I-Tech WEPERE RESTART User manual

USER MANUAL
Recover faster, anytime anywhere

3 USERMANUAL
Technical information
Manufacturer 4
Declarationofconformity 4
Classifications 5
Intendedpurposeandscopeofuse 5
Technicalspecifications 6
Devicedescription and controls 7
Labelling 8
Packcontents 10
How To Use
Introductiontothetechnology 10
Contraindications 11
Warnings 12
Deviceuse 12
Treatments 14
Looking after the device
Maintenance 14
Troubleshooting 15
Chargingthebattery 16
DisposalInformation 16
Warranty 17
Support 18
Spareparts 18
Interferenceandelectromagnetic compatibility tables 22

USERMANUAL 4
Manufacturer
I.A.C.E.R.S.r.l.
viaEnzoFerrari 2 •30037Scorzè(VE) -Italy
Tel.[phone]•Fax[phone]
Declarationofconformity
Themanufacter I.A.C.E.R.S.r.l
viaEnzoFerrari 2 -30037Scorzè(VE) -Italy
declaresunderitsownresponsibilitythattheproduct
RESTART
Isconformtothedispositionsoftheelectromagnetic compatibility Directive 2014/30/UE
oftheEuropeanParliamentandoftheCouncilofthe26thFebruary 2014,tothecurrent
TECHNICALSTANDARDon ELECTROMAGNETICCOMPATIBILITY EN 60601-1-22015
andthefollowingrules applied:
EN60601-12006 +A12013,EN60601-1-22015,IEC60601-2-52009,EN60601-1-62010+A12015,
EN60601-1-112015,ENISO 14971:2012,ISO10993-1:2009,ISO10993-5:2009,ISO10993-10:2010,
EN62366:2015.
Scorzè, 31/01/2022 MASSIMO MARCON
Place,date LegalRepresentative

5 USERMANUAL
Classifications
TheRESTARTdeviceassumes the following classifications:
• classIIwithtype BFappliedpart (Classif.EN 60601-1);
• device with IP22 protection degree against the penetration of solids and liquids into the ma-
chinebody.IPX7 protection degree for the treatmenthead.DEVICE NOTSUITABLEFORUSEIN
IMMERSION.
• equipmentandaccessoriesnotsubjecttosterilisation;
• devicenotsuitableforuseinthepresenceofaflammableanaestheticmixturewithairorwith
oxygen or with nitrous oxide;
• deviceintendedforcontinuousoperation;
• devicenotsuitablefor externaluse.
Intendedpurposeand scope ofuse
The RESTART device for ultrasound treatment is ideal for all muscle, tendon and ligament treat-
mentsincluding:
• Musclecontracture;
• Tendoncool-down;
• Relaxingmassage;
• Tissueoxygenation;
• Pre-competition preparation;
• Post-workoutrecovery;
• Tissuerecovery;
• Musclerelaxation.
Itisalsorecommendedusingthedevicefor the following aesthetictreatments:
• Cellulite;
• Drainingmassage;
• Microlifting.
Theuserofthedevicecan be either the useroraprofessionaloperator.

MANUALEDIUTILIZZO 6
Technicalspecifications
Feature Specification
PowerSupply IN:100-240V~,50/60Hz, 0.6-0.2A
OUT:15V 1.2A
Battery Ni-MH AAA850mAh 4.8V
Externaldimensions
(LengthxWidth xHeight) 204x 63x 58mm
Ingressprotection ratingIP IP22 machinebody
IPX7head
Insulation(EN60601-1) II
Appliedparts (EN60601-1) BF
Partapplied tothe user Aluminiumhead ofthedevice
Operation Continuous
Waveform Pulsed, continuous
Carrierfrequencyof use 1MHz± 10%
Modulationfrequency 100Hz±10%
Dutycycle 5%, 50%,100% (mainspowered)
5%,50%, 100%(batterypowered)
Power Canbe setin 3stepsL (low)- M(medium)-H(high)
Maximumpower density 1.6W/cm(mains powered)
0.8W/cm(batterypowered)
Maximumoutputpower 6.4W(mainspowered)
3.2W(battery powered)
RBN(max) 5.0
Headsurface 5 cm
Actual radiantarea 4cm ±20%
Beamtype Collimated
Headmaterial Aluminium
Treatmenttime 5,10,15 minutes
Usageconditions
Ambienttemperature From +5to+40°C.
Relative humidity From 15to93%
Atmospheric pressure 700-1060hPa
Transport andstorageconditions
Ambienttemperature From +5to+40°C.
Relative humidity From 15to93%
Atmospheric pressure 700-1060hPa
Usefullife ofthe deviceand itsaccessories: 3years.

7 USERMANUAL
Devicedescriptionandcontrols
1 Treatmenttimeindicator
2 Timebutton
3 Poweradjustmentbutton
4 Treatmentpowerindicator
5 Battery indicator
6 DeviceON/OFFbutton
7 Emitting head
8 Powersupplyconnector

USERMANUAL 8
Labelling
IPX7: for the device head only
I.A.C.E.R. Srl, via Enzo Ferrari 2
30037 Scorzè (VE) - Italy
Model: Restart
Power supply
In: 100-240V~, 50/60 Hz, 0.6-0.2 A
Out: 15V 1.2A
Battery: Ni-MH AAA850mAh 4.8 V
Ultrasound
Carrier frequency of use: 1MHz ± 10%%
Duty cicle:
5%, 50%, 100% (mains powered)
5%, 50%, 100% (battery powered)
Maximum output power:
6.4W (mains powered)
3.2W (batter powered)
RBN (max): 5,0
Actual radiant area: 4 cm² ± 20%
Wave form: pulsed, continous
Beam type: collimated
Modulation frequency: 100Hz ± 10%
Pulse duration: 0.5ms, 5ms
XXXXXX XXXX-XX
SN

9 USERMANUAL
Gel labelling
Followthe“instructions for use”
WEEEDirective
TypeBFappliedpart
ClassIIdevice
Incompliancewith Directive2014/30/UE
SN Serial number
Allowedtemperatures(storagetemperatures,onpackaging)
Relative humidity (storagerelative humidity,onpackaging)
Dateofmanufacture(YYYY-MM)
Powersupply
Warning,seethedocumentsaccompanyingthe product
IP22 Deviceprotected against the penetrationofsolids(with diameter
d≥12.5mm) and against the fall of vertical drops of water when the device
isheldat15°from the normaloperatingposition.
Expiry date
xxxx-xx
Shanghai International Holding Corp.
GmbH (Europe) Eiffestraße 80,
20537 Hamburg Germany
Shenzhen Dongdixin Technology Co., Ltd.
Floor 1-2, No.3 Building, Fanshen Xusheng
Industrial Estate Xilixiaobaimang 518108
Nanshan District, Shenzhen P. R. China
2 Anni a confezione integra /
2 years sealed condition

USERMANUAL 10
Packcontents
TheRESTARTpackcontains:
•1RESTARTdevice;
•1medicalpower supply;
•1batterycharger;
•1gelfor ultrasound;
•1carry bag;
•1usermanual.
Introduction tothetechnology
Ultrasoundtreatmentrepresentsamethodthatisbasedonthetransferofenergyintothetissues
whichresultsinthermal and non-thermal biological effects.
This treatment is based on the contact between the head of the device and the tissues being
treated.Theoptimalcouplingof these twosurfacesisensured bytheuseofawater-basedultra-
sound gel. Through the contact described the transmission of general mechanical waves from
the piezoelectric present inside the head of the device takes place. In order for there to be maxi-
mumtransmissionofenergyfromonemediumtoanother,theimpedanceofthetwomustbethe
same.Obviouslyinthecaseofthehumanbody, suchconditionhardlyoccurs.
Thegreatertheimpedancedifferencebetweenthetwomedia,thegreaterthereflectionandcon-
sequently the smaller the amountofenergy that will betransferred.Theimpedancedifferenceis
greatestwithaluminium-airinterface,whichisthefirstthatultrasoundwaveswouldhavetoover-
cometoreachthebody.Toreducethisdifference,acouplingsubstancemustbeused.Ifthereisa
smallamountofairbetweenthetransducerandtheskin,theproportionofultrasoundwavesthat
wouldbereflectedwouldreach99.998%,i.e.therewouldbe no transmission.
In addition to the phenomenon of reflection, if the wave does not hit the separation surface
between the media at 90°, refraction occurs. In practice, the direction of the ultrasound beam
through the second medium will be angled. The critical angle for ultrasound waves at the skin
surface appears to be 15°.If the device head is oriented at a 15° angle to the surface, most of the
beam will propagate through the epidermal tissues parallel to the skin rather than perpendicular
tothetissues.
The absorption of the energy released by the ultrasound waves follows an exponential trend, in
fact muchmoreenergyisabsorbedinsuperficialtissuesratherthanindeepones.
Precisely due to the trend of absorption, theoretically there is no point where all the energy is absor-
bed,butthereiscertainlyapointwheretheselevelsarenotsufficienttoproduceatherapeuticeffect.
Generally tissues with the highest protein content will absorb more, unlike tissues with high water
andlowproteincontent,whichwillabsorbaminimalamountofenergy(bloodandfat,forexample).

11 USERMANUAL
Contraindications
Itisstrictly prohibited touseRESTARTinusers withseverearrhythmiasorwith pacemakers,with
heart disease and severe cardiovascular problems, who suffer from epilepsy, with ongoing phle-
bitis, thrombophlebitis, in feverish states, tuberculosis, malignant tumours and neoplasms, local
infections, metalimplants(possible afterconsultingadoctor),venous thrombosis,severeosteo-
porosis,arteriopathies (exceptmedicalprescriptions).
ConsultyourdoctorbeforeusingRESTARTwithmetallicosteosynthesisdevices.
Warnings
Itisrecommended:
• to use the device keeping the applicator at least 3 metres away from televisions, monitors,
mobile phones or any other electronic equipment even if the device does not generate or re-
ceiveanyelectromagnetic interference from other equipment;
• to avoid use of the device by people who are not properly trained and who have not read this
manual;
• during treatment, the userisadvisednottowearmetal objects;
• touseONLY theaccessoriessuppliedbythemanufacturer.
Itisforbidden:
• tousethe deviceinthepresenceof equipmentformonitoringtheuser’svitalfunctions,equi-
pmentforelectrosurgeryorforshortwaveormicrowavetreatmentorotherdevicesthatsend
electricalimpulsestothebodyandingeneral in combination with other medical devices;
• for the device to be used by people of unsound mind, suffering from sensory processing di-
sorders,temporarily unfit unless assistedbyqualifiedpersonnel;
• tousewithconsumersundertheageof 18;
• to use the device if you find any damage or signs of deterioration to it or to the accessories
and/orcables:contacttheretailerorthemanufacturerasindicatedintheSupportparagraph.
Checktheconditionofthedevicebeforeeach use;
• to use the device near flammable substances, gases, explosives, in environments with high
oxygenconcentrations,inthepresenceofaerosolsorinveryhumidenvironments(donotuse
inthebathroomorwhileshowering/bathing);
• to use the device while driving vehicles or while operating and controlling equipment/machi-
nery;

USERMANUAL 12
• tousethedeviceinhyposensitiveareas,oncarotidsinuses,genitals,neartheuterus and ab-
domen, in areas of the body where there are glands. Also avoid using the device on the neck
andmouth.Finally, avoid treatment withdirectexposureoftheeyetotheultrasonicbeam;
• keep the treatment head fixed in one place during treatment;
• tousesharpobjectsonthedevicehead.
Warning:
• pay attention to the use of connection cables in the presence of children/young people: po-
tentialstrangulation hazard;
• do not confuse the connection cables with headphone cables or other devices and do not
connect the cablestootherdevices.
• Thedeviceisnot intended foroutdooruse.
Themanufactureristobeconsidered responsible forthesafety,reliability and performance of
thedeviceprovidedthat:
• anyadditions,modificationsand/orrepairs are carried outbyauthorised personnel;
• theelectricalsystemof theenvironmentinwhichRESTARTis installedcomplieswithnational
laws;
• thedeviceisusedinstrictcompliancewiththeinstructions given inthismanual.
Shouldanyforeignsubstancesgetintothe device, contact thedealerormanufacturer immedia-
tely.Should the device fall, checkthatthere arenocracksinthecontaineror damage ofanykind;
ifthereare,contactyourdealeror manufacturer.
In the event of any change in performance during treatment, stop treatment immediately and
contactyourdealerormanufacturerimmediately.
Deviceuse
Cleananddisinfecttheultrasoundheadwithadisinfectantsolutionbeforeand afteruse.
TouseRESTART:
1. connectthepowersupplytothedeviceifthedeviceis not batteryoperated.
2. Beforestartingtreatment,makesuretocleanthetreatmentareawitha70%alcoholsolutionor
mildsoap.Itisrecommendedtoremoveexcessivehairinthetreatment
area.
3. Apply a good amount of ultrasound gel in the treatment area (ONLY
USE GEL WITH CE MARKING). Gel is essential to ensure a correct cou-
pling between the treatment area and the head and therefore the ef-
fectivenessofthetreatment.
WARNING:donotapplythegeldirectlyonthehead.Thedevicemayinterpretthis as
skin-to-headcontactand emitultrasoundenergy,damaging the device.

13 USERMANUAL
4. Turn on the device by moving the switch to the ON position. The ultrasound intensity indicator
willdisplayL(Low,preset),whereasthebatterylevelindicatorwillindicatethebatterycapacity:
low(L-Lowpreset),medium(M-Medium)andhigh (H-High).
5.Select the desired intensity by repeatedly pressing the MODE key. There are three levels of in-
tensityselectableinorder:low(presetL – Low),medium(M–Medium) and high(H–High).
6. Selectthetreatmenttimebyrepeatedly pressingtheTIME key: theLEDsrelatingtothe5-10-15
minutesoftreatmentwilllightupin sequence,asshowninthefigure.Wheninuse, thechosen
treatment time indicatorwillbeconstantlylituntilthesettimehaselapsed.
7. Once the application time has been set and the head has been placed in
contact with the skin, the treatment will begin: it is important to perform the
treatment by continuously and uniformly moving the head around the ap-
plication area, with slow and circular movements. The treated area should
be twice the applicator diameter. If there is poor transmission of ultrasound
energy,itisrecommendedtoaddmoregelorrepositionthe ultrasoundhead.
Head movement should not be too slow to avoid inducing heat; nor too fast to pre-
ventbad contact whichwouldreduce theeffectivenessof the treatment.
8.At the end of the treatment all the indicator lights will turn off. Turn the switch to OFF and di-
sconnect the device from the power supply (not needed if you are using the device with bat-
tery).
9, Clean any gel off the head before storing the device and its accessories in the bag provided.
Makesure thereisno gel leftonthehead.DO NOTSUBMERGEIN WATER!

USERMANUAL 14
N.B.disconnectthecablesbeforeputting thedeviceinthe bag.Ifthisisnot done,thecablescan
beexcessivelybentneartheconnectors,whichcandamage the cables.
WARNING: to ensure user safety, the device is equipped with a system that detects cor-
rectcouplingbetweentheultrasoundheadandtheuser’sskin.Intheeventofincorrect
coupling or bad contact, the treatment time LED will start flashing and the ultra-
sound intensity will be reduced. Once head/skin contact is restored, the intensity will
automatically increaseslowly,up to the previously setlevel.
WARNING: to ensure user safety, the device is also equipped with a temperature regula-
tionsystem.Ifthe headtemperatureexceeds42°C, thedevicewill endthetreatment
and the time indicator LED will flash twice; it will not be possible to resume treatment
untiltheheadreachesatemperaturebelow 40°C.
Treatments
Belowisthelistoftreatmentssuggestedbythemanufacturer:
Treatment Intensity Minutes
Muscle H- Powersupply/Battery 15
Tendon/Ligament L/M -PowersupplyM -Battery 10 –15
Aesthetic L- Powersupply L/M -Battery 5– 10
REMEMBERTO:
•keeptheultrasoundheadalways inmotion;
•useagood amount ofgeltoensurecontact;
•actevenlyonthetreatedarea.
Maintenance
Ifusedinaccordancewiththeinformationreportedherein,thisdevicerequiresnoparticularrou-
tinemaintenanceoperations.
Itisadvisabletocarryoutafunctionalcheckofthedeviceat the Manufacturerevery24months.
The manufacturer does not consider the RESTART device to be repairable by personnel outside
the company itself. Any such operation by personnel not authorised by the Manufacturer will be
consideredtamperingwiththedevice,therebyavoidingthemanufacturer’swarrantyandfreeing
itfromliabilityforanyhazards to whichtheoperatororusermaybe subjected.
CLEANING
It is advisable to switch off the RESTART at the end of each treatment session, in addition to
removing the power cable.Use a soft dry cloth to remove any dust from the device. In case of
hard-to-removedirt,useaclothsoakedin water andalcohol.

15 USERMANUAL
Thedevicedoesnot require sterilisation.
Notes:
- Neverusesolventsforcleaning.Cleaning agentscandamagethedevice.
- Carryoutroutinemaintenance,in particular:
•inspectthebodyofthedeviceforcracksor fissures, which mayallowliquidstoenter;
•inspectthecables.
TRANSPORTANDSTORAGE
Transportprecautions
Thereisno particularcaretobetakenduringtransport asRESTARTis aportable device.However,
itisrecommendedtoputRESTARTanditsaccessoriesinthebagprovidedaftereachuse.Protect
thedevicefromintenseheat,directsunlightandliquids.Storethedeviceinacoolandwellventi-
latedenvironment.Donotplaceheavy objectsontopof the device.
Storageprecautions
Thestoragelocationshouldhave the following characteristics:
During operation ambienttemperaturefrom+5to+40°C
relative humidity from 15to93%
pressurefrom700to1060 hPa
Inthebag provided ambienttemperaturefrom+5to+40°C
relative humidity from 15to93%
pressurefrom700to1060 hPa
Troubleshooting
Any type of work on RESTART must only be carried out by the manufacturer or authorised dealer.
In any case, before sending RESTART to the manufacturer, it will be necessary to ascertain the
exactnatureoftheRESTARTmalfunction. Checkthefollowing:
PROBLEM POSSIBLECAUSE SOLUTION
Thedevice doesnot turnon
Adaptercontacterror Makesuretheadapter
isconnected.
Checkthefollowingcontacts:
•All contactsare fine
•All contactsare notbroken
•The battery isO
Thedevice doesnot work
Thebattery isdamaged
TheLED indicatorsdo notlightup
Mainsplug notinsertedcorrectly
inthepower socket. Checktheoperation ofthe power socket.
Mainscable notcorrectly
insertedin theconnector
ofthedevice.
Inserttheplug andcable
correctly intothe connector
oftheappliance.
Mainscable wornandbroken. Replacethe mainscable.

USERMANUAL 16
TheLED indicatorsdo notlightup Switchnot turned ON. Checkthatyou haveturned
theswitchON.
Thepower LEDis working finebut
thereisnooutput Timeandintensitysetincorrectly. Checkand resetthe desired values.
Somecontrolsdo notwork
properly..
Defectivebuttonsor keys. Contactthemanufacturer
Electronic controlcircuit failure.
Thedevice worksasnormal,
butthereis anoticeable
dropin theeffectiveness
ofthetreatment.
Possiblehead fault. Contact themanufacturer
Possiblefailure ofthe appliance’s
powergenerator circuit.
Allbatteryindicatorsflash The batteryis damaged Changethe battery
Thereis nobattery
Chargingthebattery
The device can be powered by the internal battery: when the battery level indicators are all off or
the battery charge indicator is flashing to L (Low), it is necessary to charge the battery by con-
necting the adapter tothedevice.
When the device is charging: the battery indicator will flash from L-M-H in sequence. Once char-
gingiscomplete,thebattery charge indicatorwilllightupasH (High).
WARNING: the battery life cycle depends on the charge/discharge cycles to which it is
subjected andonthenumberofthem.
Takethefollowingprecautionstoincreasebattery life:
•Rechargethebatteryonceamonth,evenwhennot using the device;
•Drainthebatteryasmuchaspossibleduringuse.
ReplacingtheBattery
The battery must only be replaced by personnel authorised by the manufacturer and not by the
user. In addition, the batteriesaredisposedofinaccordance withcurrentregulations(WEEE).
Therefore,forreplacement,contactIACERs.r.l.supportdirectly (Support paragraph).
DisposalInformation
RESTARTdevices,inlinewithoperatingandsafetyrequirements,havebeendesignedandbuiltto
have a minimum negative impact on the environment, following the provisions of the European
Directive2012/19/EUrelatingtothedisposalofwasteelectricalandelectronicequipment.
Thecriteriafollowedarethoseofminimisingtheamountofwaste,toxicmaterials,noi-
se,unwantedradiationandenergyconsumption.

17 USERMANUAL
Carefulresearchintooptimisingmachineperformanceguaranteesasignificantreductionincon-
sumption,inaccordancewiththeconceptofenergysaving.
Thissymbolindicatesthatthisproductshouldnotbedisposedwithotherhouseholdwaste.
Correct disposal of obsolete equipment, accessories and especially batteries helps to prevent
possiblenegativeconsequencesonhumanhealthandtheenvironment.
Theusermustdisposeofthe equipmenttobescrappedbytaking it to the collection centre indi-
catedforthesubsequentrecyclingof electrical andelectronic equipment.
For more detailed information on the disposal of obsolete equipment, contact your local council,
wastedisposalserviceorshopwhere you purchasedtheproduct.
Warranty
RESTARTiscoveredbya2(two)yearwarranty,startingfromthedate ofpurchase,on theelectro-
nic parts, when used in accordance with the instructions provided in this manual. The parts
subject towearandtearare excluded from the warrantyunlessthereareobviousmanufacturing
defects. The warranty will lapse if: the device is modified in any way or operated by staff not au-
thorisedbythemanufacturerorbytheauthorised dealer.
ThewarrantyconditionsarethosedescribedinthefollowingparagraphWarrantyconditions.The
warranty is providedbyIACER.
Shouldyouneedtoreturnthegoodsthenpleasepackthedeviceandalltheaccessoriessothatitwon’t
be damaged during transportation. In order to be entitled to the warranty assistance, the purchaser
mustenclosetothedeviceacopyofthepurchasingreceipt,provingoriginandpurchasingdate.
Warranty terms andconditions
1) Any warranty claim must be accompanied by the receipt or invoice, that will be sent together
with the goodstothemanufacturer.
2) Thewarrantyperiodis2years(two)andcoverstheelectronicpartsofthedevice.Thewarran-
tyclaimcanbe addressedtothedealerfromwhichyou havepurchasedthedeviceor directly
tothemanufacturer.
3) Thewarranty only coversdamagetotheproductthatcausesitto malfunction.
4) Thewarrantyisunderstoodtobethefreerepairorreplacementofcomponentsrecognisedas
faultyduetomanufacturingormaterialdefects, includinglabour.
5) The warranty does not apply in case of damage caused by negligence or use that does not
complywiththeinstructionsprovided,damagecausedbyoperationscarriedoutbyunautho-
risedpersons,damageduetoaccidental causesornegligenceofthepurchaser,withparticu-
larreferencetoexternalparts.
6) Thewarranty doesnotcoveranydamage caused byincorrectpowersupplytothedevice.
7) Thepartssubjecttowearandtearoncethedevicehasbeenusedareexcludedfromthewarranty.
8) Thewarrantydoesnotincludetransportcoststhatwillbebornebythebuyerinrelationtothe
modesandtimesoftransportation.

USERMANUAL 18
9) The warranty automatically expires after 2 years. In this case, any assistance operations will
be performed by charging for the replaced parts, labour costs and transport costs according
tothecurrentrates.
10) Anydisputesthatmayarise shallbesettled exclusively before the courtofVenice.
Support
The manufacturer is the only point of contact for technical support regarding the device. For all
technicalsupport matters, please contact:
I.A.C.E.R.S.r.l.
viaEnzoFerrari 2 •30037Scorzè(VE) -Italy
Tel.[phone]•Fax[phone]
Technical documentation concerning repairable parts may be provided, but only with prior com-
panyauthorisation and only after giving proper training tothemaintenancepersonnel.
Spareparts
Original spare parts for this device can be ordered at any time from the manufacturer. To order
themcontact:
I.A.C.E.R.S.r.l.
viaEnzoFerrari 2 •30037Scorzè(VE) -Italy
Tel.[phone]•Fax[phone]
Use only original spare parts supplied by the manufacturer; if non-original spare parts are used,
theoperationandsafetyoftheproductmightbeaffected andthewarranty will be nullandvoid.
Interferenceandelectromagneticcompatibilitytables
TheRESTARTultrasoundtreatmentdeviceisdesignedandbuiltincompliancewiththecurrentTECH-
NICALSTANDARDonELECTROMAGNETICCOMPATIBILITYEN60601-1-22015,withtheaimofproviding
reasonableprotectionagainstharmfulinterferenceinresidential,civilandhealthcaresettings.
Basedonitsoperatingprinciple,thedevicedoesnotgeneratesignificantradiofrequencyenergy
and has an adequate level of immunity to radiating electromagnetic fields. Under these condi-
tions,harmfulinterferencecannotoccurtoradioelectriccommunicationsandtotheoperationof
electro-medical devices used for monitoring, diagnosis, treatment and surgery, to the operation
of electronic office devices such as computers, printers, copiers, faxes, etc. and to any electrical
orelectronicapplianceusedinsuchenvironments,provided thattheycomplywiththeELECTRO-
MAGNETICCOMPATIBILITY directive.
Inanycase,topreventanyproblemwithinterference,itisrecommendedtooperateanytreatment

19 USERMANUAL
deviceatanappropriatedistantfromcritical equipment for monitoring users’ vital functions and
to use caution in therapeutic applications on users with pacemakers. However, it is advisable to
use the device keeping a distance of at least 3 metres from televisions, monitors, mobile phones
oranyotherelectronicequipment.
Formoredetailsconsultthecompatibilitytablesattheendof the manual.

USERMANUAL 20
RESTART. Allrights reserved. RESTARTandthelogo aretheexclusivepropertyof
I.A.C.E.R.S.r.l.and areregisteredtrademarks.
Issue:MNPG417-01 of31/01/2022