TD3 Series
Content Support Introduction 2 3-6 Adverse Reactions Product Specifications Parts & Setup How to Use Recommended Use Positions Cleaning and Maintenance Technical Information Troubleshooting Environmental Condition for Transport and Storage Symbols interpretation Safety Test Standards EMC and FCC statement Contact Information 7 7 8 9 - 10 11 11 12 13 - 14 15 15 16 17 - 25 26 Indications for Use Safety Warning Contraindications Warnings Precautions 3 3 3 3-4 4-6
Support Our manual should provide you with all the information you need to set up and use this product. If you have a question, have a look at our Troubleshooting page! For further assistance, why not contact our Customer Care team directly? We’re here to help! Our Customer Care team are available from 9am-5pm, Monday to Friday (excluding bank holidays). We promise to respond to all queries and will ensure to resolve any issue you may be having.
Introduction Kinetik TENS Pain Reliever delivers electric impulses to tired and sore muscles. These different frequencies of impulses covering Transcutaneous Electrical Nerve Stimulation mimic the action potential coming from the central nervous system to trigger contraction of the muscle. It may be helpful in relieving aches and pains in various parts of the body such as the waist, shoulders, joints, hands and feet.
into the chest may cause rhythm disturbances to the patient’s heart, which could be lethal. Do not apply stimulation over, or in proximity to, cancerous lesions. Do not apply stimulation when the patient is in the bath or shower. If you have one of the following conditions, please consult with your physician before purchasing or using this device.
Do not apply stimulation of this device in the following conditions: (1) across the chest because the introduction of electrical current into the chest may cause rhythm disturbances to the heart, which could be lethal; (2) over painful areas. Please consult with your physician before using this device if you have painful areas; (3) over open wounds or rashes, or over swollen, red, infected, or inflamed areas or skin eruptions (e.g., phlebitis, thrombophlebitis, varicose veins).
(9) To use caution if the user has a tendency to bleed internally, such as following an injury or fracture. (10) Use caution if stimulation is applied over the menstruating uterus. (11) Use caution if stimulation is applied over areas of skin that lack normal sensation; (12) Stop using the device if the device does not provide pain relief. (13) Use this device only with the leads, electrodes, and accessories that the manufacturer recommends. (14) Do not share the use of the electrode pads with others.
Adverse Reactions Patients may experience skin irritation and burns beneath the stimulation electrodes applied to the skin; Patients may experience headache and other painful sensations during or following the application of electrical stimulation near the eyes and to the head and face. Patients should stop using the device and should consult with their physicians if they experience adverse reactions from the device. Product Specifications Accessories included in the package.
Parts & Setup Unpack the product, take the product and accessories out, charge device and then connect the electrode pad into the device. Then simply turn-on and select mode/intensity as desired. ON/OFF Countdown Timer Battery Indicator LCD Display Intensity Indicator Decrease Intensity Mode Selection Increase Intensity A Channel B Channel Pause/Play (a lock symbol will be shown on screen when paused) Timer Output A channel USB port 8 Output B channel For support… Visit our website: www.
How to Use • The Kinetik Wellbeing TD3 TENS Machine needs to be charged for up to 8 hours before the first use. • Connect a pair of electrode pads to one output cable – this is done by snapping them on. If required, connect the other pair of electrode pads to the remaining output cable. • Insert the output cables in use into the TD3 • Attach electrode pads to the treatment area, such as shoulders or legs.
• Good skin care is important for the comfortable use of this device. Be sure that the treatment area is clean of dirt and body lotion. • Keeping the electrode pads in their plastic storage bags after use will extend lifespan. The electrode is disposable and should be replaced when it loses the adhesiveness. To purchase additional electrodes, please contact Kinetik Wellbeing. Product Programs Program name Time min. Frequency (Hz) Pulse Width (µs) Remarks Mode 1 10,20,30,40,50,60 68.
Recommended Use Positions Cleaning and maintenance Please use a slightly wettened cloth or natural detergent to clean the device first, and then use a dry cloth to wipe again. The electrode pads that come with the device are disposable and should be replaced after they lose their adhesiveness – please contact Kinetik Wellbeing for replacements. We recommend that users avoid the sticky side of the pads from touch. 11 For support… Visit our website: www.kinetikwellbeing.
Technical Information Model/type TD3 Weight 40g Power supply Powered by internal 3.7V li-ion battery Automatic shutoff After 20 minutes without use Waveform and wave shape Biphasic rectangular wave pulse Degree of protection against electric shock Type BF applied part Pulse duration 100us (Microseconds) Type of protection against electric shock Internally powered equipment Pulse frequency 1-100Hz (Hz=vibration per second) Grade of waterproof IP22 Output Voltage Max.
Troubleshooting If your device is not operating properly, please check below for common problems and suggested solutions. If the recommended action does not solve the problem, please contact Kinetik Wellbeing. Problem One pad feels stronger than the other The intensity feels very weak The skin turns red or the skin feels irritated Possible Cause Solution This is normal. Different area of your body will react differently Nothing needs to be done. Make sure the pads are moist and making good contact.
Troubleshooting Problem No power source; no display on LCD Power cuts off during use It is difficult to attach the pad to the skin Adhesive surface of pad is not sticky Possible Cause The battery capacity is depleted Solution Charge the battery The battery is weak Charge the battery The cord is broken Replace the cord Have you removed the transparent film from the pad? Peel off film on the adhesive surface of pads Was the pad applied immediately after washing? Dry the pad Is the adhesive surfa
Environmental condition for normal working, transport and storage - Normal working ambient temperature: 5~40°C - Normal working ambient humidity: 15~90% - Store and transport ambient temperature: -25 ~70°C - Store and transport ambient humidity: 0~90% - Atmospheric pressure: (70~106)kPa Symbols interpretation Fragile, handle with care Type BF applied part Keep the product in the dry place Away from water and rain Read the instructions (actual symbol colours are white on a blue background).
Safety Test Standards • Medical Devices Directive 93/42/EEC • IEC 60601-1:2005+A1:2012/EN 60601-1:2006 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance • IEC60601-1-2：2014/EN60601-1-2：2014 Medical electrical equipment - Part 1-2: General requirements for safety - Collateral standard: Electromagnetic compatibility - Requirements and tests • IEC 60601-2-10:2012/EN 60601-2-10:2000+A1:2001 Medical electrical equipment - Part 2-10: Particular requirements for
EMC and FCC statement Electromagnetic Compatibility and FCC Compliance Statement 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, and this unit can be affected by portable and mobile radio frequency (RF) communications equipment. 2) Do not use a mobile phone or other devices that emit electromagnetic fields, near the unit. This may result in incorrect operation of the unit.
EMC and FCC statement 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.
EMC and FCC statement 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 Electrostatic discharge (ESD) IEC 60601 test level Compliance level Electromagnetic environment - guidance ±6 kV contact ±6 kV contact ±8 kV air ±8 kV air Floors should be wood, concrete or ceramic tile.
EMC and FCC statement 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 Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11 Power frequency (50Hz /60Hz) magnetic field IEC 61000-4-8 IEC 60601 test level Compliance level <5% UT (>95% dip in UT) for 0.
EMC and FCC statement 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.
EMC and FCC statement 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 level Compliance level Electromagnetic environment - guidance 80 MHz to 800 MHz Radiated RF 3 V/m IEC 61000-4-3 80 MHz to 2.
EMC and FCC statement a 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.
EMC and FCC statement Recommended separation distances between portable and mobile RF communications equipment and the device. The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
EMC and FCC statement The subject device has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. The product generates, uses, and can radiate radio frequency energy and, if not installed and used accordance with the instructions, may cause harmful interference to radio communications.
Contact Information Manufacturer： Harvard Medical Devices Ltd. HK Unit 1002, 10th Floor, Railway Plaza, 39 Chatham Road South, Tsimshatsui, Kowloon, Hong Kong. EC Authorized Representative： Share Info Consultant Service LLC Repräsentanzbüro Heerdter Lohweg 83, 40549 Düsseldorf 26 TD3 IB UK 20190425 For support… Visit our website: www.kinetikwellbeing.com / Email: customercare@kinetikwellbeing.
