Dynatronics Dynatron 825 Operator's Manual
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Dynatronics Dynatron 825 Operator's Manual

Dynatron 25 series
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DYNATRON® 25 SERIES™ | OPERATOR'S MANUAL
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Summary of Contents for Dynatronics Dynatron 825

  • Page 1 DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...
  • Page 2 Dynatronics Corporation Emergo Europe ISO 13485 7030 Park Centre Drive Salt Lake City, UT 84121 Molenstraat 15 NEMKO CERTIFIED (801) 568-7000 / (800) 874-6251 / www.dynatronics.com The Hague, 2513 BH DQS CERTIFIED The Netherlands 0470 DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...

  • Page 3: Table Of Contents

    Table of ConTenTs Table of Contents Section I: Introduction Introduction to the Dynatron® 25 Series™ ..................... 1 Summary of Features by Device ...............................1 Simplified Setup ..................................2 Language Selection ..................................2 Operator’s Profile ..................................2 Before You Treat a Patient .................................3 Installation and Features ........................4 Unpacking ....................................4 Standard Components ................................4 Dynatron®...
  • Page 4 Table of ConTenTs Section II: Operation and Treatment Instructions Interferential / Premodulated Instructions ..................25 Detailed Interferential / Premodulated Setup ........................25 Interferential and Premodulated Modality Information ..............29 Interferential (Quadpolar) Therapy ............................29 Premodulated (Bipolar) Therapy ............................30 Target ......................................30 Why Is Target Better? ................................30 Target Sweep .....................................31 Interferential Electrode Placement ............................31 Interferential / Premodulated Default Settings ........................31...
  • Page 5 Table of ConTenTs Ultrasound Modality Information ....................... 53 Selecting the Appropriate Soundhead ...........................53 Penetration of Ultrasound Waves ............................54 Types of Delivery..................................55 Treatment Time ..................................55 Treatment Intensity ..................................55 Frequency of Treatment ................................56 Usage Cautions – Combination Treatments .........................56 Potential for Burns or Periosteal Pain ...........................56 Ultrasound Problem Solving .......................
  • Page 6 Table of ConTenTs Section IV: Technical Information Technical Information.......................... 76 Setting Defaults ..................................76 Save New Defaults ..................................76 Restore Factory Defaults .................................77 Battery Operation ..........................78 Battery Life ....................................79 Battery Life ....................................79 General Specifications .......................... 80 Dynatron 25 Series Specifications ............................80 Environmental Conditions ..............................80 Safety Features of the Dynatron 25 Series..........................81 Care and Cleaning Instructions .............................81...

  • Page 7: Introduction To The Dynatron® 25 Series

    Interferential, Premodulated, High Volt, Biphasic, Russian, Microcurent, and fixed frequency IFC/Premod. In addition, the 925 and 825 include Dynatronics’ Ultrasound Comboplus feature with the power to deliver up to 5 channels of Stim and Ultrasound - all at the same time. All of the Dynatron 25 Series models offer 1, 2, and 3 MHz frequencies for the greatest flexibility in depth of treatment.

  • Page 8: Simplified Setup

    This manual provides operator information and instructions for the four 25 Serises models: the 525, 625, 825, and 925. The section that discusses Ultrasound and Combo treatments applies only to the Dynatron 825 and 925 models. All other sections of this manual apply to all Dynatron 25 Series devices.

  • Page 9: Before You Treat A Patient

    InTroduCTIon To The dynaTron® 25 serIes™ response to attended or unattended treatments. The operator should be able to hear an audible signal indicating completion of treatments. There should be no other limitations for operating this device. Before You Treat a Patient Before administering a treatment to a patient with the 25 Series 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.

  • Page 10: Installation And Features

    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.
  • Page 11 Operates at 1, 2, and 3 MHz WSH10 10 cm Operates at 1, 2, and 3 MHz Optional Accessories The following optional and replacement accessories may be purchased from Dynatronics or from your Dynatronics dealer: Part No. Description D71BAG Soft Side Carrying Case...
  • Page 12 InsTallaTIon and feaTures Part No. Description 7B0209 2" (5.8cm) diameter carbon electrodes (gray) 7B0063 3" (7.62cm) diameter carbon electrodes (red) 7B0065 3" (7.62cm) diameter carbon electrodes (gray) 7B0059 3" x 5" (7.62cm x 12.7cm) carbon electrodes (red) 7B0061 3" x 5" (7.62cm x 12.7cm) carbon electrodes (gray) 7B0067 1.5"...

  • Page 13: Dynatron® 25 Series Physical Features

    dynaTron® 25 serIes PhysICal feaTures Dynatron 25 Series ® Physical Features Before operating the Dynatron 25 Series 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.
  • Page 14 dynaTron® 25 serIes PhysICal feaTures 1. START: Press the green START key on the right side of the Treatment Display Screen to start the treatment timer and treatment proceeds as set up. The START key can also be used to save new treatment DEFAULT settings. After setting up a treatment, press and hold the START key for two seconds.

  • Page 15: Premod

    dynaTron® 25 serIes PhysICal feaTures IFC (Interferential) Premod Biphasic Russian SOUND (Ultrasound) SOUND (Function Key View) COMBO (Combination) COMBO (Function Key View) DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...
  • Page 16 dynaTron® 25 serIes PhysICal feaTures HIVOLT (High Volt) HIVOLT (Function Key View) 9. TREATMENT WINDOW TOGGLE KEYS: TOGGLE KEYS are located below the five TREATMENT WINDOWS. Pressing the toggle key directly below a window allows the one to choose an output channel, and select treatment parameters for a treatment in focus.
  • Page 17 dynaTron® 25 serIes PhysICal feaTures 12. CONDUCTANCE/TEMPERATURE BAR Conductance. The 25 Series devices continuously measure conductance during electrical Stim treatments for Interferential, and Premod 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.

  • Page 18: Channels And Jacks

    dynaTron® 25 serIes PhysICal feaTures • 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.
  • Page 19 dynaTron® 25 serIes PhysICal feaTures 14. Left-Side Panel Jacks SD Card Input. Located on the left-side of the 25 Series devices is the SD Card Input. The SD Input provides a way for the 25 Series Devices to receive software updates quickly and easily. Complete instructions for updating the devices using an SD card are found in the “Technical”...

  • Page 20: Current Limit

    dynaTron® 25 serIes PhysICal feaTures Back Panel Jacks a. POWER CORD ENTRY MODULE. This entry module is designed to accommodate a hospital-grade power cord. b. 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”...

  • Page 21: Error Messages

    dynaTron® 25 serIes PhysICal feaTures CURRENT LIMIT ERROR MESSAGES CAUSE “Cannot start treatment with zero intensity” Intensity not set error 101, error 111, error 120, error 130 “lead error: current too low! lead issue; electrode issue Please check or replace your leads and pads!” error 100, error 110, error 140 lead shorted “lead error: high current delivery detected.

  • Page 22: Ultrasound Error Messages

    dynaTron® 25 serIes PhysICal feaTures Ultrasound Error Messages ULTRASOUND ERROR MESSAGES CAUSE “no soundhead connected, no soundhead attached cannot setup ultrasound/combo treatment.” “soundhead is too hot! soundhead is too hot output has been disabled to allow cooling.” “Caution: soundhead is getting hot!” soundhead is getting hot “Thermistor on soundhead is broken! Thermistor on soundhead is broken...

  • Page 23: Testing Leads

    NOTE: The LEAD TEST should be used for testing patient lead wires only. This is not an accurate means of testing carbon electrodes. Contact Dynatronics Customer Service to arrange for free testing of carbon electrodes or for instructions for testing these electrodes.

  • Page 24: Carbon Electrodes

    3. How to Clean Carbon Electrodes. Carbon electrodes from Dynatronics may be cleaned using a mild soap and a small brush (such as a nail brush). To sterilize, alcohol may be used. They may also be sterilized in an Autoclave. Daily cleaning is recommended...

  • Page 25: Self-Adhesive Electrodes

    Self-Adhesive Electrodes Dynatronics’ self-adhesive electrodes are intended for multiple but patient specific use due to the danger of cross contamination. Improper use of the electrodes can decrease the life of the electrode and could even result in harm to your patient.
  • Page 26 dynaTron® 25 serIes PhysICal feaTures discard the electrode. Using straps and weights with self-adhesive electrodes could have an unpredictable effect on the electrodes and could cause injury. 4. NEVER use monitoring electrodes such as ECG, or EMG, nor ordinary TENS electrodes. 5.

  • Page 27: Electrotherapy Information And Usage Cautions

    eleCTroTheraPy InformaTIon and usage CauTIons Electrotherapy Information and Usage Cautions The following general warnings are to be observed during Interferential, Premodulated, Russian, Biphasic, and High Voltage stimulations. WARNING • NEVER turn the power ON or OFF while the unit is connected to the patient. •...
  • Page 28 eleCTroTheraPy InformaTIon and usage CauTIons Current Density This is the amount of current being delivered to the patient divided by the area through which the current is being delivered (the surface area of the electrodes being used). Electrode Condition Worn or dried out electrodes cause the current to concentrate in small areas of the electrode instead being evenly distributed over the entire surface of the electrode.
  • Page 29 eleCTroTheraPy InformaTIon and usage CauTIons Interferential / Premodulated electrode size maximum recommended Intensity 3" round (7.62cm) 25 - 30 Carbon electrodes 3" x 5" (7.62cm x 12.7cm) 30 - 40 1.75" square (4.45cm) 10 - 15 1.75" x 3.75" (4.45cm x 9.53cm) 25 - 30 self-adhesive 1.25"...
  • Page 30 eleCTroTheraPy InformaTIon and usage CauTIons the foil backing behind the adhesive is broken. Carbon electrodes should be deep black and should be free of cracks in the electrode surface. 4. Some patients tend to be much more sensitive to electrotherapy treatments. On patients with this tendency, treat with reduced intensity and/or shorter treatment times with possibly more frequent treatments, if required.

  • Page 31: Interferential / Premodulated Instructions

    InTerferenTIal / PremodulaTed InsTruCTIons Interferential / Premodulated Instructions An Interferential treatment uses two channels and four electrodes (channel pairs 1-2 or 3-4). The device will automatically select the first available channel pair when you select IFC. A Premodulated treatment uses one channel and two electrodes. The device will automatically select the first available channel (1, 2, 3, or 4) when PREMOD is selected.
  • Page 32 InTerferenTIal / PremodulaTed InsTruCTIons If you wish to change or customize the treatment settings, proceed through the following steps: 2. Customize TIME The default treatment time is displayed at 10:00 min. Use the TIME arrow keys to increase or decrease the treatment time. 3.
  • Page 33 InTerferenTIal / PremodulaTed InsTruCTIons made using the arrow keys to the side of each displayed setting. If you set both displays to the same value, the treatment will be delivered at that single frequency rather than sweep through a frequency range. •...
  • Page 34 InTerferenTIal / PremodulaTed InsTruCTIons 7. SAVE DEFAULTS If the treatment you have just set up is a frequently used, you can save the treatment parameters as new defaults by pressing and holding the START key until a beep sounds indicating the treatment parameters have been saved. The next time you select the modality, these parameters will be selected automatically.

  • Page 35: Interferential And Premodulated Modality Information

    InTerferenTIal and PremodulaTed modalITy InformaTIon Interferential and Premodulated Modality Information Interferential (Quadpolar) Therapy Interferential therapy uses four electrodes to deliver two currents, one current with a constant frequency of 4000 Hz and the other current with a variable frequency of 4000 to 4150 Hz. The paths of these two currents cross resulting in a “beat” that produces the therapeutic frequency at the treatment site.

  • Page 36: Premodulated (Bipolar) Therapy

    (a smaller total coverage area means greater current density at the treatment site). Target The Dynatronics’ TARGET (available for Interferential treatments only) simplifies placing the interferential beat directly on the treatment site. The movement of the finger on the Target paid along with the feedback supplied by the patient allows the user to place the  ...

  • Page 37: Target Sweep

    InTerferenTIal and PremodulaTed modalITy InformaTIon Target Sweep The Sweep option literally moves the point of interference inward and outward in a somewhat spiral pattern, bathing about 80 percent of the area within the electrodes with the Interferential current. Sweep utilizes the Target feature and moves the point of interference to cover a wider treatment area while still retaining the full Interferential beat.

  • Page 38: Biphasic / Russian Instructions

    bIPhasIC / russIan InsTruCTIons Biphasic / Russian Instructions In the Russian and Biphasic Stimulation modes the output of the device is a pulsed sinusoidal wave. 25 Series allows the operator to choose a muscle contraction/rest cycle that is most suited for the individual patient and for the desired treatment. Once the cycle is chosen, each muscle-stimulating burst is followed by a rest cycle.

  • Page 39: Biphasic / Russian Quick Setup

    bIPhasIC / russIan InsTruCTIons 1. Press the CONT/REST toggle key. Select CUSTOM. 2. Press the MODE toggle key. Select CUST C/R (Custom Contraction Rest). 3. Press TREATMENT toggle key. Select Normal, Co-Cont, Recip. 4. Using the RAMP toggle key, select RAMP time (.05, 1.0, 1.5, 2.0). 5.

  • Page 40: Detailed Biphasic / Russian Setup

    bIPhasIC / russIan InsTruCTIons Detailed Biphasic / Russian Setup If you do not understand the terms contraction, rest, ramp time, pulse duration, or pulse rate; consult the diagrams in the section of this manual entitled “Biphasic / Russian Parameters. ” 1.
  • Page 41 bIPhasIC / russIan InsTruCTIons Press the PULSE RATE arrow keys to the left-side of the Treatment Screen to change the PULSE RATE. Press the PULSE DURATION arrow keys to the right-side of the Treatment Screen to change the PULSE DURATION. Press the MODE toggle key and select TIME to return the TIME display.
  • Page 42 bIPhasIC / russIan InsTruCTIons • RAMP TIME • TREATMENT TIME • RATE/DURATION (not available for Reciprocal treatments nor when two “Normal” treatments are running simultaneously on a channel pair—CH 1-2 or 3-4). • INTENSITY (separately for each channel) 12. STOP When the treatment time has elapsed, the current to the patient stops and a tone sounds signaling the end of a treatment.

  • Page 43: Biphasic / Russian Modality Information

    bIPhasIC / russIan modalITy InformaTIon Biphasic / Russian Modality Information Russian Stimulation With Russian Stimulation mode, the output of the device is a 2500 Hz sinusoidal wave. Russian stimulation currents produce strong muscle contractions. The Dynatron 25 Series devices allows complete control over all the parameters of the Russian Stimulation treatment. Three treatment modes include Normal for firing one muscle, Reciprocal for firing two different muscles at different times, and Co-contraction for firing two different muscles simultaneously.
  • Page 44 bIPhasIC / russIan modalITy InformaTIon Biphasic / Russian Default Settings mode normal Contraction / rest Times 10 / 30 Treatment Time 10 minutes ramp up and down Time 5 sec. Russian Stimulation Contraction Rest Times default setting Valid range Pulse rate 50 Pulses per sec.
  • Page 45 bIPhasIC / russIan modalITy InformaTIon If a given Russian stimulation treatment has a 50 percent duty cycle, this means the output cycle is continuously repeating for half of the pulse duration (see “Rate” in the diagram above) followed by a zero-current period for the other half of the pulse duration.

  • Page 46: High Volt Instructions

    hIgh VolT InsTruCTIons High Volt Instructions High Volt electrical stimulation is a pulsed DC current with pulse durations in the microsecond range and pulse rates ranging from 1 to 200 Hz, with peak amplitude of up to 500 Volts. The Dynatron 125 devices deliver High Volt utilizing a twin-peak monophasic waveform.

  • Page 47: Detailed High Volt Setup

    VolT InsTruCTIons electrode is at least twice the size (in area) of the combined sizes of the active electrodes. The bifurcated lead wire extension is an optional accessory available through Dynatronics. During the treatment current flows in one direction between the active and dispersive electrodes.
  • Page 48 hIgh VolT InsTruCTIons 1. Press the HI VOLT key. The High Volt channel and the default settings for High Voltage electrode pulsed stimulation are automatically selected. Using the dedicated High Volt (HV) channel attach leads and place electrodes on the patient now. . Default Setting Treatment ..High Volt Pads Treatment Duty Cycle ......
  • Page 49 hIgh VolT InsTruCTIons CUSTOM (Duty) CYCLE TIME SELECTIONS • Press the FUNCTION key located on right-side of the device faceplate. • Using the CONT/REST toggle key, select CUSTOM in the CONT/REST window. • Using the MODE toggle key, select CUST CR in the MODE window. Selections will be illuminated GREEN. •...
  • Page 50 hIgh VolT InsTruCTIons 9. MODIFY Settings While the High Volt treatment is in progress, TIME, INTENSITY, AND POLARITY can be modified. Carefully observe the channel indicator lights when modifying a treatment. When a channel’s light is illuminated GREEN, the current treatment parameters for that channel are displayed. Any changes made to the parameters will affect only the channel that is illuminated in GREEN.

  • Page 51: High Volt Modality Information

    hIgh VolT modalITy InformaTIon High Volt Modality Information High Voltage pulsed stimulation is a pulsed DC current with pulse durations in the microsecond range and pulse rates ranging from 1 to 200 Hz, with a peak amplitude of up to 1.0 A utilizing a twin-peak monophasic waveform.

  • Page 52: High Volt Default Settings

    hIgh VolT modalITy InformaTIon Custom Contraction/Rest Time Cycles. The Dynatron 25 Series allows for the choice of muscle contraction and relaxation time cycles (Duty Cycles) from options of 10/10 (ten seconds on and ten seconds off), 10/30, 10/50, Continuous or Custom cycles.

  • Page 53: Ultrasound Instructions

    ulTrasound InsTruCTIons Ultrasound Instructions The following Ultrasound Instructions are for 25 Series 825 and 925 USERS ONLY. The Dynatron 25 Series 525 and 625 do not offer the Ultrasound feature. Ultrasound therapy channels sound waves through muscle, nerve, bone, and connective tissue to aid in reducing pain, muscle spasms, and joint contractures.

  • Page 54: Soundhead Warming

    ulTrasound InsTruCTIons Make sure a soundhead is firmly plugged into the device before turning the device on. When changing to a different size soundhead, turn the machine off first, remove the soundhead, plug in the desired soundhead, then turn the machine on again.

  • Page 55: Head Temperature Hot Display

    ulTrasound InsTruCTIons During any Ultrasound treatment the soundhead should be moved continuously, covering an area approximately two to four times the size of the soundhead. The full surface of the soundhead should maintain in contact with the patient’s skin (except with underwater treatments).

  • Page 56: Detailed Ultrasound Setup

    ulTrasound InsTruCTIons Ultrasound Quick Setup Select SOUND. 1. FREQUENCY. Using the FREQUENCY toggle key select 1 MHz, 2 MHz, or 3 MHz. 2. DUTY CYCLE. Using the DUTY toggle key, select 10%, 20%, 50% or CONT (Continuous). 3. TIME. Change the treatment TIME, if desired using the Up/Down arrow keys. 4.
  • Page 57 ulTrasound InsTruCTIons 2. Choose the FREQUENCY. Press the FREQUENCY toggle key located under the FREQUENCY window to select 1, 2, or 3 MHz. Any one of the three Frequencies may be selected with the 2 cm , 5 cm or 10 cm soundhead.
  • Page 58 ulTrasound InsTruCTIons without ending the treatment. Press the PAUSE key again to restart the treatment. A tone will sound indicating that the treatment is again in progress. Output resumes and the treatment timer starts from where it was paused. NOTE: During a COMBO treatment, THE STIM OUTPUT OF THE TREATMENT IS NOT PAUSED when the PAUSE key is pressed, although the Ultrasound output is stopped and the treatment timer is paused.

  • Page 59: Ultrasound Modality Information

    Modality Information For Dynatron 825, and 925 users only. The Dynatron 525 and 625 do not offer the Ultrasound feature. Ultrasound, by its very nature, has the ability to irritate the patient’s skin. While the benefits of Ultrasound far outweigh any disadvantages, certain precautions should be observed to assure maximum safety and comfort for your patients.

  • Page 60: Penetration Of Ultrasound Waves

    ulTrasound modalITy InformaTIon The selection of the appropriate soundhead is key to the success of the treatment and is based on the size of the area to be treated. Ultrasound treatments should be kept specific to the tissue involved in pathology. A good guideline is 2 to 4 times the size of the soundhead.

  • Page 61: Types Of Delivery

    ulTrasound modalITy InformaTIon Types of Delivery Ultrasound can be delivered in four different ways. You will likely only see two of the four methods in clinical practice. 1. Direct Contact Movable. Here the soundhead is placed in direct contact with the patient. A coupling agent is used between soundhead and the patient’s skin.

  • Page 62: Frequency Of Treatment

    ulTrasound modalITy InformaTIon 4. Use a little lower intensity for the first treatment to gauge response. 5. Patient feedback is key. A treatment should feel warm, but the patient should never feel heat, pain, stabbing, pricking or dull ache. Acute Conditions: ........0.1 – 0.5 W/cm (no appreciable thermal effect).
  • Page 63 ulTrasound modalITy InformaTIon • Holding the soundhead in one place on the patient’s skin • Moving the soundhead too slowly • Treating an area where sensory nerve damage is present with a loss of normal skin sensation • Time (Caution: Don’t treat too long). Bony prominences are especially susceptible, as they reflect sound waves and increase intensity to the periosteum resulting in a burning sensation.

  • Page 64: Ultrasound Problem Solving

    ulTrasound Problem solVIng Ultrasound Problem Solving Whirlpool Treatments If you are treating in a whirlpool, you may find the temperature reaches high enough to read approximately 103˚F, causing the overheated soundhead caution to appear in the Treatment Display Screen. This is only a cautionary warning to let you know that the soundhead is approaching the temperature limit.

  • Page 65: No Soundhead

    Check to be sure the soundhead has not become disconnected from the machine. The soundhead should be firmly plugged into its port. Only Dynatronics soundheads may be used with this device. If the soundhead has been dropped, it may be damaged. If the device operates normally with one soundhead, but not with another, the problem may be a damaged soundhead and you must contact Dynatronics Customer Service.

  • Page 66: Ultrasound Specifications

    ± 10% Ultrasound Regulation and Technical Information For the Dynatron 825, and 925 Only The Dynatron 825, and 925 comply with the following: • FDA 21CFR 1050(c)(1)(i). The error in indication of the temporal-average ultrasonic power shall not exceed ±20 percent for all emissions greater than 10 percent of the maximum emission.

  • Page 67: Ultrasound Beam Profiles

    ulTrasound beam ProfIles Ultrasound Beam Profiles (For Dynatron 25 Series 825, and 925 users only. The Dynatron 25 Series 525 and 625 do not offer Ultrasound). The following diagrams show the typical spatial distribution of the radiated field for each size Dynatron 25 Series soundhead. This applies to the radiation emitted into the equivalent of an infinite medium of distilled, degassed water at 30˚...
  • Page 68 ulTrasound beam ProfIles 5 cm Head. Near Field 1MHz 2 MHz 3 MHz 2 cm Head. Near Field 1MHz 2 MHz 3 MHz DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...

  • Page 69: Combination Therapy Instructions

    Be alert for any sign of periosteal (bone) pain. Comboplus ™ Dynatronics’ Comboplus feature means you have almost unlimited options in setting up a combination treatment with 25 Series. You can: • Combine an Ultrasound treatment with the following electrotherapy modalities provided by this device: IFC, Premodulated, Biphasic, Russian, or High Volt.

  • Page 70: Stim Through The Soundhead

    CombInaTIon TheraPy InsTruCTIons • Set up a combination treatment by using the ULTRASOUND output jack and the automatically selected default STIM channel. A special “COMBO” lead wire is provided with the 825 and 925 with the standard accessories for this device to accommodate the ComboPlus feature.

  • Page 71: Combination Therapy Setup

    CombInaTIon TheraPy InsTruCTIons Combination Therapy Setup 1. Press the COMBO key on the 825 and 925. SOUND will be illuminated GREEN in the CHANNELS window and an automatically selected STIM channel will be illuminated in YELLOW. Other available channels not in use will be illuminated in WHITE.

  • Page 72: Modify A Treatment

    CombInaTIon TheraPy InsTruCTIons ALL STOP: Press the STOP key to stop all treatments at all channels on the 825 and 925 devices. The output for the channel(s) selected is stopped (both STIM and SOUND channels), and the device then displays the beginning treatment parameters.

  • Page 73: Simultaneous Treatments

    sImulTaneous TreaTmenTs Simultaneous Treatments The Dynatron 25 Series allows many combinations of simultaneous treatments to be delivered at once using available channels. Simultaneous treatments are not the same as COMBO treatments. A COMBO treatment combines Ultrasound with a Stim therapy into a single treatment. A COMBO treatment is always delivered to one patient. Simultaneous treatments are independent treatments that are set up separately, that have separate treatment timers, and which may be delivered to one or more patients at the same time.
  • Page 74 sImulTaneous TreaTmenTs All channels that are currently operational but not in focus, are listed both in the CHANNELS window and in small font on the left-hand side of the Treatment Display Screen under the heading, RUNNING TREATMENTS. Included in the list under RUNNING TREATMENTS, is the active channel(s) illuminated in YELLOW;...

  • Page 75: Contraindications, Warnings, & Precautions

    ConTraIndICaTIons, WarnIngs, & PreCauTIons Contraindications, Warnings, & Precautions for Interferential, Premodulated, Russian, Biphasic, and High Voltage Pulsed Stimulation. Contraindications Thrombosis. It is possible that the current produces chemical changes in the blood leading to alterations in the clotting time. At present there is no specific scientific evidence to support this. Nevertheless, treatment must not be given to any patient who is taking anticoagulants as it may render these ineffective.

  • Page 76: Precautions

    ConTraIndICaTIons, WarnIngs, & PreCauTIons 1. Adequate precautions should be taken in the case of persons with suspected or diagnosed epilepsy. 2. Severe spasm of the laryngeal and pharyngeal muscles may occur when the electrodes are positioned over the neck or mouth. The contractions may be strong enough to close the airway or cause difficulty in breathing. 3.

  • Page 77: Treatment Setup Warnings

    ConTraIndICaTIons, WarnIngs, & PreCauTIons 4. Use extreme caution when administering a treatment where sensory nerve damage is present or in any\case where there is a loss of normal skin sensation; this includes areas desensitized by medication or ice. When treating an area where there is loss of feeling, there is an increased danger of injuring the patient.
  • Page 78 Use Only Dynatronics Accessories The leads and electrodes provided by Dynatronics have been tested with Dynatronics devices and are appropriate for use with these devices. Dynatronics cannot guarantee the safety or performance of leads and electrodes purchased from other vendors.

  • Page 79: Contraindications, Warnings, & Precautions For Ultrasound Treatment

    ConTraIndICaTIons, WarnIngs, & PreCauTIons for ulTrasound TreaTmenT Contraindications, Warnings, & Precautions for Ultrasound Treatment Contraindications The Dynatron 25 Series Ultrasound should not be applied in the following CONDITIONS: • Pregnancy • Acute and sub-acute thrombosis and thrombophlebitis • Potentially malignant lesions, tumors malignant or benign •...

  • Page 80: Precautions

    ConTraIndICaTIons, WarnIngs, & PreCauTIons for ulTrasound TreaTmenT • Hemophilia • Where sensory nerve damage is present with a loss of normal skin sensation. The Dynatron 25 Series Ultrasound should not be applied to the following AREAS: • Transcerebrally • To the eye •...

  • Page 81: Warnings

    ConTraIndICaTIons, WarnIngs, & PreCauTIons for ulTrasound TreaTmenT Warnings • Do not use in general area where high-powered, high-frequency transmitting surgical units are being operated. Short wave diathermy should not be turned on or used at the same time as this Dynatron device. •...

  • Page 82: Technical Information

    TeChnICal InformaTIon Technical Information CAUTION There are no serviceable parts in 25 Series devices. Setting Defaults Each of the modalities has default settings that are automatically selected when a modality key is pressed. The default settings feature allows previously used treatment parameters to be set up in just seconds. For guidance in selecting the appropriate settings for each modality, consult published medical literature.

  • Page 83: Restore Factory Defaults

    1. Turn the machine off and wait five seconds. 2. Turn on the machine. Following initialization, DYNATRONICS appears in the Display Screen. 3. Press and hold the START key down until three beeps are sounded. The Factory Defaults have now been restored for all modalities.

  • Page 84: Battery Operation

    Use ONLY a Dynatronics’ Approved Battery Before purchasing or using an existing battery with a 25 Series device, contact Dynatronics or your Dynatronics Representative to obtain specifications for a battery that may be safely used with a 25 Series device.

  • Page 85: Battery Life

    baTTery oPeraTIon Battery Life Note: If using a smaller gauge wire (20 AWG and up) the BATT LOW error is possible when the battery is not low. • 12 volt and at least 5 amps hours. • Battery adaptor cord must match the plug end of the battery pack. The barrel plug end must match the 0.325” barrel jack adaptor plug on the 25 Series device.

  • Page 86: General Specifications

    General Specifications Other ranges, accuracy and precision values that are not provided here may be obtained from Dynatronics upon request. Dynatron 25 Series Specifications Power Requirements ................. 100-240 V~, 50/60 Hz Power Consumption ......................100 Watts Fuse: .......................250V, 1.6A slow blow Dimensions ........18.5"...

  • Page 87: Safety Features Of The Dynatron 25 Series

    general sPeCIfICaTIons Operation This equipment is designed to operate in normal use under the following environmental conditions: +30°C a. an ambient temperature range of +10°C b. a relative humidity range of 30% to 75% including condensation c. an atmospheric pressure range of 700 hPa to 1060 hPa Safety Features of the Dynatron 25 Series •...

  • Page 88: Suggested Maintenance Schedule

    4. For older devices contact Dynatronics or your Dynatronics dealer for information and pricing for current upgrades to your device. Even if the machine is functioning properly, you can send it to Dynatronics for preventative maintenance service for a nominal charge; call for pricing.

  • Page 89: Routine Ultrasound Calibration Inspections For 25 Series

    Dynatronics contact Dynatronics’ Customer Service Department. The device will need to be shipped to Dynatronics for the inspection. As an alternative, these periodic checks may be performed in your own locale by an independent contractor who is expert in checking the calibration of Ultrasound equipment. The calibration procedure MUST be performed by a qualified Ultrasound technician using the proper equipment, and is recommended every 6 to 12 months.

  • Page 90: Software Updates

    1. Turn off the console. 2. Insert the SD card supplied by Dynatronics into the SD CARD slot on the left-side of the console (fingers of the SD card facing up, label side down). 3. Turn on the console. There will be a 3 to 4 second pause while the card syncs with the 25 Series system software. A RED screen will appear with the following warnings: “DO NOT DISCONNECT POWER, ”...

  • Page 91: Returning A Unit For Repair

    Return Authorization If it becomes necessary to return a 25 Series unit for repair, contact Dynatronics’ Customer Service (800) 874-6251. All returns must have a Service Order Number (SVO). The following information will need to be supplied when calling Dynatronics’...

  • Page 92: Definition Of Symbols And Labeling

    Temperature humidity model number serial number fuse european Conformity maintenance battery Input secure digital Card dynatronics manufacturer location manufacturing date Safety Certification for Canada and the USA. Certified to IEC60601-1 DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...

  • Page 93: Equipment Classification

    general sPeCIfICaTIons The following labels appear on the 25 Series consoles, Ultrasound Heads. 25 Series 825 and 925 25 Series 525 and 625 Manufactures Label Ultrasound Equipment Classification This device is classified as follows: • Protection against electric shock: Class I (protectively earthed enclosure) •...

  • Page 94: Basic Troubleshooting Techniques

    basIC TroubleshooTIng TeChnIques Basic Troubleshooting Techniques Lead Testing Leads may easily be tested without any special equipment by using the “Lead Test” function of the 25 Series console. A DMM can also be used to see if the pads and leads are in good working condition. Electricity will always choose the path of least resistance to ground.

  • Page 95: Testing Carbon Pads

    basIC TroubleshooTIng TeChnIques Testing Carbon Pads The carbon pads can be checked with the DMM. This is done with the resistance setting of the meter. Set the meter to “Ohms. ” Plug one of the test leads into the pin receptacle of the pad. Touch the other lead to the black carbon surface of the pad.

  • Page 96: Can/Csa Waveform Requirements

    Can/Csa WaVeformrequIremenTs CAN/CSA Waveform Requirements “A graphical representation of typical output signals, showing voltage waveforms at half and full setting of the output control when the EQUIPMENT is connected to resistive loads of 200 ohms, 500 ohms, 1000 ohms and 2000 ohms. ” See the following pages for the graphical representations: DYNATRON®...
  • Page 97 Can/Csa WaVeformrequIremenTs Interferential Current Mid-Range Full Range DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...
  • Page 98 Can/Csa WaVeformrequIremenTs Premodulated IFC Mid-Range Full Range DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...
  • Page 99 Can/Csa WaVeformrequIremenTs Russian Mid-Range Full Range DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...
  • Page 100 Can/Csa WaVeformrequIremenTs Biphasic Mid-Range Full Range DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...
  • Page 101 Can/Csa WaVeformrequIremenTs Hi Volt Mid-Range Full Range DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL...

  • Page 102: Electromagnetic Emissions And Immunity

    eleCTromagneTIC emIssIons and ImmunITy Electromagnetic Emissions and Immunity Tables 1 through 4 below list the Dynatron 25 Series declarations of electromagnetic emissions and immunity, and give user guidance on the Dynatron 25 Series in an electromagnetic environment per IEC 60601-1-2 guidelines. Table 1 Guidance and Manufacturer’s Declaration - Electromagnetic Emissions The dynatron 25 series (and accessories) is intended for use in the electromagnetic environment speci-...
  • Page 103 eleCTromagneTIC emIssIons and ImmunITy Table 2 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity The dynatron 25 series (and accessories) is intended for use in the electromagnetic environment speci- fied below. The customer or the user of the Dynatron 25 Series (and accessories) should assure that it is used in such an environment.
  • Page 104 eleCTromagneTIC emIssIons and ImmunITy Table 3 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity The dynatron 25 series (and accessories) is intended for use in the electromagnetic environment speci- fied below. The customer or the user of the Dynatron 25 Series (and accessories) should assure that it is used in such an environment.
  • Page 105 eleCTromagneTIC emIssIons and ImmunITy Table 4 Recommended separation distance between portable and mobile RF communications equipment and the Dynatron 25 Series (and accessories) The dynatron 25 series (and accessories) is intended for use in an electromagnetic environment in which radiated rf disturbances are controlled. The customer or the user of the dynatron 25 series (and ac- cessories) can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile rf communications equipment (transmitters) and the dynatron 25 series (and ac- cessories) as recommended below, according to the maximum power of the communications equipment.

  • Page 106: Medical Device Reporting Requirements

    Under the Safe Medical Devices Act (SMDA), the manufacturer and distributor are required to report specific incidents to the FDA. In the event of any applicable incident, you should report details of the incident to the Dynatronics Customer Service Department at 1-800-874-6251. Reports should be submitted to the manufacturer immediately to allow the manufacturer to report to the FDA within 2 working days based on the following criteria: •...

  • Page 107: Reporting Any Incident Of Patient Discomfort

    Reporting any Incident of Patient Discomfort Dynatronics recommends that if discomfort of any level is reported by the patient, the treatment be stopped immediately. The device and all accessories in use during that treatment should be isolated and held for inspection. Make a note of treatment parameters that were in use during the treatment including intensity settings.

  • Page 108: Dynatron® 25 Series Plus Limited Warranty

    REGISTRATION REQUIRED. In order for this warranty to be valid, the warranty registration card (included with the product) must be filled out and returned to DYNATRONICS within 30 days of purchase by the original owner. A copy of an invoice or receipt may be requested to verify purchase date.

  • Page 109: 25 Series Warranty Registration

    25 serIes Plus lImITed WarranTy 25 Series Warranty Registration To register the warranty for your Dynatronics unit, complete all information requested, and MAIL, FAX, or EMAIL TO: Dynatronics, 7030 Park Centre Drive, Salt Lake City, Utah 84121, Fax: 801-568-7711, Email: info@dynatron.com...

This manual is also suitable for:

Dynatron 925Dynatron 625Dynatron 525

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