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Summary of Contents for Venen Engel Vein Rocker
- Page 1 Product Manual Vein Rocker Transcutaneous Electrical Nerve Stimulator ENGLISH KTR-4029...
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Page 2: Table Of Contents
Content Product Overview...............01 Technical Specifications............05 III. Safety Precautions..............07 How to Operate It..............11 Cleaning, Maintenance and Storage........15 Troubleshooting...............16 VII. EMC Statements..............18 VIII. Symbols..................18 Executive Standards..............20 Appendix..................21... - Page 3 Battery level display Signal receiving window Foot electrode Foot pulse intensity Electric pulse mode Foot stimulation intensity adjustment Electric pulse Red light Remote control Power switch Main unit Signalradiation window Accessories adaptor AAA batteries battery cover USB charging for electro cable(Type-C) - 02 - - 02 -...
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Page 4: Technical Specifications
Applied parts of the product: into the electrode outlet on the product, and connect the other end of the Applied parts of the product include foot and body electrodes. cable to electrodes. ■ Remove the protective film on electrodes and firmly apply them to your 1.4.2 Electrodes: body parts with a pain. -
Page 5: Safety Precautions
2.2 Ambient conditions Temperature Humidity Barometric pressure Rated load impedance 500Ω, with ±10% error tolerance Set treatment time 15/30/45/60minutes, with an Normal operation +5°C -+40°C 15%-93%RH 700hPa-1060hPa acceptable error of ±10% Storage -20°C -+70°C 0-93%RH 700hPa-1060hPa Transport -20°C -+55°C 15%-93%RH 700hPa-1060hPa 2.3 Electronic performance 2.4 Describe for software:... - Page 6 Contraindications Warning The product is prohibited from being used to patients Please consult the doctor for pregnant women and with bleeding tendency, local acute suppurative those in Menstrual period, and patients with inflammation, local malignant tumor, local pacemaker, sensitive skin, heart disease, abnormal blood local metal implants or skin sensory disorders, Patients pressure, cancer, cerebrovascular disease, acute with deep venous thrombosis, and to human hearts and...
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Page 7: How To Operate It
IV. How to Operate It 4.1 Preparations before use First install 2 AAA batteries on the remote control, pay attention to the positive and Caution negative polarities of the batteries, and then close the battery cover. Make sure that the lithium battery of the host is fully charged. If the lithium battery of the Please don't use the product near your heart and to your host is insufficient, it needs to be charged before use. - Page 8 Note: the main unit in standby state will shut down automatically if it fails to Note: be sure to adjust the massage intensity with the adjustment button on receive the power-on signal from the remote control within 3 minutes. To the right side of the remote control, otherwise the intensity will have no reuse the main unit, you need to press "Power"...
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Page 9: Cleaning, Maintenance And Storage
4.3 The use of battery V. Cleaning, Maintenance and Storage 4.3.1 Remote control battery 5.1 Cleaning and maintenance 1)The remote control uses 2 AAA batteries, which can be used for about 1) When the main unit becomes dirty, please wipe it with a dry cloth or towel. half a year(according to use 30 minutes a day). -
Page 10: Troubleshooting
Are the electrodes in The electrodes must be in VI. Troubleshooting contact with your foot good contact with your foot The user or operator is not allowed to perform repair or maintenance during use of the soles or body skin? soles or body skin. -
Page 11: Emc Statements
VII. EMC Statements Warning on danger 1) Electromagnetic compatibility (EMC) is of particular importance for this device. Please use it based on the EMC information provided, since it may be affected by portable and mobile RF communication devices. Category II medical device 2) The product has been thoroughly tested and inspected to ensure its excellent performance and proper operation. -
Page 12: Executive Standards
XI. Appendix Atmospheric pressure limits. It indicates the range of atmospheric pressure to which medical devices can be safely exposed. The atmospheric pressure Guidance and manufacture’s declaration limits shall be indicated near the upper and lower – electromagnetic emission horizontal lines. The Transcutaneous Electrical Nerve Stimulator is intended for use in the electromagnetic environment specified below. - Page 13 Guidance and manufacture’s declaration Voltage dips, <5% UT <5% UT Mains power quality – electromagnetic immunity short (>95% dip in (>95% dip in should be that of a typical interruptions UT) for 0.5 UT) for 0.5 commercial or hospital The Transcutaneous Electrical Nerve Stimulator is intended for use in the and voltage cycle cycle...
- Page 14 Recommended separation distances between portable and mobile RF communications equipment and the Transcutaneous Electrical Nerve Stimulator. The Transcutaneous Electrical Nerve Stimulator is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The buyer or user of the Transcutaneous Electrical Nerve Stimulator can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Transcutaneous Electrical Nerve Stimulator...
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