Chattanooga Intelect Advanced Series User manual

User Manual
Operation Instructions for:
2774 - Vacuum Electrode Module with
Therapy System Cart
2785 - Vacuum Electrode Module
Moving
Rehabilitation
Forward™
!
Vacuum Electrode Module
DJO is an ISO 13485 Certified Company

Intelect®Advanced Vacuum Electrode Module
TABLE OF CONTENTS
Foreword. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Electrotherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-5
Precautionary Instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
Electrotherapy Indications, Contraindications and Adverse Effects . . . . . . . . . . . . . . .5
Nomenclature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-7
Intelect Advanced Vacuum Electrode Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
Symbol Definitions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7
Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8
System Set Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
Electrode and Patient Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-12
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Replacement Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15-16
Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

Intelect®Advanced Vacuum Electrode Module
1
FOREWORD
This manual has been written for the owners of an Intelect Advanced Vacuum Electrode Module. It contains general information on the
operation, precautionary practices and maintenance information. In order to maximize use, efficiency and the life of your system, please
read this manual thoroughly and become familiar with the controls as well as the accessories before operating the system with the
Vacuum.
This manual contains general safety, operating, maintenance and care instructions for the optional Two (2) Channel Vacuum Electrode
Module for the owners and operators of the Intelect Advanced Therapy Electrotherapy and Combination systems. Instructions for
additional options such as sEMG, sEMG + Electrical Stimulation, Laser, Battery and Two (2) Channel Electrotherapy Modules are found in
their respective User Manuals which contain operation and installation instructions.
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 Advanced Vacuum Electrode Module is a two channel (Channels 1 and 2) vacuum electrotherapy option that allows the
clinician to have available vacuum-applied electrodes for use in electrotherapy treatment sessions.
Stay current with the latest clinical developments in the field of electrotherapy. Observe all applicable precautionary measures for
treatment.
Keep informed on 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.
The Intelect Vacuum Electrode Module is not for sale in the United States of America.
© 2011 DJO, LLC. All rights reserved. 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.

Intelect®Advanced Vacuum Electrode Module
2
ELECTROTHERAPY
• Read, understand and practice the precautionary and operating
instructions. Know the limitations and hazards associated with using
any electrical stimulation device. Observe the precautionary and
operational decals placed on the unit.
• The Intelect Advanced Vacuum Electrode Module is designed to
operate only when properly installed in the Intelect Advanced
Therapy System Cart and properly connected to an Intelect
Advanced Therapy System.
• DO NOT operate the system in an environment of shortwave
diathermy use.
• DO NOT use sharp objects such as a pencil point or ballpoint pen to
operate the buttons on the control panel as damage may result.
• This unit should be operated, transported and stored in
temperatures between 15° C and 40° C (59° F and 104° F), with
Relative Humidity ranging from 30%-60%.
• Before each use, inspect Vacuum Electrode Cups and Lead Hoses
for cracks and damage which may not allow the vacuum to properly
secure the electrodes.
• The Intelect Advanced Vacuum Electrode Module 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.
• Drain the Vacuum Electrode Module water reservoir regularly to
prevent excessive accumulation from electrode sponge water.
• Periodic flushing of the system and reservoir are required to
maintain Factory functionality of the Vacuum Electrode Module.
Refer to the Maintenance Section of this manual for proper instructions.
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 “WARNING”indicator will explain possible Safety infractions
that will potentially cause serious injury and equipment damage.
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.
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 definition of these
symbols are as follows:
DANGEROUS VOLTAGE
Text with a “DANGEROUS VOLTAGE” indicator serves to inform the
user of possible hazards resulting in the electrical charge delivered to
the patient in certain treatment configurations of TENS waveforms.

Intelect®Advanced Vacuum Electrode Module
3
ELECTROTHERAPY
• This equipment generates, uses and can radiate radio frequency energy
and, if not installed and used in accordance with the instructions,
may cause harmful interference to other devices in the vicinity.
However, there is no guarantee that interference will not occur in a
particular installation. Harmful interference to other devices can be
determined by turning this equipment on and off. Try to correct the
interference using one or more of the following: reorient or relocate
the receiving device, increase the separation between the equipment,
connect the equipment to an outlet on a different circuit from that to
which the other device(s) are connected and/or consult the factory
field service technician for help.
• This device should be used only under the continued supervision
of a 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.
• This device should be kept away from children.
• Care must be taken when operating this equipment around other
equipment. Potential electromagnetic or other interference could
occur to this or to the other equipment. Try to minimize this
interference by not using other equipment in conjunction with it.
• Powered muscle stimulators should be used only with the leads
and electrodes recommended for use by the manufacturer.
Precautionary Instructions (continued)
• Before administering any treatment to a patient, 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, inflamed areas
or skin eruptions, e.g., phlebitis, thrombophlebitis, varicose veins, etc.
• Stimulation should not be applied over, or in proximity to, cancerous
lesions.
• Output current density is 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.
• Vacuum electrodes should not be used on patients with thin, papery
skin. Vacuum may lead to contact difficulty and bruising.
• Vacuum electrodes are not suitable for patients who are taking
steroids due to the likelihood of bruising.

Intelect®Advanced Vacuum Electrode Module
4
ELECTROTHERAPY
• Stimulus delivered by the TENS waveforms of this device,
in certain configurations, will deliver a charge of 25
microcoulombs (µC) or greater per pulse and may be
sufficient to cause electrocution. Electrical current of this
magnitude must not flow through the thorax because it
may cause a cardiac arrhythmia.
• In the event that an Error message or Warning beginning with a 2 or
3 appears, immediately stop all use of the system and contact the
dealer or DJO for service. Errors and Warnings in these categories
indicate an internal problem with the system that must be tested
by DJO or a Field Service Technician certified by DJO before any fur-
ther operation or use of the system. Use of a system that indicates an
Error or Warning in these categories may pose a risk of injury
to the patient, user or extensive internal damage to the system.
Precautionary Instructions (continued)
• The safety of TENS waveforms for use during pregnancy or birth
has not been established.
• TENS is not effective for pain of central origin. This includes
headache.
• TENS should be used only under the continued supervision of a
physician.
• TENS waveforms have no curative value.
• TENS is a symptomatic treatment and as such suppresses the
sensation of pain which would otherwise serve as a protective
mechanism.
• The user must keep the device out of the reach of children.
• Electronic monitoring equipment (such as ECG monitors and ECG
alarms) may not operate properly when TENS stimulation is in use.

Intelect®Advanced Vacuum Electrode Module
5
ELECTROTHERAPY
Electrotherapy Indications, Contraindications and Adverse Effects
Indications for VMS™, VMS™ Burst, Russian, TENS,
High Voltage Pulsed Current (HVPC), Interferential, and
Premodulated waveforms
• Relaxation of muscle spasms
• Prevention or retardation of disuse atrophy
• Increase local blood circulation
• Muscle re-education
•Maintaining or increasing range of motion
Additional Indications for Microcurrent, Interferential, Premodulated,
VMS™, VMS™ Burst, and TENS waveforms
•Symptomatic relief of management of chronic, intractable pain
•Post-traumatic acute pain
•Post-surgical acute pain
Indications for Galvanic Continuous Mode
•Relaxation of muscle spasm
Contraindications
•This device should not be used for symptomatic local pain relief unless
etiology is established or unless a pain syndrome has been diagnosed.
•This device should not be used when cancerous lesions are present in the
treatment area.
•This device should not be used when open wounds are present in the
treatment area.
•Other contraindications are patients suspected of carrying serious
infectious disease and or disease where it is advisable, for general medical
purposes, to suppress heat or fevers.
•Electrode placements must be avoided that apply current to the carotid
sinus region (anterior neck) or transcereberally (through the head).
•Safety has not been established for the use of therapeutic electrical
stimulation during pregnancy.
•Powered muscle stimulators should not be used on patients with cardiac
demand pacemakers.
•There should not be any use of TENS waveforms on patients with cardiac
demand pacemakers.
Additional Precautions
•Caution should be used for patients with suspected or diagnosed heart
problems.
•Caution should be used for patients with suspected or diagnosed epilepsy.
•Caution should be used in the presence of the following: When there is a
tendency to hemorrhage following acute trauma or fracture; following recent
surgical procedures when muscle contraction may disrupt the healing
process; over a menstruating or pregnant uterus; over areas of the skin
which lack normal sensation.
•Some patients may experience skin irritation or hypersensitivity due to the
electrical stimulation or electrical conductive medium. The irritation can
usually be reduced by using an alternative conductive medium or an
alternative electrode placement.
•Electrode placement and stimulation settings should be based on the
guidance of the prescribing practitioner.
•Powered muscle stimulators should be used only with the lead wires and
electrodes recommended for use by the manufacturer.
•With TENS waveforms, isolated cases of skin irritation may occur at the site
of electrode placement following long-term application.
•The effectiveness of TENS waveforms is highly dependent upon patient
selection by a person qualified in the management of pain patients.
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.

Intelect®Advanced Vacuum Electrode Module
6
NOMENCLATURE
Intelect Advanced Vacuum Electrode Module
12
4
5
3
6
7
8
1. Exhaust/Overflow Hose (Routes to bottom of Therapy System Cart)
2. Vacuum Module to Intelect Advanced Therapy System Leads
3. Vacuum LED Indicators
4. Vacuum Mode Selector Button
5. Vacuum Intensity Knob
6. Channel 1 and 2 Lead Wire Connectors
7. Reservoir Drain Hose (Routes into Cart Storage Bin below Vacuum)
8. Channel 1 Vacuum Lead Hose Connectors (Channel 3 a second
Vacuum Electrode Module).
9. Channel 2 Vacuum Lead Hose Connectors (Channel 4 a second
Vacuum Electrode Module).
10. Vacuum Main Power Switch
NOTE:
The Intelect Advanced Vacuum Electrode Module is shown out of the
Therapy System Cart for component clarification only. The Intelect
Advanced Vacuum Electrode Module is not operable outside of the
Therapy System Cart and must be properly connected to the Intelect
Advanced Therapy System.
A second Intelect Vacuum Electrode Module may be installed for
Intelect Advanced Therapy Systems with the optional Two Channel
Electrotherapy Module installed. This would allow the application of
vacuum electrodes on all four channels simultaneously.
9
10

Intelect®Advanced Vacuum Electrode Module
7
Intelect Advanced Optional Module
and Accessory Symbols
NOMENCLATURE
Symbol Definitions
Below are the definitions for all of the symbols used on the Intelect Advanced hardware and symbols used within the software. Study and learn these
symbols before any operation system.
Contrast
Contro
lOn/Off
Switch
Data
Port
Multimedia
and Patient
Data Card
Stop
Treatment
Pause
Treatment
Start
Treatment
System Hardware Symbols System
Software Symbols
Move
Therapy
Intensity
Control
Channel 1/2
Operator
Remote
Control
(Optional)
Patient
Interrupt
Switch
Channel 1
Lead Wires
Channel 2
Lead Wires
Microcurrent
Probe
Ultrasound
Applicator
Home
Clinical
Resources
Back
UP
Move
DOWN
Move
RIGHT
Move
LEFT
Accept
and
Return
Do not
Accept
and
Return
M
Increase
Intensity
Decrease
Intensity
Pause
Treatment
Manual
Stim
Operator
Remote
Channel 3
Lead Wires
Channel 4
Lead Wires
Microcurrent
Probe
Two (2) Channel
Electrotherapy
Module
Battery
Module
Charge Level
Battery
Charging
Channel 3/4
Operator
Remote
Control
(Optional)
Type B Rating
(Stim Only) Type B Rating
(Stim Only)
Patient
Interrupt
Switch
Vacuum
Electrode
Module
Vacuum
Hoses
& Cups
Lead
Wires
Vacuum
On/Off
Switch
Continuous
Vacuum
1.65 Sec On
0.35 Sec Off
Vacuum
0.75 Sec On
0.25 Off
Vacuum
Intelect Advanced Therapy System Symbols
Type BF
Rating
Type BF
Rating

Intelect®Advanced Vacuum Electrode Module
8
SPECIFICATIONS
Vacuum Electrode Module Specifications
DEPTH
HEIGHT
NOTE:
All waveforms available on the Intelect Advanced Therapy System are
available to the Intelect Advanced Vacuum Electrode Module. Refer to
the Intelect Advanced User Manual, part number 27429, for Waveform
Specifications, precautions and set up instructions.
WIDTH
DIMENSIONS
Width. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .22.7 cm (8.9375”)
Depth . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13.3 cm (5.25”)
Height. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23.5 cm (9.25”)
Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2.8 kg (6.265 lbs)
Shipping Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.2 kg (7.0 lbs)
Vacuum . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 - 600 mbar maximum
0 - 17.7 inches mercury maximum
Vacuum Type
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Continuous
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1.65 seconds On/0.35 seconds Off
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.75 seconds On/0.25 seconds Off
Power
Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100 - 240V - 1.0A, 50/60 Hz
Output . . . . . . . . . . . . . . . . . . . . . . . .Intelect Advanced Therapy System dependent
Electrical Class . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CLASS I
Electrical Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .TYPE BF

Intelect®Advanced Vacuum Electrode Module
9
SYSTEM SETUP
Intelect Advanced Vacuum Electrode Module
Remove the Intelect Advanced Therapy System Cart with Vacuum Electrode
Module and all accessories from shipping cartons. Visually inspect for
damage. Report any damage to the carrier.
Standard Accessories
Power Cords (Select One)
Vacuum Electrode Module Setup
The Intelect Vacuum Electrode Module is designed to function with the
Intelect Advanced Therapy System only. The following setup instructions
apply to the connection of the Vacuum to System Leads for integration of
the Vacuum Module with the Intelect Advanced Therapy Systems.
Installation of the Intelect Advanced Vacuum Electrode Module into the
Therapy System Cart must be performed by the Dealer or a Service
Technician certified by DJO.
Connecting Vacuum to System Leads
Remove the Front Access Cover of the
Intelect Advanced Therapy System.
Connect the respective Vacuum to
System Leads to Channels 1 and 2.
NOTE:
If connecting to a four channel
Intelect Advanced Therapy System, it
is recommended that the vacuum to
system leads be connected to channels
1 and 2.
Replace the Intelect Advanced Therapy
System Front Access Cover. CHANNELS 1 and 2 LEAD
WIRE CONNECTORS
Part No. Country Qty
21284 Euro 1
78121 US 1
20971 Australian 1
20972 Swiss 1
20973 UK 1
20974 Danish 1
20975 Japanese 1
20976 Indian 1
20977 Israeli 1
Part No. Description QTY
2774 Intelect Advanced Therapy System Cart with
Vacuum Electrode Module 1
2785 Intelect Advanced Vacuum Electrode Module (Module Only) 1
27745 Vacuum Lead Hose, Channel 1 (Black) 2
27746 Vacuum Lead Hose, Channel 2 (Grey) 2
56582 60 mm Vacuum Electrodes 4
56806 60 mm Electrode Sponges 4
27458 User Manual (CD-ROM) 1

Intelect®Advanced Vacuum Electrode Module
10
ELECTRODE & PATIENT PREPARATION
Vacuum Electrode Instructions
DJO Vacuum Electrodes are designed specifically for use with the Intelect
Advanced Vacuum Electrode Module for optimum efficiency and performance
of the Intelect Advanced Therapy System. These electrodes are multi-
use when properly maintained and cleaned. The associated sponges are
recommended for single patient use only and should be cleaned with a 70%
alcohol solution before and after each therapy session.
Size of Vacuum Electrodes
Refer to the Intelect Advanced Therapy System User Manual, part number
27429, for waveform setup and parameter changes.
View the Electrode Placement recommendations in the Treatment Review
Screen of the Intelect Advanced Therapy System for the particular modality
being used for treatment as a reference point only, prior to administering
treatment.
Select the prescribed Vacuum Electrode
size and install one to the opposite end
of each Vacuum lead hose.
Using cleaned sponges, liberally
wet the respective sponges for the
electrode size being used with distilled
water. Squeeze out the excess water.
Place one sponge inside each Vacuum
electrode cup.
Turn the Vacuum Module on with
Power Switch.
Select Vacuum Mode: Continuous, 1.65
second On - 0.35 Off or 0.25 Second
On - 0.75 Second Off.
With the Vacuum Electrodes placed
face down on a clean, firm surface,
increase the intensity of the Vacuum
with the Vacuum Intensity Knob until
the electrodes are secure on the
surface.
Individually remove each electrode from
the surface and place on the treatment
area of the patient as prescribed.
NOTE:
Adjust Vacuum intensity until electrodes
are secure to patient.
Connecting Lead Hoses
Insert the red lead hose to the positive
(+) lead hose connector for the channel
desired on the Vacuum Module.
Connect the other lead hose to the
negative (-) lead hose connector on the
Vacuum Module.
NOTE:
If only using one channel, place the
vacuum connector covers on the
channel not being used to prevent
vacuum leakage during therapy session.

Intelect®Advanced Vacuum Electrode Module
11
OPERATION
Vacuum Electrode Module
Use the following instructions in conjunction with the Intelect Advanced
User Manual, part number 27429, when setting waveform parameters.
NOTE:
Use of sEMG, sEMG + Electrical Stimulation or Combination Therapy is not
possible through the Channel 1 and 2 Lead Wire Connectors on the Vacuum
Electrode Module. To perform sEMG, sEMG + Electrical Stimulation or
Combination Therapy, it will be necessary to connect the respective Lead
Wires directly to the Intelect Advanced Therapy System and not to the
Vacuum Electrode Module.
Turning Vacuum Module ON and OFF
The Intelect Advanced Vacuum
Electrode Module incorporates an
independent Main On/Off Switch
located on the lower left corner of the
module.
NOTE:
It is not necessary for the Vacuum
Module to be turned On if only the
Intelect Advanced Therapy System is
being used to administer therapy.
These instructions also apply to the
operation of a second Intelect Advanced
Vacuum Electrode Module installed on
a single four channel Intelect Advanced
Therapy System.
Adjusting Vacuum Intensity
Perform Electrode & Patient Preparation
as described on page 10.
Adjust Vacuum Intensity by rotating the
Vacuum Intensity Knob from 1 to 10 on
the dial as desired to secure electrodes
to patient.
Selecting Vacuum Mode
The Intelect Advanced Vacuum
Electrode Module allows for
Continuous, 1.65 second On - 0.35 Off
or 0.25 Second On - 0.75 Second Off.
Modes. To select, press the Vacuum
Mode button until the LED for the
desired mode is illuminated.
Using Lead Wire Connectors
Rotate the Vacuum Intensity Knob
completely counterclockwise. Connect
the Intelect Advanced Therapy System
Lead Wires to the Channel 1 & 2 Lead
wire connector on the Vacuum Module.
NOTE:
It will be necessary to connect the lead
wires for standard electrotherapy and
combination therapy sessions.

Intelect®Advanced Vacuum Electrode Module
12
OPERATION
Vacuum Electrode Module (continued)
Setting up Waveform Parameters
No waveform parameters or selections
can be made with the Vacuum Module.
Refer to the Intelect Advanced Therapy
System User Manual, part number
27429, for all waveform selection and
parameter setting instructions.
NOTE:
Combination Therapy, sEMG and
sEMG + Electrical Stimulation
Therapy cannot be administered
using the Intelect Advanced Vacuum
Electrode Module. These modalities
are administered using the Intelect
Advanced Therapy System only. Refer to
the Intelect Advanced Therapy System
User Manual, part number 27429.

Intelect®Advanced Vacuum Electrode Module
13
TROUBLESHOOTING
General Information
The Intelect Advanced Therapy Systems incorporate Error Messages and Warnings to inform the user of problems or potential problems with the system,
modality or accessories. Refer to the Intelect Advanced Therapy System User Manual, part number 27429 for all Error Message Troubleshooting of the Intelect
Advanced Therapy System. The Troubleshooting information below is related to the Intelect Advanced Vacuum Electrode Module only.
PROBLEM PROBABLE CAUSE POSSIBLE REMEDY
Vacuum stops and all three vacuum mode LED’s are
flashing.
Reservoir full. Drain Reservoir. Refer to Maintenance section of this
manual.
Vacuum stops running and no LED’s are flashing. Primary Reservoir Sensor faulty. Contact dealer or DJO for service.
Vacuum not efficient. Electrodes not secure to patient. Lead Hoses and/or Electrode Cups worn or damaged. Replace Lead Hoses and/or Electrode Cups.

Intelect®Advanced Vacuum Electrode Module
14
REPLACEMENT ACCESSORIES
General Information
The following provides users of Intelect Advanced Therapy System with Vacuum Electrode Module, the necessary information to order the replacement
accessories most commonly used with the system. This list of replacement accessories are designed for use with the Intelect Advanced Vacuum Electrode
Module. When ordering, provide the respective part number, description and quantity desired.
Part Number Description Qty Req’d
27745 Vacuum Lead Hose, Channel 1/3 (Black) 1
27746 Vacuum Lead Hose, Channel 2/4 (Grey) 1
56852 60 mm Electrodes 4
56806 60 mm Electrode Sponges 4
27657 30 mm Electrodes 4
27658 30 mm Electrode Sponges 4
56851 90 mm Electrodes 4
56854 90 mm Electrode Sponges 4
27312 Electrotherapy Lead Wire- Channel 1 1
27313 Electrotherapy Lead Wire- Channel 2 1
42044 Dura-Stick™ 2.75” (7 cm) Electrodes 40/case
79967 6 cm X 8 cm Carbon Electrodes 4
79970 6 cm X 8 cm Electrode Sponges 4
2775 Therapy System Cart 1
27729 Power Distribution Block 1

Intelect®Advanced Vacuum Electrode Module
15
MAINTENANCE
Vacuum Module Cleaning
With the system disconnected from the power source, clean the
vacuum module 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 vacuum module in liquids. Should the vacuum
module accidentally become submersed, contact the dealer or DJO Service
Department immediately. Do not attempt to use a vacuum module that
has been wet inside until inspected and tested by a Service Technician
certified by DJO.
Cleaning the Vacuum Module
Reservoir Draining
Open the storage bin beneath the
vacuum module to access the Reservoir
Drain Tube. Wearing surgical type
gloves, place a cup with a minimum
capacity of 250 ml (8 fl oz) beneath the
drain tube.
Pull Drain Tube from plug and allow all
liquid to drain into cup.
After draining is complete, reinstall
Drain Tube to plug.
NOTE:
If Drain Tube is not reinstalled onto the
plug the vacuum will not work properly.
Dispose of reservoir contents according
to national, state and local rules and
regulations.
To re-start the Vacuum Module after
draining reservoir, rotate the Vacuum
Intensity Knob counterclockwise until
Vacuum Pump stops then, reset to the
desired vacuum intensity.

Intelect®Advanced Vacuum Electrode Module
16
MAINTENANCE
Service
Should the unit require service, warranty, or repair, please contact
the selling dealer or your local DJO customer service.
WARRANTY
Flushing Lead Hoses and Reservoir
Connect all four lead hoses to the
Vacuum Module.
Submerse the other end of the lead
hoses into a container filled with at
least 250 ml (8 fl oz) of hot water with
one drop of dishwashing detergent
added.
Turn Vacuum Module On and set
Vacuum Intensity to maximum.
When the Vacuum Module stops and
the three Vacuum Mode LED’s are
flashing, perform the Reservoir Drain
Procedure on page 15.
Repeat this procedure until no particles
are visible when the reservoir is
drained.
Dispose of reservoir contents according
to national, state and local rules and
regulations.

Intelect®Advanced Vacuum Electrode Module
17
DJO, LLC ("Company") warrants that the Intelect Advanced Vacuum Electrode Module ("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, 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 accessories is 180 days. Accessories include Lead Hoses and Vacuum Electrodes.
This Warranty does not cover:
Replacement parts or labor furnished by anyone other than the Company, the selling dealer or a certified Company service technician.
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's Manual.
DJO, LLC is not responsible for injury or damage resulting from modifications or service performed by non-authorized DJO, LLC service personnel.
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.
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 representative 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.
WARRANTY

27455_H Vacuum (English)
DJO is an ISO 13485 Certied Company
DJO France SAS
Centre Europeen de Fret
3 rue de Bethar
64990 Mouguerre, France
T: + 33 (0) 5 59 52 86 90
F: + 33 (0) 5 59 52 86 91
djoglobal.eu/fr_FR
© 2011 DJO, LLC. All rights reserved.