Chattanooga Fluidotherapy Series User manual

Dry Heat Therapy Units
Models:
FLU110D
FLU110DE
FLU115D
FLU115DE
ISO 13485 Certified
User Manual

i
Operation ....................................................................................24
Patient Preparation ..................................................24
Starting Treatment ...................................................24
Stopping Treatment.................................................24
Preventive Maintenance ................................................25-32
Daily Maintenance.................................................... 25
Weekly Maintenance ........................................26-29
ADDITIONAL FLUIDOTHERAPY PREVENTIVE
MAINTENANCE REQUIREMENTS
Quarterly ......................................................................30
Bi-Annual .....................................................................30
Annual........................................................................... 30
As Needed ...................................................................30
Fluidotherapy Maintenance Record .................. 31
Cleaning ....................................................................... 32
Service ..........................................................................32
Accessories..................................................................................33
Replacement Accessories ......................................33
Warranty ...................................................................................... 34
Foreword....................................................................................... 1
About Dry Heat Therapy.........................................2-5
Precautionary Instructions ................................. 2-4
Description of Device Markings ........................... 2
Indications & Contraindications........................... 5
Nomenclature......................................................................... 6-8
FLU110D & FLU110DE Unit
Familiarization............................................................. 6
FLU115D & FLU115DE Unit
Familiarization............................................................. 7
Operating Controls.................................................... 8
Specifications.........................................................9-14
FLU110D & FLU110DE.............................................. 9
FLU115D & FLU115DE............................................10
Electromagnetic Compatibility Tables ........ 11-14
Setup ..................................................................................... 15-23
Treatment Mode Parameters........................ 15-17
Time Controlled Parameters................................18
Preference Mode Default Parameters.......... 18-23
©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.
TABLE OF CONTENTS Fluidotherapy® - Dry Heat Therapy

1
Thank you for purchasing a Fluidotherapy Dry Heat Therapy Unit.
This manual contains general safety, operating, maintenance, and care instructions for the owners and operators of the
Fluidotherapy Dry Heat Therapy Units.
The specifications put forth in this manual were in effect at the time of the publication. However, owing to DJO, LLC's
policy of continuous improvement, changes to these specifications may be made at any time without obligation on the
part of DJO, LLC.
Read, understand, and follow the information contained in this manual.
Stay current with the latest clinical developments in the field of Dry Heat Therapy and observe all applicable
precautionary measures for treatment.
Keep informed on appropriate indications and contraindications for the use of Dry Heat Therapy.
This equipment is to be used only under the prescription and supervision of a licensed practitioner.
FOREWORD
1
Fluidotherapy® - Dry Heat Therapy

2
ABOUT DRY HEAT THERAPY
PRECAUTIONARY INSTRUCTIONS
The precautionary instructions found in this section and throughout
this manual are indicated by specific symbols. Understand these
symbols and their definitions before operating this equipment. The
definitions of these symbols are as follows:
= CAUTION - Text with a “CAUTION” indicator will explain
possible safety infractions that could have the potential to
cause minor to moderate injury or damage to equipment.
= WARNING - Text with a “WARNING” indicator will explain
possible safety infractions that will potentially cause serious
injury and equipment damage.
= DANGER - Text with a “DANGER” indicator will explain
possible safety infractions that are imminently hazardous
situations that would result in death or serious injury.
= EXPLOSION HAZARD - Text with an “Explosion Hazard”
indicator will explain possible safety infractions if this
equipment is used in the presence of flammable anesthetics.
= NON-IONIZING ELECTROMAGNETIC RADIATION - Text with a
Non-Ionizing Electromagnetic Radiation" indicator informs
the user of possible hazards resulting from elevated,
potentially dangerous, levels of non-ionizing radiation.
= Protective Earth (ground)
NOTE: Helpful information marked as "NOTE" may be found
throughout this manual. Each "NOTE" is beneficial in the aid of
a particular area or function being described for this product.
Fluidotherapy® - Dry Heat Therapy
DESCRIPTION OF DEVICE MARKINGS
Degree of Protection Against Electrical Shock ...........................
Complies with UL 2601-1 CSA C22.2 No. 601.1
Medical Electrical Equipment ............ ..............................................
Refer to Instruction Manual/Booklet .............................................

3
Read, understand, and practice the precautionary and operating•
instructions found in this manual. Know the limitations and hazards
associated with using any electrical device. Observe the precautionary
and operational decals placed on the unit.
DO NOT operate this unit in an environment where other devices
•
are being used that intentionally radiate electromagnetic energy in
an unshielded manner. Medical Electrical Equipment needs special
precautions regarding EMC and needs to be installed and put into
service according to the EMC information provided in this manual.
Portable and Mobile RF Communications equipment can affect Medical
•
Electrical Equipment.
This unit 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 unit 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 which the other device(s) are connected
and consult the DJO, LLC Service Department for help.
Clean Inlet Filter(s) daily before unit startup.
•
Turn unit OFF before positioning a patient or removing a patient from•
the unit.
Place the patient in a comfortable position allowing for correct
•
placement of the limb being treated.
Secure all entry ports before turning the unit ON.
•
Use only Cellex® Dry Heat Medium in the Fluidotherapy units.•
Refill unit daily to proper fill level with Chattanooga Cellex Dry Heat•
Medium.
ABOUT DRY HEAT THERAPY
Use only fingers to operate button controls on the control panel(s). Use of sharp•
objects such as pencils or pens will result in damage to the unit.
Check unit temperature before treating patient to ensure correct temperature.•
This unit should be transported and stored in temperatures between -40 °F and•
158 °F (-40 °C and -70 °C) with Relative Humidity between 10% - 100% to prevent
damage to the unit or its components.
This unit should be operated in temperatures between 110 °F and 125 °F (43 °C and•
52 °C) to prevent damage to the unit or its components.
DO NOT operate the unit when connected to any unit other than Chattanooga•
devices.
Change Cellex Dry Heat Medium every six (6) months.•
Do not use accessories other than those supplied with the unit, or recommended•
by DJO, LLC. The safety of other products has not been established, and their use
could result in injury to the patient.
Fluidotherapy® - Dry Heat Therapy

4
ABOUT DRY HEAT THERAPY Fluidotherapy® - Dry Heat Therapy
Perform all Preventive Maintenance as described in this manual. Failure to perform•
the Preventive Maintenance could result in the Cellex medium entering the heat
chamber of the unit and cause severe injury to patients as well as smoke damage
to the facility and the Fluidotherapy unit.
The solvents of adhesives and flammable solutions used for cleaning and•
disinfecting the unit should be allowed to evaporate before the unit is used.
Federal law restricts this device to sale by, or on the order of, a physician or licensed•
practitioner. This device should be used only under the continued supervision of a
physician or licensed practitioner.
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.
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 Dry Heat Therapy.
The Fluidotherapy Dry Heat Therapy Unit should not be used adjacent to or stacked•
with other equipment. If adjacent or stacked use is necessary, the Fluidotherapy Dry
Heat Therapy Unit should be observed to verify normal operation in the configuration
in which it will be used.
For continued protection against fire hazard, replace fuses only with ones of the•
same type and rating.
This device should be kept away from children.•
To prevent electrical shock, disconnect the unit from the power source before•
attempting any maintenance procedures.
Use only processed dry heat medium in the unit such as Cellex to prevent excessive•
dusting.
Use only accessories that are specially designed for this• unit. Do not use accessories
manufactured by other companies on this unit. DJO, LLC is not responsible for any
consequence resulting from using products manufactured by other companies. The use
of other accessories or cables may result in increased emissions or decreased immunity
of this unit.
Dispose of all products in accordance with local and national regulations and codes.•
Fluidotherapy equipment not in use should be protected against unqualified use.•
The Fluidotherapy Dry Heat Therapy Unit is not suitable in the•
presence of a flammable anesthetic mixture with air, oxygen, or nitrous
oxide.

55
Indications & Contraindications
Indications
• Relief of local pain
• Treatment of local blood flow insufficiency
• Treatment in range of motion when combined with exercise
• Treatment for symptoms of non-rheumatoid arthritis
Contraindications
• This device should not be used for symptomatic pain relief unless
etiology is established or unless a pain syndrome has been
diagnosed.
• This device should not be used when cancerous lesions or open
wounds are present in the treatment area.
• Other counterindications are patients suspected of carrying
serious infectious disease or disease where it is advisable, for
general medical purposes, to suppress heat or fevers.
Adequate precautions should be taken when treating individuals•
with suspected or diagnosed medical conditions or diseases such as
heart problems, epilepsy, diabetes, etc.
Prior to treatment, consult a medical professional familiar with the•
precautionary measures to be taken for patients that may experience
allergic reactions to dust and pollen.
ABOUT DRY HEAT THERAPY Fluidotherapy® - Dry Heat Therapy

6
Fluidotherapy® - Dry Heat Therapy
NOMENCLATURE
FLU110D & 110DE Unit Familiarization
1. RESERVOIR LID & TREATMENT VIEWING WINDOW
Access to add/change medium, view patient treatment, and
clinician access to patient treatment area
2. MEDIUM/TREATMENT RESERVOIR
Treatment access and medium reservoir
3. HAND/ARM ACCESS PORT
Treatment port for Hand/Arm Treatment (end of unit)
4. REPLACEABLE INLET FILTERS
Filters room air entering the Fluidotherapy unit (1 each side)
5. FOUR POINT BASE
Casters included to convert to a Mobile Base
6. BLOWER HOUSING
Houses Blower & Heater
7. CONTROL PANEL
See page 8 for detailed description of controls
8. ELBOW/FOOT TREATMENT ACCESS PORT
Treatment port for Elbow and Foot
1
2
4
5
6
7
8
3

77
Fluidotherapy® - Dry Heat Therapy
NOMENCLATURE
FLU115D & FLU115DE Unit Familiarization
1. ELBOW/FOOT ACCESS PORT
Treatment port for Elbow and Foot Treatment, access to add/
change medium, clinician access to patient treatment area
2. HAND/ARM ACCESS PORTS
Treatment ports for Hand/Arm Treatment (end of unit)
3. INLET FILTERS
Filters room air entering the Fluidotherapy unit (1 each side)
4. MEDIUM/TREATMENT TUB
Treatment access and medium reservoir
5. MOBILE BASE
6. LOCKING CASTERS
7. BLOWER HOUSING
Houses Blower & Heater
8. CONTROL PANEL
See page 8 for detailed description of controls
1
3
4
5
6
7
8
2

8
Fluidotherapy® - Dry Heat Therapy
NOMENCLATURE
Operating Controls (All Units)
1. DISPLAY
Displays Treatment Time, Temperature, Airspeed, Pulse Time,
Preheat Timer, and Clock when the respective Mode is indicated
2. PREHEAT TIMER ON
Indicator light for Preheat Timer
3. INCREASE/HOUR
Use to increase Mode parameters and use to set the Hour when
setting Clock
4. DECREASE/MINUTE
Use to decrease Mode parameters and use to set the Minutes
when setting Clock
5. STOP
Use to stop treatment and Preheat Timer
6. MOTOR FUSE
7. START
Use to start treatment
8. INDICATOR BAR
Indicates Mode as they are chosen
9. HEATER FUSE
10. PREHEAT TIMER BUTTON
Press once to turn Preheat Timer On. Press twice to start
Preheat function.
11. MODE SELECT
Use to select desired Mode
12. PM
PM indicator for Clock
123
4
5
6
78
9
10
12
11

99
Fluidotherapy® - Dry Heat Therapy
SPECIFICATIONS
FLU110D & FLU110DE
MODES OF OPERATION
Continuous (Default)
Variable Adjustments for Time, Temp, and Air Speed
Pulse Mode.....................................................................OFF to 6 Sec ON/OFF
TREATMENT TIME........................................................................1 to 99 minutes
OPERATING TEMPERATURE...............................110 °F (43.3 °C) to 125 °F (51.6 °C)
AIR SPEED.............................................................0% to 100% (5% increments)
PREHEAT TIMER........................................115 °F (46.1 °C) with 50% Air Flow
MEDIUM CAPACITY.........................................Approximately 30 lb (13.6 kg)
INPUT POWER (FLU110D)..............................................120V, 50/60 Hz, 12A
INPUT POWER (FLU110DE).....................................230-240V, 50/60 Hz, 8A
PHYSICAL DIMENSIONS
Cabinet Length..........................................................................34.0” (86.4 cm)
Cabinet Width............................................................................11.5” (29.2 cm)
Height............................................................................................33.0” (83.8 cm)
Weight...............................................................70 lbs (31.7 kg) Less Medium
Shipping Weight....................................................................100 lbs (45.4 kg)
DEGREE OF PROTECTION AGAINST INGRESS OF WATER...............IPX0
ELECTRICAL CLASS.....................................................................................CLASS I
DEGREE OF PROTECTION AGAINST ELECTRICAL SHOCK......TYPE B
POWER CORD......................................2 meter cable length, 14 AWG, shielded
Length
Height
Width 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.

10
Fluidotherapy® - Dry Heat Therapy
SPECIFICATIONS
FLU115D & FLU115DE
MODES OF OPERATION
Continuous (Default)
Variable Adjustments for Time, Temp, and Air Speed
Pulse Mode.....................................................................OFF to 6 Sec ON/OFF
TREATMENT TIME........................................................................1 to 99 minutes
OPERATING TEMPERATURE..............................110 °F (43.3 °C) to 125 °F (51.6 °C)
AIR SPEED.............................................................0% to 100% (5% increments)
PREHEAT TIMER........................................115 °F (46.1 °C) with 50% Air Flow
MEDIUM CAPACITY.......................................Approximately 40 lbs (18.1 kg)
INPUT POWER (FLU115D)...............................................120V, 50/60 Hz, 12A
INPUT POWER (FLU115DE)...................................230-240V, 50/60 Hz, 10A
PHYSICAL DIMENSIONS
Cabinet Length..........................................................................34.0” (86.4 cm)
Cabinet Width.............................................................................18.5” (47.0 cm)
Height.............................................................................................33.0” (83.8 cm)
Weight................................................................60 lbs (27.2kg) Less Medium
Shipping Weight....................................................................100 lbs (45.4 kg)
DEGREE OF PROTECTION AGAINST INGRESS OF WATER. ..............IPX0
ELECTRICAL CLASS.....................................................................................CLASS I
DEGREE OF PROCTECTION AGAINST ELECTRICAL SHOCK....TYPE B
POWER CORD......................................2 meter cable length, 14 AWG, shielded
Height
Length
Width
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.

11
TABLE 1: GUIDANCE AND MANUFACTURER'S DECLARATION - ELECTROMAGNETIC EMISSIONS
SPECIFICATIONS
ELECTROMAGNETIC COMPATIBILITY (EMC) TABLES
Emission Tests Compliance Electromagnetic Environment - Guidance
RF Emissions
CISPR 11 Group 1
The Fluidotherapy - Dry Heat Therapy Unit uses RF energy only for its internal function.Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF Emissions
CISPR 11 Class A
The Fluidotherapy - Dry Heat Therapy Unit is suitable for use in all establishments, including domestic establishments and those directly connected
to the public low-voltage power supply network that supplies buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2 Class A
Voltage fluctuations
IEC 61000-3-3 Complies
The Fluidotherapy - Dry Heat Therapy Unit is intended for use in the electromagnetic environment specified in the table below. The user
of the Fluidotherapy - Dry Heat Therapy Unit should assure that it is used in such an environment.
Fluidotherapy® - Dry Heat Therapy

12
SPECIFICATIONS
ELECTROMAGNETIC COMPATIBILITY (EMC) TABLES (CONTINUED)
TABLE 2 & 3: GUIDANCE AND MANUFACTURER'S DECLARATION - ELECTROMAGNETIC IMMUNITY
The Fluidotherapy - Dry Heat Therapy Unit is intended for use in the electromagnetic environment specified in the table below. The user of the
Fluidotherapy - Dry Heat Therapy Unit should assure that it is used in such an environment.
Immunity
Test
IEC 60601
Test Level Compliance Level Electromagnetic Environment - Guidance
Portable and mobile RF communications equipment should be used no closer to any part of the Fluidotherapy - Dry Heat Therapy Unit,
including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.
Recommended separation distance:
Conducted RF
IEC 61000-4-6
3Vrms
150 kHz to 80 MHz 3 V d = [3.5]√P
V1
Radiated RF
IEC 61000-4-3
3V/m
80 MHz to 2.5 GHz 3V/m
d = [3.5]√P 80 MHz to 800 MHz
E1
d = [7]√P 800 MHz to 2.5 GHz
E1
where Pis the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and dis the
recommended separation distance in meters (m).
Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya, should be less than the compliance level in each
frequency rangeb.
Interference may occur in the vicinity of equipment marked with the following symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
aField strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be
predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the
location in which the Fluidotherapy - Dry Heat Therapy Unit is used exceeds the applicable RF compliance level above, the Fluidotherapy - Dry Heat Therapy Unit should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the Fluidotherapy - Dry Heat Therapy Unit.
bOver the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Fluidotherapy® - Dry Heat Therapy

13
ELECTROMAGNETIC COMPATIBILITY (EMC) TABLES (CONTINUED)
TABLE 2 & 3: GUIDANCE AND MANUFACTURER'S DECLARATION - ELECTROMAGNETIC IMMUNITY
The Fluidotherapy - Dry Heat Therapy Unit is intended for use in the electromagnetic environment specified in the table below. The user of the
Fluidotherapy - Dry Heat Therapy Unit should assure that it is used in such an environment.
Immunity Test IEC 60601
Test Level Compliance Level Electromagnetic Environment - Guidance
Electrostatic discharge (ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
Floors should be wood, concrete, or ceramic tile. If floors are covered with
synthetic material, the relative humidity should be at least 30%.
Electrical fast transient/burst
IEC 61000-4-4
±2 kV for power supply lines
±1 kV for input/output lines
±2 kV for power supply lines
±1 kV for input/output lines
Mains power quality should be that of a typical commercial or hospital
environment.
Surge (1)
IEC 61000-4-5
±1 kV differential mode
±2 kV common mode
±1 kV differential mode
±2 kV common mode
Mains power quality should be that of a typical commercial or hospital
environment.
Voltage dips, short
interruptions and voltage
variations on power supply
input lines
IEC 61000-4-11
<5% UT(>95% dip in UT) for 0.5 cycle
40% UT(60% dip in UT) for 5 cycles
70% UT(30% dip in UT) for 25 cycles
<5% UT(>95% dip in UT) for 5 sec
<5% UT(>95% dip in UT) for 0.5 cycle
40% UT(60% dip in UT) for 5 cycles
70% UT(30% dip in UT) for 25 cycles
<5% UT(>95% dip in UT) for 5 sec
Mains power quality should be that of a typical commercial or hospital
environment. If the user of the Fluidotherapy - Dry Heat Therapy Unit requires
continued operation during power mains interruptions, it is recommended that
the Fluidotherapy - Dry HeatTherapy Unit be powered from an uninterruptible
power supply or a battery.
Power frequency (50/60Hz)
magnetic field
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic fields should be at levels characteristic of a typical
location in a typical commercial or hospital environment.
NOTE: UTis the a.c. mains voltage prior to application of the test level.
SPECIFICATIONS Fluidotherapy® - Dry Heat Therapy

14
SPECIFICATIONS
ELECTROMAGNETIC COMPATIBILITY (EMC) TABLES (CONTINUED)
TABLE 4: RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT
AND THE FLUIDOTHERAPY - DRY HEAT THERAPY UNIT (CONTINUED)
The Fluidotherapy - Dry Heat Therapy Unit is intended for use in an electromagnetic environment in which radiated RF disturbances
are controlled. The customer or the user of the Fluidotherapy - Dry Heat Therapy Unit can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Fluidotherapy - Dry
Heat Therapy Unit as recommended below.
Rated Maximum Output Power of
Transmitter
W
Separation Distance According to Frequency of Transmitter
m
150 kHz to 80 MHz
d = [3.5]√P
V1
80 MHz to 800 MHz
d = [3.5]√P
E1
800 MHz to 2.5 GHz
d = [7]√P
E1
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance din meters (m) can be estimated using the equation applicable
to the frequency of the transmitter, where Pis the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.
Fluidotherapy® - Dry Heat Therapy

15
Rated Maximum Output Power of
Transmitter
W
Separation Distance According to Frequency of Transmitter
m
150 kHz to 80 MHz
d = [3.5]√P
V1
80 MHz to 800 MHz
d = [3.5]√P
E1
800 MHz to 2.5 GHz
d = [7]√P
E1
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
15
SETUP
Use the following instructions to set the various Mode Parameters to
the desired settings.
TREATMENT MODE PARAMETERS
Press the “INCREASE” or “DECREASE”
buttons until desired Treatment Time is
displayed.
NOTE:
The “TREATMENT TIME” can be adjusted in
one minute increments from 1 to 99.
ATTENTION!!!
ATTRITION OF PARTICLES DURING SHIPMENT
MAY RESULT IN INITIAL DUSTING AND SMALL
PARTICLE RELEASE. DUST AND ODOR WILL
DISSIPATE WITH USE.
TREATMENT TIME
Press the“PRESS TO CHANGE MODE”
button until the indicator light is beside
“TREATMENT TIME”.
NOTE:
The default time of “20:00” will be
displayed.
TREATMENT TEMPERATURE
Press the“PRESS TO CHANGE MODE”
button until the indicator light is beside
“TEMPERATURE”.
NOTE:
The default temperature of“115 °F (46.1 °C)
will be displayed when unit is first plugged
into wall outlet.
The“F” or “C” and “TEMPERATURE” indicator
will flash while the programmedTreatment
Temperature is being displayed.
When the Bed Temperature is displayed, the
“F”or “C”and the“TEMPERATURE” indicator
will illuminate steadily.
Fluidotherapy® - Dry Heat Therapy

16
Fluidotherapy® - Dry Heat Therapy
SETUP
Press the “INCREASE” or “DECREASE”
buttons until desired Air Speed is
displayed.
NOTE:
The “AIR SPEED” is adjusted in increments
of 5 from 0 to 100.
TREATMENT MODE PARAMETERS (CONTINUED)
TREATMENT TEMPERATURE (CONTINUED)
Press the“INCREASE”or“DECREASE”
buttons until desired Treatment Temperature
is displayed.
NOTE:
°F can be changed to °C and vice versa as
desired. See page 20 for instructions.
Treatment Temperature can be adjusted in 1°
increments from 88 °F to 130 °F
(31.1 °C to 54
°C).
AIR SPEED
Press the“PRESS TO CHANGE MODE”
button until the indicator light is beside
“AIR SPEED”.
NOTE:
The default speed of “50” will be displayed.
PULSE TIME
Press the“PRESS TO CHANGE MODE”
button until the indicator light is beside
“PULSE TIME”.
NOTE:
The “PULSE TIME”allows the unit to
operate by pulsing the medium during
treatment. If selected and set, the medium
will pulse on and off in equal increments.
The Factory Default is “OFF”.
EXAMPLE: “PULSE TIME” is set at “5”.
The unit will pulse the medium during
treatment, five seconds on and five
seconds off.