SpaBuddy Mini - Instruction Manual
Contents
1. SN Serial number 13 WARRANTY Please contact your dealer or the device centre in case of a claim under the warranty If you have to send in the unit enclose a copy of your receipt with clear statement of defect description The warranty terms as below 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 cases are excluded under the warranty All damage which has arisen due to improper treatment e g nonobservance of the user instruction All damage which is due to repairs or tampering by the customer or unauthorized third parities Damage which has arisen during transport from the manufacturer to the consumer or during transport to the service centre Accessories which are subject to normal wear and tear Device damage due to privately dissembling devices 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 Zewa Inc 12960 Commerce Lakes Drive 29 Fort Myers FL 33913 USA Toll Free 888 993 3592 E Mail Warranty zewa com www zewa com2. Replace all of the batteries simultaneously 6 Always replace the device with same type battery 5 2 Connect electrode to device Before proceeding to this step be sure the device is completely turned OFF Connect the electrode to the electrode button of stimulator correctly Please see following photos for the correction connecting method A Caution Always use the electrode which is comply with the requirements of the IEC EN60601 1 IS010993 1 5 10 such as the electrode with CE mark or which are legally marketed in the US under 510 K procedure 5 3 Place electrodes on skin Place the electrode on the part you need treatment and base on the instructions of this user manual Before use please make the skin that need treatment and the silica gel of electrode clean and humid to prevent the discomfort that cause by dry skin Please ensure the skin and electrode connection well A Caution 1 Please turn off to prevent electric shock when pre moving the treatment position of the electrode 2 Before applying the electrode it is recommended to wash and degrease the skin and then dry it 3 Never remove the electrode from the skin while the stimulator is still treating 4 Only use the electrodes that provided by the manufacturer use other Dormancy current Less than 10uA At power off mode ra accessories could result in injury to the patient Working current Less than 50mA At the N1 program Dimen
3. if the pain relief is not achieved or even the pain get worse please consult your doctor 2 Burst Program B Burst frequency PR 7 pulse per burst Waveform Biphasic square wave PR Frequency 100Hz Burst Frequency 2Hz PW Pulse width 200uS Output Voltage 0 to 35Vpp 500 0 Load adjustable Output Current 0 to 70MA 500 O Load adjustable 3 Han Program H cycle time 3 sec iain la Waveform Biphasic square wave cycle time 3 sec PR Frequency 2Hz 80Hz PW Pulse width 250us 200us 2Hz 250us first output 3 sec and then output 3 sec Usage advice for EMS Output order Place the electrodes on the body part you want to treat referring to the picture on 80Hz 200us page 11 E1 amp E2 Output Voltage Oto 35Vpp 500 0 Load adjustable 1 Check and re paste on it 1 2 treatment per day about a week as a period of treatment In the early days of treatment you can use the Mode E1 and after a few days you Output Current Oto 70mA 500 0 Load adjustable 1 If the electrode connect well Lednica can use the E2 the frequency of E2 is comparatively higher Nofeeling of tothe skin We advise you use the device for one session per time If you find discomfort For EMS mode a 2 If the connect between during treatment you can pause the session or decrease the int
4. values for the respective program are listed on part 7 The operation principle of electrical stimulation equipment is based on simulating the body s own pulses which are transcutaneously transmitted to nerve or muscle fibers by means of electrode The intensity of the single channel can be adjusted separately and can be applied individually to one body region The device has single channel and one butterfly shaped electrode which allows you to stimulate one muscle groups simultaneously with a large selection of standard programs The electrical pulse is transmitted to the tissue then affect the transmission of stimulation in nerve conduction as well as the Neuron and muscle tissue in the field of application part 1 2 Medical background 1 2 1 EXPLANATION OF PAIN Pain is a warning system and the body s method of reminding us that something is wrong Pain is important signal without it abnormal conditions may go undetected causing damage or injury to vital parts of our bodies Even though pain is a necessary warning signal of trauma or malfunction in the body nature may have gone too far in its design Aside from its value in diagnosis long lasting persistent pain serves useless purpose Pain does not begin until coded message travels to the brain where it is decoded analyzed and then reacted to The pain message travels from the injured area along the small nerves leading to the spinal cord Here the message is switched to different nerv
5. Kfowe USER MANUAL Mini TEN amp EMS Device 21021 For OTC PURPOSE Zewa Inc This manual is valid for the 21021 Stimulator Be sure to read this instruction manual before operation and keep properly This user manual is published by Zewa Inc Zewa Inc does not guarantee its contents and reserves the right to improve and amend it at any time without prior notice Amendments will however be published in a new edition of this manual All Rights Reserved 21021 Rev V1 00 2014 Zewa printed in June 26 2014 Declaration of conformity Zewa Inc declares that the 21021 complies with following normative documents IEC 60601 1 IEC 60601 1 2 IEC 62304 IEC 62366 IEC 60601 1 11 IEC 60601 2 10 ISO 10993 5 ISO 10993 10 1 FOREWORD 1 1 Introduction The device 21021 is a single output channel Mini TENS amp EMS device Before using please read all the instructions in this user manual carefully and keep it safe for future Mini TENS amp EMS device belongs to the group of electrical stimulation systems It has two basic function TENS Transcutaneous Electrical Nerve Stimulation and EMS Electronic Muscle Stimulation Function of the Mini TENS amp EMS device The device has 5 application programs GG TENS programs and 2 EMS programs and applies electric currents in the low frequency range for therapy The respective application program controls the generated electric impulses their intensity frequency and frequency range The
6. parameters are set to the appropriate form of therapy adjust the control correctly Please see the following table a et 1 If there s foreign body in the battery compartment 2 If the battery has used up or counter install LEDnolight 3 If there is foreign body in the replacing of the battery interface battery 4 If the battery is not the right specification or battery interface going wrong 5 Exception reset 1 Check and clean 2 Replace the new battery or install the battery correctly 3 Check and clean 4 Replace the battery with the right specification Current 0 to 70MA 500 O Load adjustable 8 CLEANING AND MAINTENANCE Fully comply with the following daily maintenance requirements are necessary to make sure your product operate intact and guarantee the product Long term performance and safety 8 1 Cleaning and caring for the device 8 1 1 Pull the stimulator out of the electrode and remove the batteries Clean the device with a soft slightly damp cloth In case of heavier dirt build up you may also add a mild detergent 8 1 2 Do not subject the Pain Relief Plaster to moisture or dampness Do not hold the Pain Relief Plaster under running water do not submerge it in water or other liquids 8 1 3 The Pain Relief Plaster is sensitive to heat and may not be exposed to direct sunlight Do not place the Pain Relief Plaster on hot surfaces 8 1 4 Care
7. 05 1pc Self adhesive Electrodes 28x 53 2 mint Butterfy shaped AC EP2853U 1pc 3 Ordinary batteries 15V AAA AC IUAAAC 2pcs 4 User manual 7 1pc 4 SPECIFICATION 4 1Technical information Device name Multi function TENS amp EMS Device Model type 21021 Power supply 3V dc 2x AAA batteries Output Channel Single channel Wave sharp Bi phase square wave pulse Output voltage Max 35Vpp at 5000hm load Output current Max 70mA at 5000hm load Treatment time 30min Output intensity Oto 10 levels adjustable Number of program 5 programs N B H E1 and E2 Treatment mode TENS and EMS mode 5 C to 40 C with a relative humidity of 30 Operating conditions 85 atmospheric pressure from 700 hPa to 1060 hPa Storage conditions 10 C to 50 C with a relative humidity of 10 90 atmospheric pressure ow 700 Pafo theo Rs Less than 10uA At power off mode 2 In case of battery leakage please avoid contacting the battery with skin eyes and mucus membranes once contacting leakage please wash the contact part with plenty of clean water and contact your doctor immediately 3 Battery can not be dismantled thrown into fire or short circuited 4 Protect battery from excess heat Take the battery out of the product if they are spent or if you dort use it for a long time This can prevent device damage because of the battery leakage 5
8. NEGATIVE ENDS OF THE BATTERY WITH THE MARKINGS IN THE BATTERY COMPARTMENT OF UNIT 5 1 2 Disposal of battery Spent batteries are not belong to the household waste Dispose of the battery according to the current regulations As a consumer you have legal obligation to return spent battery to the Recycle Bin A Caution 1 lfa battery was swallowed please seek medical attention immediately Program No Applicable disease symptoms Applicable Location Diagra N Shoulder pain il Arm pain Elbow pain 4 Low back pain B Shoulder pain Same as N but the stimulation Arm pain is blander Elbow pain 4 low back pain H Shoulder pain Same as N but the stimulation Arm pain strength is between N and B Elbow pain 4 Low back pain El Applicable for buttocks thigh and leg H 1 fs improve and facilitate muscle gt A performance i L E2 Applicable for hand arm and AS abdomen Lyle gi improve and facilitate muscle i A f performance 6 INSTRUCTIONS FOR USE 6 1 Turn on When use for the first time open the battery cover and load two new batteries Please kindly review item 5 1 1 for the operating steps and schematic diagram Then press the on set button to turn the device on and the default program indicator LED will be lighting 6 2 Select the application program In the state of power on press off set to switch the current applicat
9. airway difficulty in breathing or adverse effects on heart rhythm or blood pressure 4 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 5 Do not apply stimulation over or in proximity to cancerous lesions 6 Do not apply stimulation in the presence of electronic monitoring equipment eq cardiac monitors ECG alarms which may not operate properly when electrical stimulation device is in use 7 Do not apply stimulation when in the bath or shower 8 Do not apply stimulation while sleeping 9 Do not apply stimulation while driving operating machinery or during any activity in which electrical stimulation can put your at risk of injury and 10 Apply stimulation only to normal intact clean healthy skin 11 The long term effects electrical stimulation are unknown Electrical stimulation device do not have any curative value 12 Stimulation should not be applied transthoracically in that the introduction of electrical current into the heart may cause cardiac arrhythmias Stimulation should not take place while the user is connected to high frequency surgical equipment that may cause burn injuries on the skin under the electrodes as well as problems with the stimulator 14 Do not use the stimulator in the vicinity of shortwave or microwave therapy equipment since this may affect the output power of
10. commended to wash and degrease the skin and then dry it 2 Never remove the electrode from the skin while the device is still switched on 3 Only use the electrode that provided by the manufacturer Use other products could result in injury to the user 6 9 Where do attach adhesive electrode a Each person reacts differently to electric nerve stimulation Therefore the placement of the electrodes may deviate from the standard If application is not successful contact your physician to find out which placement techniques are best for you b Do not use any adhesive electrodes with an electrode size smaller than the original attachment electrode issue by manufacturer otherwise the current density may be too high and cause injuries c The size of the adhesive pads may not be changed e g by clipping off parts of them d Make sure that the region radiating the pain is enclosed by the electrodes In case of painful muscle groups attach the electrodes in such a way that the affected muscles are also enclosed by the electrodes Usage advice for TENS If you fell the output intensity too strong you can press Koff set J key to de crease the output intensity During the treatment if you don t feel any discomfort we advise you use the device until the session end normally the pain relief occurs after 5 10 min treatment Normally we advise 1 2 treatment per day about a week as a period of treatment After a period of treatment
11. ds electrical pulses to your body 23 Do not use sharp objects such as pencil point or ballpoint pen to operate the buttons on the control panel 24 To check the electrode connections before each use 25 This device should be used only with the electrodes recommended for use by the manufacturer 2 5 Adverse Reactions 1 Possible skin irritation or electrode burn under the electrodes may occur 2 On very rare occasions first time users of EMS have reported feeling light headed or faint We recommend that you use the product while seated until you become accustomed to the sensation 3 If the stimulation levels are uncomfortable or become uncomfortable reduce the stimulation Intensity to a comfortable level and contact your physician if problems persist 3 GETTING TO KNOW YOUR DEVICE 3 1 Front Rear Panel 1 ON SET button 1 2 Program name 3 OFF SET button 4 Electrode buttons 5 Battery compartment 6 Tape for removing battery 7 Batter cover 3 2 Key Functions ON SET Button In standby state turn on the device in treatment state to increase the output intensity OFF SET Button In power on state press the button to select the treatment program keep press the button to 2 seconds to turn off the device in treatment state to decrease the output intensity 3 3 Accessories No Description Part No ary 1 Pain Relief Plaster ED4
12. ensity of the peor electrode connect well to the output 4 EMS program program E1 and E2 yek stimulator Pfieplace tie net batten stimulating ifthe batteryis used up 4 Use the wet cotton cloth 7 PROGRAM Contract ime ithe sin stoo dy immersion water wipe Ramp time Ramp time the electrode and the 7 1 Application program r ji Relax time skin which will be use Program Pulse Wave i iad Time min Frequency wih TENS 1 Ifthe electrode pad stick wel tothe skin N W 80 200 Normal rare ih Nasir 2 If the connect between 1 Checkand re stickit B 30 2 200 Burst Seton elatda a kas nie electrode pad and stimulator 2 Check and re connect H 30 280 250 200 nes Wave characteristic All program of EMS mode output wave characteristic is right 3 Replace the new battery are same or Weak gt aratati 3 If the battery is used up 4 Replace the new A Keep pa PR Frequency For program E1 50Hz For program E2 20Hz I A ifthe electrodepad hasbeen electrode pad Program Time Frequency Pulse Wave P it Time Te For program E2 20Hz 0 to 35Vpp 500 O Load adjustable used too long and with no Name min Ha widthius creNS GNP O PW Pulse width 2500 stickiness time s Ramp up time 25sec Bta 30 so 250 ems 2 5 10 Ramp down time Pec Halt 1 If the electrode pad loosen 1 Check and stick the E2 30 20 250 EMS 2 5 10 Contract time on time 5sec automatically from the body electrode pad well in the treatment 2 I
13. es that travel up the spinal cord to the brain The pain message is then interpreted referred back and the pain is felt 1 2 2 EXPLANATION OF TENS TENS Transcutaneous Electrical Nerve Stimulation gives good results in relief of pain It is clinically proven and used daily by physiotherapists 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 1 2 3 EXPLANATION OF EMS Electrical Muscle Stimulation is an internationally accepted and proven way of treating muscular injuries It works by sending electronic pulses to the muscle needing treatment that causes the muscle to exercise passively It is a product derived from the square waveform originally invented by John Faraday in 1831 Through the square wave pattern it is able to work directly on muscle motor neurons The Ultra EMS System has low frequency and this in conjunction with the square wave pattem allows direct work on muscle groupings 2 SAFETY INFORMATION 2 1 Intended use For program N1 B and H of TENS mode To be used for temporary relief of pain associated with sore and aching muscles due to strain from exercise or normal household
14. f the battery is used up 2Replace the new battery Relax time off time 10sec 7 2 The waveform of the stimulation program Output Voltage Oto 35Vpp 500 N Load adjustable For TENS mode 1 Normal Program N1 N2 PR ahs PW Waveform Biphasic square wave PR Frequency PW Pulse width Output Voltage N1 80Hz N2 2Hz NI 200uS N2 250uS 0 to 35Vpp 500 0 Load adjustable 0 to 70mA 500 Q Load adjustable Output Current off and the battery is taken out when cleaning the device 8 2 Maintenance 8 2 1 The manufacturer didn t authorize to any maintenance agencies abroad If your device has any problem please contact the distributor The manufacturer will not be held responsible for the results of maintenance or repairs by unauthorized persons 83 2 The user must not attempt any repairs to the device or any of its accessories Please contact the retailer for repair 83 3 Opening of the equipment by unauthorized agencies is not allowed and will terminate any claim to warranty Each product in manufacturing has been through the systematic validation The performance is stable and did not need to undertake the performance parameters of calibration and validation IFyour product can t reach the expected performance and the basic function have change in normal use please contact the retailer 9 TROUBLESHOOTING Should any malfunctions occur while using the device Check whether the
15. fully clean the surface of the adhesive electrode with a damp cloth Make sure the device is turn offl 8 1 5 For reasons of hygiene each user should use his her own set of electrode 8 1 6 Do not use any chemical cleaners or abrasive agents for cleaning 8 1 7 Ensure that no water penetrates into the machine If this should ever happen only use the device again once it is completely dry 8 1 8 Not to clean the device during treatment be sure that the device is turned 1 Do the treatment once a day short the treatment time reasonable 2 Check and paste on the electrode well 3 Use the wet cotton cloth immersion have water wipe it Then can use it 1 Ifthe treatment time lasts too long The skin of the 2 Ifthe electrode stick well to the treatment skin i partreddenor 3 If the interface of the panes paiar tickle electrodes is dirty or dry istar y of a Eria thE 4 wi light sensitive please 4 If the skin is sensitive to the electrode change the sticking place or shorten the treatment time The strong sensitive should stop the treatment or to see the doctor 10 STORAGE Remove the batteries from the device if you are not going to use it for a longer period Leaking batteries can damage the unit Do not make any sharp kinks in the connecting leads or electrodes After use pull the electrode in original package Do not expose the device to direct sunlight and protect it against dirt and m
16. ion pro gram The LED indicator of corresponding program will lighten when switching Please see below picture 6 3 Starting the treatment Press on set button to adjust the output intensity and the device will enter the working state and the current application program indicator LED will be flicker for 1Hz frequency esha ynang Ao OEO 6 4 Adjust Channel Intensity Place the electrode stick the application of body parts press Kon set key increase output intensity The output intensity is increasing a level in each press the Lon set key it has 10 levels output intensity Please adjust the intensity in your feel comfortable condition The LED of corresponding application program will be flash as 1Hz frequency to indicate that in treatment status If you fell the output intensity too strong you can press Loff set key to de crease the output intensity The output intensity is decrease a level in each press the Loff set key When the output intensity decreased to zero it will return the wait mode and the LED of the application program will be lighting As the schematic below EZR ess O O E o Caution If the stimulation levels are uncomfortable or become uncomfortable reduce the stimulation intensity to a comfortable level and contact your medical practitioner if problems persist 6 5 Turn the device off Press the off set button for 2 seconds to turn off the device at any mode and the all indicatio
17. laced on opposite sides of your head 8 The safety of electrical stimulation during pregnancy has not been established 9 You may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical conductive medium silica gel 10 If you have suspected or diagnosed heart disease you should follow precautions recommended by your physician 11 Ifyou have suspected or diagnosed epilepsy you should follow precautions recommended by your physician 12 Use caution if you have a tendency to bleed internally such as following an injury of fracture 3 Consult with your physician prior to using the device after a recent surgical procedure because stimulation may disrupt the healing process 14 Use caution if stimulation is applied over the menstruation or pregnant uterus and 15 Use caution if stimulation is applied over areas of skin that lack normal sensation 16 Forsingle patient use only 17 Keep yourself informed of the contraindications 18 This stimulator is never use by patients who have noncompliant emotionally disturbed dementia or low IQ 19 The instruction of use was listed any improper use may be dangerous 20 Caution should be used for patients with suspected or diagnosed heart problems 21 Isolated cases of skin irritation ray occur at the site of the electrode placement following long term application 22 Do not use this device at the same time as other equipment which sen
18. n LED will be turn off Ea io 6 6 Load detect function When the device haven t detect the load or the electrode with skin connect not good it will automatically detect the load if the intensity is added to 1 level if it is judged to no load the intensity will automatically return to zero and the device will return to wait mode 6 7 Battery To replace the battery open the battery cover and extract the battery Replace it with AAA batteries Make sure you insert the battery correctly Notice of batteries Batteries may be fatal if swallowed Therefore keep the batteries and the product out of the range of children If a battery was swallowed go to hospital immediately If the battery has leakage avoid contact with skin eyes and mucus membranes Rinse the affected spots with lots of clear water immediately and contact a physician right away c Batteries may not be charged dismantled thrown into fire or short circuited d Protect batteries from excess heat Take the batteries out of the product if they are spent or in case you no longer use the article This prevents damage caused by leaking batteries e Always replace the full set of batteries with different set at the same time f Press on set button to check the electric quality of battery when the battery become low voltage the LED indicator will be dim or the device can not power on 6 8 Use of the adhesive electrode a The electrode may only be connection
19. oisture Store the machine in a cool well ventilated place Never place any heavy objects on the machine 11 DISPOSAL Spent batteries are not belong to the household waste Dispose of the battery according to the current regulations As a consumer you have obligation to dispose of batteries correctly Consult your municipal authority or your dealer for information about disposal At the end of the product lifecycle do not throw this product into the normal household garbage but bring it to a collection point for the recycling of electronic equipment Waste Electrical and Electronic Equipment can have potentially harmful effects on the environment Incorrect disposal can cause harmful toxins to build up in the air water and soil and can be harmful to human health 12 Normalized symbols Attention see Instructions for use BE Consult instructions for use Applied part of type BF Meaning of the symbols on the product the packaging or in the operating instructions electric devices are recyclable material and should not be disposed as household waste X 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 Common device protected against access to IP20 hazardous parts with a finger and non protected of waterproof
20. sions 57x45x16 5 mm mpa Weight 20g without batteries 42g with batteries 5 3 4 Electrode placement A on FDES106 is a kind of OTC stimulator suitable for home IE use you only need to use according to the user manual Classification oun re Pp place the electrode on the position where you feel pain SNP and need to exercise treating and adjusting base on The amplitude level will be reset to OV your own feeling nied cen as when the amplitude lve is Vor greater Setar Circuit at either channel is The different programs with corresponding applicable letected Size of electrodes pad 3 X 4 Butterfly shaped symptoms as below All the output parameters allow 20 error Output precision forthe specification Technical specification PW pulse width 200 250us PR Frequency 2 80Hz Hz vibration per second Burst frequency 2Hz Output characteristics Constant Voltage CV Nom The pulse rate and pulse width output will ome be constant based on the design value Han 2Hz 250us first output 3 sec and then output 3 sec 80Hz 200us 5 OPERATING INSTRUCTION 5 1 Battery 5 1 1 Check replace batteries Open the battery cover insert two batteries 4 ee type AAA into the battery compartment Make mi sure you are installing the battery properly Be sure to match the positive and negative ends of the battery to the markings in the battery Aa gt compartment of device BE SURE TO MATCH THE POSITIVE AND
21. the stimulator Never use near the heat Stimulation electrodes should never be placed anywhere on the front of the thorax marked by ribs and breastbone but above all not on the two large pectoral muscles Here it can increase the risk 13 15 of ventricular fibrillation and lead to cardiac arrest 16 Never use on the eye area 17 Never use near the genitals 18 Never use on the areas of the skin which lack normal sensation 19 Keep electrodes separate during treatment electrode in contact with other could result in improper stimulation or skin burns 20 Keep the stimulator out of reach of children 21 Consult your doctor if you are in any doubt whatsoever 22 Discontinue and do not increase the intensity level if you feel discomfort during use 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 p
22. with the Mini TENS amp EMS device Make sure that the device is turned off when attaching or removing the adhesive electrode b If you want to reposition the electrode during the application turn the device off first c The use of electrode may lead to skin irritations If you experience such skin irritations e g redness blistering or itching discontinue using the adhesive electrode Do not use the Mini TENS amp EMS device permanently on the same body part as this may also lead to skin irritations d Electrode is personal belongings just for single person use Please note that prevent cross use e The electrode must connect entirely to the skin surface to prevent high local currents which may lead to skin burns f Do not use the adhesive electrodes for more than approx 20 times as contact between the electrodes and the skin deteriorates over time g The adhesive force of the electrodes depends on the skin properties storage and the number of applications If your adhesive electrodes no longer fully stick to the skin s surface replace them with new electrodes The adhesive electrodes must adhere entirely to the skin surface to prevent high local currents which may lead to skin burns Stick the adhesive electrodes back onto the protective foil after use and store them in the storage bag to prevent them from drying out This retains the adhesive force for a longer period Caution 1 Before applying the electrode it is re
23. work activities For program E1 and E2 of EMS mode To be used to stimulate healthy muscles in order to improve and facilitate muscle performance 2 2 Contraindications 1 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 The device should not be used when cancerous lesions or other lesions are present in the treatment area Stimulation should not be applied over swollen infected inflamed areas or skin eruptions e g phlebitis thrombophlebitis varicose veins etc Electrode placements must be avoided that apply current to the carotid sinus region anterior neck or transcerebrally through the head 5 This device should not be used over poorly enervated areas 6 Inguinal hernia 7 Do not use on scarred areas following surgery for at least 10 months after the operation 8 Do not use with serious arterial circulatory problems in the lower limbs 2 3 Warning A 1 Ifyou have had medical or physical treatment for your pain consult with your physician before using this device 2 Ifyour pain does not improve becomes more than mild or continues for more than five days stop using the device and consult with your physician 2 3 4 3 Do not apply stimulation over your neck or mouth because this could cause severe muscle spasms resulting in closure of your
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