Dongdixin Technology IT300AB 3-in-1 Wireless Electrotherapy Devices User Manual
Shenzhen Dongdixin Technology Co.,Ltd. 3-in-1 Wireless Electrotherapy Devices Users Manual
Users Manual
I (E \ ISoothe ;_ 3-in-1 Wireless Electrotherapy » 9 Drug-free Pain Relief Technology ‘\ 30"}; ‘y Mode‘ iTaooAB / i _J User Manual Thls manual is applicable to lSoothe“ 3,.n,1 Wireless Eleclrolherapy Devlce Model ITBOOAB. This inslruclion manual is published by lnnuvo Medical lnnovu Medical reserves me right la updale Inis manual al any lime wilnoul prior notice. Amendmenls may however be published in new edmons 01 mi: manual. All RighlS Reserved Rev W .0 © 2018 TABLE OF CONTENTS introduction .. . important safety precautions and wammgs. How TENS works for pain reheL How EMS works tor muscle conditioning Package contents Know yaur device . Charging Easy steps to get started wrtn iSoome" eiectrotneraoy Cleaning and storage Speciiications.. How to manage your pain Troubleshooting Product/Battery dispesai . Glossary of symhois. important inlormatiori regaiding electromagnetic compatibiiity (EMC). FCC Compiiance intorrnation. . Warranty. INTRODUCTION Thank you lor purchasing me iSooIhe” 37ml wireless Electrnlherapy Device Model lTSOOAB for your pain reliel soluiion In order in use ihis eleciroiherapy device salely, please read ihe user manual careiully peldre use Keep lhis user manual in a secure place or sldre willi lhe device lcr fulure relerence Indications far use: TENS The dewce is designed lo be used lor lhe lemparary reliel oi pain assecialed Willi sore and aching muscles in line shoulder, w3lsti pack neck, upper exiremilies (arms) and lower exlremilles (legs) due 10 slrain lrom exercise or regular housework. EMS The device is designed lo he used to slirnulale heallhy muscles in order m improve and lacililale muscle perlcrmance Devrce should be applied lo normal, healthy clean and dry skin of adull users. Device is designed to be used at home. Package Contains llie lollowmg cemponenls: Standard Parts: No. Descripllon Quantity A iTaouAa eleclroiherapy device lpc B Elecircde padslllumm x 70mm 190mm x 95mm) was 0 lnslruciion manual m: D MicrosUSE caple we E Quick start guide we F Elecircde placemenl guide we IMPORTANT SAFETY PRECAUTIONS AND WARNINGS It Is important that you read aH warmngs and precautmns Included In this user manuaI beIDre using the producl They are Intended In keep you safe, prevenI imury and avoid a srtuatien thaI can damage the devree SAFETY SYMBOLS USED IN THIS MANUAL DANGER Intimates a potehtrany hazardous srtuatron which‘ II not avordeu. couId result m mm or serious Injury. WARNING Intimates a potentiany hazardous srtuatron which i! not avmded, couId result m senous injury and devme damage. & CAUTION IndwcaIes a potentialIy Hazardous sIIuaIIon which it run avorded, couId result m minor or moderate mrury lo the user, or damage lo the devroe or other propeny A DANGER THIS ELECTROTHERAFY DEVICE MUST NOT BE USED IN COMBINATION WITH THE FOLLOWING MEDICAL DEVICES: Camlac pacemaker Implamed denbnnator. or oIher ImplanIed metahe. [ads or electromc devmes. EIecIronic Ixfersuppon eqmpmenl, such as resprrators. EIecIvonic medICaI devrces aItached lo the body, such as electrocarmographs. Usmg [ms eIeclroIherapy dewce with other electromc medical devrees may cause erroneous operation at those aevrees. WARNING Do NOT us: THIS DEVICE UNDER THESE CONDITIONS: Consult With your physician oetore use. Deince may cause lethal rhythm disturbances in certain susceptible indiyiduals. ll you have a cardiac pacemaker. implanted defibrillator. or other implanted metallic or electronic device Such use could cause electric shock, ourns. electrical interierence or death. II you are on a hie-supporting medical electronic device such as an artificial hearl. lung or respirator. In the presence at electronic monitoring equipment (e.g cardiac monitors ECG alarms). which may not operale properly when device is in use While connected to high—Irequency surgical equipment. It may cause burn Wurles on skin under the electrodes, as well as problems with the device In the vicinity ol shortwave or microwave therapy equipment. This may alIect the output power oI device. 0n open wounds or rashes; oyer swollen, red. iniected. inilamed areas; or skin eruptions (e.g. phleoitis. thromoophleoitis. varicose veins). pron top of. or in proximity to, cancerous lesions Over areas of skin that lack normal sensation. On the head since the elIects oI electrical stimulation on the brain are unknown. Do NOT USE THIS DEVICE ON THESE INDIVIDUALS: Pregnant women, cecause the saiely ot eleclrical slimulation during pregnancy has ricl oeen eslaolished. Children or iniants. oecause deVice has not been evaluated lor pediatric use. People incapable oi expressing their thoughts or intentions. DO NOT USE THIS DEVICE WHILE: Bathing, showering or swnnming. Sleeping. Driving. operating maoninery or in any aCIlvllleS wnere electrical stimulation can out you at risk lor inyury. PAIN MANAGEMENT WARNINGS: it you have nad prior medical or physical lrealrnent ior pain, consult Wiln your onysioian belore using tnis device ll your pain does not improve, oecomes seriously chronic or severe, or conlinues ror more than five days, stop using device and consult wiln your onysioian Pain may be an indicalor of illness, If you are sufienng lrorn any serious illness, consult win your onysician pelore uslng deirice WARNINGS REGARDING THE ELECTRODE PAD: Apply electrode pad only to normal, liealtnyclean and dry Skin (oi aduk users). it may otherwise disrupt tne Skln nealing process. ll you experience any SKI" irritation or redness alter a session, do not Conllnue electrotnerapy in lnat area at ttie skin NEVER APPLV THE ELECTRODE FAD T0: Tne near: or any area DI tne face. Tne lronl side ollne neck oi any area olllie lnrcal because this can cause severe musole ® spasms resulting in closure urine airway, difficulty in tnealning, or adverse elleots on nean rnylnni orolood pressure Dotti sides oltne thorax simultaneously (lateral ® or lront and back), oi across yourcnest tiecause [he lntroducllun of electrical current may cause ® rnyllini disturbances, whicn could to letnal. & CAUTION PRECAUTIONS REGARDING THE ELECTRODE PAD: Do not bend or told pad because it may prevent pad irorn funcllonlng properly. Place pad onto plastic lilm provided and store in the sealed package when not in use. Pad is preagelled and ready to use. It will adhere to skin. No additional gel/icrmula is quulled Do not apply ointment or any solvent to pad or your skin because it will prevent pad Irorn iunctioning properly. To avoid damage to adhesive suriace oi pad, place pad only on clean and dry skin or on plastic Iilm provrded. Always place clean pad in accordance with illustrations provided (Reter to Electrode Pad Placement Illustrations on page 20). Make sure electrode pad is well connected to device. Pad should be properly placed on part oi the body you Wish to treat or the therapy Will not be etiective DO NOT USE THE ELECTRODE PAD THIS WAY: Do not place pad on your spine or backbone. Pad should not touch any metal object, such as a belt buckle, necklace or other yewelry rnade Irorn metal. Do not share pad wrth another person. Thls may cause skin irritation or inlection The pad is intended tor use by one person only. Do not place or relocate the pad while device is on. Always turn the power oil belore removing or changing location oi the pad. Do not leave pad attached to skin alter treatment. The lile ol pad may vary depending on the lreouency olwashing. skin condition and storage state. CAUTION WHILE USING THE DEVICE: II devrce is not Iunctioning properly or you Ieel discomtort, stop using device immediately. Do not use devrce while wearing electronic devices such as watches as this may damage the device. Do not use device in the yicinity at a cellphone as this may cause device to rnallunction. Do not throw device into a are The batteries may explode. Dispose devlce and components according to applicable local laws and regulations. Unlawtul disposal may cause eninronmental pollution. The size, shape and type of electrode pad may anect the salety and etieetiveness ol electrothempy. Usmg pad that is too small or incorrectly applied could result in discornlort or skin ourns.Use deyice only with the specially designed pad. Refills can be purchased separately (iSootheB wireless Electrode Pad Model iT300AGS. iTGUOAGrL). GENERAL PRECAUTIONS: The user is the intended operator. The longaterm ellects cl electrical stimulation are unknown Do not use the electrotherapy deyice tor any other purpose not described in this manual Apply the electrotnerapy device only to normal, intact. clean. dry and healthy skin TENS is not effective in treating the original source or cause ol pain. including headache. TENS is not a substitute tor pain medications and other pain management therapies TENS does not cure diseases or inyuries. TENS is a symptomatic treatment and. as such. suppresses the sensation ol pain that would othenwise serve as a warning mechanism The etlectiyeness of etectrotherapy is highly dependent upon the indiyiduat. You may experience skin irritation or hypersensitiyity due to electrical stimulation or electrical conductive medium (gel) on the electrode pad. if you are at risk or diagnosed With a heart condition or epilepsy you should toltow precautions recommended by your physician Use caution it you are at risk or internal bleeding. such as alter an iniury or lracture Consult with your physician prior to using device after a surgical procedure. Electrical stimulation may disrupt the healing process The device should not he applied to the aodomen during pregnancy or menstruation. The device should not be applied to areas oi skin that lack normai sensation Use device oniy With electrode pad and Micro- usa cable recommended by manuiacturer. Do not modiiy deyice Without authorization irom the manuiacturer. Do not use device or electrode pad it it is damaged. The use of a damaged device may cause inyury, improper resuits or serious danger store deyice and components in a ciean and dry place Do not expose devrce and components to any chemical soiyent, water, iint, dust direct sun or high temperature. CAUTION Keep device and components out oi reach oi young children. The came may cause strangulation. SmaH pieces may be a choking hazard. Contact your physician immediately it ingested. POSSIBLE ADVERSE REACTIONS: no not use device to treat one region tor an extended period oitirne (more than 30 minutes a session. up to 3 limes/day). This may cause muscies in the treated region to become exhausted and sore You may experience skin irritation redness or bums in the treated region. You shouid stop using device and consuit with your physician it you experience adverse reactions irom using the device HOW TENS WORKS FDR PAIN RELIEF What is TENS? TENS slams lor Transculaneous Eleetrreal Nerve Sllmulatlon. TENS ls a cllnlcally tested, nun-Invasive drug-free melhod a! managing paln. It uses tlny eleclrlcal lmpulses sent through me skln to me nerves (0 rellef pam. TENS rs hlghly recommended by medlcal prolessrerrals as a safe and ellectnre means for paln management TENS dues n01 cure any physiolagical problem ll only nelps Io manage paln Please note lnat uslng TENs Io manage pam may not wurk lar all users. How does TENS work? Sclentmc theory suggesls lnat eleclncal stlmulatmn lnerapy may work ln several ways Tne gentle electrlcal pulses block “paln message" earned by tne nerves lrom leachlng the brew. Tne gentle electrlcal pulses lnduce an lncrease In file producllon of endorphlns‘ the body‘s natural pain klller NOW EMS WORKS FOR MUSCLE CONDITIONING What is EMS? EMS stands lor Electrrcal Muscle Slimulauon EMS is wroely ulillzed as a muscle conortiomng lool. It uses genlle electrical lmpulses senl through the skln to the muscle, callslrlg ll to conlracl. mimicklng physical exerclse. This allows your muscles to exerclse passively even when you are sedentary. EMS lacrlrtates muscle oerlormance, alds ln strength lralnlng and recovery lrom mrnor muscle Inlllrles and post exercise. How does EMS work? EMS device sends eleclrrcal rmpulses lhal mrmrc lhe acllon polemlal lrorn the central nervous syslem ll uses square wave pattern (ladderrshaped) whrch ls ellectrve rn targellng muscle motor neurons. When muscle lecelves eleclrrcal srgnal. il llexes When electncal slgnal ceases. u relaxes Thrs cycle ls repealed, mlmicklng normal muscular actrvrty during physical exerclse. How dues MASSAGE work? The MASSAGE eleclrolherapy program ls a type ol low level EMS lhat provldes relaxrng vroratron lo loosen lrghl muscles. ll mlmlcs manual massage lo promote relaxation and reduce muscle tension. PACKAGE CONTENTS {G ”E 3 ‘ “ ‘ " ’ E/‘fé \TSODAB E‘ectrcde pads Micmusg cable eledmlherapy device (110mm x 70mm,190mm x 95mm) lsoacha' Instrumion manual QUICK start gulde Electrode p‘acement gulde KNOW YOUR DEVICE Features Channe‘s One channel Tleatmem modes TENS 5 programs EMS 2 programs MASSAGE 2 programs ompm Amphtude: Max. 45v (at soon load) Wavelorm type: Symmetrical Bwphasic square muse Control madam App comm (iOS or Andrmd} and demos comm ® v rm WWW _@ 38 S (D [was] hum In standby mode: . Shun press |a swrtcrr prugram frum1 «u 9 a Long press tn swmch tleaflnennlme IONIn/Zflmmflflmm In wnrk mod ' - Shun press ‘0 decrease InlensHy . Lang press to cpnunue decreasmg mtsrrsuy [31"] humm In standby mode: . Shun press «p s|art «reatmem In work made: . Shun press «a rncrease mensuy . Long press m cammue moreasmg rmerrsuy @ Display treatment time ® Display treatment intensity © Display treatment program © Lock icon - wh-u device is in locked state, the icon appears; in unlocked state, the icon disappears (3 Battery indicator icon -when device is charging. the icon displays in orange. When device is lully charged, the icon changes to green (IN/OFF button . snort press to turn device on . Long press (about 35) to tum device 0" ‘ in work made shun press to terminate treatment sessmn ® Lock/Unlock button . Sheri press to lock/unlnck devlce @ Micro-USE charging port CHARGING Using MlcrusUSB cable connecnhe Mlcm-USB plug |o rhe Mlcro-USB ’ chargrng pan on devlce. Then‘ ‘s D connecl lhe Slandard uss plug of cable lo an appropriale power supply source lhal can ou|pm 5v d.c. 3ODmA. Whrle chargrng, the ballery mdicalar lighl drsplays orange When ballery ls lully charged, lhe rndrcalor lrghl mms green. Nola: Use only the Micro-USE cable lhal ls included wlth the devlce Devlce musl be lully charged prlor (a hrsl use, ll |akes abeul 2 5 hours |o charge lhe devlce. A lull ballery charge lypically allows up lo 4 30-mirlme lrealrnenl sessrons under normal condillons Please charge devlce lully before slamng each sesslon. Olherwlse, lhe ballery may be depleled before session ends. Nole devrce canrlm be used whlle ll rs chargrng. WARNING If ballery leaks and comes rnro conlacr wrlh 5km or eyes, wash rmmedralely wrlh large ameunl ofwater Drspose used banery safely rn accordance wlth local regulalibns. The lrre ora rechargeable barlery depends on the number el rechargrnglrundewn cycles The servlce Me or lhe rechargeable battery rs abeul sou rechargrng/rundown cycles, ll deVlce ls nel used lreouenlly. please recharge ballery ar least once a rnonlh lo exlen d ballery life. EASY STEPS TO GET STARTED WITH ISOOTHE" ELECTROTHERAPV The i5oothe~ electrotherapy device can be used with or without the mobile application (App). To use with the App, start with Step 1. To use without the App, skip Step 1. STEP 1 Download the mobile application. Download the App to your smartphone or tablet. Go to App Store or Google Play Search lor ‘lnrtnvo iSoothe'. The App operates on ins and Android plattorms (At least ios 8.0. Android 5.0). STEP 2 Prep Ihe skin. Clip excess hairlrom treatment area Remove any yewelry that may come in contact With device Clean skin with soap and wa|en and dry completely STEP 3 Prepare the device. Make sure device is off Connect device to electrode pad by pressing male snaps ol electrode pad to temale snaps oi device STEP 4 Apply device and electrode pad to treatment area. Remove the clear plastic lilm trom adhesive side ol electrode pad by peeling lrorn one end. Apply adhesive side at pad to treatment area by pressing down firmly to ensure lull contact with 5le See page 20 lor placement suggestions. Note: Do not discard the plastic lilm it Will be used to protect adhesive surtace of pad when not in use. The pad is designed to adhere well to clean. dry skin Use oi additional medium (such as electrode gel in a lube) is not recommended and may damage the device. You may need assistance when applying pad to certain treatment areas. WARNING Make sure device is 0" before connecting to electrode pad. Always connect device to electrode pad betore applying to treatment area. Replace the electrode pad it: it is dirty. damaged or torn it is past the expiration date. it has lost its adhesiveness Never use bandage or tape to attach pad to your skin. when stimulation leels weak or uncomlorlable. i.e. when you experience unpleasant stinging or biting sensation WARNING Use only electrode pad recommended tor this device by the manulacturer. Apply device and pad to treatment area according to Electrode Pad Placement illustrations on page 20. Electrode Fad Placement Illustrations , , ARM PAIN SHOULDER PAIN ELBOWIJDINY PAIN Nate: To lreel areas el shoulder or back please use large SlZe electrode pad. Skip Steps 5-9 if using device without the App. STEP 5 Connect device Io App. Ensure that aluetooth (A a) connection is activated on your smartphone or tablet Turn on the App. Turn device on by pressing the ONIOFF button. App Will automatically detect the device. Select your iSoolhe’” device by pressing ‘CONNECT' button in case oi inactivity (more than 3 min]. device will switch olT. Press the ON/OFF button again to continue. Device is now paired with the App . screen shows your iSootherv as ‘Connecled'. Press arrow ‘>‘ on the right to continue. STEP 6 Select treatment type and treatment area. Select treatment type by pressing TENS. EMS or MAS (Massage) Select treatment area accordingly. Note ‘FRONT‘ and ‘BACK‘ show available treatment areas (tagged with bright circles) Note: You can select lrom your saved lavorite treatment programs list by pressing the heart icon at the top right. STEP 7 Select your pain level. Estimate the intensity or pain you are currently experiencing in the treatment area Selec| from a scale pro to ‘lU (O-rio pain, iii—intense pain). Press ‘START' to continue. Note: A recommended program tor the treatment area is preselected You can switch treatment program by pressing leh or right arrow .< >2 STEP 3 Start trealment session. Press ‘+‘ button to start treatment. Note that this increases intensity level to 1 Press '+' button again 0 to increase intensrty to desired level. Press‘ —‘ outton to decrease intensity You can pause treatment by pressing ‘ii ' button. Tne countdown “000 timer will stop. Press again to 1 resume treatment. Press ‘9 ' button to rock the intensity controls for safety during treatment You can unlock at any time by pressing tne button again it you experience any discomfort, you can stop treatment session at any time by pressing ‘STOP' button. Note: The default treatment time is set to 20min. You can select otner treatment time from temin to 30min. Prior to starting treatment press the a - '6‘ icon, tnen select accordingty. Press ‘OK' to continue. in work mcue. ueVice wrll lock automatically alter 15 seconds cl nc operational activrty. Pressing ‘0' button struts down demo and ends treatment session Prior to starting treatment you can switcn treatment program oy pressing tne program icon accordingly ttop cl page). Pressing tne program icon during a treatment wrll eno current session. To start anotrrer session. press -+' buucn — Decrease intensity + increase intensity " Pause treatment STOP Stop treatment a Lock/Unlock a; snot down device G Set treatment tr me STEP 9 End treatment session. After treatment session is completed, you will be prompted to select your satisiaction level Press the icon accoldlngly. You can also save treatment program to tavorite by pressing ‘ADD THiS PROGRAM TO FAVORITE button Press ‘EXIT‘ button. Details oi the treatment session is displayed Treatment session is also storeo in treatment history. Press Retry‘ to restart the same treatment program on the same treatment area or ‘New Session' to start a new treatment session Note: You can end treatment session at any time by pressing the ‘STOP‘ button Continue in Step12lolurn device off. Fallow steps 10-11 if using device without the App. STEP 10 Start treatment session using controls on Ine device. Note: Please reter to pages 1545. Turn devlce on by pressing the ON/OFF button Press [-/MODE] button to switch treatment program horn t to 9 Long press [r/MODE] button to switch treatment time trom 10min to 20min to 30min. Press [HSTART] button to start treatment session During treatment. you can increase intensity level by pressing [HSTART] button ordecrease intensity level by pressing [-/MODE] oulton There are t5 intensity levels. Note: liyou experience any oiseomion. you can stop treatment session at any time by pressing the oN/OPP button. Press Luck/Unlock button to lock device. This inactivates the [-iMODE] and [MSTART] buttons to prevent accidental press during treatment sesslon to work made devrce wrll lock automallcally after 15 seconds of no operetronal acllvlly Treatment program list: Fragrant type 1 common, 2 Acufittnnuve 3 Ems! lkNS 0 Hart: 5 Mndulmlon s Streng'rmmng [M5 7 Eullulnfi 3 ”’7 Message Knead STEP 11 End treatmenl session using controls on the device. Alter treetrnent sesslon ls completed. devlce wlll mm on automatlcally. You can end treatment sesslun at any [true by pressing the ON/OFF button STEP12 Turn the device on. Press the ON/OFF button on the devlce unlll ll turns ott. Note: To turn devtce oft ustng App, go to the treatment operatlon‘ page, then press ‘uy button. Devlce le mm on eutematreelly alter a mrnutes of no actrvrty. STEP 13 Remove device and pad from (realment area and store. Remove electrode pad from skln by peeling gently lrom one edge. Remove devtce flom electrode pad. Protect adheswe surface of electrode pad uslng the clear plastre lllm store device and electrode pad in cool and dry place away from direct sunllgm Make: You can charge Ihe devlce ll necessary AMI battery charge Is advlsable before slaning a new treatment sesslon. CLEANING AND STORAGE Cleaning the device 1) Turn device 0H. Remove MicrosUSB eaole il device has been charging. 2) wipe device gently With slightly moistened, linta lree sofl cloth Do not use chemicals (such as thinner. benzene). Do not allow any water to seep into the device Note: Device and accessories do not require sterilization Cleaning the electrode pad I) Turn device 0". Remove pad horn device. 2) Wash pad when adhesive surlace becomes dlrly and/or no longer adheres well to shin. Wash adhesive surlace of pad soltly With lingertips under slow running cold water lor several seconds. Do ncl use sponge/clolh/sharp ooyeot like lingernail an adhesive surlace. Do not use detergent, chemicals or soap 3) Allow pad and adhesive suriace to air-dry eomplelely Do not Wlpe wilh tissue paper or cloth 4) Protect adhesive surlace oi pad using the clear plastic lilm Q CAUTION The lile oi pad may vary depending on lrequeney otwashing. skin condition and storage state. it pad no longer adheres to skin or it is damaged/broken. discomlnue use immediately Refills can be purchased sepaiately tiSoothei wireless Electrode Pad Model iTaoUAGs. ITSDOAGVLJ Storage Slare ereerrede pad m seared hag. smre device and aeeessaries m com and dry place. Keep devlce and acoessones um 01 reach of chi‘dren CAUTION u dewce is n01 used lor a hang penod 07 tune. it rs recommended that you recharge we battery at least once a warm. SPECIFICATIONS Power Source 3 7v Ll-iorl Power Supply lnpul 100724ov Ac. suleon. D.ZA;Outpu15V DC. auumA Frequency: 2Hz—132Hz Pulse wldtn: 3Uus~250us Waveform Blphaslc square wave OlleutVollage max 45V(al§UU ohm load) Output lntensrty Level u~1s levels Operatmg CondlIlons 5°c~40“cr ao%RH—75%RH; 700hPa ~losonpa Storage and transport condltlons (devlce): 1A°F~131‘F (-10”C ~55”C)‘1U%RH~90%RH‘ 70mm ~1OSOhPa Size mas 7x12.3mm (devlce) WelgM 25g (devlce) Servlce lrle el devlce 2 yEars Sen/Ice Me dl electrode pads up to 15 uses Applied pan Electrode SlZe nIelectmde: Large: 190mm x 95mm; Small 110mmx70mm lP classlflcatlon system lPZZ Maxlmum separatlon dlslance 10m (ln open enwdnment) The recommended separallon dlstance: 3m Description oi Ihe Wireless Funclions and Technology: 2.AGH172.AEGH1 2 MHz (-ZDdb) RF flequency Channel bandwidth Operation voltage DC3 7 V Types al spread speclrum DSSS Modulation type GFSK Number ol channel 40 Chanel spacing 2 MHz Channel frequency 0—39 Channel 2 402-2 ABDGHz An|enrla gain ZdBl Bluekooth version V4.0 The momma device uses oneonrone connection ol ELEM), and the device as a peripheral. responds to the App‘s connemlon request passively. establishing a Charonrone connection With the App. Alter lTSOOAE dewce connects to the App, it will not be connected to or controlled by other wireless devices. When the App connecls to peripheral device, App will send command. When iTauuAB dewce ensures this command is right il will open lhe conlrol command. You can then control the mains device Otherwise, the App cannot control the mums device HOW TO MANAGE YOUR PAIN When should the device be used? ll ls recommended cnal you use me devroe as soon as you experlence paln Slan wlth one lrealment session and evaluale your pain level. Slanrng early may prevent your paln lrorn becomlng worse or even cnronrc. ll ls advlsabie lo slan managlng your paln early oelore rl reaches a mu lnresnolo where rl may ilmlt your oarly ac|lvltles How oiten can the device be used? ll ls recommended cnal you use me devroe once a day (up to 30 mlnules) for each lreatment area. Dependlng on your palm level, you may need to use rl longer. Do nol exceed 3 lvnes a day (maxlmum so rnrnules lolal). Slarl wlih one lrealrnenl sesslon Keep track of your progress by raung your palrl level lrorn o (no pain) lo 10 (Intense oarn; before eacn lrealrnenl Stop eleolrolnerapy sesslon il pain reduces or steps. ll it does nor lmpmve and you experience soreness from oversuse‘ refraln lrorn treating me affected areas lor 2 days. ll thls reoccurs, reduce lrealmenl tlme and lnlensily (or fulure treatment. Setting the intensity level Trealment rnlensny snoulo be based on your level ofcomlon Always slan the lirsl session with short lrealrnenl time and low lntenslty level wnen you are lamilrarwnn lne eleolrolneraoy sessmn, you can adjust lrearmenl lime and inlensrly accordlngly Please pracllce caution when usmg devroe with hlgh rnlensny Do not exceed your eomlon level. & CAUTION Slap using the device under these conditions: lr you experlence any adverse reachonl such as 5le rrnlalion/redness/ourns. neadacne or olner oalnlul sensallnn‘ or il you leel any unusual discomlort lfyollr conoltlon does not lrnorove. becomes cnronic and severe or contlnues lor more than five days Note: lf you feel lncreasing oaln, dlzzlness‘ discomlort or nausea. discontinue use and consult wlth your nealtncara provlder. What (ype of pain is [he deVice suitable for? Electrolneraoy works best on acute oaln , oarn rn one local area less than 3 montns lt lS not sullaole to address onronlo oaln - paln ln more man one area lastrno longer than 6 months cnronrc paln ls usually caused by olner Issues lnat electrolnerapy cannot address. Note: TENS does nol cure any onyslologleal oroolem ll only helps to manage oaln Uslng TENS to manage oaln may nol work lor all users. TROUBLESHOOTING PROBLEM POSSIBLE CAUSES POSSIBLE SOLUTION The devlce dees nm paweron. The ballery IS exhausted. Charge (he delrlee. Eleelneel sllrnulellon IS weak cl eennol leel any slirnulellon Electrode pad has drled cm or ls dlrly. Replace with new elecvode pad. Elemrede pad does not adhere to sklrl well Replace wml new eleclrede pad. Eleclrlcal sllrrlulellerl IS uneernlorlable lnlenslly level ls too hlgh. Decrease lne lnlenslly level Devlce ls nol opereled acwrdlng le lnslrucllarls Please read user manual before use Eleclrlcal sllrnulellen ls lnellecllve Improper electrode pad placemenL Reposmon eleelrede pad Unknown Consult your heallhcare pmvlder. PROBLEM POSSIBLE CAUSES POSSIBLE SOLUTION The Skin becomes red and/or you leel a stabolng pain Electrode pad is applled on the same slte too oflen Reposltion the electrode pad If you feel paln or discomfort discontinue use lmmediately EIecIdee pad Is not adhered Io skin properly Ensure lha| electrode pad is securely adhered |o Skin. Eleclrode pad is dlny. Clean electrode pad according Io lnstructions ln thls manual or replace wlth new electrode pad. The surlace oleleclrode pad ls scratched Replace with new electrode pad. Output current stops during electrotherapy. Electrode pad detaches lrom sklrl. Turn delrlce all and reapply electrode pad. ll necessary replace With new electrode pad. The battery ls exhausted. Charge the deylce. PRODUCT/BATTERY DISPOSAL Used and lully discharged oalterles must be dlsposed ol ln a speclally labeled oollectlon contalner, at texlc waste collectlon polnls or through an electronlc retailer. Please dispose oi the device ln accordance wllh local laws and regulations. _ GLOSSARY OF SYMBOLS IP22 Dtsposal m accordance thh Dtreclive 2012/19/EU (WEEE) Type BF Apphed Fan (The applreu part rs ttre electrode) Refer ‘0 Insrmctmn Manua‘ Senal number The first number 2: Protected agarnst sohd torergrr objects of1Z,5 mm a: and greater. The second number Protected against venieauy lalhng waterarops when encrosure trltea uplo15’.VerItca\ly'alllng drops shau have no harmlul effects when the enclosure rs med starry engre up in 15» an erther srde loe ver|ica\ Transpanatren and storage lemperalure (mm -10°Cm 55“c Transportatron and storage mtmrmty Irmns tram 10% to 90% Transponatren and storage atmospnenc pressure Iirrrrts Mm 700 hPa tmoeo rrPa IMPORTANT INFORMATION REGARDING ELECTROMAGNETIC COMPATIBILITY (EMC) Use at accessories ther Ihan those specrned er provrded by tne manufacturer nIIms eqmpmenl could resutt in moreased electmmagneuc emlsslons or decreased electromagnem: Immunlly ct tnrs equrprnent and resmt m rrnpreper cperatron. Use of the equrpmem adjacent to or stacked wdn etnerequrpment snoutd be avaided because iI could result in rmproper dperatrcn usden use rs necessary‘ [ms edmpment and tne other eqmpment shank} be observed to venfy tnal may are operatrng normaHy. Portame RF eommunreatrons equlpmenl (mdudmg peripherats sucn as antenna cabtes and external antennas) should be used no cldser Ihzn 30 cm (12 incnes) In any pan DIIhe device, mcludmg cables specined by the manMacturer. otnerwrse. degradatren at me pertormance of tms eqmpmem eeuld resutt. Table 1 declamlmn , electromagnetlc emlSSlon The devlce is inlended for use lrl the electromagnetic envlmrlmenl specified below. The customer or the user ofdeVlce should ensure that it ls used in such an enVlronmenL Emlssians lest Compliance Electromagnetlc enwunment - guidance RF emissions Group 1 The devlce uses RF energy only for its inlemel CISPR 11 function. Therefore, KS RF emlsslorls are Very low and are not llkely to cause any interference in nearby eleslroms equipmenl. RF emlsslons Class B The devlce ls sullable for use In all CISPR 11 establlsnmenls, lncluding domestic Harmonlc emisslcns Cl A establlshmenls and those directly ccnnecled to IEC 51000 —2 ass lhe public lowsvoltage power supply network lhal ‘ , s lles b lldln 5 sea for domestlc r uses. Vollage llucluauonsl Complies upp u g u pu p lllCKer emlssions IEC 51000-3—3 Table 2 declaration , electromagnetlc immunlt The device ls intended Var use lrl (he electromagnellc envlrorlmerll specllled below. The cuslomer or Ihe user of dewce shuuld ensure Ihal ii is used in such an enVlronmeht. lmmunlty Iesl IEC 60601 lesl level Compllance level Eleciromaghehc ehvrrorrmehl - gmdance Electrostatic discharge (ESD) lEC 61000-4-2 :8 kV Contact :2 kv‘ :4 kV‘ :8 W :15 kV alr :8 kV Contact :2 kV‘ :4 le :8 kV, :15 kV arr Floors should be wood, concrete orceramlc tile. Iffluors are Covered wltl'l Synthellc malerlal, (he relatlve humldlly should be al leasl 30 %. Eleclrlcal lasl : 2 W for power supply : 2 kV for power Mains powerqualily should be llanSlenl/bum “Hes sul’p'y'mes Ihatofal roaleommeroral or IE0 61000-4-4 :1kaorlnpul/uulpul :1kaDr ho “ law”) 8 t llrles lnpul/oulput lines 5" a "W "m "- Surge : 0.5kV, : 1 kV |Irle(s) to : 0.5km :1 kV . . IEc 51000.4.5 Ilnes line(s) Io lines Mains powerquallly should be : U.5kV.:1kV,: 2 kV llne(s) lo earlh : 0.5kV. :1 kV. : 2 kV lihels) in earth that oi a typical commercial or hospiial environment. Voltage dips, shun lnterruptions and voltage variaiions on power supply input lines IEC 61000-441 0 "/a UT‘ 0.5 cycle AH)", 45”, 90", 135”, 180°, 225”, 270°3nd 315“ 0 % UT 1 cycle and 70 % UT: 25/30 cycles Single pnase- at 0° 0 “/p UT‘ 250/300 cycles 0 % UTl 0.5 cycle AID”, 45°, 90", 135“, 1801225”, 270°2md 3l5“ o % UT 1 cycle and 70 % UT, 25/30 Cycles Single pnase at 0., 0 "/a UT‘ 250/300 5 Cles Mains power quality snauld be that ol a typical commerclal or hospilal environment Ii Ihe user of lne device requires Conlillued operallon durlng power mains inierruplions, ii is recommended thai ihe devlce be powered from an uninierruplibie power supply or a banery. Power frequency (50/60 Hz) magnolia field IEC 51000-4-8 30 Nm 30 Nm Power lreguency magneiic fieids should be at leveis Characterlstic of a typical location in a typical commercial or hespilai envlmnmenl. NOTE: UT is (he a.c. mains voltage prlor to applicaiion cl ine test level Table 3 declarallen - electromagnetic lrnrnunily The devlce ls lnlended ror use m lhe eleelromagnellc envlmnmenl specllled below The cllslomer or the user of davlca should ensure lhafi N Is used ln such an envlmnmem. lmmunlly lesl IEC 60501 lesl Compllanee Electromagnelle level level ehwonrnenl - guldance Condueled RF 3 V 3 v Forlable and memle RF eemmumeahons lEc 61000-445 015 MHz to 80 0.15 MHz tn emu-pnleflshould be used no closer to any MHz 80 MHz pan oldevlce‘ lheh lhe recommended . sepereuoh dls|ance calcula|ed from [he 5 V ‘" ‘SM 3”“ E V '" ‘SM equalloh appllceble h) the lrequerlcy or the amaleur radle and amaleur vansmme, bands between Vad‘O bands Recommended separatlon dlslance 3'3; ””1 am 5° $365308? {1 , | ,2JF «50 KHz lo so MHz MHz .471 HP an MHzloauo MHz d:23JFaaMHzlezveHz where F' ls lhe maleum eulpul power ralmg dune trans er in we“: (W) eeedrdlhg lo E???“ R: 333%“: m 2 7 “MM me hansmmer manufacmrer and d ‘5 the DU” ’3 GHZ ' recommended seperelien dislahee lrl melers (m) Field slrenglhs lrdrn llxed RF hehsrnmers, as delermlned by an eleelremagnellc slle surveyv 3should be less than lhe compllenee level m each lrequency range. lnlerierence may occur in ttie vicinity or eduiement marked wrtri tne rollcwmg symbol (< D NOTE I At 30 MHz and 300 MHz, tne bigner frequency range applles. NOTE 2 These guidelines may not apply to all situations. Eleclrcmagnetic bropagalibn is aitecled by absorption and reflection tram structures, cbyects and peonle a Field strengtns lrom lixed RF transmitlers, such as base stations for radio (cellular/cordless) telepndnes and land mobile radius, amateur radio, AM and FM radio broadcast and TV bruadcast cannot be predieied theoretically wilh accuracy To assess Ihe electromagnetic environment due Io iixed RF transmilters. an electromagnetic sile survey should be cansidered ll tne measured lield strengtn in me location in wnicn device is used exceeds tne applicable RF compliance level above, device shuuld be observed to verity normal operation it abnormal beriorrnance is observed, additional measures may be necessary. sucti as re- orienting or relocating device. b Over tne frequency range 0.15 MHz to 80 MHz, lield strengths should be less tnan 3 Wm. Table 4 Recommended separation distances between portabie and mobile RF communications equipment and device The device Is intended for use in an electromagnetic environment In whlch radlaled RF disturbances are controlied. The customer or the user of device can nelp prevent eiectromagnetic Interference by maintaining a minimum distance between poriabie and mobile RF communications equipment (transmitters) and device. as recommended below. according to the maximum output power of the communications equipment. Rated maximum cutpul Separation distance according to trequency of transmitter power of transmitter m W 0.15 MHZ I0 80 80 MHZtn 800 MHZ 80 MHZ to 2.7 GHZ MHZ 4:1.2‘5 4:255 d :12fi 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 Itsted above, the recommended separatton mstance d m meters (m) can be estrmated usmg the equation applicable to the trequency of the transmttter, where P is the maximum output power rating of the Iransmiller in watts (W) accordmg to the transmitter manutacturer NOTE 1 At 50 MHZ and 800 MHz‘ the higher trequency range applies. NOTE 2 These guidelmes may not apply in alt sttuatiuns. Electromagneuc prupagatton is affected by absorption and reflection from structures, objects and people. FCC Cumpliancn illIonlIaIiolI Caution: The user is cautioned that changes or moditicaticns not expressly approved by the party responsible tor cumpllance could void the user‘s authority to operate the equipment. This deVICe complies with Part is otthe FCC Rules. Operation is sublect to the tollowirig 2 conditions: this device may not cause harrntul lntel'ferenCE, and this deVice must accept any lnterference received, including interterence that may cause undesired operation. NOTE: This equipment has been tested and tound to comply With the limits tor a Class B digital deVice, pursuant to Part 15 of the FCC Rules These limits are designed to proVide reasonable protection against harmlul interlerence in a residential installation This equipment generates, uses and can radiate radio frequency energy and, it not installed and used in accordance With the instructions. may cause harmlul interterence to radio communications. However, there is no guarantee that interierence Wlll not occur in a particular installation. it this equipment does cause harmlul interterence |o radlo or televlslon receptlon. whlch can be determined by turning the equipment off and on, the user is encouraged to try to correct the interterence by one or more of the tollowmg measures Reorlenl or relocate the receivrng antenna. Increase the separation between the equipment and recelver Connect the equipment into an outlet on a circuit diltererit trom that to which the receiver is connected Consult the dealer or an experienced radiorlv technician tor help FCC Radiation Expusure Statement: This equipment compiles With FCC radiation exposure limits set kmh tor an uncontrolled environment. Thls transmitter must not be colocated or operating in conyunction With any other antenna or transmitter. WARRANTY Prease contact mnovo Mearcal In case or a dam underlhe warranty. The rouowmg warranty terms appry: 1) The warranty period for |he devrce\51 year trom date of purchase In case of a warramy alarm, me date 0! purchase has to be proven by means a! a sales recerpt or mvmce. 2) Repairs under warranty do not extend the warramy penod tor the devree or far we replacemem parts a) The «anawrng is excluded under tne warranty All damage due to improper use, 6.9 nanobsewance of we user rrrstruatrorrs. All damage due |a reparrs er |amperrrrg by cusmmer or unauthorized thrrd parlies Accessorres wrnen are subject to normar wear and tear 4) Liabrhly {or dilect or indrrect Consequentia‘ losses caused by the umr rs excrudea even me damage In Ine umt rs accepred as a warranty clarm. Manulacmved lor Innovo Medlea‘ 10101 Slaflord Germs Dv Ste B Staffovd, TX 77477 Phone +1-858-888-9781 Eman: cs@mnovogroups.com www.mnovo-medwcal.cum Eli AH R‘ghts Reserved‘ Rev‘ V1.0 © 2018
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