Roundwhale R-C101F Instruction Manual
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Roundwhale R-C101F Instruction Manual

Combo electrotherapy device
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INSTRUCTION MANUAL
FOR
Combo Electrotherapy Device
R-C101F
Shenzhen Roundwhale Technology Co., Ltd.
This manual is valid for the R-C101F Stimulator
Be sure to read this instruction manual before operation and
keep it where safe.
This user manual is published by Shenzhen Roundwhale
Technology Co., Ltd.

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  • Page 1 INSTRUCTION MANUAL Combo Electrotherapy Device R-C101F Shenzhen Roundwhale Technology Co., Ltd. This manual is valid for the R-C101F Stimulator Be sure to read this instruction manual before operation and keep it where safe. This user manual is published by Shenzhen Roundwhale...
  • Page 2 Amendments will be published in a new edition of this manual. All Rights Reserved. R-C101F Rev. V1.0© 2021, printed on Nov. 23, 2021. Declaration of conformity: Shenzhen Roundwhale Technology Co., Ltd. declares that the device complies with following normative documents:...

  • Page 3: Table Of Contents

    TABLE OF CONTENTS 1. FOREWORD 2. SAFETY INFORMATION 3. GETTING TO KNOW YOUR DEVICE 4. SPECIFICATION 5. OPERATING INSTRUCTION 6. INSTRUCTIONS FOR USE 7. CLEANING AND MAINTENANCE 8. TROUBLESHOOTING 9. STORAGE 10. DISPOSAL 11. ELECTROMAGNETIC COMPATIBILITY (EMC) TABLES 39 12. NORMALIZED SYMBOLS 13.

  • Page 4: Foreword

    1. FOREWORD 1.1 Introduction The device R-C101F is a dual channel output TENS (Trans- cutaneous Electrical Nerve Stimulation), and EMS (Elec- tronic Muscle Stimulation) stimulator. Before using, please read all the instructions in this user manual carefully and keep it safe for future use.

  • Page 5: Safety Information

    by physiotherapists, caregivers and top athletes around the world. High-frequency TENS currents activates the pain-in- hibiting mechanisms of the nervous system. Electrical im- pulses from electrodes, placed on the skin over or near the pain area, stimulate the nerves to block the pain signals to the brain, causing the pain go unperceived.
  • Page 6 EMS mode The EMS stimulation program stimulates healthy muscles in order to improve and facilitate muscle performance. The device can be used in the home or hospital, using the object (patient) must be 18 years or older of adults. 2.2 Important Safety Precautions and Warnings It is important that you read all the warnings and precautions included in this manual because they are intended to keep you safe, prevent risk of injury and...
  • Page 7 7) Do not use on scarred areas following a surgery for at least 10 months after the operation. 8) Do not use with serious arterial circulatory problems in the lower limbs. 2.2.2 WARNING If you have had medical or physical treatment for your pain, consult with your physician before use.
  • Page 8 skin. 11) The long-term effects of electrical stimulation are un- known. Electrical stimulation device cannot replace drugs. 12) Stimulation should not take place while the user is con- nected to high-frequency surgical equipment, which may cause burn injuries on the skin under the elec- trodes, as well as problems with the stimulator.
  • Page 9 headache. 2) TENS is not a substitute for pain medications and other pain management therapies. 3) TENS is a symptomatic treatment and, as such, sup- presses the sensation of pain that would otherwise serve as a protective mechanism. 4) Effectiveness is highly dependent upon patient selec- tion by a practitioner qualified in the management of pain patients.
  • Page 10 14) The instruction of use is listed and should be obeyed; any improper use may be dangerous. 15) Rare cases of skin irritation may occur at the site of the electrode placement following long-term application. 16) Do not use this device in the presence of other equip- ment which sends electrical pulses to your body.

  • Page 11: Getting To Know Your Device

    3. GETTING TO KNOW YOUR DEVICE 3.1 Accessories Description Combo Electrotherapy Device Electrode pad （40mm×40mm ) 4pcs Electrode wires 2pcs 9 Volt Battery User manual 3.2 LCD display No. Function description No. Function description 5 Treatment time 1 Icon of Channel 1 Treatment mode Low battery icon Pulse width or...
  • Page 12 3.3 Device illustration FRONT BACK SIDE...

  • Page 13: Specification

    Battery Strip 10 Battery Case 11 Belt Clip 12 Protective Cover 4. SPECIFICATION 4.1Technical information Device name Combo Electrotherapy Device Model/type R-C101F Power sources One 9 volt battery Output channel Dual channel Waveform Bi-phase square-wave pulse Output current 0-50V (Load:500 ohm)
  • Page 14 Output precision ±20% error is allowed for all the output pa- rameters P.W. (Pulse Width) Adjustable, from 50 to 300 μs, 10 μs/step P.R. (Pulse Rate) Adjustable, from 2 to 150 Hz, 1 Hz/step Time A d j u s t a b l e , f r o m 1 t o 6 0 m i n u t e s o r continuous.
  • Page 15 10 seconds. Pulse rate (2~150Hz) and pulse width (50-300μs) are fully adjustable. SD2 Mode The SD2 (Strength-Duration) mode consists of automatic modulation intensity and pulse width in 70% range. The intensity and pulse width in 70% range. The intensity is always increasing while the pulse width is decreasing and vice versa.
  • Page 16 The waveforms of the 5 stimulation modes are as follows. 1. Burst 2. Normal 3. Modulation 4. SD1 (Strength-Duration) 5. SD2 (Strength-Duration)
  • Page 17 Synchronous mode Alternate mode...

  • Page 18: Operating Instruction

    5. OPERATING INSTRUCTION 5.1 Battery 5.1.1 Check/ replace batteries Open the battery cover, insert one 9 into the bat- volt battery tery compartment. Make sure you are installing the batter- ies properly. Be sure to place the batteries according to the markings of positive terminal (+) and negative terminal (-) in the battery compartment of device.
  • Page 19 battery leakage. 5. Replace all of the batteries simultaneously! 6. Always replace the device with the same type battery. 5.2 Connect electrode pads to electrode wires Insert the electrode wires connector into electrode connec- tor. Make sure they are properly connected to ensure the good performance.
  • Page 20 areas at the same time. Caution Do not insert the plug of the electrode wires into any AC power supply socket. 5.4 Electrode 5.4.1 Electrode options The electrodes should be routinely replaced when they start to lose their adhesiveness. If you are unsure of your electrode adhesive properties, please order new replace- ment electrodes.
  • Page 21 5.4.3 Electrode placement R-C101F is a kind of OTC stimulator, suitable for home use. You only have to use according to the user manual, place the electrode on the position where you feel pain. Conduct exercise, treatment and adjustment based on your own feeling.
  • Page 22 Position of electrode placement under TENS programs Neck Shoulder Hand Back Abdomen...
  • Page 23 ２ Foot Joint (knee) Joint (elbow) Joint (ankle) Joint (wrist)
  • Page 24 Position of electrode placement under EMS programs Neck Shoulder Hand Back Foot...

  • Page 25: Instructions For Use

    6. INSTRUCTIONS FOR USE 6.1 Power On/Off Switch and Intensity Controls: If both controls are in the off-position, the device is switched off. By turning the controls clockwise, the appro- priate channel is switched on and the indicator of power (CH1 or CH2) will reveal on the LCD.
  • Page 26 6.3 Configuration Control By pressing the [SET] button , you can enter the value of configuration to perform. You can begin to set the value by pressing the controls of [ ] and [ ] when the value flashes . 6.4 Increment Control This button controls the increase of settings .
  • Page 27 on the settings intensity level. 6.8 To Set TENS parameters a. Set Pulse Width Press [SET] button and the number for “Width” on the LCD screen will flash. To change the default number, press ] or [ ] until the desired Pulse Width number is dis- played on the screen.
  • Page 28 (Continuous).Press [SET] control to enter this menu, then press [ ] or [ ] to adjust the setting. Press[ ] when the timer shows 60 minutes, it will be switched to continuous stimulation. 6.9 To Set EMS parameters Choose EMS Mode by pressing [MODE] . EMS and “S” for Synchronous will display on the screen.
  • Page 29 number or higher. If the default “ON” time is the desired time and no change is needed,press[SET] to move on to the next parameter. c. Set Relaxation “OFF” Time Press [SET] button and the number for “OFF” on the LCD Screen will flash.
  • Page 30 rameter. e. Set Pulse Rate Press [SET] and the number for “Rate” on the LCD screen will flash. To change the default number, press [ ] or [ until the desired Pulse Rate number is displayed on the screen. If the default Pulse Rate is the desired number and no change is needed, press[SET] to move on to the next pa- rameter.
  • Page 31 This unit can store 60 sets of operation records. Total treat- ment time up to 999 hours can be stored. Check and Delete Individual Records Press [MODE] control and tum on the power simultaneous- ly. The LCD will show the number of records and operation time.
  • Page 32 3. Remove the battery from the com- partment. 4. Insert the battery into the compart- ment. Note the polarity indicated on the bat- tery and in the compartment. 5. Replace the battery compartment cover and press to close. Notice of batteries: 1.
  • Page 33 experience such skin irritations, e.g. redness, blistering or itching, discontinue using them. Do not use the TENS stimulator permanently on the same body part, as this may also lead to skin irritations. 4. Electrode pads are private and intended for single person use.
  • Page 34 lation. Therefore, the placement of the electrodes may deviate from the standard. If application is not success- ful, contact your physician to find out which placement techniques are best for you. 2. Do not use any adhesive electrodes with a size smaller than those the original manufacturer attached.

  • Page 35: Cleaning And Maintenance

    treatment; 3. We advise you to use the device for one session per time. If you feel discomfort during treatment, you can either pause the session or decrease the intensity of the output. 7. CLEANING AND MAINTENANCE Fully comply with the following necessary daily mainte- nance requirements to make sure the device is intact and guarantee its long-term performance and safety.

  • Page 36: Troubleshooting

    7.2 Maintenance 7.2.1 The manufacturer didn’t authorize any maintenance agencies abroad. If your device has any problems, please contact the distributor. The manufacturer will not be responsible for the results of maintenance or repairs by unauthorized persons. 7.2.2 The user must not attempt any repairs to the device or any of its accessories.
  • Page 37 1. There’s foreign 1. Check and clean the body in the compartment. battery com- partment. 2. Replace the new battery or 2. The battery has install the battery correct- been used up or installed oppo- sitely. 3. Check and clean the No display 3.

  • Page 38: Storage

    1. The electrode loses connec- Automatic 1. Check and place the elec- tion with the halt in the trode properly on the skin. skin. treatment 2. Replace the battery. 2. If the battery is used up. 1. Do the treatment once a 1.The treatment day and shorten the treat- time lasts too...

  • Page 39: Disposal

    9.2 Storing the Unit 1. Place the unit, electrodes, lead wires and manual back into the carrying case. Store the box in a cool, dry place, -10℃ ~ 55℃ ; 10% ~ 95% relative humidity. 2. Do not keep in places that can be easily reached by chil- dren.
  • Page 40 The device is intended for use in the electromagnetic environment specified below. The customer or the user has to assure that it is used in such environment. Emissions test Compliance Electromagnetic environment - guidance The device uses RF energy only for its internal function.
  • Page 41 not applicable Surge ± 1 kV line(s) not applica- (for INTERNALLY IEC 61000-4-5 to line(s) POWERED ME EQUIPMENT) <5% U (>95% dip in for 0.5 cycle Voltage dips, 40% U short interrup- (60% dip in U not applicable tions and volt- for 5 cycles not applica- (For INTERNAL-...
  • Page 42 Immunity 60601 Compli- Electromagnetic environment - test test ance level guidance level Radiated 10V/m 10V/m & Portable and mobile RF communi- & table table 9 cations equipment should be used not closer to any part of the device, 61000-4-3 including cables, than the recom- mended separation distance calcu- lated from the equation applicable to the frequency of the transmitter.
  • Page 43 Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, 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.
  • Page 44 1720 GSM1800; 1845 CDMA 1900; Pulse 1700- GSM 1900; modu- 1990 DECT; LTE lation 1970 Band 1,3, 217Hz 4,25; UMTS Bluetooth, Pulse WLAN, 2400- modu- 2450 802.11 b/g/ 2570 lation n, RFID 2450, 217Hz LTE Band 7 5240 Pulse 5100- WLAN 802.11 modu- 5500...

  • Page 45: Normalized Symbols

    12. NORMALIZED SYMBOLS Electrical devices are recyclable material and should not be disposed of with household waste after use! Help us to protect the environ- ment and save resources and take this device to the appropriate collection points. Please contact the organization which is responsible for waste disposal in your area if any ques- tions.

  • Page 46: Warranty

    13. WARRANTY Please contact your dealer or the device center in case of a claim under the warranty. If you have to return the unit, en- close a copy of your receipt with clear statement of defect description. The warranty terms are as below: 1.
  • Page 48 Shenzhen Roundwhale Technology Co., Ltd. Add: 202, 2/F, Building 27,Dafa Industrial Park，longxi community,longgang street, longgang district, Shenzhen, China. Email: info@roovjoy.com...

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