Related Manuals for iReliev ET-1313
Summary of Contents for iReliev ET-1313
- Page 1 Pain Management System Model: iReliev™ Model #: ET-1313 Operating & Instruction Manual Read Before Using...
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Page 2: Table Of Contents
Pain Management System Intended Use The iReliev™ Pain Management System (Model # ET-1313) is intended for temporary relief of pain associated with sore and aching muscles in the upper and lower extremities (arm and/or leg) due to strain from exercise or normal household and work activities. -
Page 3: Reactions
Use the electrode pads only on normal, healthy, clean and dry skin. Do not use the electrode pads on open wounds or rashes, or over swollen, red, infected or inflamed skin. If you have ever had back surgery, consult your Physician before using the iReliev™ system. - Page 4 The pain may indicate that you have some other health problem. You should know the reason and source of your pain before using the iReliev™ system. Do not rely solely on the treatment of the iReliev™ system for pain.
- Page 5 Important: Do not use your iReliev™ system at the same time with any other device that transfers an electrical current into the body (e.g. another muscle stimulator). Stop using your iReliev™ system if you are feeling light headed or faint. Consult your Physician if this happens.
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Page 6: Introduction To Your Pain Management System
Introduction to your iReliev™ Pain Management System PACKAGE CONTENTS iReliev™ Device 1 clip holder 4 electrode pads 3 AAA batteries 2 lead wire cables Storage bag ABOUT THE iReliev™ DEVICE FRONT VIEW REAR VIEW Power on / adjust / increase setting key... -
Page 7: How The Ireliev™ System Works
How Your iReliev™ System Works The iReliev™ stimulator generates continuous stimulation pulse, which can create pain relief. We cannot ensure that pain relief is 100% effective for everyone. However, when used according to information within this instruction manual, it can be a safe, non-addictive and a non-invasive pain reliever. -
Page 8: Operating Instructions
Proper preparation of the skin to be covered by the electrode pads allows more stimulation to reach targeted tissues, prolongs electrode pad life, and reduces the risk of skin irritation. After connecting the lead wire(s) to the iReliev™ stimulator, use the following steps to prepare your skin at the electrode pad placement sites: 1. - Page 9 Selecting the Treatment Program Mode The iReliev™ stimulator (Model # ET-1313) offers eight different preset treatment program modes. The programs differ with respect to varying pulse widths and frequencies. The user may choose suitable stimulation mode depending on their personal condition, as indicated in the following steps: Start from P1;...
- Page 10 Selecting the Therapy Intensity Level 1. Intensity is adjustable according to the channel selected. Select the channel you wish to adjust by pressing CH1 or CH2. “CH1” or “CH2” will flash on the display. 2. To increase or decrease the intensity, press ON + (to increase) or OFF – (to decrease) repeatedly until the desired intensity level flashes on the display.
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Page 11: Care And Maintenance
How to Store Your iReliev™ System 1. Store your iReliev™ system at room temperature in a dry place, out of the reach of children. 2. If the iReliev™ stimulator will not be used for more than a week, remove the batteries from the stimulator. -
Page 12: Replacement Parts
Replacement Parts Be sure to use only iReliev™ Arm & Leg Pain Management System parts originally supplied. The following replacement parts can be ordered: Self -adhesive Pads (set of 4) CM5050 , size 50x50 mm , wired iReliev™ Part no. measured by length... -
Page 13: Ireliev™ Et-1313 Stimulator Technical Specifications
Power Source : 3 x AAA / 4.5 Volt batteries All electrical specifications are ±20% at 500Ω load. Description of symbols: (i) There are a number of technical symbols on your iReliev™ unit explained as follows: This symbols means “Serial number“ This symbols means “Attention” consult the accompanying documents This symbols means “Manufacturer“... -
Page 14: Electromagnetic Compatibility
Electromagnetic Compatibility Information Guidance and manufacturer’s declaration – electromagnetic emissions The ET-1313 is intended for use in the electromagnetic environment specified below. The customer or the user of the ET-1313 should assure that it is used in such an environment. Emissions Compliance... - Page 15 Guidance and manufacturer’s declaration – electromagnetic immunity The ET-1313 is intended for use in the electromagnetic environment specified below. The customer or the user of the ET-1313 should assure that it is used in such an environment. Electromagnetic environment IEC 60601...
- Page 16 Guidance and manufacturer’s declaration – electromagnetic immunity The ET-1313 is intended for use in the electromagnetic environment specified below. The customer or the user of the ET-1313 should assure that it is used in such an environment. IEC 60601 Electromagnetic environment...
- Page 17 ET-1313 The ET-1313 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the ET-1313 help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the ET-1313 as recommended below, according to the maximum output power of the communications equipment.
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Page 18: Warranty
Warranty This iReliev™ Arm & Leg Pain Management System carries a one-year warranty from the date of purchase. The warranty applies to the iReliev™ Arm & Leg Pain Management System and necessary parts and labor relating thereto. The distributor reserves the right to replace or repair the unit at their discretion.
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