Table of ConTenTs Table of Contents Introduction ............................I Essential Performance ................................I Operator’s Profile ..................................I Before You Treat a Patient ................................. I SmarTRAC Features ..........................2 Unpacking ....................................2 Principles of Operation ................................2 Device Design .....................................3 Touch Screen Control ................................3 Safety Features ....................................4 Traction Therapy Programs ............................4 Installation .............................
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Table of ConTenTs General Specifications .......................... 22 Standard Components ................................22 Technical Specifications ................................Environmental Conditions ..............................23 SmarTRAC Labeling ................................23 Definition of Symbols and Labeling ............................24 Maintenance and Troubleshooting ...................... 25 Cleaning and Disinfection ..............................25 Warning Messages, Error Messages, and Troubleshooting ....................25 Technical Maintenance ................................26 End of Life ....................................27 EMC Details ............................
InTroduCTIon Introduction This manual has been written for the owners and operators of the SmarTRAC traction device. It contains general instructions on operation, precautionary practices, maintenance, and parts information. In order to maximize the use, efficiency, and lifespan of the unit, please read this manual thoroughly and become familiar with the controls as well as the accessories before operating the unit.
Complete the warranty registration form located at the back of this manual and return it to Dynatronics within 30 days of purchase. This will insure that you are not billed for services that are covered by the warranty policy. Warranty registration should include the serial number for the device.
smarTraC feaTures Device Design The SmarTRAC is a combination of computer technology, functional design, and operational convenience. The device is intended for use by professional users only, such as qualified personnel in physiotherapy, rehabilitation, and adjacent areas. The device is ideal for lumbar and cervical traction. Sequential programming is possible in order to program combinations of traction which can be stored as favorites for later use.
smarTraC feaTures Favorites With one touch “Favorites” can be selected from the main screen. It will show the list of earlier stored manual protocols. Manual Operation When no “Clinical Protocol” or “Favorite” is requested, a single click on “Manual Operation” from the main screen will start a wizard which leads the user through all configurations that must be set up.
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smarTraC feaTures Single Continuous Traction The force is increased to the Traction Force with the configured Speed and stays there for the Traction Force Hold Time. Depending on the configured Speed and the Traction Force, the total treatment time is calculated and shown in the treatment screen.
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smarTraC feaTures NOTE Single Progressive Traction and Single Regressive Traction are not often used as single therapy programs, but most often in combination with other traction types to start and finish a combined traction treatment. NOTE Starting a combined traction protocol with regressive traction is not possible. It only lowers a previous programmed Traction Force towards zero in a configured number of Steps or towards the Traction Force value programmed.
InsTallaTIon Installation Standard Components Device 1671902 SmarTRAC Standard SmarTRAC Accessories 7B0087 Patient Stop Switch 7B0084 Fixing Knobs, set of 4 7B0085 Nylon Cord, 170 cm with Carabiner Hook 7B0086 Power Cord UL-CSA 115V straight socket black or grey (for USA) 5D00310 SmarTRAC Operator’s Manual Connection to Power Supply...
InsTallaTIon CAUTION Do not place the device in a location where the power cord could be tripped over or pulled out during treatment. Do not attempt to use the device if it is not properly grounded. Make certain that the device is electrically grounded by connecting it only to a grounded electrical service receptacle that conforms to the applicable national and local electrical codes regarding medical environments.
InsTallaTIon Cord Guidance CAUTION To avoid damage to the device, guide the cord over the pulley exactly as illustrated in the graphic to the left. Cervical Traction Operating For cervical traction, forces over 45 lbs. (200 Newton) are not allowed. By selecting a traction force higher than 45 lbs. (200 Newton), a warning will be issued about exceeding this limit.
operaTIng InsTruCTIons Operating Instructions Operator Controls 1. Cord 2. Pulley 3. Display with Touch Screen 4. Power Switch 0 Device disconnected from power supply 1 Device connected to power supply touch screen 5. Power Input and Power Fuses 6. Type Number Plate Provides device information: type and serial number, as well as data on voltage and maximum current consumption.
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operaTIng InsTruCTIons Navigation The following buttons are displayed on the navigation bar. Button Significance Back, return to previous screen. Continue, continue to next screen. Home, return to Home screen. Page Number / number of pages in multi-page menu screens or treatment step number / number of treatment steps in sequential protocols.
operaTIng InsTruCTIons Please select a menu item by pressing the relevant button to navigate to the next screen. You can return to the previous screen by pressing the back arrow at the top of the screen. You can return to the Home menu anywhere during navigation by pressing the home button.
operaTIng InsTruCTIons Removing Favorite To remove a favorite, first press the recycle bin and then the favorite you want to remove. Manual Operation Form of Therapy After selecting Manual Operation in the main menu, the possible forms of therapy appear. Depending on the selected form of therapy, you will be prompted to enter the required parameters.
operaTIng InsTruCTIons Speed The speed with which the tractive power changes can be set very accurately using the arrow keys. Moreover, you can use the three pictograms at the bottom of the screen: SLOW, MEDIUM, AND FAST. When all required parameters have been set, you will arrive at the treatment screen.
operaTIng InsTruCTIons Diagram The center screen has five small keys located within it, one located in each corner and one at the bottom center. These keys offer the option to zoom in and out of the depiction, or to move across the time line. These keys appear when the screen is touched once in the center.
operaTIng InsTruCTIons When the PAUSE button is pressed, the force is lowered towards zero and the PAUSE button is replaced again for the START button. When the STOP button is pressed the START/PAUSE button disappears and the force is slowly lowered toward zero. Only the EMERGENCY STOP button is still shown and can be pressed to lower the force fast.
operaTIng InsTruCTIons Naming Your Favorite Using the keyboard, type in the name of your favorite setting. Press ACCEPT to store your favorite setting under the name entered by you. Once stored, favorites may be retrieved from the Favorites menu. Programming A treatment can be programmed in two ways.
operaTIng InsTruCTIons Screen 2-3: LCD Brightness: Button to select the brightness of the backlight. Keyboard Sound: Button to turn on or off a keyboard press sound. End of Treatment – Sound: Button to select a number of sounds. Screen 3-3: System Info: Press this button to show current version and other system information.
WarnIngs, preCauTIons,and ConTraIndICaTIons Warnings, Precautions, and Contraindications Treatment Preparation • The Patient Stop Switch should be handed to the patient and its use should be explained. Make sure the Stop Switch can be used by the patient during the whole treatment. •...
WarnIngs, preCauTIons,and ConTraIndICaTIons • In the event of a loss of power to the unit, traction tension should only be released by having the patient move towards the traction device to release the tension on the rope. Once the tension on the rope has been released, the mechanical connection to the motor is loosened and the rope can be pulled out.
WarnIngs, preCauTIons,and ConTraIndICaTIons Contraindications Traction is contraindicated for the following: • Any condition for which movement is contraindicated • Cardiac or pulmonary problems • Discitis • Primary or metastatic bone tumor • Spinal cord tumor • Osteoporosis • Untreated Hypertension •...
general speCIfICaTIons General Specifications Standard Components Device 1671902 SmarTRAC Standard accessories SmarTRAC: 7B0087 Patient Stop Switch 7B0084 Fixing Knobs, set of 4 7B0085 Nylon Cord, 170 cm with Carabiner Hook 7B0086 Power Cord UL-CSA 115V straight socket black or grey (for USA) 5D00310 SmarTRAC Operator’s Manual Technical Specifications...
general speCIfICaTIons Environmental Conditions Transport and Storage This equipment, while packed for transport or storage, should not be exposed to environmental conditions outside the following ranges: +70° C (158° F) a. an ambient temperature range of -10° C (14° F ) b.
WarnIngs, preCauTIons,and ConTraIndICaTIons Definition of Symbols and Labeling Some or all of the following symbols are included in the labeling for this device. Definitions accompany each symbol. read the instructions TYpe b applIed parT according IeC60601-1 fuse Warning / Caution non-ionizing electromagnetic radiation end of life - Waste electrical and electronic equipment (Weee) Transport Values / Temperatures...
maInTenanCe and TroublesHooTIng Maintenance and Troubleshooting Cleaning and Disinfection Cleaning of Apparatus To clean, turn off the unit and unplug the power supply. Clean the unit with a clean, damp cloth. Do not use abrasive cleaners. A small amount of mild household detergent may be used, if needed. Cleaning Display Panel The display panel has an anti-glare coating and should be cleaned carefully.
This may be carried out by your supplier, or by another agency, authorized by the manufacturer. If a problem occurs or technical service is requested please contact Dynatronics (800) 874-6251. It is also recommended that a service history record is maintained.
maInTenanCe and TroublesHooTIng End of Life The SmarTRAC contains materials that can not be recycled and/or are noxious to the environment. Specialized companies can dismantle the unit and sort out these materials. When you dispose of the unit, follow local regulations and laws concerning waste management. SMARTRAC | OPERATOR’S MANUAL REV.
emC deTaIls EMC Details Medical electrical devices such as the SmarTRAC are subject to special precautions with regard to electromagnetic compatibility (EMC) and must be installed and commissioned in accordance with the EMC advice given in the instructions for use and accompanying documents. Portable and mobile RF communication systems (e.g.
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emC deTaIls Table 2 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity The SmarTRAC is intended for use in the electromagnetic environment specified below. The customer or the user of the smarTraC should assure that it is used in such an environment. IeC 60601 Compliance electromagnetic environment...
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emC deTaIls Table 3 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity The SmarTRAC is intended for use in the electromagnetic environment specified below. The customer or the user of the smarTraC should assure that it is used in such an environment. emissions IeC 60601 Compliance...
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emC deTaIls Table 4 Recommended separation distance between portable and mobile RF communications equipment and the SmarTRAC The SmarTRAC is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the smarTraC can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (trans- mitters) and the SmarTRAC as recommended below, according to the maximum output power of the communications equipment.
manufaCTurer produCT lIabIlITY Manufacturer Product Liability A law on Product Liability has become effective in many countries. This Product Liability law implies, amongst other things, that once a period of 10 years has elapsed after a product has been brought into circulation, the manufacturer can no longer be held responsible for possible shortcomings of the product.
REGISTRATION REQUIRED: In order for this warranty to be valid, the warranty registration page (included in this operator’s manual) must be filled out and returned to DYNATRONICS within 10 days of the date this product is delivered to the original owner. A copy of an invoice or receipt may be requested to verify purchase date.
Dynatronics for instruction. As a trained medical practitioner, you are solely responsible for determining appropriate application of this product for your patients. Before returning this product or any part of this product to Dynatronics for service, you must first obtain a return authorization number. Call 1-800-874-6251.
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