CAUTION: Federal law restricts these devices for sale by or on the order of a physician, chiropractor,
physical therapist, or dentist licensed by the law of the state in which said person practices to use or
order the use of the devices.
Risk of burns and fire - Do not use near conductive materials such as metal bed parts, inner spring
mattresses and the like.
DANGER - Explosion Hazard: Do not use in the presence of flammable anesthetics.
IMPORTANT: Before treating a patient with any Dynatron Solaris® Device, see the “Contraindications, Warnings, and Precautions” in this manual. Read the operating instructions for each modality carefully.
INDICATIONS FOR USE
ELECTROTHERAPY:
Electrical muscle stimulation therapy (Russian, Biphasic, High Volt) for:
1. relaxation of muscle spasm;
2. prevention or retardation of disuse atrophy;
3. increasing local blood circulation;
4. muscle re-education;
5. immediate post surgical stimulation of calf muscles to prevent venous thrombosis
6. maintaining or increasing range of motion.
Transcutaneous electrical nerve stimulation and Interferential Current Therapy (Interferential, Premodulated,
High Volt, Microcurrent) for: Symptomatic relief of chronic intractable and/or management of posttraumatic or post-surgical pain
.
DIRECT CURRENT THERAPY:
Direct Current is indicated for relaxation of muscle spasms.
ULTRASOUND THERAPY:
Ultrasound therapy is intended to generate deep heat within body tissues for the treatment of selected medical
conditions such as relief of pain, muscle spasms, and joint contractures, but not for the treatment of
malignancies.
LIGHT THERAPY:
Light therapy provides topical heating for temporary increase in blood circulation, temporary relief of minor
muscle and joint aches, pain and stiffness, relaxation of muscles, and treatment of muscle spasms and minor
pain and stiffness associated with arthritis.
The D890 laser product is designated as class 1M during all procedures of Operation and Maintenance.
AVOID INADVERTENT EXPOSURE TO POTENTIALLY HAZARDOUS LIGHT
Before You Treat a Patient ..................................................................................................................... 3
Installation and Features............................................................................................................................ 4
Current Limit........................................................................................................................................ 24
Current Limit Warning......................................................................................................................... 24
Lead Wires / Electrodes........................................................................................................................ 25
Lead Wires ........................................................................................................................................... 25
Test Leads............................................................................................................................................. 25
“LEAD” Warning - No Patient Current ............................................................................................... 26
High Volt Instructions...............................................................................................................................52
Set Up High Volt Treatment with Electrodes .......................................................................................52
Set Up High Volt Probe Treatment.......................................................................................................53
Basic High Volt Setup ..........................................................................................................................53
High Volt Treatment Time....................................................................................................................54
Detailed High Volt Setup......................................................................................................................54
High Volt Modality Information...........................................................................................................59
High Volt Waveform ............................................................................................................................59
High Volt Settings.................................................................................................................................59
High Volt Default Settings....................................................................................................................60
High Volt Waveform Specifications.....................................................................................................60
General Specifications ............................................................................................................................ 128
Dynatron Solaris Specifications ......................................................................................................... 128
The Dynatron Solaris 700 Series offers the practitioner a wide range of treatment options.
These devices provide Interferential and Premodulated therapy; High Voltage pulsed
stimulation; Russian and Biphasic therapies; Microcurrent and Direct Current treatments; and
Infrared Light Probe applications. The Solaris 700 Series devices may, with the use of the
®
Dynatron
In addition, the Solaris 701, 708, and 709 include Ultrasound and the Dynatronics
Comboplus
The 700 Series devices include the standard advantages of Dynatronics engineering, such as
customizable treatments, electrode conductance meters and the popular Target feature. In
addition all units offer the option of battery operation, making the devices truly portable. The
manufacturer’s warranty for these devices is two years (see full warranty details at the back of
this manual).
This manual provides operator information and instructions for five Solaris models: the 701,
705, 706, 708, and 709. The section that discusses Ultrasound and Comboplus treatments
applies only to the Dynatron 701, 708 and 709 models. All other sections of this manual apply
to all Dynatron Solaris devices.
Summary of Features by Device
Electrotherapy
IFC X X X X
Premod X X X X
Biphasic X X X X
Russian X X X X
High Volt X X X X
Microcurrent X X X X
Direct Current X X X X
Combo Electrotherapy/Ultrasound X X
Light Therapy
Ultrasound
Special Features
Electrotherapy Channels 4 2 4 2
High Volt Channel 1 1 1 1
Stim Probe Channel X X X X
Infrared/Laser Light Therapy Port X X X X X
Conductance Meter X X X X
*
*Note: The Dynatron Solaris Booster Box must be used in conjunction with the Dynatron Xp Light pad on all Solaris
700 Series devices. Software upgrades are required on all devices manufactured prior to September 2005.
Booster Box, operate the Dynatron® Xp™, a powerful 8”X10” Infrared Light Pad.
™ feature providing almost unlimited combinations of treatment options.
Feature 701 709 708 706 705
Booster Box / Light Pad Capability X X X X X
®
700 Series
X X X X X
X X X
Introduction
2
Simplified Setup
The unique design of the Solaris front panel means treatment setup has never been easier. A
few simple key presses are all you need to fully set up a treatment. The careful grouping of
available options for each modality ensures that you can easily see and select from the
appropriate options for that modality.
Each modality offers default settings which are automatically preset when the modality is
selected—saving time in the treatment setup. You can change these defaults to match your
own most common treatment setups reducing setup time to a matter of seconds.
Before You Treat a Patient
Before administering a treatment to a patient with the Solaris devices, you should familiarize
yourself with all the operating instructions for the modality used, as well as the
contraindications, warnings, and precautions for that modality.
You should also read the general information about each of the modalities provided in this
manual. In addition to this information, consult other published sources for additional
application and safety instructions regarding use of each type of therapy.
Dynatron Solaris® 700 Series
Introduction
3
Installation and Features
Unpacking
When you receive the unit, immediately unpack it and all accessories and check for possible
damage, obvious or concealed. In case of damage, immediately notify the freight carrier and
take any steps necessary to file a claim for the damage sustained. Do not destroy or discard the
shipping carton. The carton should be reused if the device must be shipped for any reason.
The carton is specially designed to protect the unit from shipping damage. Improper
packaging of the unit during transport can result in damage and invalidate the warranty.
Complete the warranty registration form located at the back of this manual and return it
to Dynatronics within 30 days of purchase. This is essential to insure you are not billed
for services that are covered by the warranty policy. Warranty registration should
include serial numbers for both the device and soundheads.
Connect the AC power cord, which is equipped with a hospital grade, UL listed plug, to a
properly grounded 110/120V 60 Hz AC outlet (the device will automatically switch to
220/240V 50 Hz when connected to a power source with that voltage). The power cord must
also be firmly plugged into the device itself. When the cord is properly connected, it can not
be easily pulled out. Do not place the cord or the device in a place where the cord could be
tripped over or accidentally pulled out of its socket during a treatment.
If Infrared Light Therapy probes or pads are being used in conjunction with a Solaris
device and/or Booster Box, they should be plugged into the Solaris console and/or
Booster Box prior to powering-on the device(s).
Read the operating instructions in this manual before proceeding with a treatment.
Standard Components
REF The following accessories are included with the Solaris units:
Qty Part No. Description
One of the following devices:
1 D701 Solaris 701
1 D705 Solaris 705
1 D706 Solaris 706
1 D708 Solaris 708
1 D709 Solaris 709
1 7B0241 Power Cord (black)
1 9G0011 Operator's Manual
1 7B0268 Protocol Reference Manual for Electrotherapy & Ultrasound
1 7B0217 Dynagel Ultrasound Gel 100 ml sample - Solaris 701, 708 and
Dynatron Solaris® 700 Series
(Guffey, 2003)
709 only
Installation & Features
4
Qty Part No. Description
2 7B0232 120” double leads (2 red) - Solaris 706 and 709 only
2 7B0233 120” double leads (2 black) - Solaris 706 and 709 only
1 7B0230
7B0231 72” double lead (1 black) - Solaris 705 and 708 only
1
72” double lead (1 red) - Solaris 705 and 708 only
1 7B0234 COMBOplus lead wires –Solaris 708 and 709 only
1 7B0284 Ultra Polys
(pkg. of 4)
1 8E0017A MultiStim Point Tip Attachment
1 7B0250 MultiStim probe (requires one or more applicators)
1 8E0018 High Volt applicator 5/8” round
1 8E0019 High Volt applicator 2”x1-1/2”
2 7B0063
3” round carbon electrodes (2 red)
2 7B00653” round carbon electrodes (2 black)
4 7B0210 Sponge fabric for use with 3” carbon electrodes
1 7B0193 Sponge Pocket 1 1/2” x 2”
1 7B0192 Sponge Pocket 5/8”
2 DW248 2.5” x 48” straps (pkg. of 2) Solaris 706 and 709 only
1 DW248 2.5” x 48” straps (pkg. of 2) Solaris 705 and 708 only
1 7B0191 5” x 8” dispersive electrode for High Volt (gray)
1 7B0201 Sponge Fabric for use with 5”x 8” dispersive electrodes
1 8D0027 Microcurrent Ground Probe
1 7B0079 Banana-to-Pin Adapter (black)
Soundheads
The Solaris devices may be purchased with one or more applicator soundheads in the
following sizes:
Part No. Size Frequencies
9GSH02 2 cm
9GSH05 5 cm
9GSH10 10 cm
Optional Accessories
The following optional and replacement accessories may be purchased from Dynatronics or
from your Dynatronics dealer:
Part No. Description
D880 Dynatron 880 Cluster Probe
D890 Dynatron 890 Light Therapy Probe
D405 Dynatron 405 Infrared Cluster Probe
D881 Dynatron 880Plus Infrared Cluster Probe
9G0104 Protective Eyewear (D405)
Xp Dynatron Xp Infrared Light Pad (Booster Box required)
XpB Dynatron Solaris Booster Box
7B0271 Light Therapy Applications Manual (Enwemeka & Pöntinen)
7B0272 Hard Side Carrying Case for Solaris Units
7B0273 Soft Side Carrying Case
7B0208 2” diameter carbon electrodes (red)
7B0209 2” diameter carbon electrodes (gray)
7B0063 3” diameter carbon electrodes (red)
Dynatron Solaris® 700 Series
Note: The following are not applicable to the D701.
™ Self-adhesive electrodes 2” x 4” w/pin connector
2
Operates at 1, 2, and 3 MHz
2
Operates at 1, 2, and 3 MHz
2
Operates at 1, 2, and 3 MHz
Installation & Features
5
Dynatron Solaris® 700 Series
Part No. Description
7B0065 3” diameter carbon electrodes (gray)
7B0059 3” x 5” carbon electrodes (red)
7B0061 3” x 5” carbon electrodes (gray)
7B0067 1.5” x 2.0” carbon electrodes (red)
7B0069 1.5” x 2.0” carbon electrodes (gray)
7B0260 2” x 4” Ultra Polys
connector)
7B0261 2” x 2” Ultra Polys
(with snap or pin connector)
7B0077 Bifurcated extension lead wire for High Volt use
7B0082 Pin-to-Banana adapter (black)
7B0079 Banana-to-Pin Adapter (black)
7B0001 Snap adapter
5LTRGEL Ultrasound Coupling Gel (5 liter container)
9G0079 Light Probe Covers (Disposable / 25 per package)
8A0061 Remote Stop Cable Assembly (Applicable only to customized,
special order units).
Dynatron Solaris® Physical Features
Before operating the Dynatron Solaris devices, acquaint yourself with the control panel by
reviewing the illustrations and descriptions on the following pages. The numbered features in
the diagrams correspond to the numbered descriptions. Before administering treatment to a
patient, read the sections later in this manual that provide specific instructions for performing
treatments, discussions of each modality, definitions of the available options, along with
contraindications, warnings, and precautions for all modalities. Note that some options use
“toggle” keys for making selections. More specific instructions for using toggle keys are
provided later in this section.
™ adhesive electrodes (with snap or pin
™ square adhesive electrodes
Installation & Features
6
4
8
26
Dynatron Solaris 701 Control Panel
Dynatron Solaris® 700 Series
Solaris 701
5
9
10
11
1
2
3
27
17
18
16
Installation & Features
7
Dynatron Solaris® 700 Series
Solaris 705
14
13
RATE/DUTY
9
S LARIS
CH 1
SERIES
CH 2
10
Dynatron
11
27
1
2
3
20
19
21
22
24
25
23
5
4
7
6
12
26
8
CH1CH2HV
Dynatron Solaris 705 Control Panel
Installation & Features
28
CH 2
CH 1
15
705
29
8
Dynatron Solaris® 700 Series
Solaris 706
14
13
RATE/DUTY
9
S LARIS
CH 1
SERIES
CH 2
10
Dynatron
11
27
1
2
3
20
19
21
22
24
25
23
5
4
7
6
12
26
8
CH1CH2CH3CH4HV
Dynatron Solaris 706 Control Panel
CH 2
28
CH 1
15
706
29
Installation & Features
9
4
7
6
14
13
12
26
17
16
18
CH1CH2HV
Dynatron Solaris 708 Control Panel
28
Dynatron Solaris® 700 Series
Solaris 708
RATE/DUTY
9
S LARIS
CH 1
SERIES
CH 2
CH 1
CH 2
15
10
Dynatron
708
11
27
29
1
2
3
20
19
21
22
24
25
23
5
8
Installation & Features
10
4
7
6
16
18
CH1CH2CH3CH4HV
14
13
12
26
17
Dynatron Solaris 709 Control Panel
Dynatron Solaris® 700 Series
Solaris 709
RATE/DUTY
9
S LARIS
OUTPUT
CH 1
SERIES
CH 2
CH 1
CH 2
15
28
10
Dynatron
709
11
27
1
2
3
20
19
21
22
24
25
23
29
5
8
11
Installation & Features
General Selections
1. START
probe treatments, the START key only activates the probe in preparation for the treatment.
The treatment begins after the 1/0 (ON/OFF) key on the probe handle is pressed.
2. STOP: Pressing this key during a treatment IMMEDIATELY stops the output and sets the
treatment time to zero for all modalities. To stop just one
the FUNCTION key while you press the STOP key, or simply reduce that channel’s
treatment time to zero. For Light Probe treatments, press the 1/0 (ON/OFF) key located on
the probe handle. On custom devices equipped with the remote stop feature, treatments
may also be stopped by pressing the button on the REMOTE STOP cable, terminating all
treatments.
3. PAUSE/FUNCTION
unique features including: Select polarity (High Volt, Microcurrent and Direct Current),
audio volume control (Microcurrent), and to stop one treatment. Specific instructions for
using this key are provided later in this manual.
Ultrasound: For Dynatron Solaris 701, 708 and 709 only: This key is also used to PAUSE
an Ultrasound treatment. For the Solaris 708 and 709, first press the CHANNEL TOGGLE
(CH) to select SOUND. For the D701, press the SOUND key. With Ultrasound as the
focus, press PAUSE/FUNCTION; the Ultrasound output is stopped, the treatment time is
paused, and the light on the PAUSE key is lighted. When this key is pressed again, the
Ultrasound treatment countdown resumes and the light on the PAUSE key is off.
: Press this key to start the treatment timer and treatment proceeds as set up. For
Dynatron Solaris® 700 Series
treatment only, press and hold
: This key is used in combination with other key presses for accessing
Combination Treatment: During a COMBO treatment, only the Ultrasound output and the
treatment timer are stopped when you press PAUSE; the stim output continues.
Infrared Light Therapy Probe/Pad: Pressing the PAUSE/FUNCTION key will not pause a
Solaris Light Therapy Probe treatment that is in progress. A Light Therapy Probe Treatment
is paused by pressing the “1/0” key on the Light Probe handle. However, pressing the
PAUSE/FUNCTION key will pause a pad treatment.
Please note: Following the completion of either a Pad or Probe treatment when using
the Dynatron Booster Box, the practitioner must press the PAUSE/FUNCTION-STOP
keys to exit the current focus (pad or probe) and switch to the opposite Light Therapy
mode (pad or probe). For example: If the Booster Box is operational, and an Infrared
Probe treatment has just timed out
, the practitioner must press PAUSE/FUNCTIONSTOP before using the CH toggle key to switch to an Infrared Light Pad treatment.
PAUSE/FUNCTION-STOP would also have to be pressed following the Pad treatment
to return back to a Probe treatment mode.
4. TIME ARROW KEYS
: These UP/DOWN arrow keys are used to increase/decrease the
treatment time or other parameters that are displayed in the TIME display.
5. TIME DISPLAY
: This display is used to show the treatment time for one treatment at a
time; the display shows treatment time for the selected channel (the selected channel is
indicated by the GREEN LED—all other channels in use at the time will have YELLOW
LEDs). The TIME display can also show the pulse rate and duration for Russian and
Biphasic treatments as well as the frequencies for Interferential, Premodulated, and
Microcurrent treatments, pulse duration for Direct Current treatments, and the pulse rate
for High Volt. The treatment parameters for any treatment in progress may be displayed
Installation & Features
12
Dynatron Solaris® 700 Series
at any time by first using the CHANNEL TOGGLE key to choose the desired channel (the
D701 will always automatically default to show the active modality), then using the TIME
TOGGLE key to select the desired parameter (Time, Freq, Rate, Rate/Duty, Duration,
On/Off).
6. CHANNEL TOGGLE KEY (CH
): When a treatment is in progress, you can press this key
to choose an output channel and display the parameters for the treatment being delivered
by that channel. When an output light is GREEN, the displays show the settings for that
output. The available options depend on the modality selected. When two or more
treatments are in progress simultaneously, the TOGGLE KEY is used to select the output
or channel you wish to view.
7. CHANNEL SELECTIONS
: These lights indicate which output channels are currently in
use. A solid GREEN light indicates current is being delivered to that channel; the time,
intensity and other treatment parameters for that channel are also displayed. A solid
YELLOW light indicates a channel is in use and delivering current, but the time, intensity,
and treatment parameters are not displayed at this time (only one channel’s time and
intensity may be displayed at a time). Flashing GREEN or flashing YELLOW indicates the
OFF segment of a Biphasic, Russian, or High Volt treatment cycle. The channel’s intensity
and other treatment parameters may only be modified when it has a GREEN indicator light.
Press the CHANNEL TOGGLE key (CH) to select a channel to be viewed.
8. TIME TOGGLE KEY
: Press this key to display various treatment parameters in the TIME
display including Time (treatment time), Freq (frequency), Rate/Duty (pulse rate),
Duration (pulse width), ON and OFF (current on/off cycle). Available options during a
given treatment or treatment setup depend on the modality selected.
9. TIME GROUP SELECTIONS
: These LEDs indicate the parameters that are displayed
(one at a time) in the TIME display. The default selection is the treatment time. Press the
TIME TOGGLE key to select the desired option (available options depend on the modality
selected). When a parameter is selected, its indicator light is GREEN, its value is
displayed in the TIME display above, and the TIME arrow keys may be used to change
the value. The device returns to the TIME display after 10 seconds with no key presses.
10. POWER/INTENSITY DISPLAY
the treatment output in watts/cm
Direct Current, volts for High Volt and J/cm
(D701 POWER/DOSE DISPLAY): This window shows
2
or watts for Ultrasound, µA for Microcurrent and mA
2
or Joules for Light therapy. For all other
modalities it displays intensity from 0-99 in respect to the currently selected channel (the
selected channel is indicated by the GREEN LED. All other channels in use at the time will
have YELLOW LEDs). Press the CHANNEL TOGGLE key to select the desired channel to
be viewed. The D701 will default to the active modality.
11. POWER/INTENSITY ARROW KEYS
: These arrow keys are used to increase/decrease
the intensity or power of one treatment. Changes made to power and intensity affect only
the currently selected channel (the selected channel is indicated by the GREEN LED—all
other channels in use at the time will have YELLOW LEDs). Press the CHANNEL
TOGGLE key to select the desired output channel. The D701 will default to the active
modality. The arrow keys may then be used to change the intensity or power for that
channel.
12. IFC/PREMOD: Press this key once to begin setup of an Interferential treatment (the IFC
LED is lighted); press this key twice to begin setup of a Premodulated treatment (the
Premod LED is lighted). When you select IFC, a channel pair (CH1-2 or CH3-4) is
automatically selected and the GREEN LED lights for the two auto-selected channels will
be lighted. Connect two leads to the output jacks for the channels that are selected. When
you select PREMOD, a single channel (1, 2, 3, or 4) is automatically selected and that
channel’s GREEN LED will be lighted. Connect one lead to the output jack that
corresponds to the channel indicated by the GREEN LED. Note: Channel 3-4 are only
found on the Solaris 706 and 709 devices.
13. HIGH/LOW TOGGLE (used with Interferential, Premodulated and High Volt): Press this
key one or more times to select the desired frequency range for Interferential and
Premodulated treatments or the pulse rate range for High Volt treatments. The GREEN
LED indicates the option selected. For example, HIGH will be displayed as the default
selection. Press the HIGH/LOW TOGGLE key once to select LOW, press again to select
HIGH/LOW ALTERNATING, and press again to select HIGH/LOW CONSECUTIVE.
For High Volt treatments, you can select High or Low only, but not both. During a
treatment, the current sweeps through the range(s) selected.
For Interferential and Premodulated, the HIGH frequency range is initially set at 80 to 150
Hz; and the LOW frequency range is 0 to 10 Hz. For High Volt, the HIGH pulse rate
range is initially set at 80 to 120 Hz; and the LOW pulse rate range is 1 to 10 Hz. These
frequency ranges may be modified for every treatment, if desired and new default settings
for the device may also be saved. See treatment setup instructions later in this manual for
a complete description of the options that may be selected.
14. TARGET/SWEEP TOGGLE: This key is pressed to select Target, Target Sweep, or Static
treatment when an Interferential treatment is selected. The LED next to Target or Target
Sweep will be lighted when selected. If both LEDs are OFF, the Static mode will be
activated. If Target is selected, the Target pad is used to locate the exact treatment site.
15. TARGET PAD: For use during Interferential treatments when the “Target” option is
selected. Touch the TARGET pad at different points on the pad to reach the precise
treatment site. When you lift your finger from the Target pad, the selected point is locked
until you change it again. This feature is used to place the point of interference at a
specific site during an Interferential treatment.
Ultrasound Selections (Solaris 701, 708 and 709 only):
16. ULTRASOUND/COMBO D701, D708 and 709: Press this key once to begin setup of an
Ultrasound treatment (the Sound LED on this key is lighted as well as the Sound LED in
the channel indicator area); press this key twice to begin setup of a combination treatment
(the COMBO LED is lighted as well as the Sound LED and a single Channel LED in the
channel indicator area). When either of these options is chosen, the sound- head should
first be plugged into the Ultrasound output jack on the side panel. For combination
treatments, the special COMBO lead wire should be attached to the output jack selected
for that treatment and the banana plug
side of the device behind the Ultrasound jack. In the COMBO mode, the electrotherapy
treatment is delivered through the soundhead and through a single electrode which is
placed on the patient. Only single-channel electrotherapy options are available in the
COMBO mode, i.e. Premod, Russian, Biphasic, and High Volt.
Installation & Features
should be plugged in where indicated on the right
14
Dynatron Solaris® 700 Series
ULTRASOUND/COMBO D701:The D701 is designed with a Combo Input Jack on the
right side of the device to which a separate Dynatron Stim unit can be attached, allowing
the stim to flow through the soundhead. After attaching the Stim unit set up the
Ultrasound and Stim treatments separately.
17. ULTRASOUND FREQUENCY TOGGLE: This key is pressed one or more times to
select the desired Ultrasound frequency; 1 MHz, 2 MHz, or 3 MHz.
18. ULTRASOUND DUTY CYCLE TOGGLE: This key is pressed one or more times to
select the desired duty cycle for Ultrasound treatment. Options are 10, 20, or 50 percent,
or Continuous.
Russian / Biphasic / High Volt Selections:
19. BIPHASIC/RUSSIAN: Press this key once to begin setup of a Biphasic treatment (the
Biphasic LED is lighted); press this key twice to begin setup of a Russian treatment (the
Russian LED is lighted). Biphasic and Russian treatments use a single channel (1, 2, 3 or
4) when the Normal mode is selected; and a channel pair (1-2 or 3-4) when the Reciprocal
or Co-contraction mode is selected. Channels 3-4 pair treatments are only available on the
Solaris 706 and the Solaris 709.
20. TREATMENT MODE TOGGLE (for Biphasic and Russian Treatment Modes): Press this
key one or more times to select Normal, Co-Contraction, or Reciprocal contraction. The
output channel is automatically selected. When Normal is selected, one output jack only is
selected.
When Co-contraction or Reciprocal is selected, a channel pair is selected (either channels
1-2 or channels 3-4). Connect the patient lead wire(s) to the output jack(s) for the
channel(s) selected. Channels 3-4 pair treatments are only available on the Solaris 709 and
the Solaris 706.
21. HIGH VOLT: Press this key to begin setup of a High Voltage Pulsed Stimulation
treatment (the High Volt LED is lighted). The HV output channel is automatically selected
(the LED for the channel selected is GREEN). Connect the patient lead wire to the HV
output jack indicated by the green LED. Press the Channel Toggle key to select HV Probe
treatment, if desired. For probe treatments, increase (+) and decrease (-) intensity indicator
switches are located on the probe handle.
HIGH VOLT POLARITY: Polarity on a High Volt treatment defaults to negative (-). To
select or change the polarity of a High Volt treatment, hold down the FUNCTION KEY
and press the HI VOLT key one or more times to select positive only (the “+” LED is
lighted), negative polarity only (the “-” LED is lighted), or dual polarity (both (+) and (-)
LEDs are lighted).
22. CONTRACTION/REST CYCLE TOGGLE (for Russian, Biphasic, and High Volt
treatments
): Press this key one or more times to select the desired contraction/rest (on/off)
cycle. Available cycles include 10/10, 10/30, 10/50, Continuous and Custom. The
CUSTOM DUTY CYCLE is a new feature that allows you to customize the treatment by
selecting from an ON time from 3to 20 seconds, and an OFF time from 3 to 120 seconds.
The OFF time cannot be less than the ON time. In addition, you can modify the pulse rate,
the pulse duration, and the ramp time. The first value indicates the on-time in seconds,
and the second value indicates the off-time. For example; 10/30 indicates the current is on
(muscle is contracting) for 10 seconds, and current is off (muscle is relaxed) for 30
seconds. With Continuous mode, current is applied continuously with no off cycle. The
15
Installation & Features
Dynatron Solaris® 700 Series
continuously with no off cycle. The continuous duty cycle is not recommended for
electrical muscle stimulation, but may be used for settings that are intended to effect other
results than a muscle contraction.
23. RAMP TOGGLE: (for Russian, Biphasic, and High Volt treatments): This key is pressed
to select the ramp time. The ramp time is applied before and after the “On” segment of the
cycle (it provides both a ramp up and a ramp down). Available ramp times are .5, 1, 1.5,
and 2 seconds. NOTE: The ramp up and down time is the same.
Microcurrent Selections:
24. MICRO: Press this key to begin setup of a Microcurrent treatment. This key is also used
to turn the conductance tone OFF and ON after a Microcurrent treatment is started. When
the MICRO key is pressed, Channel 1 is automatically selected for the default electrodes
treatment and the LED for that channel is lighted. For a Microcurrent treatment setup with
electrodes, connect the patient lead wire to the CHANNEL 1 output jack.
For a Microcurrent probes treatment, press the CHANNEL TOGGLE key to select
PROBE after selecting MICRO and both the PROBE and MICRO LEDs are lighted. For a
Microcurrent Probe treatment connect the MultiStim probe to the STIM PROBE OUTPUT
JACK on the side panel of the device.
NOTE: Channel 1 is committed to the Microcurrent output during a probes treatment as
well as during a treatment with electrodes, and is not available for use by any other
modality while any Microcurrent treatment is in progress.
MICROCURRENT POLARITY: To select or change the polarity of a microcurrent
treatment, use the MICRO key together with the FUNCTION key. Press and continue
holding the FUNCTION key while pressing the MICRO key one or more times to select
positive only (the “+” LED is lighted), negative polarity only (the “-” LED is lighted), or
dual polarity (both LEDs are lighted).
MICROCURRENT AUDIO TONE: The audible tone is defaulted to ON for probes
treatments and OFF for electrode treatments, but may be changed. After the Microcurrent
treatment has started the MICRO key acts as a toggle key to turn the tone ON and OFF.
Press MICRO to turn the tone ON or OFF.
You may also adjust the tone volume after the treatment has started. To adjust the volume,
PRESS and HOLD the FUNCTION key. Then while continuing to press the FUNCTION
key, use the POWER/INTENSITY ARROW keys to raise or lower the volume until a
comfortable volume setting is found. The POWER/INTENSITY display will temporarily
show an incremental value representing the volume selection. You must continue holding
the FUNCTION key down while adjusting the volume. When you release the FUNCTION
key, the POWER/INTENSITY display returns to its normal display.
Direct Current Selections:
25. DIRECT CURRENT: This key selects the Direct Current modality. Since this modality is
a probes-only treatment, the MULTISTIM probe must be plugged into the STIM PROBE
JACK before a treatment may proceed. All control for intensity and actuation is from
switches located on the probe. Intensity is displayed in mA (maximum 20 mA). Duration
is displayed in mSec in the TIME DISPLAY with pulse duration selection from 0.1 mSec
to 500 mSec. To change the polarity, hold down the FUNCTION KEY and press the
DIRECT CURRENT button. Pressing one or more times will toggle through the options
of positive, or negative.
Installation & Features
16
Light Therapy Selections:
26. LIGHT THERAPY: Caution: Always begin by plugging the Light Therapy Probe or
Conductance
27. The Solaris devices continuously measures conductance during electrical stim treatments
Dynatron Solaris® 700 Series
Pad into the base console unit before turning ON the device. Please note, when using
a Dynatron Xp pad, a Solaris Booster Box is required. Press the Light Therapy key to
begin setup for either a probe or pad treatment.
PROBE: The Solaris device will recognize the type of probe that has been inserted into
the Solaris console. The CLUSTER LED or LASER LED (SLD on the D701) and the
PROBE LED are lighted.
PAD: After pressing LIGHT THERAPY, press the CH toggle key to complete setup for a
Pad treatment. The PROBE LED will go OFF, while the CLUSTER LED will remain
lighted.
START: Pressing START on the base Solaris console will immediately begin an Infrared
Light Pad treatment; however, for a Probe treatment pressing START on the console will
only activate the Probe in preparation for a treatment. The YELLOW LED on the Light
Therapy Probe handle will be lighted. A Probe treatment will begin when the 1/0
(ON/OFF) key on the Probe handle is pressed and the LED on the probe handle is
GREEN. A green LED next to OUTPUT on the faceplate will indicate that a LIGHT
THERAPY treatment is in progress.
CAUTION: Vents surrounding the Light Therapy probes must be kept clear and free of
any obstruction at all times. Do Not cover the XP pad with towels or blankets during
treatment.
for Interferential, Premod, and Microcurrent to ensure that the treatment outcome is
optimal and to minimize the possibility of patient discomfort due to poor conductance
and/or changes in current density. As conductance is measured, Solaris displays the results
in graph form on the CONDUCTANCE bar located on the front panel of the device.
Optimum conductance is displayed as a GREEN bar filling the entire graph. If the green
bar only partially fills the graph area, the conductance is at a percentage of optimum.
Conductance: Conductance is how readily electrical current is passed from the electrode
to the skin surface during a treatment. Conductance affects current density. A worn
electrode that does not conduct the current evenly over its entire surface will have “hot
spots” where a greater amount of current flows through a smaller area which means the
current density is higher at that point than elsewhere on the electrode. “Hot Spots” can
lead to patient discomfort. Never risk patient comfort by using worn electrodes or lead
wires.
Intensity: The intensity level is a convenient incremental measurement. However, raising
the intensity increases the current delivered to the patient but does not improve
conductance.
Current Density: Current density is the amount of current that passes through a given
area of the electrode. Current density varies depending on the size of the electrode, the
conductance and the intensity setting, and has an effect on patient comfort. With proper
setup and good accessories, current is dispersed evenly over the entire surface of the
electrode. The smaller the electrode, the greater the density of the current delivered
through the area. To reduce current density and improve patient comfort, you can either
use larger electrodes, or a lower intensity setting, or both.
Installation & Features
17
Dynatron Solaris® 700 Series
During a Microcurrent probe treatment, the graph is also useful in observing conductance
changes since the goal of some microcurrent treatments is to increase conductance (reduce
resistance/impedance) at a given point.
During an Ultrasound treatment, the graph is used to assist with monitoring patient
coupling. This feature is described in the section of this manual entitled Ultrasound
section of this manual entitled “Patient Coupling.”
If the number of Green displayed segments begin to decrease on the graph during a
treatment, it is important to determine the cause of the poor conductance. Remember with
poor conductance you may inadvertently increase current density at a small point under the
electrode and cause patient discomfort. Following are some considerations to insure
proper conductance.
The bar graph uses twelve lighted segments to indicate best conductance, and no lighted
segments to indicate poorest conductance.
• Check to be sure electrodes are not worn or that self-adhesive electrodes have not lost their
adhesiveness. These are the most common causes of poor current delivery. Both selfadhesive and carbon electrodes eventually lose their ability to conduct current effectively.
See “Electrotherapy Usage Cautions” in this manual for recommended intensity settings and
usage limits.
• Check to ensure the entire surface of the poly adhesive electrode is adhering.
• Self-adhesive electrodes do not require sterilization, however, electrodes should be clean and
hydrated (see package instructions or “Self-Adhesive Electrodes” section of this manual).
• Check to be sure electrodes are not worn or that self-adhesive electrodes have not lost their
adhesiveness. These are the most common causes of poor current delivery. Both selfadhesive and carbon electrodes eventually lose their ability to conduct current effectively.
Installation & Features
18
Dynatron Solaris® 700 Series
• See “Electrotherapy Usage Cautions” in this manual for recommended intensity settings and
usage limits.
• Check to ensure the entire surface of the poly adhesive electrode is adhering.
• Self-adhesive electrodes do not require sterilization, however, electrodes should be clean and
hydrated (see package instructions or “Self-Adhesive Electrodes” section of this manual).
• Check to be sure the snap adapters haven’t fallen off or that the lead wire has not become
disconnected from the electrodes or the device.
• Make sure carbon electrodes have a secure connection with the pin ends of the leads. Over
time the carbon electrodes may become too loose to use safely and the electrodes must be
replaced.
• Check for corrosion on lead ends.
• Make sure carbon electrodes are adequately moistened and free from build-up to allow
complete contact across the surface of the electrode.
• Observe the electrode placement. Some areas of the patient’s body conduct current better
than others. In areas where resistance is high you may be unable to obtain optimum
conductivity.
• Check the dryness of the patient’s skin. Dry skin does not conduct current well.
• Check to see if the electrodes do not adhere properly when a patient shifts position during a
treatment. Worn electrodes could become loose and a significant change in conductance
could result.
Remember to treat at the patient’s comfort level. It is not important to reach a given
intensity level. It is only important to set the treatment at a level that is comfortable to
the patient. See “Electrotherapy Usage Cautions in this manual for suggested intensity
limits.
Output Connectors and Jacks
Connectors and jacks on the Solaris device are “Keyed/Locking”
connectors (see illustration to the right and on the following page).
Use caution when inserting the connectors into the output jacks. When
the keys are properly aligned, the connector and jack will slide together
smoothly and exactly. When removing the connector, the locking
mechanism is released when the outside connector shell is pulled away
from the device. Do not force
may occur. This damage is not covered
Note: Devices that have been custom ordered with the Patient
REMOTE STOP cable will have an additional jack located on the
back of the base unit. The remote stop is controlled by the patient
during unattended therapy to allow the patient to stop the treatment at
any time. When the button on the remote stop cable is pressed, output
for all stim modalities and pad treatments is stopped and the tone
sounds briefly. During Combo treatments, both sound and stim
outputs are stopped.
the connector or damage to the pins
by warranty.
19
“Keyed” Ultrasound Jack
“Keyed” Probe Jack
Installation & Features
Dynatron Solaris® 700 Series
Keyed” Probe Connectors
When attaching the probe, align the raised portion of the connector
with the notched jack opening. When removing the
probe connector, the locking mechanism is released when the outside
connector shell is gently pulled away from the base unit.
“Keyed” Pad Connectors
The Pad connector is attached by aligning the connector
“Keyed” Probe Jack
with the keyed openings in the jack and pushing the connector
into the jack. To remove the connector, turn the sleeve to the
left in the direction of the “Release” arrow and gently remove
the connector. Do not use force when attaching or removing
the connector.
28. OUTPUT JACK CHANNELS 1, 2, 3, and 4
: These are the
“Keyed” Pad Connector
output jacks for delivering Interferential, Premodulated,
Russian, Biphasic, and Microcurrent treatments. These channels are located in the front of
the device. Front (left to right as you face the device).
29. HIGH VOLT OUTPUT JACK CHANNEL HV
. This is the output jack dedicated to
delivering High Volt pad treatments, located in front on the far right side.
Solaris Left Side View
30. STIM PROBE JACK - MICROCURRENT/HV/DC PROBES TREATMENTS: The
universal MultiStim probe plugs into this jack for Microcurrent, High Volt or DC probe
therapy. After the probe is connected and either Microcurrent or High Volt keys have
been pressed, press the TIME TOGGLE key to select PROBE. If the Direct Current
modality is selected, the device will automatically default to PROBE. See illustration
above.
31. DYNATRON LIGHT THERAPY (IR/RED) OUTPUT JACK: This output jack is
designed to accommodate a single probe. When one of the Dynatron Solaris probes is
connected, the device will recognize the probe and will auto calculate time/dosage (J/cm
Joules, and total treatment time. See illustration above.
32. COMBINATION TREATMENT JACK: The special combo lead wire for combination
treatments is plugged into this jack located on the right side of the device for a
combination treatment setup providing stim output through the Ultrasound head of the
D708, D709. For combination treatments using the D701, the Dynatron stim device is
plugged into the Combination Treatment Jack using a pin-to-banana adapter.
Installation & Features
IR/Red Probe (31)
20
Stim Probe (30)
2
),
Dynatron Solaris® 700 Series
The special lead wire on the D708 and D709 is also plugged into the jack on the front of
the device which has been selected for the specific COMBO treatment. See combination
treatment instructions later in this manual for detailed information regarding combination
treatment setup. See illustration on the following page.
Solaris Right Side View
33. ULTRASOUND OUTPUT JACK (Ultrasound models only): The applicator soundhead
plugs into this jack for Ultrasound therapy. Located on the right side of the device. See
diagram on previous page.
Power Switch / Battery
34. POWER 1/0 (ON/OFF) SWITCH: Located on the back of the unit this switch is labeled
“1” and “0”. Set the switch to “1” for ON; set the switch to “0” for OFF.
battery (35)
Solaris Back Panel
35. BATTERY
: This jack may be used to supply power to the device using an optional
battery pack. More information about the optional battery operation is provided later in
this manual. (See illustration on the previous page).
Booster Box / Booster Box Jacks
36. BOOSTER BOX / BOOSTER BOX JACKS (The Dynatron Booster Box is required for
use with the Dynatron Xp Pad on all Solaris 700 Series devices): The Dynatron Booster
Box is engineered to provide the additional power needed to operate the Dynatron Xp
Infrared Light pad. The Booster Box mirrors the outline of the outer-contours of the
Solaris console and stands approximately 2” in height. The flat upper surface of the
Booster Box is designed with four pre-molded circular receptacles at each corner in which
to place the rubber feet of the Solaris console, thus allowing the two units to fit
Ultrasound Probe (33)
power (34)
Combo Input (32)
21
Installation & Features
Dynatron Solaris® 700 Series
together with the appearance of a single device. The two units are electrically and
functionally connected by a communication cable (labeled SOLARIS CONNECTION)
attached to the Booster Box and designed to be plugged into the IR/RED output jack
located on the left side of the main Solaris console.
Booster Box and Jacks
The Booster Box has two output jacks: A LIGHT PROBE jack located on the left side of
the device in front of the communication cable and a LIGHT PAD output jack located on
the right side of the Booster Box. Please note: Only one Light Therapy treatment
(either probe or pad) may be given at a time.
Instructions for Using Toggle Keys
Toggle keys are used to make selections from two or more options in a given area. Toggle
keys are pressed one or more times to make a desired selection. A GREEN light (LED) next
to the toggle key shows the option that has been selected. Pressing the toggle key one or more
times allows you to scan through the available options.
Each toggle key has unique capabilities. Most toggle keys allow only one selection. For
example, the Ramp toggle key requires you to select just one of the four ramp times available.
However, some toggle keys allow you to select two options. For example, in Interferential you
can press the HIGH/LOW TOGGLE key once to select High, press again to select Low, and
press again to select both High and Low.
The following is a list of all the toggle keys available with each modality:
IFC and Premod
• Target/Sweep (IFC only)
• High/Low Frequency Ranges
Russian and Biphasic Stim
• Treatment mode
• Contraction/Rest cycle
• Ramp Time
High Volt Stim
• Contraction/Rest cycle
• Ramp Time
• Polarity
• High/Low Pulse Rate Ranges
• Channel toggle to select Pads/HV Channel or Probes Treatment (during setup only)
Installation & Features
22
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