User Manual Template
Moving
Rehabilitation
Forward™
User Manual
Operation & Installation
Instructions for:
2783- Two Channel
Transportable
Electrotherapy Unit
ISO 13485 Certified
TABLE OF CONTENTS
Intelect Transport® 2-Channel Electrotherapy
Foreword . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Safety Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Precautionary Definitions . . . . . . . . . . . . . . . . . . . . . 2
Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Dangers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Indications, Contraindications,
and Adverse Effects . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Indications for Russian, High Voltage Pulsed
Current (HVPC), IFC, and Premodulated Waveforms . . . 9
Additional Indications for IFC and
Premodulated Waveforms . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Additional Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Adverse Effects . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Common Terms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Nomenclature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Unit Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Waveform Specifications . . . . . . . . . . . . . . . . . . . . . . 20
Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
MOUNTING THE UNIT ON the WALL . . . . . . . . . . . . . . . . 22
INSTALLING the battery pack . . . . . . . . . . . . . . . . . . . 26
CHARGING the battery pack . . . . . . . . . . . . . . . . . . . . 28
USING THE BATTERY PACK . . . . . . . . . . . . . . . . . . . . . . . . . 28
Patient Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Electrotherapy Patient Preparation . . . . . . . . . 29
Electrode Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
DURA-STICK® Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Reusable Carbon Electrodes (Optional) . . . . . . . . . . . . . . 30
DURA-STICK® Electrode Instructions . . . . . . . . . . . . . . . . . 31
Connecting Lead Wires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Securing Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Reusable Carbon Electrodes (Optional) . . . . . . . . . . . . . . 32
Connecting Lead Wires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Conductive Medium . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Securing Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
OPERATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
STARTING, Stopping, and
interrupting therapy . . . . . . . . . . . . . . . . . . . . . . . . . . 33
CREATING a user protocol . . . . . . . . . . . . . . . . . . . . . . 37
Using Protocols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
SYSTEM UTILITIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Audible Tones . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Changing Protocol Parameters . . . . . . . . . . . . . . . . . . . . . . 41
Changing Default Protocols . . . . . . . . . . . . . . . . . . . . . . . . . 42
Brightening or Dimming the LCD . . . . . . . . . . . . . . . . . . . . 44
Restoring Factory Protocols . . . . . . . . . . . . . . . . . . . . . . . . . 45
Changing Languages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
i
TABLE OF CONTENTS
Intelect Transport® 2-Channel Electrotherapy
Restoring Factory Settings . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Viewing Unit Version Information . . . . . . . . . . . . . . . . . . . 48
TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Error codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
ACCESSORIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Standard Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Optional Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Maintaining THE UNIT . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Cleaning the Unit and the Accessories . . . . . . . . . . . . . . . 52
Factory Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
ii
Foreword
Intelect Transport® 2-Channel Electrotherapy
This manual has been written for the users of the Intelect Transport 2-Channel Electrotherapy units. It contains general information on the
operation, precautionary practices, and maintenance information. In order to maximize use, efficiency, and the life of the unit, read this
manual thoroughly and become familiar with the controls, as well as the accessories before operating the system.
Specifications put forth in this manual were in effect at the time of publication. However, owing to DJO, LLC's policy of continual
improvement, changes to these specifications may be made at any time without obligation on the part of DJO, LLC.
Before administering any treatment to a patient, the users of this equipment should read, understand, and follow the information
contained in this manual for each mode of treatment available, as well as the indications, contraindications, warnings, and precautions.
Consult other resources for additional information regarding the application of electrotherapy.
Product Description
The Intelect Transport 2-Channel Electrotherapy unit, designed and manufactured by DJO, LLC, offers a new dimension in clinical
electrotherapy made possible by software design and digital signal processing.
Effectiveness of this treatment is dependent upon correct use. If treatment times are exceeded, the therapy may not result in positive
clinical outcomes.
Stay current with the latest clinical developments in the field of electrotherapy. Observe all applicable precautionary measures for
treatment.
Keep informed of appropriate indications and contraindications for the use of electrotherapy.
This equipment is to be used only under the prescription and supervision of a licensed practitioner.
©2009 DJO, LLC Vista, California, USA. Any use of editorial, pictorial, or layout composition of this publication without express written consent from DJO, LLC is strictly
prohibited. This publication was written, illustrated, and prepared for distribution by DJO, LLC.
1
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
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:
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.
Text with a “DANGER” indicator will explain possible safety
infractions that are imminently hazardous situations that would
result in death or serious injury.
NOTE:
Throughout this manual, “NOTE” may be found. These Notes are
helpful information to aid in the particular area or function being
described.
Text with a “WARNING” indicator will explain possible safety
infractions that will potentially cause serious injury and
equipment damage.
2
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
• The unit should be routinely checked before each use to
• Read, understand, and practice the precautionary and
determine that all controls function normally; especially
that the intensity control properly adjusts the intensity of
the electrotherapy power output in a stable manner. Also,
determine that the treatment time control actually terminates
electrotherapy power output when the timer reaches zero.
• The Intelect battery pack is designed for use only with
Chattanooga Intelect Transport 2-Channel Electrotherapy,
Combo, Laser, and Ultrasound systems.
• Inspect cables and connectors before each use.
• The Intelect Transport 2-Channel Electrotherapy unit 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 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.
operating instructions. Know the limitations and hazards
associated with using any electrical stimulation device.
Observe the precautionary and operational decals placed on
the unit.
• DO NOT operate the Intelect Transport 2-Channel
Electrotherapy unit when connected to any unit other than
DJO, LLC devices.
• DO NOT operate this unit in an environment where
other devices are being used that intentionally radiate
electromagnetic energy in an unshielded manner.
• DO NOT use sharp objects such as a pencil point or ballpoint
pen to operate the buttons on the control panel.
• This unit should be operated, transported, and stored in
temperatures between 59° F and 104° F (15° C and 40° C ),
with relative humidity ranging from 30%-60%, and where the
atmospheric pressure is between 950 h Pa and 1050 h Pa.
3
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
• The battery pack should be removed when storing the unit
• This equipment generates, uses and can radiate radio
for extended periods of time.
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 consult the factory field service
technician for help.
• 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 disassemble, modify, or remodel the unit or
accessories. This may cause unit damage, malfunction,
electrical shock, fire, or personal injury.
• DO NOT remove the cover. This may cause unit damage,
malfunction, electrical shock, fire, or personal injury. There
are no user-serviceable parts inside the unit. If a malfunction
occurs, discontinue use immediately and consult the dealer
for repair service.
• Failure to use and maintain the Intelect Transport 2-Channel
Electrotherapy unit and its accessories in accordance with
the instructions outlined in this manual will invalidate your
warranty.
4
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
• These devices are restricted to sale by, or on the order of,
Before administering any treatment to a patient you should
become acquainted with the operating procedures for
each mode of treatment available, as well as the indications,
contraindications, warnings, and precautions. Consult other
resources for additional information regarding the application
of Electrotherapy.
• To prevent electrical shock, disconnect the unit from the
power source before attempting any maintenance procedures.
• Keep electrodes separated during treatment. Electrodes in
contact with each other could result in improper stimulation
or skin burns.
• Long term effects of chronic electrical stimulation are
unknown.
• Stimulation should not be applied over the anterior neck or
mouth. Severe spasm of the laryngeal and pharyngeal muscles
may occur and the contractions may be strong enough to
close the airway or cause difficulty in breathing.
• Stimulation should not be applied transthoracically in that
the introduction of electrical current into the heart may cause
cardiac arrhythmia.
• Stimulation should not be applied over swollen, infected,
and inflamed areas or skin eruptions, e.g., phlebitis,
thrombophlebitis, varicose veins, etc.
a physician or licensed practitioner. This device should be
used only under the continued supervision of a physician or
licensed practitioner.
• 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.
• 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.
• The user must keep the device out of the reach of children.
• Electronic monitoring equipment (such as ECG monitors and
ECG alarms) may not operate properly when TENS stimulation
is in use.
• Powered muscle stimulators should be used only with
the leads and electrodes recommended for use by the
manufacturer.
5
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
• Stimulation should not be applied over, or in proximity to,
cancerous lesions.
• Output current density is inversely related to electrode size.
Improper application may result in patient injury. If any
question arises as to the proper electrode size, consult a
licensed practitioner prior to therapy session.
• Dispose of all products in accordance with local and national
regulations and codes.
• For continued protection against fire hazard, charge the
battery pack only while installed on the Intelect Transport 2Channel Electrotherapy unit.
• Use of controls or adjustments or performance of procedures
other than those specified herein may result in hazardous
conditions causing damage to the battery pack or cells.
• To prevent electrical shock, disconnect the battery pack from
the system before attempting any maintenance procedures.
6
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
• In the event that an Error message or Warning appears on the
increase the individual cell temperature and cause
cell rupture or leakage.
• NiMH Batteries contain Class E corrosive materials. In
the event of battery cell rupture or leakage, handle
battery pack 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/or chemical burns.
• Never, under any circumstances, open the battery
pack housing or cells. Should an individual battery
from a battery pack become disassembled,
spontaneous combustion of the negative electrode
is possible. There can be a delay between exposure
to air and spontaneous combustion.
• Never dispose of the battery pack in fire. Never
short circuit the battery pack. The battery pack may
explode, ignite, leak, or get hot causing serious
personal injury.
• Dispose of NiMH batteries according to national,
LCD beginning with a 2 or 3, immediately stop all use of the
unit and contact the dealer or DJO, LLC for service. Errors and
Warnings in these categories indicate an internal problem with
the unit that must be tested by DJO, LLC or a Field Service
Technician certified by DJO, LLC before any further operation
or use of the system. 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 system.
• DO NOT connect the unit to an electrical supply without first
verifying that the power supply is the correct voltage. Incorrect
voltage may cause unit damage, malfunction, electrical shock,
fire, or personal injury. Your unit was constructed to operate
only on the electrical voltage specified on the Voltage Rating
and Serial Number Plate. Contact your DJO, LLC dealer if the
unit is not properly rated.
• Charge the battery pack according to the instructions found in
this manual. Never attempt to charge the battery pack on any
other charging mechanism.
• Use the battery pack only with the Intelect Transport Series
units.
• Do not reverse the polarity of the battery pack. Doing so can
7
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
state, and local codes and regulations.
8
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
Indications, Contraindications, and Adverse Effects
• Safety has not been established for the use of therapeutic
Indications for Russian, High Voltage Pulsed Current (HVPC),
electrical stimulation during pregnancy.
IFC, and Premodulated Waveforms
• Relaxation of muscle spasms
• Powered muscle stimulators should not be used on patients with
cardiac demand pacemakers.
• Prevention or retardation of disuse atrophy
• Increase local blood circulation
Additional Precautions
• Caution should be used for patients with suspected or diagnosed
• Muscle re-education
heart problems.
• Maintaining or increasing range of motion
• Caution should be used for patients with suspected or diagnosed
Additional Indications for IFC and Premodulated Waveforms
epilepsy.
• Symptomatic relief of chronic, intractable pain
• Caution should be used in the presence of the following:
• Post-traumatic acute pain
xxWhen there is a tendency to hemorrhage following acute
• Post-surgical acute pain
trauma or fracture
xxFollowing recent surgical procedures when muscle contraction
Contraindications
may disrupt the healing process
• This device should not be used for symptomatic local pain
xxOver a menstruating or pregnant uterus
relief unless etiology is established or unless a pain syndrome
xxOver areas of the skin which lack normal sensation.
has been diagnosed.
• This device should not be used when cancerous lesions are
• Some patients may experience skin irritation or hypersensitivity
present in the treatment area.
due to the electrical stimulation or electrical conductive medium.
The irritation can usually be reduced by using an alternative
• This device should not be used when open wounds are
conductive medium or an alternative electrode placement.
present in the treatment area.
• Electrode placement and stimulation settings should be based on
• Other contraindications are patients suspected of carrying
the guidance of the prescribing practitioner.
serious infectious disease and or disease where it is advisable,
for general medical purposes, to suppress heat or fevers.
• Powered muscle stimulators should be used only with the lead
wires and electrodes recommended for use by the manufacturer.
• Electrode placements must be avoided that apply current
to the carotid sinus region (anterior neck) or transcereberally
(through the head).
9
Safety precautions
Intelect Transport® 2-Channel Electrotherapy
Indications, Contraindications, and Adverse Effects (continued)
Adverse Effects
• Skin irritation and burns beneath the electrodes have been
reported with the use of powered muscle stimulators.
• Potential adverse effects with TENS are skin irritation and
electrode burns.
10
OVERVIEW
Intelect Transport® 2-Channel Electrotherapy
The Intelect Transport 2-Channel Electrotherapy unit, designed and manufactured by DJO, LLC, offers a new dimension in portable
electrotherapy made possible by advanced software design and digital signal processing. The result is a unit with extraordinary versatility
based on simplicity of operation.
The Intelect Transport 2-Channel Electrotherapy unit offers "On the Go" clinical electrotherapy. The unit provides an innovative case design,
with a logical control system and a large, easy to read graphical LCD. User defined protocols allow you to customize any electrotherapy
treatment to the specific needs of your patient. The repositional base allows the unit to be configured for desktop or wall-mount use.
The following features are available on the Intelect Transport 2-Channel Electrotherapy unit:
• Two channels of electrotherapy stimulation output
• Independent intensity and parameter controls for each channel
• Four currents - IFC, Premodulated, High Voltage Pulsed Current (HVPC), and Russian
• Fifteen user-defined memory positions
• Lightweight design
• Battery powered option
Common Terms
Accommodation - condition where nerves lose their ability (sensitivity) to respond to electrotherapy.
Beat Fixed - Associated with the Interferential waveform, Beat Fixed is the parameter at which the beat frequency remains constant. When
the Sweep setting is turned off, you must select a fixed beat for the therapy session. The available settings for Beat Fixed are 1 to 200 Hz.
Beat High - During a sweep, the Beat High setting is the highest number to which the beat frequency increases. The available range for
the Beat High parameter is 2 to 200 Hz. This parameter is unique to the Premodulated and IFC waveforms.
Beat Low - During a sweep, the Beat Low setting is the lowest number to which the beat frequency decreases. The available range for the
Beat Low parameter is 1 to 199 Hz. This parameter is unique to the Premodulated and IFC waveforms.
Burst - A burst is a series of pulses at a predetermined pulse frequency.
11
OVERVIEW
Intelect Transport® 2-Channel Electrotherapy
Burst Frequency (Freq.) - This is the number of bursts per second (bps). The available burst frequencies on the Intelect Transport
2-Channel Electrotherapy unit are 20 to 100 bps. This parameter is unique to the Russian waveform.
Carrier Frequency (Freq.) - Associated with the Interferential and Russian waveforms, Carrier Frequency is the frequency of the
un-modulated medium frequency current. The available carrier frequencies are 2,500, 4,000, and 5,000 Hz for IFC, but fixed at 2,500 Hz for
Russian and Premodulated waveforms.
CC/CV - This is the abbreviation for Constant Current/Constant Voltage. Constant current is a stimulator capable of delivering an electric
current that flows at the same amplitude regardless of changes in tissue impedance over time. Constant voltage is a stimulator capable of
delivering a source of voltage at the same amplitude regardless of changes in tissue impedance over time. Most modern electrotherapy
units are of the constant current type because they provide a consistent, or stable level of current amplitude throughout the therapy
session, thus making it comfortable for the patient and predictable for the clinician. Keep in mind that the amount of stimulation is directly
proportional to the current.
Channel Mode - The available channel modes are Single Channel (in which electrotherapy is distributed from one channel), Reciprocal
(where electrotherapy alternates between channels), and Co-Contract (where electrotherapy is distributed from both channels at the same
time). This parameter is unique to the Russian waveform.
Cycle Time - Cycle Time is the alternating time which the current is "on" and "off." Using the 10/30 setting as an example, the current is on
for 10 seconds and off for 30. The available cycle times are Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, and 10/50. This parameter is unique
to the Russian, Premodulated, and HVPC waveforms.
Display - Available only on the HVPC waveform, the Display feature allows you to change the displayed Intensity parameter from Volts to
Peak Current (Amps).
Duty Cycle - This is the ratio of the “On” time to “Total” time of the cycle, expressed as a percentage. The duty cycle describes the pulsed
modes of electric stimulation. The lower the percentage, the lower temporal average intensity. 100% is continuous electrotherapy. The
available Duty Cycles are 10, 20, 30, 40, 50%. This parameter is unique to the Russian waveform.
Frequency - Frequency is the number of times per second a pulse will repeat itself. The unit is selectable from 10-120 pps. This parameter
is unique to the HVPC waveform.
12
OVERVIEW
Intelect Transport® 2-Channel Electrotherapy
Intensity - Intensity is the output of electrotherapy distributed by the unit to the patient. Depending on the waveform, intensity is
measured in milliamps (mA), volts (V), and microamps (µA).
Leadwires - The leadwires consist of the main plugs that are connected to the unit, and 4 leads (2 black and 2 red) that connect to
electrodes.
Medium Frequency Current - These are the currents used by the Traditional Interferential (IFC), Interferential Premodulated, and Russian
waveforms that is higher than 1000 Hz, but lower than 10000 Hz.
Operating Channels - Operating Channels are the paths by which the electrotherapy is distributed from the unit to the patient. The unit
provides two channels of electrical stimulation.
Polarity - Polarity refers to the charge of an individual lead: positive or negative. This parameter is unique to the HVPC waveform.
Ramp - Ramp is the gradual increase and decrease in current. The purpose of ramping up the current is to maximize patient comfort by
preventing the abrupt and sudden exposure to the current. This parameter is unique to the Russian and HVPC waveforms.
Sweep - This is the modulation of therapeutic frequency commonly used to prevent accommodation. Sweeps are measured in pulses per
second (pps) and Hertz (Hz). The available sweeps are 1-120 pps for IFC and Premodulated, and 1-10 pps for HVPC.
Treatment Time – Measured in minutes and seconds, it is the suggested time in which therapy is given.
Type - Displayed as a parameter on the unit, Type is used to signify the specific kind of waveform.
Vector - A vector is a geometrically descriptive feature used to increase the effective therapeutic current at the crossing point of Traditional
Interferential (IFC).
Vector Position - The available vector positions are 0 to 90 degrees.
Vector Scan - Measured in percentages, vector scans are the rhythmic changes of the position of vector. The available vector scans are
Manual, Auto 40%, and Auto 100%.
13
OVERVIEW
Intelect Transport® 2-Channel Electrotherapy
Waveforms - Waveforms are current or voltage that is varied by time and are the geometrical descriptions of a DC, AC, or pulsed DC/AC
current. Current waveforms are described as either monophasic or biphasic. A biphasic wave is further described as either symmetrical
or asymmetrical and as balanced or unbalanced. For more specifications and types of waveforms available on the Intelect Transport
2-Channel Electrotherapy unit, refer to the section entitled "Waveform Specification" on page 20.
14
NOMENCLATURE
Intelect Transport® 2-Channel Electrotherapy
LCD Intensity/
Contrast Dial
Power
On/Off
LCD
Up
Arrow
Clinical
Resources
TIME
INTENSITY
Parameter
Display/Enter
Back
Channel 1
Lead Wire
Connection
STOP
Down
Arrow
PAUSE
START
Accessory Panel
15
Channel 2
Lead Wire
Connection
NOMENCLATURE
Intelect Transport® 2-Channel Electrotherapy
Power On/Off
The Power On/Off button controls the flow of electricity to the unit.
NOTE: Make certain there are no electrodes on the patient when turning the unit on or off.
LCD
The LCD (Liquid Crystal Display) allows the user to view and monitor the information displayed before, during, and after therapy.
Clinical Resources
Select this button to access the following functions:
•
Retrieving User Protocols
•
Restoring Factory Settings
•
Restoring Factory Protocols
•
Changing Languages
•
Viewing Unit Information
TIME
Press the Up or Down arrow buttons to set total treatment time of therapy.
Back
Use this button to return to the previous window.
STOP
Select this button to stop a treatment session.
Down Arrow
When the window displays a list of options, press the Down Arrow button to scroll down the list.
PAUSE
Use this button to pause the treatment session. When pressed, the icon displays. To restart therapy, press the PAUSE button.
16
NOMENCLATURE
Intelect Transport® 2-Channel Electrotherapy
Accessory Panel
The Accessory Panel serves as a port of connection for the electrodes.
Channel 1 Lead Wire Connection
This port serves as the connection point between the unit and the Channel 1 Lead Wire.
Channel 2 Lead Wire Connection
This port serves as the connection point between the unit and the Channel 2 Lead Wire.
START
Select Start to begin a treatment session.
Parameter Display/Enter
Select this button to display the parameters of the waveform during treatment. Also, this button is used to accept the highlighted selection.
INTENSITY
Use the up or down arrow to increase or decrease output power dosage.
Up Arrow
When the window displays a list of options, press the Up Arrow button to scroll up the list.
Battery Indicator
When displayed on the LCD, this symbol indicates the battery pack option is present on the unit. This symbol also displays the
charge status of the battery.
LCD Intensity/Contrast Dial
If the intensity of the LCD display diminishes, turn the dial until the display contrast is optimal.
17
NOMENCLATURE
Intelect Transport® 2-Channel Electrotherapy
Charge Indicator
This symbol displays when the unit is connected to mains power and the battery pack is charging.
NOTE: During battery operation, if the unit is left on, but is not active for more than five minutes, it will power off to conserve battery power. To restore power, press the Power On/Off button.
18
SPECIFICATIONS
Intelect Transport® 2-Channel Electrotherapy
Unit SPECIFICATIONS
gth
Dimensions
Width . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11.3 in (28.8 cm)
Length. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12.8 in (32.8 cm)
Height. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6.4 in (16.3 cm)
Weight
Standard Weight (with base). . . . . . . . . . . . . . . . . . . . . . . . 5.07 lb (2.3 kg)
Battery Pack. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.87 lb (0.85 kg)
Len
Power
Input. . . . . . . . . . . . . . . . . . . . . . 100 - 240 V - 1.0 A, 50/60 Hz 100 W Max
Output. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . +24 V, 3.125 A
Electrical Class . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CLASS I
Electrical Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . TYPE BF
Battery Type. . . . . . . . . . . . . . . . . . . . . . . . . . . Nickel Metal Hydride (NiMH)
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . (1.2 V x 20 size AA)
Operating Environment
Temperature. . . . . . . . . . . . Between 59° F and 104° F (15° C and 40° C)
Relative Humidity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30%-60%
Width
NOTE: All waveforms except High Voltage Pulsed Current
(HVPC) have been designed with a 200 mA peak
current limit. All waveform output intensities are
measured, specified, and listed to peak, not peak to
peak.
19
SPECIFICATIONS
Intelect Transport® 2-Channel Electrotherapy
Waveform Specifications
IFC
Premodulated IFC
Premodulated current is a medium frequency waveform. Current
comes out of one channel (two electrodes). The current intensity
is modulated: it increases and decreases at a regular frequency
(the Amplitude Modulation Frequency).
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 V
Carrier Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2,500 Hz
Beat Fixed (Sweep Off ). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-199 Hz
Sweep Low Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-199 Hz
Sweep High Beat Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-200 Hz
Cycle Time. . . . . . Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, and 10/50
Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Constant Voltage
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
IFC (Interferential) current is a medium frequency waveform.
Current is distributed through two channels (four electrodes).
The currents cross each other in the body at the area requiring
treatment. The two currents interfere with each other at this
crossing point, resulting in a modulation of the intensity (the
current intensity increases and decreases at the beat frequency).
Carrier Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2,000-10,000 Hz
Beat Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . 2,500, 4,000, or 5,000 Hz
Sweep Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 sec
Sweep Low Beat Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-199 Hz
Sweep High Beat Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-200 Hz
Scan Percentage. . . . . . . . . . . . . . . . . . . . . . . . . . . . Static, 40%, and 100%
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 V
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Constant Voltage
20
SPECIFICATIONS
Intelect Transport® 2-Channel Electrotherapy
Waveform Specifications (continued)
High Voltage Pulsed Current (HVPC)
Russian
The High Voltage Pulsed Current (HVPC) has a very brief pulse
duration characterized by two distinct peaks delivered at
high voltage. The waveform is monophasic (current flows in
one direction only). The high voltage causes a decreased skin
resistance making the current comfortable and easy to tolerate.
Output 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 pps
Cycle Time. . . . . . 5/5, 4/12, 10/10, 10/20, 10/30, 10/50, Continuous
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 Min
Russian Current is a sinusoidal waveform, delivered in bursts or
series of pulses. This method was claimed by its author (Kots)
to produce maximal muscle strengthening effects without
significant discomfort to the patient.
Output Intensity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-100 V
Channel Mode. . . . . . . . . . . . . . . . . . . . . Single, Reciprocal, and Co-Contract
Duty Cycle. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10%, 20%, 30%, 40%, 50%
Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Constant Voltage
Cycle Time. . 5/5, 4/12, 10/10, 10/20, 10/30, 10/50, and Continuous
Burst Frequency. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20-100 bps
Ramp. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.5, 1, 2, and 5 sec
Treatment Time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-60 min
21
SETUP
Intelect Transport® 2-Channel Electrotherapy
MOUNTING THE UNIT ON the WALL
The Intelect Transport 2-Channel Electrotherapy unit can be operated while the unit is resting on a flat surface or mounted on a wall. To
mount the unit on a wall, do the following:
1.
Remove the repositional base from the back of the unit.
2.
Using the repositional base as a guide, mark the 4 wall holes with a pencil or pen.
22
SETUP
Intelect Transport® 2-Channel Electrotherapy
MOUNTING THE UNIT ON the WALL (continued)
3.
Using an appropriate size drill bit, drill four holes you marked in the previous step.
4.
Press 4 appropriately sized drywall anchors into the wall so that the drywall anchor is flush with the wall.
23
SETUP
Intelect Transport® 2-Channel Electrotherapy
MOUNTING THE UNIT ON the WALL (continued)
5.
6.
Screw four #8 pan head sheet metal screws (1 inch or 2.54 cm) into the wall anchors. Make sure you leave 1/4 of an inch (0.635 cm ) between the wall and the head of the screw.
Replace the repositional base on the back of the unit.
24
SETUP
Intelect Transport® 2-Channel Electrotherapy
MOUNTING THE UNIT ON the WALL (continued)
7.
Line up the screw heads with the holes on the repositional base, and slide the unit down slightly until the screw heads are securely fastened to the repositional base.
25
SETUP
Intelect Transport® 2-Channel Electrotherapy
INSTALLING the battery pack
The Intelect Transport 2-Channel Electrotherapy unit accommodates both AC mains power and an optional battery pack. The pack
contains 20 Nickel Metal Hydride (NiMH) drycell batteries.
To install the battery pack in the unit, do the following:
1.
Locate the battery access door at the bottom of the unit and loosen the screw with a flat head screwdriver.
2.
Remove the battery access door and retain it.
26
SETUP
Intelect Transport® 2-Channel Electrotherapy
INSTALLING the battery pack (continued)
3.
4.
Connect the battery pack cable to the unit’s battery connector in the bottom of the battery recess.
Put the battery pack into the unit, making sure to orient it as shown.
27
SETUP
Intelect Transport® 2-Channel Electrotherapy
INSTALLING the battery pack (continued)
5.
Replace the battery access door and re-tighten the screw using the screwdriver.
6.
Reverse the steps in this section in order to remove the battery pack.
CHARGING THE BATTERY PACK
The battery pack is automatically charged by the unit whenever there is mains power connected. Charging may be interrupted during
operation of the unit by the control circuitry to limit total power consumption. A fully charged battery will provide 2-5 hours of treatment
depending on the mode used.
NOTE: Even when the battery pack is connected, the unit will default to mains power when plugged in.
USING THE BATTERY PACK
To save battery power, the Intelect Transport 2-Channel Electrotherapy unit is equipped with a “power off” function. This function is activated
when the unit is powered on and has been left idle for approximately 5 minutes, at which time the unit powers off. To restore power, press
the Power On/Off button.
28
Patient Preparation
Intelect Transport® 2-Channel Electrotherapy
Electrotherapy Patient Preparation
Electrode Placement
Use the following guidelines when preparing patients for
electrotherapy:
• Examine the skin for any wounds and clean the skin.
• Apply the electrodes to the treatment area.
• Ensure the electrodes are applied securely to the skin.
• Ensure good contact between each electrode and the skin.
• Check the electrode contact regularly during the treatment.
• Examine the skin again after the treatment.
• Choose electrodes that fit the anatomy.
• Follow electrode manufacturer instructions.
• Keep electrodes separated during treatment. Electrodes in contact
with each other could result in improper stimulation or skin burns.
• Output current density is inversely related to electrode size (i.e.,
the larger the electrode, the lower the current density). Improper
application may result in patient injury.
• Powered muscle stimulators should be used only with the leads and electrodes recommended for use by the manufacturer.
29
Patient Preparation
Intelect Transport® 2-Channel Electrotherapy
Electrotherapy Patient Preparation (continued)
DURA-STICK Electrodes
Chattanooga Dura-Stick Electrodes are a self adhesive, single
patient, one time use disposable product designed specifically for
use with Chattanooga Electrotherapy systems.
It is recommended that Chattanooga Dura-Stick Electrodes be
used whenever possible to ensure the highest level of contact
with the treatment area and most uniform delivery of the
prescribed electrotherapy treatment.
Properly dispose of used Dura-Stick Electrodes upon completion
of the therapy session.
Reusable Carbon Electrodes (Optional)
If used for delivery of electrotherapy, the Carbon Electrodes
must be used with a conductive medium such as Conductor™
Transmission Gel.
These Carbon Electrodes should be secured to the treatment area
using Nylatex® Wraps.
30
Nylatex® Wraps contain dry natural rubber and may
cause allergic reactions in patients with allergies to
latex.
Patient Preparation
Intelect Transport® 2-Channel Electrotherapy
Electrotherapy Patient Preparation (continued)
DURA-STICK Electrode Instructions
Connecting Lead Wires
Insert the lead with the Red (+) electrode
NOTE: Use of conductive medium or
connector into one Dura-Stick Electrode.
sponges is not required or recommended.
Insert the lead with the Black (-) electrode
Dura-Stick Electrodes are manufactured to
connector into the other electrode.
ensure the optimum conductivity during
Make certain the lead wires are
therapy when properly applied.
seated completely into the electrodes. Also,
ensure that the numbers on the electrodes
correspond to the appropriate color being
used (i.e., the black electrode labeled
number 1 should be used with the red
electrode labeled number 1).
LEAD WIRE seated
Red (+)
LEAD WIRE
Electrode
number
BLACK (-)
LEAD WIRE
31
Securing Electrodes
Remove the Dura-Stick Electrodes from
the protective backing and apply to the
treatment area as prescribed. Ensure the
entire electrode surface is in contact with
patient skin by pressing into place.
Patient Preparation
Intelect Transport® 2-Channel Electrotherapy
Electrotherapy Patient Preparation (continued)
Reusable Carbon Electrodes (Optional)
Connecting Lead Wires
Insert the lead with the Red (+) electrode
connector into Red electrode. Insert the
lead with the Black (-) electrode connector
into the Black electrode.
Conductive Medium
Liberally apply Conductor™ Transmission
Gel to electrode prior to placement on
patient.
Securing Electrodes
Use Nylatex® Wrap to secure each electrode
in position on the patient.
Make certain the lead wires are seated
completely into the electrodes.
RED (+)
LEAD WIRE
SECURE with
nylatex
BLACK (-)
LEAD WIRE
Nylatex® Wraps contain dry natural rubber and may
cause allergic reactions in patients with allergies to
latex.
32
OPERATION
Intelect Transport® 2-Channel Electrotherapy
Starting, Stopping, and interrupting therapy
The Operator Interface consists of buttons with a liquid crystal display (LCD). The operator is able to view parameter options on the display
and make selections by pressing the buttons on the control panel. The LCD will provide continuous information during the treatments
concerning power and elapsed time. Parameters are adjusted using control panel buttons on the front of the unit. The output can be
stopped by pressing the “PAUSE” or “STOP” buttons located on the control panel.
Do not turn the unit on or off while it is connected to the patient.
To apply electrotherapy, do the following:
1.
2.
3.
Turn system power “ON” by pressing the Power On/Off button.
The message "Initializing System" displays. The unit will go through self diagnostics, and the home screen displays on the LCD.
Connect the Lead Wires to the appropriate electrodes.
To see a list of recommended electrodes and their preparation, see pages 29-32.
NOTE: Do not use unnecessary force to connect the electrodes to the lead wires.
Place the self adhesive electrodes on the sites prescribed by a qualified practitioner. Make sure you press them firmly on the patient’s skin to ensure good conductivity.
33
OPERATION
Intelect Transport® 2-Channel Electrotherapy
Starting, Stopping, and interrupting therapy (continued)
4.
Depending on the type of waveform you intend to use and the number of patients
you intend to treat, insert the Lead Wire into Channel 1, Channel 2, or both Lead Wire Connections on the Accessory Panel.
5.
6.
Use the Up and Down Arrow buttons to highlight the appropriate channel.
Press the Enter button.
The Waveform screen displays.
34
OPERATION
Intelect Transport® 2-Channel Electrotherapy
Starting, Stopping, and interrupting therapy (continued)
7.
8.
Use the Up and Down Arrow buttons to highlight the appropriate waveform.
Press the Enter button.
The Parameter screen displays.
9.
10.
On the parameter screen, use the Up and Down Arrow buttons to highlight the parameter you want to change and adjust it accordingly, making sure to press the Enter button after each adjustment.
Press Enter to accept the parameters.
The Parameter screen refreshes and the new parameters are displayed.
35
OPERATION
Intelect Transport® 2-Channel Electrotherapy
STARTING, Stopping, and interrupting therapy (continued)
11.
12.
13.
To begin electrotherapy, press the START button.
The timer counts down, the output power ramps up, and "Running" displays below the timer.
NOTE: When the therapy time has expired, the unit beeps three times.
During therapy, you can press the TIME button to raise or lower treatment time (in one minute increments) using the up and down arrows.
During therapy, you can press the INTENSITY button to raise or lower the output using the up and down arrows.
Therapy can be interrupted at any time by pressing the STOP or PAUSE buttons.
When the STOP button is pressed, the unit stops emitting output, and the unit returns to the home screen. To resume therapy, repeat steps 5-11.
During treatment, the following occurs whenever the PAUSE button is pressed:
• the timer pauses
• the unit beeps quickly 5 times
• "Paused" displays below the timer
• the unit stops emitting output
To resume therapy, press the PAUSE button or the START button.
When you have completed treatment, remove all electrodes from the patient.
Turn system power “OFF” by pressing the Power On/Off button.
The unit beeps once and the blue light on the Power On/Off button flashes intermittently.
36
OPERATION
Intelect Transport® 2-Channel Electrotherapy
CREATING a user protocol
This is a library you create. You may store up to 15 protocols in the User Protocol Library. To create User Protocols, do the following:
1.
On the home screen, press the Enter button.
NOTE: User protocols can be used on either channel. It does not matter on which channel they are created.
The Waveform screen displays.
2.
3.
Use the Up and Down Arrow buttons to highlight the appropriate waveform.
Press the Enter button.
The Parameter screen displays.
4.
5.
6.
On the parameter screen, use the Up and Down Arrow buttons to highlight the parameter you want to change and adjust it accordingly, making sure to press the Enter button after each adjustment.
Press Enter to accept the parameters.
The Parameter screen refreshes and the new parameters are displayed.
Press the Clinical Resources button.
The Save Protocol screen displays.
37
OPERATION
Intelect Transport® 2-Channel Electrotherapy
CREATING a user protocol (continued)
7.
8.
Use the Up Arrow and Down Arrow buttons to highlight any unused user protocol.
If you select the Save as Default protocol, this will become the protocol displayed when the waveform is selected on the Waveform screen.
Press the Enter button to accept the highlighted selection and save your custom protocol.
The User Protocol Confirmation window displays to indicate that the protocol is now saved as the number you specified.
9.
Press any button on the Operator Interface.
The Parameter screen displays and your new protocol is now saved.
38
OPERATION
Intelect Transport® 2-Channel Electrotherapy
Using Protocols
To utilize a user protocol, do the following:
1.
On the home screen, press the Clinical Resources button.
The Clinical Library screen displays.
2.
Using the Up Arrow and Down Arrow buttons, highlight the Retrieve User Protocol option.
3.
Press the Enter button to accept the highlighted selection.
A list of user-defined protocols displays.
4.
5.
6.
Use the Down Arrow button to highlight the appropriate protocol.
As you highlight each protocol, a description of the protocol’s parameters
displays to the right.
Press the Enter button to select the highlighted protocol.
The Parameters screen displays the parameters of the protocol you selected.
Verify the parameters of this program, and use the appropriate buttons on the Operator Interface to adjust any setting, if necessary. For example, to adjust the time, press the up and down arrows on the TIME button.
39
OPERATION
Intelect Transport® 2-Channel Electrotherapy
Using Protocols (continued)
7.
To begin therapy, perform all the procedures outlined in the section entitled "Patient Preparation" on page 29. Then continue with step 11 of the section entitled "Starting, Stopping, and Interrupting Therapy" on page 36.
40
OPERATION
Intelect Transport® 2-Channel Electrotherapy
SYSTEM UTILITIES
Audible Tones
Audible tones will be heard in the following conditions:
• Any button is pressed.
• The rechargeable battery’s power is low (in which case the Low Battery icon will display).
• Any error message is displayed.
• Therapy begins.
• The therapy time reaches 0:00.
Changing Protocol Parameters
You may change any parameter prior to or during therapy. To make Intensity and Treatment Time changes, touch the respective buttons and use the up or down arrows to advance to the desired settings.
To change other parameters during therapy, do the following:
1.
2.
On the home screen, use the Up and Down Arrow buttons to highlight the channel on which therapy is currently running. Press the Enter button to select the highlighted option.
The parameters of the current therapy session display.
41
OPERATION
Intelect Transport® 2-Channel Electrotherapy
SYSTEM UTILITIES (continued)
3.
Using the Up Arrow and Down Arrow buttons, highlight the appropriate parameter and make the necessary changes, making sure to press the Enter button after each adjustment.
Changing Default Protocols
To change the power up presets of the waveforms, do the following:
1.
On the home screen, press the Enter button.
The Waveform screen displays.
42
OPERATION
Intelect Transport® 2-Channel Electrotherapy
SYSTEM UTILITIES (continued)
2.
Use the Up and Down Arrow buttons to highlight the appropriate waveform.
3.
Press the Enter button.
The Parameter screen displays.
4.
5.
6.
7.
On the parameter screen, use the Up and Down Arrow buttons to highlight the parameter you want to change and adjust it accordingly.
Press Enter to accept the parameters.
The Parameter screen refreshes and the new parameters are displayed.
Press the Clinical Resources button.
The Save Protocol screen displays.
Use the Up Arrow and Down Arrow buttons to highlight Save as Default protocol.
This will become the protocol displayed when the waveform is selected on the Waveform screen.
43
OPERATION
Intelect Transport® 2-Channel Electrotherapy
SYSTEM UTILITIES (continued)
8.
9.
Brightening or Dimming the LCD
Press the Enter button to accept the highlighted selection.
The Default Protocol Confirmation window displays.
Press any key to confirm the settings.
You are returned to the Clinical Resources menu.
To brighten or dim the LCD, turn the contrast control dial until the display contrast is optimal.
44
OPERATION
Intelect Transport® 2-Channel Electrotherapy
SYSTEM UTILITIES (continued)
Restoring Factory Protocols
If necessary, you can choose to restore the unit’s original (default) waveform parameters when it was shipped to you.
NOTE: This procedure will erase all user-defined protocols.
To restore the unit’s original waveform parameters, do the following:
1.
2.
3.
Press the Clinical Resources button.
The Clinical Library window displays.
Press the Up Arrow or Down Arrow buttons to highlight the Restore Factory Protocols option.
Press the Enter button to accept the highlighted selection.
The unit displays the message "Restoring Protocols Please wait."
The user-defined protocols are erased and the waveforms are restored to the original parameters. Then the Restore Factory Protocols Confirmation window displays.
4.
Press any button on the Operator Interface.
You are returned to the Clinical Library window.
45
OPERATION
Intelect Transport® 2-Channel Electrotherapy
SYSTEM UTILITIES (continued)
Changing Languages
You may change the language displayed by the Intelect Transport 2-Channel Electrotherapy unit to either English or Spanish.
To change the language displayed on the LCD, do the following:
1.
Press the Clinical Resources button.
The Clinical Resources screen displays.
2.
Use the Down Arrow and Up Arrow buttons to highlight the Language option.
3.
Press the Enter button to accept the highlighted selection.
The Language submenu displays.
4.
Press the Down Arrow and Up Arrow buttons to highlight the appropriate language.
5.
Press the Enter button to accept the highlighted selection.
Your unit now displays the language you selected.
46
OPERATION
Intelect Transport® 2-Channel Electrotherapy
SYSTEM UTILITIES (continued)
Restoring Factory Settings
To restore the original language on the unit, do the following:
1.
On the main window, press the Clinical Resources button.
The Clinical Library screen displays.
2.
Press the Up Arrow or Down Arrow buttons to highlight the Restore Factory Settings option.
3.
Press the Enter button to accept the highlighted selection.
The Restore Factory Settings Confirmation screen displays.
4.
Press any button on the Operator Interface.
The default power up settings are restored and you are returned to the Clinical Library screen.
47
OPERATION
Intelect Transport® 2-Channel Electrotherapy
SYSTEM UTILITIES (continued)
Viewing Unit Version Information
Use this utility to determine the unit’s software version. To do this, do the following:
1.
Press the Clinical Resources button.
The Clinical Library screen displays.
2.
Use the Up Arrow and Down Arrow buttons to highlight the View Unit Information option.
3.
Press the Enter button to accept the highlighted selection.
The Unit Version Information window displays.
4.
Press any key to return to the Clinical Library window.
48
TROUBLESHOOTING
Intelect Transport® 2-Channel Electrotherapy
Error codes
The Intelect Transport 2-Channel Electrotherapy unit incorporates error messages and warnings to inform the user of problems or
potential problems with the unit, modality, or accessories. These are numbered so the user can possibly correct the problem without the
aid of service personnel. Use the following Troubleshooting Charts to define the error codes, and locate the probable cause and possible
remedies before contacting the dealer or factory for technical service.
Code
Number
Probable Cause
Possible Remedies
104
User attempted to perform a therapy session, but both channels
are already in use.
A. Wait until the previous therapy session finishes.
B. Press the STOP button to end the therapy session on either channel.
105
User selected a two channel treatment, but at least one channel is
already in use.
A. Wait until the previous therapy session finishes.
B. Press the STOP button to end the therapy session on either channel.
106
Overcurrent
A. Check Electrodes and Lead Wires. Make certain Lead Wires are not damaged and are properly
connected to the system. Make certain Lead Wires are properly connected to the Electrodes
and that electrodes are not damaged and are making proper contact with treatment area.
B. Replace Lead Wires and Electrodes.
107
Bad Contact Quality
A. Make certain Electrodes are making proper contact with the treatment area.
B. Make certain Lead Wires are properly connected to Electrodes.
C. Replace Electrodes and Lead Wires.
108
Shorted Lead Wires
A. Check Electrodes and Lead Wires. Make certain Lead Wires are not damaged and are properly
connected to the system. Make certain Lead Wires are properly connected to the Electrodes
and that electrodes are not damaged and are making proper contact with treatment area.
B. Replace Lead Wires and Electrodes.
49
TROUBLESHOOTING
Intelect Transport® 2-Channel Electrotherapy
Error codes (continued)
In the event that an Error message or Warning appears on the LCD
beginning with a 2 or 3, immediately stop all use of the unit and contact
the dealer or DJO, LLC for service. Errors and Warnings in these categories
indicate an internal problem with the unit that must be tested by DJO,
LLC or a Field Service Technician certified by DJO, LLC before any further
operation or use of the system.
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 system.
50
ACCESSORIES
Intelect Transport® 2-Channel Electrotherapy
Standard Accessories
Ref.
Optional Accessories
Qty
Ref.
27376
Electrotherapy Accessory Kit- Includes the following:
Description
1
27312
Channel 1 Lead Wire
1
27313
Channel 2 Lead Wire
1
42044
2.75 in (7 cm) Round Disposable Electrodes (4 per pack)
1
27939
User Manual (CD-ROM)
1
27478
27467
10648
72852
72853
51
Description
NiMH Battery Pack
Intelect Transport 2 Channel Electrotherapy Carrying Bag
Nylatex® Wrap
3 in (8 cm) Round Carbon Electrodes-Black
3 in (8 cm) Round Carbon Electrodes-Red
MAINTENANCE
Intelect Transport® 2-Channel Electrotherapy
Maintaining THE UNIT
Factory Service
When the Intelect Transport 2-Channel Electrotherapy unit
requires factory service, contact the selling dealer or DJO, LLC Service
Department.
WARRANTY REPAIR/OUT OF WARRANTY REPAIR
All units returned to the factory for service must include the following:
1. Written statement containing the following information:
• RA (Return Authorization) Number- Obtain from Factory
• Model Number
• Serial Number
• Contact Person with Phone and Fax Numbers
• Billing Address (for Out of Warranty Repair)
• Shipping Address (Where to Ship Unit after Repair)
• Detailed Description of Problem or Symptoms
2. Copy of original invoice issued at purchase.
3. Ship the unit to address specified by an authorized service technician.
Service to these units should be performed only by Service
Technicians certified by DJO, LLC.
The Intelect Transport 2-Channel Electrotherapy unit Service Manual
is available for purchase and can be requested from the selling dealer
or DJO, LLC Service Department. The Service Manual contains safety
precautions, nomenclature, specifications, troubleshooting, removal
and replacement instructions, general maintenance, calibration
instructions, parts lists, schematics, warranty and other information
which would assist a certified service technician to repair the unit.
Cleaning the Unit and the Accessories
With the unit disconnected from the power source, clean the
unit with a clean, lint free cloth moistened with water and mild
antibacterial soap. If a more sterile cleaning is needed, use a cloth
moistened with an antimicrobial cleaner.
Do not submerse the unit in liquids. Should the unit accidentally
become submersed, contact the dealer or DJO, LLC Service
Department immediately. Do not attempt to use a unit that has
been wet inside until inspected and tested by a Service Technician
Certified by DJO, LLC.
To clean the Lead Wires, disconnect them from the unit and wipe
them down with a clean, lint free cloth moistened with water and
mild antibacterial soap.
To clean the reusable carbon electrodes, remove them from the
Lead Wires and wipe them down with isopropyl alcohol. Repeat this
procedure for the sponges as well.
EU Directive on Waste Electrical and Electronic Equipment
(WEEE) ensures that product is appropriately disposed of
or recycled at the end of its life.
52
WARRANTY
Intelect Transport® 2-Channel Electrotherapy
DJO, LLC, a division of Encore Medical, L.P. ("Company"), warrants that the Intelect Transport 2-Channel Electrotherapy unit ("Product") is free of defects in material and
workmanship. This warranty shall remain in effect for two years (24 months) from the date of original consumer purchase. If this Product fails to function during the two year
warranty period due to a defect in material or workmanship, at the Company's option, the 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 certofoed by the Company. Any modifications or repairs performed by unauthorized centers or groups will
void this warranty.
The warranty period for accessories is 90 days. Accessories include Lead Wires, Electrodes, and Nylatex®.
This warranty does not cover:
Replacement parts or labor furnished by anyone other than the Company, the selling dealer, or a service technician certified by the Company.
Defects or damage caused by labor furnished by someone other than Company, the selling dealer, or a certified Company service technician.
Any malfunction or failure in the Product caused by product misuse, including, but not limited to, the failure to provide reasonable and required 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:
DJO, LLC
1430 Decision St
Vista, CA 92081 USA
Phone: 1-800-592-7329 USA
Phone: 1-423-870-2281 or 1-317-406-2250
Fax: 1-317-406-2014 and
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.
53
Moving
Rehabilitation
Forward™
ISO 13485 Certified
DJO, LLC
1430 Decision St
Vista, CA 92081 USA
Phone: 1-800-592-7329 USA
Phone:1-423-870-2281 or
1-317-406-2250
Fax: 1-317-406-2014
chattgroup.com
© 2009 DJO, LLC
27937_C
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