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Snailax KTR-4021 Instruction Manual

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Transcutaneous Electrical Nerve Stimulator
KTR-4021

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Summary of Contents for Snailax KTR-4021

  • Page 1 Transcutaneous Electrical Nerve Stimulator KTR-4021...

  • Page 2: Safety Precautions

    I. Safety Precautions ■ Warning signs and symbols referred in this manual are for safe IMPORTANT INFORMATION! and proper use of the product by users, thus preventing damages to users or others. RETAIN FOR FUTURE USE! ■ Warning signs, symbols and their meanings are as follows: Read the instruction manual carefully before using this device, especially the Caution signs Meaning...
  • Page 3 Contraindications Warning 1. Please consult the doctor for pregnant women and 1. The product is prohibited from being used to patients those in Menstrual period, and patients with sensitive skin, with bleeding tendency, local acute suppurative heart disease, abnormal blood pressure, cancer, inflammation, local malignant tumor, local pacemaker, cerebrovascular disease, acute disease and those local metal implants or skin sensory disorders, Patients...

  • Page 4: Product Overview

    Transcutaneous Electrical Nerve Stimulator diseases. 1.2 Product model 2. Please don't move the product during use. When KTR-4021 changing the body part of treatment, please power off the product first before restarting it, otherwise the stimulation 1.3 Intended use may be strong.
  • Page 5 Skin detection Electric pulse sensor Battery level display Remaining time display Foot pulse intensity Body pulse intensity Pulse mode Electric pulse mode Body pulse Foot stimulation intensity intensity adjustment adjustment On/Off/Timer Foot electrode Power switch Charging Remote control power port Signal receiving window Main unit Signal-radiation...

  • Page 6: Technical Specifications

    Atmospheric pressure: 50~106kPa Transcutaneous Electrical Product name Nerve Stimulator (1) Maintenance and cleaning KTR-4021 Electrodes should be always clean on their surfaces, without any dirt, Model oil, sticky substance, etc., otherwise, their viscosity will decrease. Power supply Input: 5V DC 1A Dirty electrodes could be cleaned with clean water and then dried in Battery Capacity:3.7V DC 2200mAh...
  • Page 7 ±10% Storage -20℃-+70℃ 0-93%RH 700hPa-1060hPa Transport -20℃-+55℃ 15%-93%RH 700hPa-1060hPa 2.4 Describe for software: (1) Software name: KTR-4021-2081A V1.0 (2) Version: V1.0 2.3 Electronic performance Pulse frequency Foot:5-35Hz Body:70-100Hz WARNING Foot:360-400μs Pulse width Please ensure that the polythene packing is kept Body:100-120μs...

  • Page 8: How To Operate It

    Note: the main unit in standby state will shut down automatically if it IV. How to Operate It fails to receive the power-on signal from the remote control within 3 minutes. To reuse the main unit, you need to press "Power" on it to 4.1 Preparations before use enter the standby state.
  • Page 9 4.3 The use of battery your body parts with a pain. Then, follow the instructions on them to 4.3.1 Remote control battery operate the remote control. 1)The remote control uses 2 AAA batteries, which can be used for Note: be sure to adjust the massage intensity with the adjustment about half a year(according to use 30 minutes a day).

  • Page 10: Cleaning, Maintenance And Storage

    VI. Troubleshooting V. Cleaning, Maintenance and Storage The user or operator is not allowed to perform repair or maintenance 5.1 Cleaning and maintenance during use of the product. If it doesn't work, please send it to the 1) When the main unit becomes dirty, please wipe it with a dry cloth dealer for maintenance or repair.

  • Page 11: Emc Statements

    VII. EMC Statements 1) The product requires special attention to EMC and requires to be Are the electrodes in The electrodes must be in installed. contact with your foot good contact with your Please use it based on the EMC information provided, since it may foot soles or body skin.
  • Page 12 Atmospheric pressure limits. It indicates the Warning on danger range of atmospheric pressure to which medical devices can be safely exposed. The atmospheric pressure limits shall be indicated Category II medical device near the upper and lower horizontal lines. It means prohibition (something that must be Direct Current prohibited) Electrodes...
  • Page 13 X. Appendix Guidance and manufacture’s declaration Guidance and manufacture’s declaration – electromagnetic emission – electromagnetic immunity The Transcutaneous Electrical Nerve Stimulator is intended for use The Transcutaneous Electrical Nerve Stimulator is intended for use in the electromagnetic environment specified below. The buyer or in the electromagnetic environment specified below.
  • Page 14 Recommended separation distances between portable and Mains power quality <5% U <5% U mobile RF communications equipment and the Transcutaneous should be that of a (>95% dip (>95% dip Electrical Nerve Stimulator. in U in U typical commercial or Voltage dips, for 0.5 cycle for 0.5 cycle hospital environment.

  • Page 15: Warranty

    Pictures and/or descrip�on are required to claim defec�ve merchandise; c) Model number and Series Number label a�ached to each product 2. If the warranty claim is jus�fied by Snailax Customer Support, customer(s) will obtain from Snailax a Warranty/Return Authoriza�on Number (RMA Number) 3.Snailax reserves the right to specify that items be returned to the designated warehouse for...
  • Page 16 WEBSITES IT PROVIDES ACCURATELY ILLUSTRATE AND DESCRIBE PRODUCTS. Snailax reserves all the right for final interpreta�on of these Terms of Warranty and Return Policy above and the aright to change, modify, add or remove por�ons of these terms at any �me without prior no�fica�on.

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