient move towards the traction head to release the tension on
• Use only tables, stands, power cords and accessories that are the rope. Once the tension on the rope has been released, loosen the
specially designed for the Triton traction unit. Do not use patient harness adjustment straps.
accessories manufactured by other companies on the Triton traction
unit. Chattanooga Group is not responsible for any consequence
resulting from using products manufactured by other companies.
The use of other accessories or cables may result in increased
emissions or decreased immunity of the Triton traction unit.
7. Fit the appropriate traction harness on the patient by following the

fitting instructions supplied with the type of harness to be used.
8. Tighten any slack in the harness that may have occurred during
positioning so that it fits the patient according to the manufacturer’s
instructions.
9. Push and hold the Rope Release button on the Touch Screen and
slowly pull the end of the Traction Cord out from the traction unit.
10. Attach the Accessory Clip to the connection point of the traction
harness, according to the manufacturer’s instructions.
25
OPERATING CONTROLS  HOME SCREEN
Cervical Traction
The Cervical Traction button will go straight to the Cervical Traction
menu. The Cervical Traction menu offers the following options:
Traction Rationale - Button provides a description of the traction
being used as well as definitions of terms used in
areas of the Treatment Screen.
Traction Technique - Button provides visual steps as to how to set up
a patient for cervical traction.
NOTE: After viewing the steps for set up, the Forward Arrow button
will automatically go to the Treatment Screen.
Edit - Button provides access to the Treatment Screen to set up
parameters for treatment.
Back and Home - Buttons go back to the Home Screen.
Rope Release - Releases the Traction Cord from the unit.
Lumbar Traction
The Lumbar Traction button will go straight to the Lumbar Traction
menu. The Lumbar Traction menu offers the following options:
Traction Rationale - Button provides a description of the traction
a patient for lumbar supine or lumbar prone
traction.
26
OPERATING CONTROLS  HOME SCREEN CONTINUED
Edit - Button provides access to the Treatment Screen to set up Edit - Button provides access to the Treatment Screen to set up
parameters for treatment. parameters for treatment and to the sEMG Graph to set up the
Back and Home - Buttons go back to the Home Screen. sEMG target.
Rope Release - Releases the Traction Cord from the unit. Back and Home - Buttons go back to the Home Screen.
sEMG Traction (Models 4778 and 2841 Only)
The sEMG Traction button goes to a Clinical Protocols™
menu to select the desired body area. The Clinical Protocols™ button goes to
Press the desired body area button to a menu to select the desired body
go to the desired body area + sEMG area. Press the desired body area
Traction menu. button to go to the desired body area
menu.
The desired body area + sEMG Traction menu offers the following
options:
Traction Rationale - Button provides a description of the traction NOTE: FOR CERVICAL AND LUMBAR ONLY - There are four menu
being used as well as definitions of terms used in options to choose from before entering the Cervical or Lumbar Traction
areas of the Treatment Screen. menu: Disc Involvement with Muscle Guarding, Disc Involvement
Traction Technique - Button provides visual steps as to how to set up without Muscle Guarding, Joint Segment with Muscle Guarding and
a patient for the desired body area + sEMG Joint Segment without Muscle Guarding.
traction.
NOTE: After viewing the steps for set up, the Forward Arrow button The desired body area menu offers the following options:
will automatically go to the Treatment Screen. Traction Rationale - Button provides a description of the traction
27
OPERATING CONTROLS  HOME SCREEN CONTINUED

a patient for traction treatment of the desired
body area.
NOTE: There are no traction techniques for the Hip Body Area.
Edit - Button provides access to the Treatment Screen to set up
parameters for treatment.
Back and Home - Buttons go back to the Home Screen.
Multimedia Card (MMC) Graphics Library

The MMC Graphics Library button provides access to visual anatomical
libraries of the four body areas: Cervical, Lumbar, Hip and Hand/Wrist.
Patient Card
The Patient Card button allows access to retrieve previously saved
patient treatment information from the Patient Card.
Rope Release
Releases the Traction Cord from the unit.
28
OPERATING CONTROLS  TREATMENT SCREEN

The Touch Screen User Interface allows the operator to access and set up
for therapy in the following areas of the Treatment Screen:
1
14 NOTE: Should you make a mistake while entering data, you may correct
2 by re-pressing the appropriate key and re-entering the data.
3 NOTE: On the Touch Screen User Interface, any parameters surrounded in

blue boxes are active and can be changed at any time. Any
13
parameters surrounded in gray boxes are inactive and cannot be
4 changed.
(1) Traction Meter

Displays the amount of tension being delivered to a patient
12
(in pounds, kilograms, or newtons).
(2) Time Remaining

11
5 Displays the approximate number of minutes that remain in the current
traction therapy session.
(3) Time Remaining During Hold/Rest Cycles

6 10 Displays an amount of time when a Hold or Rest cycle is occurring
during treatment as well as show the number of minutes that remain in
that cycle.
7 16 9
18
17
(4) Treatment Status
15 8
Displays one of the following to show the current status of the treatment
being performed: Setup, Running, Paused, and Completed.
29
OPERATING CONTROLS  TREATMENT SCREEN CONTINUED

(5) Home (9) Regressive
The Home button will return to the Home Screen of the unit. There are two buttons to use under the Regressive section. The first
button allows you to choose from Static or Intermittent Traction Mode
(6) Back to use during the Regressive phase of the traction therapy session. The
The Back button will return to the previous screen. second button allows you to enter the step number (1-9) desired in the
Regressive phase of the traction therapy session.
(7) Progressive NOTE: The third box in the Regressive section is an inactive button that
There are two buttons to use under the Progressive section. The first displays the approximate amount of time (in minutes) selected
button allows you to choose from Static or Intermittent Traction Mode for the regressive phase of the traction program.
to use during the Progressive phase of the traction therapy session. The
(10) Rope Release
second button allows you to enter the step number (1-9) desired in the
The Rope Release button is used to release the Traction Cord in order to
Progressive phase of the traction therapy session.
pull out of the unit freely for setup.
NOTE: The third box in the Progressive section is an inactive button that
To release the cord, either pull on the Traction Cord and it will slowly
displays the approximate amount of time (in minutes) selected
feed out, or hold the Rope Release button down and pull the Traction
for the progressive phase of the traction program.
Cord out.
(8) TX (Traction) NOTE: If there is more than 5 lbs (2kg or 19N) of tension, the Rope
There are two buttons to use under the TX section. The first button Release button is disabled.
allows you to choose from Static, Intermittent or Cyclic Traction Mode to
use during the traction phase of the traction therapy session. The second
button allows you to enter the amount of time in minutes (1-99) desired
for the traction phase of the traction therapy session.
NOTE: The TX Time can be changed during treatment. Press the TX • In the event of a loss of power to the unit or when quick release is
Time button and use the Up or Down Arrows to change the time needed, traction tension should only be released by having the
in one minute increments. Press the Return Arrow to accept patient move towards the traction head to release the tension on
changes. the rope. Once the tension on the rope has been released, loosen the
patient harness adjustment straps.
30

(11) Speed Edit Hold/Rest Times button,
The percentage of speed of when press the appropriate button,
the Traction Cord is being pulled or and use the Up or Down Arrow
released. There are three speed options buttons any changes. Press the
to choose from: 30%, 50% or 100%. Return Arrow button to accept.
(12) Pre-tension (14) Edit Min/Max Levels

Pre-tension allows the clinician to Displays the Minimum and Maximum
set a certain level in weight and time Traction Tension entered during
to allow the opportunity to make setup. To enter the Minimum or
adjustments to harnesses before Maximum Traction Tension, press the
treatment starts. Edit Min/Max Levels button, press the
appropriate button, then enter the
desired setting, using the number
keypad. Press the Return Arrow button
(13) Edit Hold/Rest Times to accept.
Displays the amount of hold and rest NOTE: The Minimum and Maximum
times (0-99 seconds) of Progressive, Traction Tension can be
TX and Regressive traction entered changed during the traction
during setup. To enter the hold or rest therapy session by pressing the
time, press the appropriate button, Edit Min/Max Levels button,
then enter the desired time, using press the appropriate button,
the number keypad. Press the Return then use the Up or Down
Arrow button to accept. Arrow buttons to make
NOTE: The Hold and Rest Time can be changes in 1 lb (1 kg or 1 N)
changed during the traction increments. Press the Return
therapy session by pressing the Arrow button to accept.
31
FOR LUMBAR TRACTION ONLY: (15) Clinical Resources

The Minimum and Maximum Traction This button offers the following features of the traction unit: (See
Tension levels can be entered in two Patient Data Card and User Protocols in the Operation Section for
different ways: Force Levels in Weight more information)
or Percentage of Body Weight. • Patient Card
• Patient Card (Patient Name)
For Force Levels in Weight, simply • Edit Current Pain Profile
enter the Minimum and Maximum • Edit/Save Completed Pain Profile
levels as described previously. • Erase Patient Card
• Protocols
For Percentage of Body Weight, Press • Retrieve Protocol
the Body Weight button and enter • Save Protocol
the body weight of the patient. Press • Clinical Protocols™
the Max. Level % of BW button to • Utilities
enter the percentage of the patient's • Unit Settings (see Pages 22-23 for more information)
body weight to be the maximum
(16) Stop
traction tension level. Press the Min.
Stops the treatment program. Traction tension slowly decreases to zero.
Level % of BW button to enter the
percentage of the patient's body (17) Pause
weight to be the minimum traction Pauses the treatment program. Traction tension slowly decreases to zero.
tension level. Press the Pause Button again to resume treatment program and traction
tension.
(18) Start
Starts the treatment program.
32
sEMG TRACTION TREATMENT

NOTE: sEMG is only used as a trigger to begin traction therapy.
Preparing for sEMG Traction Therapy
Plug the sEMG lead wire into the front
of the unit. • Handle, clean, and dispose of components and accessories that have
come in contact with bodily fluids according to National, Local and
Facility rules, regulations and procedures.
Give the Patient Interrupt Switch

to the patient, instructing that
pressing the red button will stop the
treatment.
The Patient Interrupt Switch also
serves as a visual indicator for the
• Do not apply electrodes over broken or compromised skin (e.g., patient with sEMG. Once a patient
sunburn, cuts, acne) due to increased risk of skin reactions. is hooked up to electrodes, the blue
lights on the Patient Interrupt Switch
Examine the patient's skin for show the amount of tension of the
any wounds and clean the skin. patient. The increased number of blue
Chattanooga Group recommends
lights indicate higher levels of tension
using only Dura-Stick® II Electrodes
to obtain the most accurate sEMG in a patient.
feedback.
Connect the Dura-Stick II disposable
electrodes to the lead wire. Leave
the electrodes on the protective
backing until treatment area has been • The Patient Interrupt Switch must be in the patient’s grasp throughout
prepared. Ensure the electrodes are the traction therapy.
applied securely to the skin.
33
sEMG TRACTION TREATMENT CONTINUED

Press the sEMG Traction button from Target button - This toggle button
the Home Screen. allows the clinician to select the
NOTE: Once the sEMG Traction target either manually or take the
button is pressed, a average of muscle activity achieved
continuous audible tone will over a 15 second period.
sound from the Patient
Interrupt Switch to indicate
sEMG Traction activity
readings. Adjust/Capture Target button -
Once the target is selected, this
button allows the clinician to either
Set the parameters for sEMG Traction
adjust the manual target or capture
treatment, using the following
the average target.
buttons on the Treatment Screen:
View Graph
The View Graph button allows the
clinician to toggle between the
Treatment Graph to the sEMG graph.
To Adjust the Manual Target -
sEMG Graph Press the Target button until Manual
The sEMG Graph allows the setting is selected, press the Adjust Target
target level of muscle activity for button, press the Up or Down Arrow
triggering traction therapy to start. buttons to adjust the Target to the
There are three buttons and a scale to prescribed level, and press the Return
set the sEMG target: Arrow to accept. The target range is
from 5 to 2,000 μV.
34
sEMG TRACTION TREATMENT CONTINUED

To Capture the Average Target - Press the Start button on the front of the unit to begin treatment.
Press the Target button until Average NOTE: Once the Start button is pressed, the continuous audible tone
is selected. Press the Capture Target from the Patient Interrupt Switch will stop during treatment.
button. Press the Begin Capture NOTE: When traction treatment begins, if sEMG readings are above
button to initiate the 15 second target, a message will display saying, "Ask the patient to relax".
period. Once the 15 second period Once the patient has relaxed and the sEMG readings go below
is completed, the average target the target, the message will disappear and treatment will start.
of muscle activity is captured, and
the Up and Down Arrow buttons
Check the sEMG Graph from the Treatment Screen to assure that the
can be used to increase (up to
sEMG signal is being received.
200%) or decrease (down to 5%) the
percentage of the captured target
value. The Reset button can be NOTE: The continuous audible tone from the Patient Interrupt Switch
pressed to clear the captured target. will begin again once treatment is complete, if the Patient
NOTE: The capture may be stopped Interrupt Switch has been pressed during treatment, or if the
at any time during the 15 Stop button is pressed.
second period by pressing the
End Capture button. Examine the patient's skin again after treatment.
Alarm button - This button allows
the clinician to choose if the alarm
should sound above or below the
target.
Above: The alarm will sound when
the sEMG activity exceeds the target.
Below: The alarm will sound when
the sEMG activity is below the target.
35
STARTING, PAUSING AND STOPPING TREATMENT Traction therapy can be stopped at any time by pressing the Stop button
or by pressing the red button of the Patient Interrupt Switch.
NOTE: Read and follow steps of the Patient Preparation section on
When the Stop button is pressed:
Pages 24-25 , the Operating Controls of the Home and
Treatment Screens on Pages 26-32, and the sEMG Traction • traction tension will decrease gradually
section on Pages 33-35 as well as learn Operating Controls of the • the Traction Cord will release
Treatment Screen to set up traction treatment. • the audible tone sounds
• the Treatment Screen will return to Setup Mode
When the Start button is pressed:
• the audible tone sounds If necessary, check the patient’s harness and position on the table, and
change the traction parameters. Restart traction therapy by pressing the
• A message will display saying, "Beginning traction. Ensure
Start button.
table is unlocked. Touch anywhere to continue".
NOTE: If the screen is not touched, the message will When the red button of the Patient Interrupt Switch is pressed:
• the audible tone sounds
disappear in 3 seconds.
• the motor is stopped
• the Traction Cord tightens • a warning will display saying The Patient Switch has been
• traction therapy begins pressed. The treatment has been terminated. Touch the screen
• the Treatment Screen displays the maximum traction tension, to acknowledge the warning and the tension will decrease to
the minimum traction tension, the hold time, the rest time, zero
the current tension, the time remaining in the traction • the Traction Cord will release
therapy, and the running status If the unit loses power:
• the Treatment Graph of the traction therapy becomes • the motor stops
shaded as it goes through the treatment
NOTE: Monitor the traction therapy closely.
When the Pause button is pressed:
• the audible tone sounds
• traction therapy is paused • In the event of a loss of power to the unit or when quick release is
• the Traction Cord will release needed, traction tension should only be released by having the
• the tension slowly decreases to zero patient move towards the traction head to release the tension on
NOTE: The Pause button may be used to adjust the patient's harness or the rope. Once the tension on the rope has been released, loosen the
position during treatment. patient harness adjustment straps.
Resume the traction therapy by pressing the Pause button again.
36
STARTING, PAUSING AND STOPPING TREATMENT CONTINUED
When the traction therapy is finished, the audible tone sounds, the
traction tension will decrease gradually, the Traction Cord will release,
and a message will display saying, "Treatment has been completed. Do
you want to save data to Patient Card?" Touch the Yes or No button to
respond. (See Saving Treatment to a Patient Data Card for more
information.)
NOTE: The beeper will beep every 30 seconds until the screen is touched
to acknowledge the message.
NOTE: Wait until all tension has released automatically before attempting
to remove the harness from the patient. Release the patient from
the traction harness according to the manufacturer’s instructions.
37
SAVING TREATMENT TO A PATIENT DATA CARD
The Triton traction unit incorporates a Patient Data Card interface that Pain Scale - There are eleven pain scale
allows transfer of patient therapy data from the unit to the Patient Data settings to choose from a numeric scale
Card. The unit allows storage and recall of the following patient session of 0 to 10. Press the arrows left to right
data onto the Patient Data Card: all therapy session parameters, before from what the patient describes pain
and after Patient Pain Profiles, and Session Notes (stored on card via from being No Pain (0) to Worst Pain
PC only). Each Patient Data Card can store multiple sessions and each Possible (10).
session can be recalled within the unit. NOTE: If the patient is unsure of rating
pain from a numeric scale, a
New Patient Data Card Setup visual pain scale is available.
Toggle the middle button
between the left and right
Insert a new Patient Data Card (with the
arrows to choose between
gold chip facing up) into the Patient
a Numeric or a Visual Analog
Data Card port located on the front of
Scale. Press the arrows left to
the traction unit.
right to move the visual bar from
NOTE: Insert the Patient Data Card
what the patient describes
before treatment.
pain from being No Pain to Worst
Pain Possible.
Press the Clinical Resources button on
Pain Type - There are eleven pain
the front of the traction unit.
types to choose from based on how
Press the Edit Current Pain Profile button
the patient describes pain: Numbing,
located in the Patient Card section of
Dull Ache, Throbbing, Pulsing, Tingling,
the menu.
Nagging, Pinching, Burning, Shooting,
Stabbing, Radiating, or None Selected.
Enter the following information under
the Pain Before Treatment column:
38
SAVING TREATMENT TO A NEW PATIENT DATA CARD CONTINUED
Pain Map - Press the Edit Pain Map Once a therapy session has been
button. Press the area of the body to completed, press the Clinical Resources
highlight where the patient describes button. Press Edit/Save Completed
pain. Each time an area of the body Pain Profile button to enter all post-
diagram is pressed, a highlighted square treatment pain information after the
is produced. Press the area again to therapy session.
remove the highlighted square.
(See previous instructions for Pain
NOTE: The Clear button clears all Scale, Pain Type, and Pain Map and
highlighted areas of the body enter information under the Pain
diagram. After column) to show any progress
made from the treatment.
Press the Back button or Home button
to begin set up and to perform the NOTE: Once pain information is
patient therapy session. entered, review all information
to ensure of accuracy. Once
NOTE: All pain information can be saved, pain information
edited during a patient cannot be changed.
therapy session by pressing
the Clinical Resources button Press the Save to Patient Card button
and Edit Current Pain Profile to save patient therapy session. This will
button. However, it is save all session parameters, and pain
recommended to enter all pre- information.
treatment pain information
before the patient therapy
session.
39
SAVING TREATMENT TO A NEW PATIENT DATA CARD CONTINUED

After the Save to Patient Card button is Approximately ten treatments can be saved on a Patient Data Card. Use
pressed, a keyboard will be displayed one card per patient. The Patient Data Card can also be used with the
to enter the patient's name, if the card optional Patient Data Management System.
is blank. Once the patient's name is
entered, press the Return Arrow to Information may be transferred to a PC via the optional Patient Data
accept. Management System. The PC software is designed to allow easy access
to patient data and printing of reports as well as adding Session Notes to
A message will be displayed saying the Patient Data Card.
treatment has been saved to the Patient NOTE: No Session Notes will be available unless the optional Patient
Card for (patient's name). Touch the Data Management System has been utilized to enter Session
screen to acknowledge. This will return Notes onto the Patient Data Card.
you to the Treatment Screen.
Remove the Patient Data Card for filing

with patient records.
40
RETRIEVING DATA FROM EXISTING PATIENT DATA CARD

Existing Patient Data Card Use The treatment list is located on the
Insert the Patient Data Card (with the right side. Press the Up or Down Arrow
gold chip facing up) into Patient Data button to select the desired treatment.
Card port located on the front of the Press the Return Arrow to accept. This
traction unit. will show the following information:
Before and After Treatment Pain
Information (Pain Map, Pain Scale and
Pain Type) and Session Notes.
Press the Clinical Resources button on NOTE: The box located on the left
the front of the traction unit. side of the treatment list is a
Press the Patient Card (Patient's Name) review of treatment parameters
button located in the Patient Card of the selected treatment.
section of the menu. The review of the treatment
shows the following information:
NOTE: If the Patient Data Card is not
Patient's Name, Date, Start
inserted, this button is
Treatment Time, End Treatment
deactivated.
Time, Treatment Parameters and
Session Notes (stored on card
via PC only).
Press Run This Treatment button.
Read and follow the steps of the

Patient Preparation section on Pages
24-25 to set up traction treatment.
Press the Start button to begin

treatment.
41
ERASING PATIENT DATA CARD
Insert the Patient Data Card (with the When the Patient Data Card is erased,
gold chip facing up), to be erased, into a message will be displayed saying,
the Patient Data Card port located on "Patient Card has been erased".
the front of the traction unit. Touch the screen to acknowledge
the message and it will return to the
Clinical Resources Screen.

Press the Erase Patient Card button

located in the Patient Card section of
the menu.
A message will display asking, "Are you

sure you want to erase the Patient
Card?" Press Yes or No.
42
USER PROTOCOLS
This library is a series of protocols created by the user and stored in the After the Return Arrow is pressed, a
unit memory. The following information gives general instructions as to keyboard will be displayed to enter the
setup, saving and access of User Protocols. Should the Restore Default name of the User Protocol. Once the
Protocol button be pressed, through the Utilities section of the Clinical User Protocol name has been entered,
Resources Screen, all User Protocols will be permanently removed from press the Return Arrow to accept.
the unit.
NOTE: Twenty User Protocols can be saved per body part as well as a
Default Protocol for Cervical and Lumbar only.
Setup and Saving User Protocols

Select and edit the parameters of the A message will be displayed saying
desired treatment from the Treatment Current treatment settings have been
Screen. saved as "Protocol Name". Touch the
screen to continue.
Press the Save Protocol button located

in the Protocols section of the menu.
Press the Up or Down Arrow button

to select the number of User Protocol
to save the desired treatment to or
the Default Protocol button to save
treatment as the default. Press the
Return Arrow to accept.
NOTE: The Default Protocol is only
available for Cervical or Lumbar
Traction.
43
USER PROTOCOLS CONTINUED
Accessing User Protocols

Press the Clinical Resources button on The list of the User Protocols is located
the front of the traction unit. on the right side and the body part
buttons are located on the left side
Press the Retrieve Protocol button to toggle between body part User
located in the Protocols section of the Protocols. Press the Up or Down button
menu. to review the User Protocols.
Select the desired User Protocol by

pressing the Return Arrow.
Select the body part for the desired User

Protocol to retrieve.
44
CLINICAL PROTOCOLS™
The Clinical Protocols™ section is a series of traction protocol presets Select the desired body area for a
where the body area is selected by the user and the Clinical Protocols™ Clinical Protocol.
algorithm will select the parameter settings.
These Clinical Protocols™ are to be used only as guidelines. Each patient
should be individually assessed by a licensed practitioner to determine
the appropriateness of the protocol parameters prior to use. All
Clinical Protocols™ can be edited to suit appropriate patient treatment
prescription and patient comfort.
The following information gives general instructions to access, select and
setup Clinical Protocols™. Each Clinical Protocol can be set up and edited There are four options to choose from
in the same basic manner. for Cervical and Lumbar only:
• DIsc Involvement with Muscle Guarding
Press the Clinical Protocols™ button • Disc Involvement without Muscle
from the Home Screen. Guarding
• Joint Segment with Muscle Guarding
• Joint Segment without Muscle Guarding
The next screen will show the body area

menu of the Clinical Protocol.
45
CLINICAL PROTOCOLS™ CONTINUED
Press the Traction Rationale button to

view the text explaining the rationale
for the type of traction associated with
the Clinical Protocol selected as well as
a definition of terms associated to the
Treatment Screen.
Press the Traction Technique button to

view patient preparation instructions.
NOTE: There are no traction techniques
for the Hip body area.
Press the Edit button to enter the

Maximum and Minimum Traction Levels
or to change any of the Clinical Protocol
presets.
46
MULTIMEDIA CARD MMC GRAPHICS LIBRARY
The Multimedia Card (MMC) Graphics Library offers an anatomical library Once the body area is selected, a list of related items to the body
that is designed to aid the operator in visually identifying and recognizing area will be displayed. Choose from the following:
specific skeletal structures and muscles.
Lumbar
Press the MMC Graphics Library button • Bones • Radicular Pain
from the Home Screen. • Muscles • Herniated Disc
• Scoliosis • Sciatica
• Sacroiliac Joint • Spinal Stenosis
• Degenerative Disc • Ankylosing Spondylitis
Cervical
• Bones • Tension Headache
• The Spine • Anterior Cervical Muscles
• The Cervical Spine • Whiplash
• Herniation • Whiplash II
Select the button of the desired body
area. Hand/Wrist
• Bones • Carpal Tunnel
• Ligaments • CTS: Cross Section
• Palmer View • CTS
• Muscles • CTS: Palmer View
• Tendons • Dupuytren's Contracture Scarring
• Tendonitis
Hip
• Bones
• Muscles
• Hip: Bursitis
47
DTS PULL PATTERNS IF APPLICABLE
The DTS Pull Patterns, only available with Model 2841 Triton DTS Traction Selecting a DTS Pull Pattern
Unit with sEMG or with P/N 2842 Triton DTS Card, offer a selection
of various intermittent traction programs. It is up to the clinician to From the Home Screen, press the DTS
determine the applicability and appropriate parameters of the presets as Pull Pattern button.
applied to the patient.
Installing Triton DTS Card
Turn the traction unit off with the On/

Off Switch on the back of the unit.
Remove the Multimedia Card (MMC) Choose the desired body area for the
from the front of the traction unit. DTS Pull Pattern.
NOTE: The Multimedia (MMC) Card can
be discarded once removed.
Insert the Triton DTS Card into the

Multimedia Card (MMC) Port.
Turn the traction unit on with the On/ Select one of the five desired DTS Pull
Off Switch on the back of the unit. Patterns.
NOTE: The DTS Pull Pattern parameters
A message will display on the Touch can be edited and saved as the
Screen User Interface saying, "Unit has default Pull Pattern or as a User
been changed to a DTS unit. Touch Protocol. (See the User
anywhere to continue." Protocol Section on Pages
43-44 for more information)
48
ACCESSORIES Triton® Traction
The following provides the users of the Triton traction unit the necessary information to order the replacement accessories most commonly used with
the system. This list of replacement accessories are designed for use with Chattanooga Group traction devices. When ordering, provide the respective part
number, description and quantity desired.
Ref. Description Ref. Description
7040 Saunders Cervical Traction Device 42061 Dura-Stick II Electrodes - 1.25 in (3 cm) Round (40/case)
1450 Carpal-Trac 1440 TXA-1 Accessory Package

Includes: 1 Adjustable Cervical Traction Halter, 1 Heavy Duty Pelvic
12540 Carpal-Trac Replacement Wrist Strap Traction Set, 2 TX Pillows and Covers, and 1 17 in (43 cm) Spreader Bar.
48039 Traction Clevis 60044 12 in (31 cm) Stainless Steel Spreader Bar
1410 QuikWrap Belt System 60030 17 in (43 cm) Stainless Steel Spreader Bar
48083 Patient Interrupt Switch 1301 TX Cervical Pillow without Cover

1341 TX White Cotton Pillow with Cover
48084 Patient Interrupt Switch with sEMG
10889 TX Pillow Cover
48018 Patient Switch Hook Kit
48031 Replacement Traction Cord
27465 Patient Data Cards (25/pack)

2768 Patient Data Management System
27321 sEMG Lead Wire
4766 sEMG Module
2842 Triton DTS Card
48129 Multimedia (MMC) Card
42042 Dura-Stick II Electrodes - 2 in (5 cm) Round (40/case)
49
TROUBLESHOOTING Triton® Traction
The Triton traction unit is designed with patient safety in mind. An error can be caused by both external and internal disturbances. Errors can be caused
by disruptions in the power supply (such as a voltage break), and excess or inadequate voltage. Errors may also be caused by patient movement during
the traction therapy.
All traction unit errors and warnings are categorized by three numerical digits: Messages beginning with a 1 are general errors, a 2 symbolizes internal
warnings and errors and a 3 signifies a critical error where the problem has locked up the unit. (See Warning on Page 53 for more information)
Before calling for service, carefully review this User Manual. In the event you are still unable to correct the problem, contact your Chattanooga Group
dealer for all repair service. Be certain to specify your model number, serial number, and a detailed description of the issue you encountered.
Problem Possible Remedy

The Power On/Off Switch is in the “ON” position - • Verify the Mains Power Cord is properly connected to the power supply outlet.
nothing happens. • Contact dealer or Chattanooga Group for service.
The LED Indicator (Power On/Off) Light glows, but there • Verify the voltage from the power supply of the electrical outlet is the same as that
is nothing displayed on the LCD, or the LCD displays is listed on your Voltage Rating and Serial Number Plate.
confusing wording.
The LED Indicator (Power On/Off) blinks - • The unit is in Screen Saver Mode. Touch the screen or any button to reactivate the
nothing is displayed on the screen. unit.
The Patient Interrupt Switch is not working. • Make sure the Patient Interrupt Switch is properly connected to the Patient
Interrupt Switch Receptacle.
The Rope Release will not work. • Release all tension on the Traction Cord.
• If there is more than 5 lbs (2kg or 19N) of tension, the Rope Release button is
disabled.
• If patient is attached, have patient move towards the traction head to release tension.
• Shake the Traction Cord while holding down the Rope Release button.
• Turn unit off and return to Chattanooga Group for repair.
50
Problem Possible Remedy

Unable to properly read Patient Data Card. • Properly insert a Patient Data Card.
• Use a known good Patient Data Card.
• If problem persists, contact dealer or Chattanooga Group for service.
Attempted to use an Invalid Patient Data Card. • Properly insert a Patient Data Card.
• Use a known good Patient Data Card.
• If problem persists, contact Chattanooga Group for service.
No Session Data is available on the inserted Patient • Save session data to Patient Data Card.
Data Card. • Use a known good Patient Data Card.
• If problem persists, contact dealer or Chattanooga Group for service.
Patient Data Card is full. • Purchase additional Patient Data Cards from an authorized Chattanooga Group
dealer.
• Save to the Patient Data Management System (PDMS).
sEMG Traction button is grayed out. • An sEMG Module is required to initiate EMG Traction.
• Make sure sEMG Module is properly inserted into the Triton traction unit. If
problem persists, contact dealer or Chattanooga Group for service.
51
ERROR MESSAGES
ERROR ERROR DEFINITION PROBABLE CAUSES POSSIBLE REMEDY

CODE TYPE
100 WARNING Treatment has been running for 8 seconds, but no tension is Too much slack in Traction Cord. Remove Traction Cord slack.
detected on the rope.
101 WARNING Patient pressed Patient Interrupt Switch. Patient Interrupt Switch button pressed. Touch the Touch Screen to clear the message.
102 WARNING Patient Interrupt Switch is unplugged. Patient Interrupt Switch not properly connected to unit. Properly connect Patient Interrupt Switch and touch the
Touch Screen to clear message.
104 WARNING User selected Patient Card button on Utilities Screen, but no Wrong or bad Patient Data Card inserted into unit. Insert correct Patient Data Card.
traction treatments were found on the card.
105 WARNING User selected Save To Card, but no card is inserted into the No Patient Data Card is inserted. Properly insert correct Patient Data Card into unit.
unit.
106 WARNING User selected Save To Card, but the card currently inserted is Wrong or bad Patient Data Card inserted into unit. Insert correct Patient Data Card.
not a Patient Card.
107 WARNING User selected Save To Card, but the card currently inserted Memory full on Patient Data Card used. Save Data to PDMS and erase Patient Data Card.
is full.
108 WARNING User typed in a blank Patient Name. No Patient ID assigned. Enter Patient ID.
112 WARNING Error upgrading Control Board Software. Unknown Contact Dealer or Chattanooga Group for Service.
113 WARNING Error upgrading Motor Board Software. Unknown Contact Dealer or Chattanooga Group for Service.
114 WARNING User pressed START, but has not yet set the Max Level value User has not completed Treatment Setup. Complete Treatment Setup prior to pressing Start.
to a value greater than zero.
115 WARNING User pressed HOME button from treatment review screen Home button has been pressed. Press Stop To End Treatment prior to pressing Home.
while a treatment was running.
52
ERROR MESSAGES
• 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 unit that must be
tested by Chattanooga Group or a Field Service Technician certified
by Chattanooga Group before any further operation or use of
the unit. Use of a unit that indicates an Error or Warning in these
categories may pose a risk of injury to the patient, user or extensive
internal damage to the unit.
53
MAINTENANCE Triton® Traction
CLEANING SERVICE
NOTE: Before cleaning, disconnect the unit from the power source.
Periodically, clean the system with a clean, lint free cloth moistened with Should the Triton Traction Unit require service, contact the selling dealer
water and mild antibacterial soap. If a more sterile cleaning is needed, or Chattanooga Group Service Department.
use a cloth moistened with an antimicrobial cleaner. All returned units to the factory for service must include the following:
Do not submerse the system in water. Should the unit accidentally WARRANTY REPAIR/OUT OF WARRANTY REPAIR
become submersed, contact the dealer or Chattanooga Group Service 1. Written statement containing the following information:
Department immediately. Do not allow cleaning solutions or water • RA Number - Obtain from Factory
to enter the ventilation holes in the unit. This could permanently • Unit Model Number
damage the unit. Do not attempt to use a unit that has been wet inside • Unit Serial Number
until inspected and tested by a Field Service Technicians certified by • Contact person with Phone and Fax Numbers
Chattanooga Group. • Billing Address (for Out of Warranty Repair)
Touch Screen Cleaning • Shipping Address (Where to Ship Unit after Repair)
Clean unit display lens using a soft damp cloth, moistened with warm • Detailed Description of Problem or Symptoms
water and soap if necessary. DO NOT USE alcohol or chlorine based
2. Copy of original invoice issued at purchase of the unit.
solvents as this may damage the display.
3. Ship unit to Factory in the original container with all accessories
PREVENTIVE MAINTENANCE SCHEDULE and information as required in item one (1) above to:
The design of this device is mechanical in nature and thereby has Chattanooga Group
moving parts that may become worn or require lubrication from time 4717 Adams Road
to time. It is recommended that this device be placed on a periodic Hixson, TN 37343 USA
maintenance schedule to examine for lubrication needs or replacement Phone: 1-423-870-2281
of components. Please reference the Service Manual for particular parts Fax: 1-423-875-5497
and maintenance. The schedule of the maintenance depends upon the When shipping the unit to the dealer or factory, make certain the
frequency and duration of device usage and should be determined by original packaging is used. If the original packaging is not available,
the user. contact Chattanooga Group to obtain the packaging materials listed on
Page 17 for shipment. Any damage sustained from improper packaging
CALIBRATION REQUIREMENTS may render the warranty null and void.
Annual factory calibration is required for Triton traction units. The unit
should be sent to the factory or a Field Service Technician certified by Service to these units should be performed only by a Field Service
Chattanooga Group for this procedure. Technician certified by Chattanooga Group.
54
WARRANTY Triton® Traction
Chattanooga Group (“Company”) warrants that the Triton Traction Unit (“Product”) is free of defects in material and workmanship. This warranty shall remain in effect for
one year (12 months) from the date of original consumer purchase. If this Product fails to function during the one year warranty period due to a defect in material or
workmanship, Company or the selling dealer will repair or replace this Product without charge within a period of thirty (30) days from the date on which the Product is
returned to the Company or the dealer.
All repairs to the Product must be performed by a service center authorized by the Company. Any modifications or repairs performed by unauthorized centers or groups will
void this warranty.
The warranty period for the accessories shipped with the unit is 90 days. Accessories consist of the materials shipped with the unit.
This Warranty Does Not Cover:
Replacement parts or labor furnished by anyone other than the Company, the selling dealer or a certified Company service agent.
Defects or damage caused by labor furnished by someone other than Company, the selling dealer or a certified Company service agent.
Any malfunction or failure in the Product caused by product misuse, including, but not limited to, the failure to provide reasonable and necessary maintenance or any use
that is inconsistent with the Product User Manual.
COMPANY SHALL NOT BE LIABLE IN ANY EVENT FOR INCIDENTAL OR CONSEQUENTIAL DAMAGES.
Some locations do not allow the exclusion or limitation of incidental or consequential damages, so the above limitation or exclusion may not apply to you.
To obtain service from Company or the selling dealer under this warranty:
1. A written claim must be made within the warranty period to the Company or the selling dealer. Written claims made to the Company should be sent to:
4717 Adams Road
P.O. Box 489
Hixson, TN 37343 USA
Phone: 1-423-870-2281
Fax: 1-423-875-5497
2. The Product must be returned to the Company or the selling dealer by the owner.
This warranty gives you specific legal rights and you may also have other rights which vary from location to location.
The Company does not authorize any person or representative to create for it any other obligation or liability in connection with the sale of the Product. Any representation
or agreement not contained in the warranty shall be void and of no effect.
THE FOREGOING WARRANTY IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED,
INCLUDING ANY WARRANTY OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.
55
Moving
Rehabilitation
Forward™
ISO 13485 CERTIFIED
4717 Adams Road

P.O. Box 489
Hixson, TN 37343 U.S.A.
1-423-870-2281
1-800-592-7329 U.S.A.
1-800-361-6661 CANADA
+1-423-870-7200 OUTSIDE USA
chattgroup.com
48037A ©2006 Encore Medical, L.P.

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Moving

ISO 13485 CERTIFIED

FOREWORD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Operating Controls - Home Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26-28

OVERVIEW OF TRACTION THERAPY

BASE UNIT FRONT VIEW

BASE UNIT FRONT VIEW CONTINUED

Accessory Clip Patient Interrupt Switch

Clevis Attachment Slots

sEMG Lead Wire Receptacle

• Do not use the Clevis as a handle to pick up or carry the unit.

Power On/Off Switch

BASE UNIT REAR VIEW CONTINUED

System Hardware Symbols System Software Symbols

Contrast Stop Patient

On/Off Pause Move DOWN

Meets Directive 93 /42 /EEC

Meets Directive 93 /42 /EEC

CAN C22.2 No. 601.1-M90w/A2

Refer to ACCOMPANYING DOCUMENTS !

MOUNTING UNIT ON TABLE

ATTACHING THE PATIENT INTERRUPT SWITCH HOOK

A screw hole cap with the

Using a screwdriver, pop the screw

The Patient Interrupt Switch can now

Place the Patient Interrupt Switch

INSTALLING THE sEMG MODULE

Plug the traction unit back into the

REMOVING OF THE sEMG MODULE

Gently press the tabs underneath

INITIAL UNIT SETUP

Accessing User Utilities Clinic Name

Set Date and Time

INITIAL UNIT SETUP CONTINUED

Language Reset Default Protocols

NOTE: The default of Language is set as English.

Reset Unit Settings

To prepare the patient for traction therapy, do the following:

• The Patient Interrupt Switch must be in the patient’s grasp throughout

PATIENT PREPARATION CONTINUED

• In the event of a loss of power to the unit or when quick release is

7. Fit the appropriate traction harness on the patient by following the

OPERATING CONTROLS  HOME SCREEN

OPERATING CONTROLS  HOME SCREEN CONTINUED

OPERATING CONTROLS  HOME SCREEN CONTINUED

Traction Technique - Button provides visual steps as to how to set up

Multimedia Card (MMC) Graphics Library

OPERATING CONTROLS  TREATMENT SCREEN

3 NOTE: On the Touch Screen User Interface, any parameters surrounded in

(1) Traction Meter

(2) Time Remaining

(3) Time Remaining During Hold/Rest Cycles

OPERATING CONTROLS  TREATMENT SCREEN CONTINUED

OPERATING CONTROLS  TREATMENT SCREEN CONTINUED

(12) Pre-tension (14) Edit Min/Max Levels

OPERATING CONTROLS  TREATMENT SCREEN CONTINUED

FOR LUMBAR TRACTION ONLY: (15) Clinical Resources

sEMG TRACTION TREATMENT

Give the Patient Interrupt Switch

sEMG TRACTION TREATMENT CONTINUED

sEMG TRACTION TREATMENT CONTINUED