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Related Manuals for Compex Tens / Heat
Summary of Contents for Compex Tens / Heat
- Page 1 TENS / HEAT...
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Page 3: Table Of Contents
TABLE OF CONTENTS Introduction..................................4 Indications for Use................................4 Safety Warning................................5 Contraindications................................5 Warnings..................................5 Precautions..................................6 Adverse Reactions.................................8 Symbol and Title................................8 Environmental Condition for Transport and Storage....................9 Electromagnetic Compatibility..........................10 How the Device Works..............................14 Device Description...............................15 Operating Instruction..............................16 Performance Specifications............................21 Cleaning and Maintenance............................21 Trouble Shooting................................22 Contact Information..............................23... -
Page 4: Introduction
INTRODUCTION Compex Tens / Heat delivers electric pulses and heat to the user’s body areas such as knee and back through the conductive silver pads. The portable and compact device has multiple modes of different pulse frequencies, covering Transcutaneous Electrical Nerve Stimulation (TENS) and Electrical Muscle Stimulation (EMS). -
Page 5: Safety Warning
SAFETY WARNING CONTRAINDICATIONS » Do not use this device on patients who have a cardiac pacemaker, implanted defibrillator, or other implanted metallic or electronic device, because this may cause electric shock, burns, electrical interfer- ence, or death. » Do not use this device on patients whose pain syndromes are undiagnosed. WARNINGS »... -
Page 6: Precautions
» Stimulation should not be applied over swollen, infected, or inflamed areas or skin eruptions, e.g., phlebitis, thrombophlebitis, varicose veins, etc. » Stimulation should not be applied over, or in proximity to, cancerous lesions. PRECAUTIONS » Safety of stimulation use during pregnancy has not been established. »... - Page 7 » Do not attempt to move the conductive silver pads while the device is operating. » Do not apply stimulation of this device in the following conditions: across the chest because the introduction of electrical current into the chest may cause rhythm disturbances to the heart, which could be lethal;...
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Page 8: Adverse Reactions
ADVERSE REACTIONS » You may experience skin irritation and burns beneath the conductive silver pads applied to the skin; » You should stop using the device and should consult with your physicians if you experience adverse reactions from the device. SYMBOL AND TITLE Information essential for proper use shall be indicated by using the corresponding symbols. -
Page 9: Environmental Condition For Transport And Storage
ENVIRONMENTAL CONDITION FOR TRANSPORT AND STORAGE ° Normal working ambient temperature: 10~40°C (50~104°F) ° TEMPERATURE LIMITATION Normal working ambient humidity: 30~85% ° Store and transport ambient temperature: -10 ~50°C (14~122°F) ° TEMPERATURE LIMITATION Store and transport ambient humidity: 30~90% Fragile; handle with care Keep away from rain Non-sterile Product packaging is able to be recycled... -
Page 10: Electromagnetic Compatibility
ELECTROMAGNETIC COMPATIBILITY 1. This product needs special precautions regarding electromagnetic compatibility (EMC) and needs to be installed and put into service according to the EMC information provided. This unit can be affected by portable and mobile radio frequency (RF) communications equipment. 2. - Page 11 GUIDANCE AND MANUFACTURE’S DECLARATION – ELECTROMAGNETIC EMISSION The device is intended for use in the electromagnetic environment specified below. The customer of the user of the device should assure that it is used in such an environment. Immunity IEC 60601 test Compliance level Electromagnetic environment - guidance test...
- Page 12 GUIDANCE AND MANUFACTURE’S DECLARATION – ELECTROMAGNETIC IMMUNITY The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment. Immunity test IEC 60601 test Compliance level Electromagnetic environment - guidance level...
- Page 13 observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the device. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m. RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT AND THE DEVICE.
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Page 14: How The Device Works
HOW THE DEVICE WORKS The device has multiple modes, covering TENS and EMS. If you are using the device for the first time, it is recommended that you start with the default Mode 1, which combines different pulse frequencies. Some modes are particularly effective for certain users, but you may need to select the mode that is best for you. -
Page 15: Device Description
DEVICE DESCRIPTION Remove the device and accessories from the packaging. The accessories include a USB cable used for charging, and a wrap with conductive silver pads. BATTERY INDICATOR INTENSITY INCREASE MODE CHANGE INTENSITY DECREASE TIMER CHANGE HEAT LEVEL ON / OFF: HOLD 2 SEC. CHARGING PORT USE ON/OFF BUTTON TO LOCK SCREEN... -
Page 16: Operating Instruction
OPERATING INSTRUCTION The following steps are used to guide the device operation, and the details about each step are listed in the following table. Charge control unit before first use Lightly dampen conductive silver pads with water Apply brace to body part NOTE: Skin should be clean. - Page 17 1ST STEP – Charge control unit before first use The control unit comes with a built-in rechargeable battery, and can be used as received. If the battery icon on the turned-on control unit keeps flashing, it means the battery is running out. Charge the control unit with the enclosed USB cable.
- Page 18 6TH STEP - Select program There are eight stimulation modes. Press the “M” button to select a M = MODE CHANGE desired pulse mode. The mode selected will be shown on the display. 7TH STEP - Change simulation time Default timer is set to 30 min. Press the “T” button to select a desired time (30, 40, 50, 60, 10 and 20 min) interval.
- Page 19 When using the device for the first time, we recommend starting from the default Mode 1, which combines the different frequencies. If you use one of the specific TENS or EMS modes, please refer to the following for details. USE AS TENS The control unit includes the following TENS frequencies, 69Hz (Mode 2), 1.2 Hz (Mode 4), 100Hz (Modes 5 and 6), and 160Hz (Mode 8).
- Page 20 Recommended Practice for Both TENS and EMS: • Start from the lowest intensity and gradually adjust the intensity to a comfortable level at a scale from from 1 to 20. • Good skin care is important for a comfortable use of device. Be sure the treatment site is clean of dirt and body lotion.
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Page 21: Performance Specifications
PERFORMANCE SPECIFICATIONS Power Source 3.7V Battery Number of Output Modes 8 auto pulse modes Timer Range (minutes) 10-60 Dimensions (mm) [L x W x D] 89 x 77 x 18 mm Waveform Biphasic Shape Rectangular Maximum Output Voltage 64V@500Ω Maximum Output Current 128mA@500Ω... -
Page 22: Trouble Shooting
TROUBLE SHOOTING If your device is not operating properly, please check below for common problems and suggested solu- tions. If the recommended action does not solve the problem, please contact the seller. STIMULATION IS WEAK OR NON-EXISTENT • Be sure skin is clean and pads are firmly attached to skin. •... -
Page 23: Contact Information
CONTACT INFORMATION Distributed by DJO, LLC JKH Health Co., Ltd. Address: 4-5F, Building 12, Hengmingzhu Industrial Park, Xinqiao Tongfuyu Industrial Area, Shajing, Baoan District, Shenzhen, China Tel: +86-755-27926589 Fax: +86-755-29970323 E-mail: info@JKHhealth.com... - Page 24 PL-029K13 VERSION 1.0...
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