instruction manual - TENS Machines & Pain Relief Blog
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1. LG TEC Multi INSTRUCTION MANUAL ecu TEC Multi DES www LGMedSupply com This manual is valid for the LG TEC Multi This user manual is published by Current Solutions LLC Current Solutions LLC does not guarantee its contents and reserves the right to improve and amend it at any time without prior notice Amendments may however be published in new editions of this manual All Rights Reserved Rev V1 0 2011 A United States Federal Law restricts this device to sale by or on the order of a physician or licensed practitioner Conformity to safety standards Current Solutions LLC declares that the device complies with following normative documents IEC60601 1 IEC60601 1 2 EC60601 2 10 IEC60601 1 4 15010993 5 15010993 10 5010993 1 10 11 12 TABLE OF CONTENTS FOREWORD 1 1 Introduction 1 2 Medical background SAFETY INFORMATION visi 6 2 1 Indication for use 2 2 Contraindications 2 3 Warnings 2 4 Precautions PRESENTATIONS 3 1 Front and Rear panel 3 2 LCD display 3 3 The key functions SPECIFICATION met dose tae inet tenet restent Z 4 1 Accessories 4 2 Technical information INSTRUCTION FOR USE raa nos R RA 13 5 1 Check Battery 5 2 Connect electrodes to lead wires 5 3 Connect lead wires to device 5 4 Place electrodes on skin 5 5 Switch on 5 6 Checking the memory 5 7 Selection2. LCD ON OFF button Increasing the output intensity of channel 1 Select User 1 or User 2 Decreasing the output intensity of channel 1 Program selection backward Reducing the output intensity of channel 2 Enter the user program parameter setting Pause Increasing the output intensity for channel 2 Program selection forward Belt clip 14 Battery cover Socket for channel 1 Socket for channel 2 3 2 LCD Display oe te Hi L ud iii TENS EMS and MASSAGE display Lock intensity Program number Output pulse frequency and width User 1 User2 Pause Treatment sign Memory checking Low battery indicator Treatment time Working time or memory time Treat position of hand Treat position of body Channel 1 output Channel 2 output M Uude oo BR wD aM 5 5 3 3 The Key Functions The buttons on the device has the different functions in the different states except the basic function 45 Button In working mode ON OFF the device Stop the treatment Press and hold on 3 seconds turn off device In set mode Confirmed the setting parameter and return the normal state A Button In working mode To select the program in the up way Setting doctor parameter mode Press itto adjust user program parameter Button In working mode To select the program in the down way Setting doctor par
3. Voltage fluctuations flicker Not emissions applicable IEC 61000 3 3 Guidance and manufacturer s declaration electromagnetic immunity The device is intended for use in the electromagnetic environment specified below The customer or the user should assure that it is used in such an environment Electromagnetic environment guidance Compliance Immunity IEC 60601 at eve test test level Floors should be wood concrete or Electrostatic 6 kV ceramic tile If floors 6 kV discharge are covered with ESD IEC contact coritact synthetic material 61000 4 2 therelative humidity 8 kV air ia should be at least 30 95 2kV for Electrical Not applicable Mains power quality fast power supply should be that of a transient lines typical commercial burst IEC for or hospital 61000 4 4 _ input output environment lines Surge 1kV Not applicable Mains power quality IEC differential should be that of a 61000 4 5 mode typical commercial 2kV common or hospital mode environment Voltage dips lt 5 UT Not applicable Mains power quality short gt 95 dip in should be that of a interruptions UT for 0 5 typical commercial or and voltage cycle hospital environment variations on power supply 40 UT input lines 60 dip in IEC UT for 5 61000 4 11 Cycles 70 UT 30 dip in UT for 25 Cycles lt 5 UT gt 95 dip in UT for 5 sec Power 3 A m 3 A m P
4. the treatment User U1 or U2 5 8 Select the treatment mode 5 9 Set the parameter in the doctor mode 5 10 Select the program 5 11 Select the treatment 5 12 Adjust the intensity 5 13 Pause 5 14 Lock the button 5 15 Switch off 5 16 Replace batteries 5 17 Low battery indicator PROGRAMS AND SPECIAL 21 6 1 TENS pain relief program 6 2 EMS muscle training program 6 3 Massage program CLEANING AND CARE roseus 220 6 1 Tips for skin care 6 2 Cleaning the device 6 3 Electrodes 6 4 Cleaning the Electrodes cords 6 5 Maintenance CLEANING AND MAINTENANCE eene 28 7 1 Cleaning the device 7 2 Electrodes 7 3 Cleaning the Electrodes cords 7 4 Maintenance TROUBLESHOOTING STORAGE E DISPOSAL reorum in ELECTROMAGNETIC COMPATIBILI GLOSSARY OF SYMBOLS 1 FOREWORD 1 1 Introduction The LG TEC Multi is a battery operated pulse generator that sends electrical impulses to the body and reach the nerves and underlying muscle group this is a unit to be used for pain relief muscle stimulation and massage The device provides two controllable output channels each independent of each other an electrode pair can be connected to each output channel The parameters of units are controlled by button Its intensity level is adjustable according to the needs of patients 1 2 Medical background What is TENS TENS Transcuta
5. 0Hz Treatment time 5 90 Intensity Adjustable from 0 to 60mA 1000 ohm 5 C to 40 C with a relative Operating humidity of 3096 7596 conditions atmospheric pressure from 700 hpa to 1060 hpa 10 C to 55 C with a relative Storage humidity of 2096 9396 conditions atmospheric pressure from 700 hpa to 1060 hpa Dimensions 117x60x25mm without belt 110g without batteries Weight 140g with batteries 5 INSTRUCTIONS FOR USE 5 1 Check Battery Insert a fresh 4xAAA batteries into the battery compartment Make sure you are installing the battery properly The battery is inserted in the casing on the back of the stimulator Be sure to match the positive and negative ends of the battery to the markings in the battery compartment of unit To remove the battery cover press and pull down following the direction of on the battery cover Caution Remove the battery from the stimulator during storage to prevent battery leakage Failure to do so may damage the stimulator Replace a battery that has been immersed in water or liquid Never heatthe battery or throw it into a fire e Ifthe battery is leaking a liquid do not touch the liquid with bare skin Neverrecharge battery An explosion may result e Dispose ofthe battery according to current federal state and local regulations 5 2 Connect electrodes to lead wires Insert the lead wire connector into electrodes connec
6. ame nerve cannot carry a pain and a non pain impulse at the same time the stronger non pain impulse from the device controls the gate The second method of pain control is the endorphin release method The device can be set to trigger the body s natural pain killers called endorphins These chemicals interact with receptors blocking the perception of pain This is similar to the way the pharmaceutical drug morphine works but without the side effect associated with morphine No matter which pain control method is employed the Device has been proven useful in pain management By reading this manual and carefully following the treatment instructions provided by your clinician you can attain maximum benefit from your device What is EMS EMS Electrical muscle stimulation is achieved by sending small electrical impulses through the skin to the underlying motor units nerves and muscles to create an involuntary muscle contraction Neuromuscular stimulation has many usesbeyond its traditional application to prevent disuse atrophy How does EMS work Because the transdermal stimulation of nerves and muscles may be accomplished by electrical pulses this modality can help prevent disuse atrophy Accordingly incapacitated patients can receive therapeutic treatment to create involuntary muscle contractions thereby improving and maintaining muscle tone without actual physical activity The goal of electrical muscle stimulation is to ach
7. ameter mode Press itto adjust user program parameter Button In normal mode Press to select the U1 or U2 In doctor mode Press it to select the U1 or U2 S Button In normal mode Press it to pause the treatment or to continue the treatment In doctor mode Press it to select setting user program parameter and enter the next parameter set CH1 Button In working mode To decrease the output intensity of channel 1 To unlocked the button In doctor mode Press it with S button together for 3 seconds to lock the user program Press it with button together for seconds to reset the U1 or U2 original parameter CH2 Button In working mode To decrease the output intensity of Channel 2 To unlocked the button In doctor mode Press it with S button together for 3 seconds to enter check the recording state CH1 Button In working mode To increase the output intensity of channel 1 CH2 Button In working mode To increase the output intensity of Channel 2 4 SPECIFICATION 4 1 Accessories No DESCRIPTION Q TY 1 TENS stimulator device 1 piece 2 Electrodes Leads 2 pieces 3 40mm x 40mm adhesive electrodes 4 pieces 4 AAA Battery 4 pieces 5 Instruction Manual 1 piece 6 Carrying case 1 piece 4 2 Technical Information Channel Two channel Power supply DC6V 4 x AAA batteries Waveform Biphase square wave pulse Pulse duration 50 300uS Pulse frequency 1 15
8. atteries exhausted D 9 STORAGE 1 Fora prolonged pause in treatment store the device in a dry room and protect it against heat sunshine and moisture 2 Store the device in a cool well ventilated place 3 Never place any heavy objects on the device 10 DISPOSAL Used fully discharged batteries must be disposed of in a specially labeled collection container at toxic waste collection points or through an electrical retailer You are under legal obligation to dispose of batteries correctly Please dispose of the device in accordance with the legal obligation 11 ELECTROMAGNETIC COMPATIBILITY EMC TABLES Guidance and manufacturer s declaration electromagnetic emissions The device is intended for use in the electromagnetic environment specified below The customer or the user assures that it is used in such an environment Emissions Electromagnetic environment t st Compliance guidance The device uses RF energy only for its internal function Therefore RF its RF emissions are very low and emissions Group 1 are not likely to cause any CISPR 11 interference in nearby electronic equipment RF emissions CISPR11 The device is suitable for use in all establishments other than domestic and those directly Harmonic connected to the public low emissions Not voltage power supply network IEC applicable that supplies buildings used for 61000 3 2 domestic purposes
9. e 50 3 modulation 0 P13 100 75 30 P14 Burst rate 2Hz Fixed rate 150Hz 200 30 P15 Burst rate 2Hz Burst Fixed rate 35Hz 50 30 Burst rate 2Hz P16 Burst Fixed rate 80Hz 50 30 P17 Continuous 110 175 30 P18 Hans 150 2 150 200 30 P19 Burst 100 150 30 P20 6 2 EMS muscle training program 1 Athletic Training Neglected for many years muscle preparation has today become indispensable for the competitive athlete In this respect muscular electro stimulation is a complementary training technique widely used by an increasing number of athletes aiming to improve their level of performance Increasing the maximum strength of a muscle developing muscular volume increasing the explosive strength of muscles or improving the capacity of muscle fibres to sustain effort over long periods of time are objectives that differ according to the sporting discipline being practiced Ensuring optimal muscle preparation immediately before competition combining electro stimulation with voluntary muscle training optimizing the effects of training techniques such as stretching reproducing the muscular stress resulting from polymeric training or imposing a restoration activity on muscles is easily accessible today thanks to the high specificity of the new programs offered by your device Use of programs of the Sport category is not suitable for atrophied muscles that have suffered any kind of pathological proc
10. e by or on the order of a physician A prescription is required If your pain does not improve becomes more than mild or continues for more than five days stop using the device and consult with your physician Do not apply stimulation over your neck because this could cause severe muscle spasms resulting in closure of your airway difficulty in breathing or adverse effects on heart rhythm or blood pressure Do not apply stimulation across your chest because the introduction of electrical current into the chest may cause rhythm disturbances to your heart which could be lethal 6 Do not apply stimulation over painful areas If you have painful areas you should consult with your physician before using this device 7 Do not apply stimulation over open wounds or rashes or over swollen red infected or inflamed areas or skin eruptions e g phlebitis thrombophlebitis varicose veins 8 Do not apply stimulation over or in proximity to cancerous lesions 9 Do not apply stimulation in the presence of electronic monitoring equipment e g cardiac monitors ECG alarms which may not operate properly when the electrical stimulation device is in use 10 Stimulation should not take place while the user is connected to high frequency surgical equipment it may cause burn injuries on the skin under the electrodes as well as problems with the stimulator 11 Do not use the stimulator in the vicinity of shortwave or microwav
11. e therapy equipment since this may affect the output power of the stimulator 12 Do not apply stimulation when in the bath or shower 13 Do not apply stimulation while sleeping 14 Do not apply stimulation while driving operating machinery or during any activity in which electrical stimulation can put you at risk of injury and 15 Do not use the device on children if it has not been evaluated for pediatric use 16 Consult with your physician before using this device because the device may cause lethal rhythm disturbances to the heart in susceptible individuals and 17 Apply stimulation only to normal intact clean healthy skin 18 This device requires a written prescription from a physician 2 4 Precautions 1 TENS is not effective for pain of central origin including headache 2 TENS is not a substitute for pain medications and other pain management therapies 3 TENS devices have no curative value 4 TENS is a symptomatic treatment and as such suppresses the sensation of pain that would otherwise serve as a protective mechanism 5 Effectiveness is highly dependent upon patient selection by a practitioner qualified in the management of pain patients 6 The long term effects of electrical stimulation are unknown 7 Since the effects of stimulation of the brain are unknown stimulation should not be applied across your head and electrodes should not be placed on opposite sides of your head 8 You ma
12. ess Fitness programs Today there are more fitness enthusiasts than ever before and their number is rising Apart from some rare individuals who have real competitive targets the vast majority have only one aim to restore their body to peak physical condition or maintain it at that level Cardio training therefore alternates with more specific exercises to develop or maintain a good quality musculature With this in mind the sought after aims may differ according to who is doing the training increasing muscle volume toachieve an imposing stature body building or better muscle endurance to improve physical comfort during sustained efforts Combined with a voluntary physical activity aerobic exercises in the fitness facility footing cycling swimming etc which becomes more pleasant and therefore more effective the programs of the Fitness category enable users to obtain a toned and harmonious figure 3 4 Esthetic Program Thanks to their great diversity and their high specificity the Aesthetic programs provide the solution for everyone who wants to regain and keep the benefits of intense muscular activity These programs allow you to restore and maintain a firm body shapely figure and toned skin Indeed a sedentary life style is very bad for the figure especially if you have a poorly balanced diet The muscles which are not used much lose their qualities loss of strength reduced tone slackness They can no
13. h frequency range b NOTE At 80 MHz ends 800 MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people 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 If the measured field strength in the location in which the device is used exceeds the applicable RF compliance level above should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the device b Over the frequency range 150 kHz to 80 MHz field strengths should be less than Vi V m 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 The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the as rec
14. ieve contractions or vibrations in the muscles Normal muscular activity is controlled by the central and peripheral nervous systems which transmit electrical signals to the muscles EMS works similarly but uses an external source the stimulator with electrodes attached to the skin for transmitting electrical impulses into the body The impulses stimulate the nerves to send signals to a specifically targeted muscle which reacts by contracting just as it does with normal muscular activity 2 SAFETY INFORMATION 2 1 Indications for use This device is used in following instance 1 2 3 4 5 6 7 Symptomatic relief of chronic intractable pain acute post traumatic pain or acute post surgical pain Increase of blood flow in the treatment area Relaxation of muscle spasm Immediate post surgical stimulation of muscles to prevent venous thrombosis Prevention or retardation of disuse atrophy Muscle re education Maintaining or increasing range of motion 2 2 Contraindications Do not use this device if you have a cardiac pacemaker implanted defibrillator or other implanted metallic or electronic device Such use could cause electric shock burns electrical interference or death 2 3 Warnings 1 2 3 Not suitable for use during pregnancy or labor or if you suspect you may be pregnant Consult with your physician before using this device Federal law USA restricts this device to sal
15. lems persist 85 c ga Press A and V button to set the treatment frequency Press S button to enter the setting the pulse duration e Press A and V button to set the treatment pulse width cz ey Ces 5 10 Select the program Press A or V button to select the treatment program form TENS EMS MASSAGER and USER program D ji xj ip 30 08 P4 5 13 Pause e Press Q0 button to stop the output e Press S button to pause treatment and press again to continue the treatment 5 14 Lock the button If there is no operation in the panel for 10 seconds the button will be locked automatically The user can press the CH1 or CH2 to unlock B e E 30 D i CH1 P 2 Lt 5 15 Turn off Press the 9 button for seconds to turn off e In the working mode if there is no operation in the panel for 2 minutes the device will be switch off automatically Unplug the electrode lead wires grasping them by the e plug the cord If treatment will be resumed shortly the electrodes may be left on the skin When the electrodes are removed clean the skin thoroughly with mild soap and water If there is skin irritation consult your medical professional 5 16 Replace batteries To replace the batteries open the lid cover and extract the battery Replace it with new AAA batteries Make sure you i
16. longer carry out their tasks of supporting the body and holding the organs in place The body becomes soft and loose with clear consequences on body shape Rehabilition and Relaxtion program The low frequency current used for the Rehabilition and Relaxtion category of programs significantly improves blood circulation in the stimulated area Many people more particularly women who remain standing for long periods suffer from circulatory problems These mainly affect the legs and are caused by stagnation of the blood and the lymph and are manifested by a feeling of heavy legs swelling or the dilatation of surface veins The consequences are multiple fatigue tension pain lack of oxygenation of tissue and the appearance of varicose veins and edemas EMS Program program Freg Wih ment default P1 50 150 30 2 1 P2 80 150 30 1 1 P3 80 150 30 0 5 0 5 P4 80 60 4 2 180 200 220 240 P5 30 30 30 2 150 170 200 200 P6 80 60 30 2 150 170 200 200 P7 80 2 200 P8 80 2 200 P9 5 60 3 200 250 200 P10 5 15 3 200 250 200 P11 5 90 3 200 250 200 P12 5 120 3 200 250 200 P13 5 80 5 2 200 270 190 210 P14 5 60 150 250 P15 2 60 150 P16 5 60 150 200 P17 8 60 5 150 200 150 P18 3 30 100 2 200 P19 5 60 3 300 300 250 P20 3 30 80 2 200 6 3 Massage program The programs of the Massage category subject the muscles of the stimulated region to m
17. neous Electrical Nerve Stimulation gives good results in acute and chronic pain conditions of many kinds It is clinically proven and used daily by Physical Therapists other caregivers and top athletes around the world High frequency TENS activates the pain inhibiting mechanisms of the nervous system Electrical impulses from electrodes placed on the skin over or near the painful area stimulate the nerves to block the pain signals to the brain and the pain is not perceived Low frequency TENS stimulates the release of endorphins the body s natural painkillers TENS is a safe treatment method and has in contrast to drugs and other pain relief methods no side effects It may be sufficient as the only treatment form but it is also a valuable complement to other pharmacological and or physical treatments TENS does not always treat the cause of pain Consult your doctor if pain persists How Does TENS Control Pain The device provides pain relief in two ways The first is the gate control method When the body is injured both pain and non pain impulses are sent to the brain from the nervous system These pulses travel through the cutaneous nerves to the deeper afferent nerves and then to the spinal cord and brain Along the ath are many areas referred to as gates which determine which impulses are allowed to continue on to the brain The gates prevent the brain from receiving too much information too quickly Since the s
18. nsert the battery correctly 5 17 Low battery indicator When the low power indicator flashes the batteries should be replaced with new batteries as soon as possible However the stimulator will continue to operate for several more hours 6 PROGRAMS AND SPECIAL APPLICATIONS 6 1 TENS pain relief program Physical pain is an abnormal and unpleasant sensation caused by an injury a disorder or incorrect functioning of a part of our organism It is a signal sent to us by our body which should not be ignored and that in all cases requires us to consult a doctor if it does not disappear quickly The approach to pain adopted by the medical profession has changed considerably in recent years Treatment of the cause is always fundamental however the pain as such must be otherwise removed or at least considerably reduced and made bearable for the patient The means to combat pain have developed greatly and there is no longer any hesitation today in using powerful analgesics to improve the quality of life of patients TNES Program Pulse Treatment program Waveform sd Width time Min us default P1 Continuous 100 200 30 P2 Continuous 80 150 30 P3 Continuous 35 200 30 P4 Continuous 2 250 30 P5 Alternate 100 200 P7 100 2 150 200 P8 Burst 150 30 P6 100 2 150 200 30 30 30 P9 Modulation 200 100 30 P10 Modulation 200 100 30 Pulse rate En modulation 250 30 P12 Pulse rat
19. oderate activity which produces beneficial effects that help to improve physical comfort and well being Remaining in the same working position for a long time for example sitting in front of a computer screen conditions of stress repeated jostling insufficient muscular conditioning before physical activity are all very frequent situations that are often responsible for uncomfortable bodily sensations Massage program program ret i ine mu default P1 7 5 3 300 21 P2 298 250 22 PS 1 50 250 44 P4 5 8 200 30 P5 5 8 300 30 P6 5 8 200 30 P7 5 8 300 30 P8 85 130 100 200 30 P9 25 70 200 30 P10 1 15 200 30 7 CLEANING AND MAINTENANCE 7 1 Cleaning the device 1 Remove the batteries from the device every time before cleaning 2 Clean the device with a soft slight moistened cloth In case of more extreme soiling you can also moisten the cloth with mild soapy water 3 Do not use any chemical cleaners or abrasive agents for cleaning 7 2 Electrodes 1 Use the device only with the leads and electrodes provided by the manufacturer Use only the electrode placements and stimulation settings prescribed by your practitioner 2 It is recommended that at minimum 1 5 x 1 5 self adhering based square electrodes are used at the treatment area 3 Inspect your electrodes before every use Replace electrodes as needed Reusable electrodes may cause slight skin i
20. ollow 2 Press D button first and then press the V button to select the doctor mode The display as follow UD Bos 5 9 Set the parameter in the doctor mode 1 Select the treatment program e Press D button first and then press the V button to select the doctor mode Press g button to select U1 or U2 for different user e Press A and V button to select U01 U10 or L01 L10 program 2 Setthe parameter e Press S button and holding for seconds to enter the setting the treatment time 1 u1 n uw es e Press A and V button to set the treatment time e Press S button to enter the setting the pulse frequency Caution Consult your physician for your suitable stimulation program 5 11 Select the treatment Press CH1 or CH2 button to adjust the output intensity of channel 1 or channel 2 Press CH1 or CH2 to decrease the output intensity of channel 1 or channel 2 The step is 1mA 5 12 Adjust the intensity e Press the intensity control button to control the intensity output Slowly press the intensity button control until you reach the setting recommended by your medical professional Repeat for the other channel if both channels are to be used Caution If the stimulation levels are uncomfortable or become uncomfortable reduce the stimulation intensity to a comfortable level and contact your medical practitioner if prob
21. ommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter Rated m maximum output 150 kHz to 80 MHz 800 MHz power of 80 MHz to 800 MHz to 2 5 GHz transmitter af oD 3 5 eror W d 39 yp de 3 9 4p vp V1 E1 E1 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be estimated using the equation applicable to the frequency of the transmitter where P is the maximum output power rating of the transmitter in watts W accordable to the transmitter manufacturer NOTE At 80 MHz 800 MHz the separation distance for the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be estimated using the equation applicable to the frequency ofthe transmitter where P is the maximum output power rating of the transmitter in watts W accordable to the transmitter manufacturer NOTE At 80 MHz 800 MHz the separation distance f
22. or the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people 12 GLOSSARY OF SYMBOLS Batch code Serial number Electrical devices are recyclable material and should not be disposed of with household waste after their useful life Help us to protect the environment 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 you have any questions Dx Attention Read the operating instruction for use Type BF Applied Part 13 WARRANTY Please contact LG MedSupply in case of a claim under the warranty If you have to send in the unit enclose a copy of your receipt and state what the defect is The following warranty terms apply 1 The warranty period for device is one year from date of purchase In case of a warranty claim the date of purchase has to be proven by means of the sales receipt or invoice 2 Repairs under warranty do not extend the warranty period either for the device or for the replacement parts 3 The following is excluded under the warranty All damage which has arisen due to improper treatment All damage which is due to repairs or tampering by the customer or unauthorized third parities Damage which has arisen d
23. ote of the contra indications and safety measures detailed at the beginning of this manual Safety information as this powerful equipment is neither a toy nor a gadget Di x ed 30 Noe n n Le In order to turn on the device keep the 45 button pressed down until the operation page appears on the screen 5 6 Checking the memory e Press 5 button and CH2 in the same time and holding for 3 seconds to enter check menory e Press A and V button to check the up or next recording e Press 5 and holding for 3 seconds to clear the all data Press button back doctor mode D 5 7 Selection the treatment User U1 or U2 LG TEC Multi has special design which can be used and has memory for two users The user 1 U1 or user 2 U2 can operate device independently with their own program and treatment memory Press button to select the U1 or U2 ni B u2 30 Ge CH1 5 8 Select the treatment mode There are two working modes in this device One is normal modes and another is doctor mode For the normal treatment mode it can be using the preset treatment programs and also user program U01 U10 For the doctor mode it can be set treatment time pulse width and frequency of U01 U10 into L01 L10 programs and check the patient treatment memory by the doctor 1 Insert the batteries first and then press key to enter normal mode The display as f
24. ower frequency frequency magnetic fields 50 60Hz should be at levels magnetic characteristic of a field IEC typical location in a 61000 4 8 typical commercial or hospital environment NOTE UT is the a c mains voltage prior to application of the test level Guidance and manufacturer s declaration Electromagnetic immunity The device is intended for use in the electromagnetic environment specified below The customer or the user should assure that it is used in such an environment Immunity IEC 60501 Compliance Electromagnetic test test level level environment guidance Portable and mobile RF Communications equipment should be used no closer to any part of the device including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance Conducted 3 Vrms 3 Vrms RF IEC 150 kHz 3 5 yp 61000 4 6 to 80 MHz 1 Radiated 3 V m80 3 5 80MHz RF IEC MHz to 3 vim le 800MHz 61000 4 3 2 5 GHz 800MHz d Zl YP to 2 5MHz Where P is the maximum output power rating of the transmitter In watts W according to the Transmitter manufacturer and dis the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey a should be less than the compliance level in eac
25. own the intensity Rotate lead wires in socket 90 If still intermittent replace lead wire 3 If still intermittent after replacing lead wire a component may have failed Call the repair department Some programs will seem intermittent This is expected Refer to the Program Program option in use Option Controls in the Operation section for a description of the program option Stimulation is ineffective Improper electrode and applicator placement Unknown Use the electrodes Reposition electrode and applicator Contact clinician Re position the electrodes If The skin becomes red and or you feel a stabbing pain on the same site every time The electrodes aren t stuck onto the skin properly at any time you feel pain or discomfort stop use immediately Ensure the electrode is stuck securely on the skin The electrodes are dirty The surface of the electrode was scratched Clean the electrode pads with a damp lint free cloth or replace new electrode pads Clean the electrode belt according the description in user manual Replace new electrode Output current stops during therapy The electrode pads come off the skin Turn off the device and stick the electrode pad firmly to the skin The cable is disconnected Turn off the device and connect the cable The power of the batteries has been Please replace them with new b
26. re the electrodes are placed firmly to the skin and make good contact between the skin and the electrodes Place the electrodes over the skin attach them properly firmly and evenly Caution Before applying the self adhesive electrodes it is recommended to wash and degrease the skin and then dry it Do not switch the device on when the self adhesive electrodes is not positioned on the body e Never remove the self adhesive electrodes from the skin while the device is still switched on e tis recommended that at minimum 1 5 x 1 5 self adhering based square electrodes are used at the treatment area 5 4 8 Electrode placement The placement of electrodes can be one of the most important parameters in achieving success with therapy Of utmost DB importance is the willingness of the physician to try the various styles of electrode placement to find which method best fits the needs of the individual patient Every patient responds to electrical stimulation differently and their needs may vary from the conventional settings suggested here If the initial results are not positive speak to your physician about alternative stimulation settings and or electrode placements Once an acceptable placement has been achieved mark down the electrodes sites and the settings so the patient can easily continue treatment at home 5 5 Turn on Before using the unit for the first time you are strongly advised to take careful n
27. rritation lose adhesion and deliver less stimulation if overused Adhesive Pad gt Connector for inserting Lead wire Pin Reusable Self adhering electrodes To use these electrodes Attach the electrode to the lead wire e Remove the protective backing from the electrode surface Do not throw away the protective backing because it is reused after the treatment session has been completed e Place the tacky surface to the prescribed skin area by pressing the electrode firmly against the skin To remove your electrodes e Lift the corner of the electrode and gently remove it from the skin e Apply the protective backing to the tacky side of the electrode Place the electrode on the side of the protective backing that is labeled with the word on e Store the electrodes in the resalable pouch or a plastic bag Caution Do not pull on the electrode wire Doing so may damage the and electrode e Always use the electrodes with CE mark or are legally marketed in the US under 510 K procedure 7 3 Cleaning the Electrodes cords Clean the electrode cords by wiping them with damp cloth Coating them lightly with talcum powder will reduce tangles and prolong the life 7 4 Maintenance 1 Maintenance and all repairs should only be carried out by an authorized agency The manufacturer will not be held responsible for the results of maintenance or repairs by unauthorized persons 2 The user may no
28. t attempt any repairs to the device or any of its accessories Please contact the retailer for repair 3 Opening of the equipment by unauthorized agencies is not allowed and will terminate any claim to warranty 4 Check the device before each use for signs of wear and or damage Replace wear items as required 8 TROUBLESHOOTING If your device does not seem to be operating correctly refer to the chart below to determine what may be wrong Should none of these measures correct the problem the device should be serviced Stimulation is uncomfortable Problem Possible Cause Solution Displays fail Battery contact 1 Try fresh batteries to light up failure 2 Ensure batteries are inserted correctly Check the following contacts All contacts are in place All contacts are not broken Stimulation Electrodes weak 1 Dried out or Replace and contaminated re connect 2 Placement Lead wires Old worn damaged Replace Intensity is too high Decrease intensity Electrodes are too close together Damaged or worn electrodes or lead wires Electrode active area size is too small Reposition the electrodes Replace Replace electrodes with ones that have an active area no less than 16 0cm 4cm 4cm Mayn t operate the device according to the manual Please check the manual before use Intermittent output Lead wires 1 Verify connection is secure Insure firmly 2 Turn d
29. tor Make sure no bare metal of the pins is exposed Caution Always use the electrodes CE mark or which are legally marketed in the US under 510 K procedure 5 3 Connect lead wires to the device Before proceeding to this step be sure the device is completely turned OFF Holding the insulated portion of the lead wire connector insert the plug into the receptacle on the top of the main unit Ensure the lead wires are inserted correctly The device has two output receptacles controlled by Channel 1 and Channel 2 You may choose to use one channel with one pair of lead wires or both channels with two pairs of lead wires Using both channels gives the user the advantage of stimulating two different areas at the same time 5 4 Electrode 5 4 1 Electrode options The electrodes are disposable and should be routinely replaced when they start to lose their adhesive nature If you are unsure of your electrode adhesive properties order new replacement electrodes Replacement electrodes should be re ordered through or on the advice of your physician to ensure proper quality Follow application procedures outlined in electrode packing to maintain optimal stimulation and to prevent skin irritation 5 4 2 Place electrodes on skin Apply electrodes to the exact site indicated by your Physician Before applying electrodes be sure the skin surface over which electrodes are placed is thoroughly cleaned and dried Make su
30. uring transport from the manufacturer to the consumer or during transport to the service centre Accessories which are subject to normal wear and tear 4 Liability for direct or indirect consequential losses caused by the unit is excluded even if the damage to the unit is accepted as a warranty claim CURRENT SOLUTIONS Manufactured for Current Solutions LLC 3814 Woodbury Drive Austin TX 78704 Ph 800 871 7858 www currentsolutionsnow com
31. y experience skin irritation or hypersensitivity due to the belt or electrode pads 9 If you have suspected or diagnosed heart disease you should follow precautions recommended by your physician and 10 If you have suspected or diagnosed epilepsy you should follow precautions recommended by your physician 11 Use caution if you have a tendency to bleed internally such as following an injury or fracture 12 Consult with your physician prior to using the device after a recent surgical procedure because stimulation may disrupt the healing process 13 Use caution if stimulation is applied over the menstruating and 14 Use caution if stimulation is applied over areas of skin that lack normal sensation 15 Keep this device out of the reach of children and 16 Use this device only with the leads electrodes and accessories recommended by the manufacturer or distributer 17 You may experience headache and other painful sensations during or following the application of electrical stimulation near your eyes and to your head and face and 18 Please stop using the device and consult your physician if you experience adverse reactions from the device e g skin irritation 3 PRESENTATION 3 1 Front and Rear Panel Q TN 9 ICH2 9 gt C 9 9 LED for channel 1 LED for channel 2 _
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