iReliev ET-7070 Instruction & Operation Manual
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iReliev ET-7070 Instruction & Operation Manual

Strength & recovery system
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Instruction & Operating Manual
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iReliev™ Strength & Recovery System

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Summary of Contents for iReliev ET-7070

  • Page 1 Instruction & Operating Manual Read Before Using iReliev™ Strength & Recovery System...

  • Page 2: Table Of Contents

    Pain Management System Intended Use The iReliev™ Strength & Recovery System, model no. ET-7070 is intended for: For temporary relief of pain associated with sore and aching muscles in the lower back due to strain  from exercise or normal household and work activities. (Choose TENS Modes P1 through P7) For temporary relief of pain associated with sore and aching muscles in the upper and lower extremities ...

  • Page 3: Safety Instructions: Contraindications & Warnings

    Read instruction manual before operation. Be sure to comply with all “CAUTIONS” and “WARNINGS” in the manual. Failure to follow instructions can cause harm to user or device. Please read the following information carefully before using iReliev® Strength & Recovery System. What is TENS? The more precise term is Transcutaneous (meaning “through the skin”) Electrical Nerve Stimulation...
  • Page 4 Do not apply stimulation across the chest because the introduction of electrical current into the chest  may cause rhythm disturbances to the heart. Do not place the pads on or around your head. The effects of stimulation of the brain are unknown. ...
  • Page 5 Application of moderate heat (thermal wrap) to muscles as well as moistening skin prior to  treatment improves treatment efficacy; use of cold packs on treated muscles after treatment is likewise recommended. This unit should only be used with the leads, electrodes and accessories provided by the manufacturer.  The device is not intended for medical use, for the treatment of any medical condition or for any ...

  • Page 6: Adverse Reactions

    7 and page 9 and then restart the program again.  Only use iReliev™ brand electrode pads with your device. Any others many not be compatible with your unit and could degrade the minimum safety levels.

  • Page 7: Package Contents

    PACKAGE CONTENTS ET-7070 iReliev™ Strength & Recovery Device 1 clip holder Electrodes CM-5050, sized 2” x 2”, 4 pieces/pack 3 AAA batteries 2 lead wires1 storage bag ET-7272 size 130x90 mm 2 pcs/pack 7. Optional Conductive Back Wrap Accessory, Model # ET-1515 ABOUT THE iReliev™...

  • Page 8: Step By Step Operation Guide For Treatment

    STEP BY STEP OPERATION GUIDE FOR TREATMENT Preparing the Skin for Running a Session Proper preparation of the skin covered by the electrodes allows more stimulation to reach targeted tissues, prolongs electrode life, and reduces the risk of skin irritation. After connecting the lead wire(s) to the stimulator, use the following steps to prepare your skin at the electrode placement sites: 1.

  • Page 9: Placement Of The Pads For Tens (Treatment Of Pain)

    Connecting the Cable to The Device 1. Connecting the lead wire to the electrodes before applying to the Skin. 2. Insert the connector plugs into sockets at the top of unit. Placement of the Electrode Pads for TENS (Treatment of Pain) Note: 1.
  • Page 10 Step 3. Insert the connector plugs into sockets at the top of unit. For the Conductive Back Wrap, additional pads, and replacement parts, visit www.iReliev.com Note for EMS users: The belt can be used for your back or your stomach.

  • Page 11: Placement Of Pads For Ems (Muscle Stimulation)

    Placement of the Electrode Pads for EMS 1. Connecting the lead wire to the electrodes before applying them to the Skin. Use the large Electrode Pads for EMS. 2. The pad placement chart hereafter illustrates the correct placement of the pads for a selection of target muscle Note: Always start with a low intensity level, increase gradually.

  • Page 12: Turning On The Device

    Turning On the Device 1. Press and hold the ON+ button for one (1) second to turn on the device. 2. The most recently selected treatment time and program will flash when the unit is turned on. ▲Note : Do not turn the unit on until all electrodes and lead wires are properly attached. ▲Note : When stimulating the muscles of the arms or legs in the EMS Mode, bear in mind that the muscle contraction may cause involuntary limb movement which could cause injury to you or others.

  • Page 13: Selecting The Program

    SelectingTENS OR EMS Programs The device offers 14different pre-set treatment programs for both TENS (P1-P8) and EMS (P1-P6) modes; the programs differ with respect to varying pulse widths and frequencies. Choosethe mode that is appropriate to your needs or gives you the greatest pleasure 1.
  • Page 14 For TENS (P1-P8) Programs: When using any of the 8 programs for pain relief always start with the lowest intensity and gradually increase the level of intensity until you feel a “tingling” sensation. All programs are different and therefore feel differently. You may try all 8 programs in the beginning and choose one that feels pleasant. Never increase the intensity to a level so that it hurts, always stay under the point of discomfort.
  • Page 15 For EMS (P1-P6) programs: When using the device for muscle stimulation (EMS) any of the 6 programs may be used. The intent is to cause a muscle to contract, and then release. All 6 programs will achieve contraction and vary mainly by the rate and duration of the contractions.

  • Page 16: Selecting The Therapy Intensity Level

    Selecting the Therapy Intensity Level This device offer a maximum of 25 intensity levels. The design of the device does not allow the user to modify any of the electrical parameters. The only adjustment that can be made is the electrical intensity which is set to a predetermined maximum current that is well with in safe limits.

  • Page 17: Special Features

    SPECIAL FEATURES Treatment Time The device offers 12 preset times: 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55 and 60 minutes. Time will countdown on the display in 1-minute increments for the duration of your session.  The device turns off automatically when the therapy time has elapsed. ...

  • Page 18: Care And Maintenance

    The electrode pads are disposable and use an adhesive that will dry after prolonged usage or storage. Pads should be replaced when they lose their adhesive quality, or you sense a change in stimulation sensation. If you’re in doubt about the integrity of the pads, order fresh pads please order online at www.iReliev.com or contact authorized distributor(s).

  • Page 19: Troubleshooting

    TROUBLE SHOOTING Always check the unit and accessories before use to prevent damage and defects; these are some of the simple checks: 1. Make sure the battery has sufficient charge and is not corroded. 2. Make sure the cables fit tightly into the connection sockets of the device. The table below shows some common defects. If you cannot remedy the defects as described, contact your unit provider if it is not possible to remedy in the manner described. Defect Cause Remedy The device does not No battery or bad battery Replace battery turn on Battery not inserted...

  • Page 20: Et-7070 Stimulator Technical Specifications

    ET-7070 STIMULATOR TECHNICAL SPECIFICATIONS Channel: Dual, isolated between channels. Pulse Amplitude: Adjustable 0 – 80mA peak into 500Ω load each channel; RMSV at 3.5 V (max.), RMSA at 1.3mA (max.) Pulse Rate: As pre-programming operation mode. Pulse Width: As pre-programming operation mode. Timer: 5~60 min. selectable. LCD: Shows modes, pulse rate, pulse width, timer, CH1/CH2, intensity level.
  • Page 21  Radio equipment may affect the operation of this device. ELECTROMAGNETIC COMPATIBILITY INFORMATION Guidance and manufacturer’s declaration – electromagnetic emissions The ET-7070 is intended for use in the electromagnetic environment specified below. The customer or the user of the ET-7070 should assure that it is used in such an environment. Emissions Compliance Electromagnetic environment - guidance The ET-7070 uses RF energy only for its internal function.
  • Page 22 AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the ET-7070 is used exceeds the applicable RF compliance level above, the ET-7070 should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the ET-7070.
  • Page 23 Guidance and manufacturer’s declaration – electromagnetic immunity The ET-7070 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the ET-7070 help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the ET-7070 as recommended below, according to the maximum output power of the communications equipment.

  • Page 24: Warranty

    WARRANTY The iReliev® Strength & Recovery System, Model no. ET-7070, carries a one-year warranty from the date of purchase. The warranty does not apply to damage resulting from failure to follow the operating instructions, accidents, abuse, alterations or disassembly by unauthorized individuals.
  • Page 25 ExcelHealth Inc. www.iReliev.com P.O Box 80907 Billings, MT 59108...

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