TABLE OF CONTENTS

INTrOduCTION . . . . . . . . . . . 3

prOduCT OvErvIEw . . . . . . . .3

TEChNICAL SuppOrT . . . . . . . .3

SuppLIES & rEpLACEmENT pArTS . . 3

INdICATIONS FOr uSE . . . . . . . . 4

CONTrAINdICATIONS . . . . . . . . 4

wArNINgS . . . . . . . . . . . . . . 4

prECAuTIONS . 4 1 .System .Precautions . . . . . . . . .4 . 4 2 .Procedural .Precautions . . . . . 4-5

INFECTION CONTrOL . 5 1 .General .Information . . . . . . . 5 . 5 2 .Water .Supply .Recommendation . 5

INSTALLATION INSTruCTIONS . 6 1 .Water .Line .Requirements . . . . . .5 . 6 2 .Electrical .Requirements . . . . . . .5 . 6 3 .Unpacking .the .System . . . . . . 6 . 6 4 .System .Installation . . . . . . . . .6 . 6 5 .Power .Cord .Connection . . . . . 6 . 6 6 .Water .Supply .Line .Connection . 6-7 . 6 7 .Foot .Control .Battery .Installation/ . . . . . . . .Replacement . . . . . . . . . . . .7 . 6 8 .Foot .Control .Synchronization . . . .7

CAvITrON® pLuS SCALEr dESCrIpTION . 7 1 .System .Controls . . . . . . . . . 8 . 7 2 .Diagnostic .Display .Indicators .and . . . . . . . . .Controls . . . . . . . . . . . . . 9 . 7 3 .Handpiece ./ .Cable . . . . . . . . . 10 . 7 4 .Cavitron® .30K™ .Ultrasonic . . . . . . . .Inserts . . . . . . . . . . . . . .10 . 7 5 .Wireless .Foot .Control .Information . . . . . . . . . . . . . . . . . . .and .Operation . . . . . . . . . .11 . 7 6 .Accessories .and .User . . . . . . . . .Replaceable .Parts . . . . . . . . . 11 . . 7 6 1 .Accessories . . . . . . .11 . . 7 6 2 .User .Replaceable .Part . . . . . . . . . . . . .Kits . . . . . . . . . . . . 11

SYSTEm SETup, OpErATION ANd TEChNIQuES FOr uSE . 8 1 .Handpiece .Setup . . . . . . . . . 11 . 8 2 .Patient .Positioning . . . . . . . . 12 . 8 3 .Performing .Ultrasonic . . . . . . . . .Scaling .Procedures . . . . . . . . 12 . 8 4 .Patient .Comfort .Considerations . . 12

SYSTEm CArE . 9 1 .Daily .Maintenance . . . . . . . . 12 .

. . Start-up .procedures . . . . at .the .beginning .of .the .day . . . 12 .

. . Between .patients . . . . . . . . 13 .

. . Shut-down .procedures .at . . . . the .end .of .the .day . . . . . . . 13 .

. 9 2 .Weekly .Maintenance . . . . . . . 13 . 9 3 .Water .Line .Filter .Maintenance . . 13

TrOuBLEShOOTINg . 10 1 .Troubleshooting .Guide . . . 13-14 . 10 2 .Technical .Support .and .Repairs .14

wArrANTY pErIOd . . . . . . . . 15 .

SpECIFICATIONS . . . . . . . . . . 15

CLASSIFICATIONS . . . . . . . . . . 15

dISpOSAL OF uNIT . . . . . . . . . 15

QuICK rEFErENCE guIdE . . . .16-17

English

INTrOduCTIONCongratulations!

YourdecisiontoaddtheCavitron®Plus™UltrasonicScalertoyourpracticerepresentsawiseinvestmentingooddentistry.

Foroverfourdecades,dentalprofessionalshavepreferredtheclinicalbenefitsandlabor-savingadvantagesinherentinCavitronultrasonicscalers.Clinicalstudiesandindependentresearchhaveproventhatnoothermethodofsupra-andsubgingivalcalculusremovalcansurpassthespeed,efficiency,andversatilityofultrasonicscaling.

DENTSPLYProfessionalisanISO13485registeredcompany.AllDENTSPLYProfessionalmedicaldevicessoldinEuropeareCEmarkedinconformancewithCouncilDirective93/42/EEC.

Website:www.professional.dentsply.com

RxOnly:Thisproductisintendedforusebyqualifieddentalprofessionalhealthcareproviders.

prOduCT OvErvIEwTheCavitronPlusUltrasonicScalerisaprecisionengineeredandmanufacturedinstrument.Itcontainscontrolsandcomponentsforultrasonicscaling.Thesystemproduces30,000strokespersecondattheultrasonicinsert’sworkingtipthatwhencombinedwiththecavitationaleffectofthecoolantlavagecreatesasynergisticactionthatliterally“powersaway”theheaviestcalculusdepositswhileprovidingexceptionaloperatorandpatientcomfort.

TheCavitronPlusUltrasonicScalerisequippedwithaSustainedPerformanceSystem™(SPSTechnology),whichoffersaconstantbalancebetweenscalingefficiencyandpatientcomfortbymaintainingclinicalpowerwhentheinserttipencounterstenaciousdeposits,allowingthecliniciantoeffectivelyscaleevenatadecreased/lowerpowersetting.TheCavitronPlusSystemhasextendedtheSPStechnologybyspreadingouttheBlueZonerange,providingfinerresolutiontothepowersettings.AdvancedfeaturesthatmaketheCavitronPlusawiseinvestmentincludeawirelessfootcontrol,illuminateddiagnosticdisplay,rinsesetting,andautomatedpurgefunction.

Thesefeaturescombinewithestablishedfeatures,suchastheSteri-Mate®detachable,sterilizablehandpieceandswivelcablewithlavagecontrol,lowpowerrange,andhands-freeboostmodetoprovidetheultimateinultrasonicscalingexperiencesforyourpatients,whilestillprovidingthequalityandreliabilityyou’vecometoexpectfromCavitronbrandultrasonicsystems.

TheCavitronPlusUltrasonicScalerisUL/ULccertifiedandapproved.TheCavitronPlusUltrasonicScalerisclassifiedbyUnderwritersLaboratoriesInc.withrespecttoelectricshock,fire,mechanicalhazardsinaccordancewithIEC60601Standard.TheCavitronPlusUltrasonicScalercomplieswithPart15oftheFCCRules.Operationissubjecttothefollowingtwoconditions:1)thisdevicemaynotcauseharmfulinterference,and2)thisdevicemustacceptanyinterferencereceived,includinginterferencethatmaycauseundesiredoperation.CavitronPlusbaseFCCcertification/registrationnumber:FCCID:TF3-DPD73227323;IC:4681B-73227323.CavitronPlusfootcontrolFCCcertification/registrationnumber:FCCID:TF3-DPD81675;IC:4681B-81675.ThetermICbeforethecertification/registrationnumbersignifiesthattheIndustryCanadatechnicalspecificationsweremet.

TEChNICAL SuppOrTFortechnicalsupportandrepairassistanceintheU.S.,callDENTSPLYProfessionalCavitronCareSMFactoryCertifiedServiceat1-800-989-8826,MondaythroughFriday,8:00A.M.to5:00P.M.(EasternTime).Forotherareas,contactyourlocalDENTSPLYProfessionalRepresentative.

SuppLIES &rEpLACEmENT pArTSToordersuppliesorreplacementpartsintheU.S.,contactyourlocalDENTSPLYProfessionalDistributororcall1-800-989-8826,MondaythroughFriday,8:00A.M.to5:00P.M.(EasternTime).Forotherareas,contactyourlocalDENTSPLYProfessionalRepresentative.

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SECTION 1: Indications For use

Allgeneralsupraandsubgingivalscalingapplications

Periodontaldebridementforalltypesofperiodontal diseases

Endodonticprocedures

SECTION 2:Contraindications

UltrasonicSystemsshouldnotbeusedforrestorative dentalproceduresinvolvingthecondensationof amalgam.

SECTION 3: warnings

Personsfittedwithcardiacpacemakers,defibrillators andotheractiveimplantedmedicaldevices,havebeen cautionedthatsometypesofelectronicequipment mightinterferewiththeoperationofthedevice. Althoughnoinstanceofinterferencehaseverbeen reportedtoDENTSPLY,werecommendthatthe handpieceandcablesbekept6to9inches(15to23 cm)awayfromanydeviceandtheirleadsduringuse.

Thereareavarietyofpacemakersandothermedically implanteddevicesonthemarket.Cliniciansshould contactthedevicemanufacturerorthepatient’s physicianforspecificrecommendations.Thisunit complieswithIEC60601MedicalDeviceStandards.

TheuseofHighVolumeSalivaEvacuationtoreduce thequantityofaerosolsreleasedduringtreatmentis highlyrecommended.

ItistheresponsibilityoftheDentalHealthcare Professionaltodeterminetheappropriateusesofthis productandtounderstandthehealthofeachpatient, thedentalproceduresbeingundertaken,andindustry andgovernmentalagencyrecommendations, requirements,andregulationsforsafepracticeof dentistry.

Whereasepsisisrequiredordeemedappropriatein thebestprofessionaljudgmentoftheDentalHealthcare Professional,thisproductshouldnotbeused.

Duringboil-wateradvisories,thisproductshouldnot beoperatedasanopenwatersystem(e.g.connected toapublicwatersystem).ADentalHealthcare Professionalshoulddisconnectthesystemfromthe centralwatersource.TheCavitronDualSelect™system canbeattachedtothisunitandoperatedasaclosed

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systemuntiltheadvisoryiscancelled.Whenthe advisoryiscancelled,flushallincomingwaterlines fromthepublicwatersystem(e.g.faucets,waterlines anddentalequipment)inaccordancewiththe manufacturer’sinstructionsforaminimumof5minutes.

Priortobeginningtreatment,patientsshouldrinsewith anantimicrobialsuchasChlorhexidineGluconate 0.12%.Rinsingwithanantimicrobialreducesthechance ofinfectionandreducesthenumberofmicroorganisms releasedintheformofaerosolsduringtreatment.

PerFCCPart15.21,changesormodificationsnot expresslyapprovedbythepartyresponsiblefor compliancecouldvoidtheuser’sauthoritytooperate thisequipment.

SECTION 4: precautions

4.1 System precautions

Donotplacethesystemonornexttoaradiatoror otherheatsource.Excessiveheatmaydamagethe system’selectronics.Placethesystemwhereairisfree tocirculateonallsidesandbeneathit.

Thesystemisportable,butmustbehandledwithcare whenmoving.

Equipmentflushinganddentalwatersupplysystem maintenancearestronglyrecommended.SeeSection9: SystemCare.

Closemanualshut-offvalveonthedentalofficewater supplyeverynightbeforeleavingtheoffice.

Theuseofanin-linewaterfilterisrecommended.

Neveroperatesystemwithoutfluidflowingthrough handpiece.

4.2 procedural precautions

TheCavitronPlusunitworkswithCavitroninsertsasasystem,andwasdesignedandtestedtodelivermaximumperformanceforallcurrentlyavailableCavitronandCavitronBellissima™brandultrasonicinserts.Companiesthatmanufacture,repairormodifyinsertscarrythesoleresponsibilityforprovingtheefficacyandperformanceoftheirproductswhenusedasapartofthissystem.Usersarecautionedtounderstandtheoperatinglimitsoftheirinsertsbeforeusinginaclinicalsetting.

Likebristlesofatoothbrush,ultrasonicinserttips“wear” withuse.Insertswithjust2mmofwearloseabout50% oftheirscalingefficiency.Ingeneral,itisrecommended thatultrasonicinsertsbediscardedandreplacedafter oneyearofusetomaintainoptimalefficiencyandavoid

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breakage.ADENTSPLYProfessionalInsertEfficiency Indicatorisenclosedforyouruse.

Ifexcessivewearisnoted,ortheinserthasbeenbent, reshapedorotherwisedamaged,discardtheinsert immediately.

Ultrasonicinserttipsthathavebeenbent,damaged,or reshapedaresusceptibletoin-usebreakageandshould bediscardedandreplacedimmediately.

Retractthelips,cheeksandtonguetopreventcontact withtheinserttipwheneveritisplacedinthepatient’s mouth.

SECTION 5: Infection Control

5.1 general Information

Aswithalldentalprocedures,useuniversalprecautions (i.e.,wearfacemask,eyewear,orfaceshield,gloves andprotectivegown).

Foroperatorandpatientsafety,carefullypracticethe infectioncontrolproceduresdetailedintheInfection ControlInformationBookletaccompanyingyour System.Additionalbookletscanbeobtainedbycalling CustomerServiceat1-800-989-8826,Mondaythrough Friday,8:00A.M.to5:00P.M.(EasternTime).For areasoutsidetheU.S.,contactyourlocalDENTSPLY Professionalrepresentative.

Aswithhighspeedhandpiecesandotherdentaldevices, thecombinationofwaterandultrasonicvibrationfrom theCavitronPlusScalerwillcreateaerosols.Following theproceduralguidelinesinSection8ofthismanualcan effectivelycontrolandminimizeaerosoldispersion.

5.2 water Supply recommendations

Itishighlyrecommendedthatalldentalwatersupply systemsconformtoapplicableCDC(Centers forDiseaseControlandPrevention)andADA (AmericanDentalAssociation)standards,andthatall recommendationsbefollowedintermsofflushing, chemicalflushing,andgeneralinfectioncontrol procedures.SeeSections6.1and9.

Asamedicaldevice,thisproductmusttobeinstalled inaccordancewithapplicablelocal,regional,and nationalregulations,includingguidelinesforwaterquality (e.g.drinkingwater).Asanopenwatersystem,such regulationmayrequirethisdevicetobeconnectedto acentralizedwatercontroldevice.TheCavitron® DualSelect™DispensingSystemmaybeinstalledtoallow thisunittooperateasaclosedwatersystem.

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SECTION 6: Installation Instructions

IftheinstallationofyourCavitronPlusSystemisperformedbysomeoneotherthantrainedDENTSPLYProfessionalDistributorpersonnel,careshouldbetakentoobservethefollowingrequirementsandrecommendations.

6.1 water Line requirements

Awatersupplylinewithuser-replaceablefilteris suppliedwithyoursystem.SeeSection9SystemCare forreplacementinstructions.

Incomingwatersupplylinepressuretothesystemmust be20psi(138kPa)to40psi(275kPa).Ifyourdental watersystem’ssupplylinepressureisabove40psi, installawaterpressureregulatoronthewatersupplyline toyourCavitronPlusUltrasonicScalingSystem.

Amanualshut-offvalveonthedentalwatersystem supplylineshouldbeusedsothatthewatercanbe completelyshut-offwhentheofficeisunoccupied.

Inadditiontothewaterfiltersupplied,itisrecommended thatafilterinthedentalwatersystemsupplylinebe installedsothatanyparticulatesinthewatersupplywill betrappedbeforereachingtheCavitronsystem.

Aftertheaboveinstallationsarecompletedonthedental watersupplysystem,thedentalofficewaterlineshould bethoroughlyflushedpriortoconnectiontotheCavitron system.

6.2 Electrical requirements

Incomingpowertothesystemmustbe100voltsACto 240voltsAC,singlephase50/60Hzcapableof supplying1.0amps.

ThesystempowershouldbesuppliedthroughtheAC powercordprovidedwithyoursystem.

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6.3 unpacking the System

CarefullyunpackyourCavitronPlusSystemandverifythatallcomponentsandaccessoriesareincluded:

1. Cavitron®Plus™Scalerwithhandpiece cableassemblywithswivel 2. DetachableACPowerCord 3. WirelessFootControl 4. “AA”Batteries(4-Pack) 5. AuxiliaryCableforFootControl 6. WaterLineAssembly(Blue)withFilterand QuickDisconnect 7. AdditionalWaterLineFilter 8. Steri-Mate®DetachableSterilizableHandpiece 9. Steri-Mate®GripAccessory(notshown) 10. Cavitron®UltrasonicInserts(quantityoptional) 11. EfficiencyIndicatorforCavitronInserts 12. LiteraturePacket

6.4 System Installation

TheCavitronPlusSystemisdesignedtorestonalevel surface.Besureunitisstableandrestingonfourfeet.

Placingunitindirectsunlightmaydiscolorplastic housing.

Thesystemhasbeenequippedwithawirelessfoot controlwhichwasfactorysynchronizedtooperatewith thesystem’sbaseunit.Ifyourofficecontainsmorethan oneCavitronPlussystem,itisrecommendedthatyou markthefootcontrolandbaseunitforeasyreferenceas towhichfootcontroloperateswithwhichbaseunit. Shouldresynchronizationbenecessary,followthe instructionsinSection6.8.

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6.5 power Cord Connection

VerifytheMainPowerON/OFFswitch,locatedatthe centerfrontundersideoftheSystem,issettotheOFF (O)positionbeforeproceeding.

InserttheACpowercordintothepowerinputonthe backoftheSystem.

InserttheprongedplugintoanACwalloutlet.

6.6 water Supply Line Connection

GrasptheWaterSupplyLine(bluehose)bytheendoppositethequick-disconnectandinsertitintothewaterinletconnectoruntilfullyseated.

ConnectthequickdisconnecttothedentalofficewatersupplyoraCavitronDualSelectDispensingSystem.

Inspectallconnectionstomakecertainthereareno leaks.

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ToremovethewaterlinefromtheCavitronPlusSystem, turnoffthedentalofficewatersupply.Disconnectthe watersupplylinefromthedentalofficewatersupply.If aquick-disconnectconnectorisattachedtotheendof thehose,relievethewaterpressurebypressingthetip oftheconnectorinanappropriatecontainerandallow watertodrain.Toremovethehosefromthesystem, pushontheouterringofthesystem’swaterinletand gentlypulloutthewaterline.

6.7 Foot Control Battery Installation/replacement

TurnfootcontroloverandusingaPhilipsscrewdriver carefullyremovebatterycoverscrewandbatterycover. Ifapplicable,removeusedbatteriesandinstalltwonew “AA”batteriesasshown.Donotdepressfootcontrol whileinstallingbatteries.

Thecommunicationlightwillblinkforapproximatelytwosecondstoindicatethefootcontrol’sabilitytocommunicatewiththeunit.Ifthelightdoesnotblink,checkthebatteries.Ifthebatteriesaregoodandthelightdoesn’tblink,acommunicationserrormayexist.Re-establishcommunicationwithFootControlSynchronizationprocedureSection6.10.

Theremotefrequencycommunicationcanbebypassedusingtheauxillaryfootcontrolcable.RefertoSection10.2TechnicalSupportandRepairforfurtheraction.

ReplacethebatterycoverandscrewandhandtightenwithPhilipsscrewdriver.

Removebatteriesiffootcontrolistobestoredforan extendedperiodoftime.

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6.8 Foot Control Synchronization

Thewirelessfootcontrolsuppliedwithyoursystemhasbeenfactorysynchronizedwiththebaseunit.Shouldareplacementfoot control be necessary, synchronization will be requiredprior to system operation. Perform the following steps tosynchronizethefootcontrolwiththebaseunit.

1. TurntheMainPowerswitchlocatedatthecenter frontundersideofthesystemtotheOFF(O)position. 2. Installanewsetof“AA”batteriesintothefootcontrol (SeeSection6.7)Leavethebatterycoverofthe footcontrolopensotheredpushbuttonis accessible.

3. Maintainadistanceofnomorethan10feetbetween thebaseunitandfootcontrolduringthe synchronizationprocess. 4. TurntheMainPowerswitchtotheON(I)position andwaitfortheDiagnosticDisplaygraphicstolight (refertoSection7.2).

5. Whileallgraphicsarelit,pressthePurgebutton,locatedontheDiagnosticDisplay.Thegraphicswillbegintoblinkinasequentialpattern,representingthesynchronizationmode.Thismodewilllast5to6seconds.

6. Duringthismode,presstheredbuttonlocatedinthe batterycompartmentofthefootcontrol.Thiswill completethesynchronizationprocess. 7. Synchronizationissuccessfulwhenallgraphicsblink atthesametime. 8. Toverifypropercommunication,pressthefoot controltotheBoostposition(footcontrolfully pressed–2ndposition)andensuretheBoostgraphic onbaseunitlights. 9. Replacebatterycoverandthescrew.

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Press ring to releasewater supply tube.

Look for blinkingcommunicationslight.

Main Power ON/OFF SwitchON/OFFSwitchlocatedatthecenterfrontundersideofthesystem.

Ultrasonic Power Level ControlTurnknobtoselecttheultrasonicpowerlevelforoperation.Turningtheknobclockwiseincreasesthedistancetheinserttipmoves(stroke)withoutchangingthefrequency;turningtheknobcounterclockwisedecreasesthedistancetheinserttipmoves(stroke)withoutchangingthefrequency.

The Blue Zoneisalow-powerrangeforeffectivesubgingivaldebridementandimprovedpatientcomfortduringdefinitivetherapy.

RinseTurnultrasonicpowerlevelcontrolknobfullycounterclockwiseuntila“click”isheard.Rinsemodeisforuseduringanultrasonicscalingprocedurewhenlavageisdesiredwithminimalcavitation.

Diagnostic DisplaySeeSection7.2.

Handpiece OperatesallCavitron®30K™Ultrasonicinsertsandtransmitspowerandlavagefromthesystemtoinsert.

Handpiece HolderSecurelyholdsthesystem’shandpiece(withorwithoutinsert)whenthesystemisnotinuse.Alsoholdscableconnectorwhenhandpieceisnotinstalled.

Dual PositionFoot Control SeeSection7.5

SECTION 7: Cavitron plus Scaler description

7.1 System Controls

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7.2 diagnostic display Indicators and Controls

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Power IndicatorLights(3Sec.delay)whentheMainPowerON/OFFSwitchisON(“I”position).

Low Battery IndicatorLightswhenthefootcontrolbatterypowerisapproachingendoflife.ReplacebatteriesasinstructedinSection6.7.

Service IndicatorLightswhenthesystemisnotfunctioningproperly.Thisdiplayhasthreedistinctmodes.

•Afastblink(3blinkspersecond)indicatesan improperset-up.

•Aslowblink(1blinkpersecond)meansthesystemisoperatingoutoffactoryspecifications.

•Asteadylightindicatesthesystemisoverheating.Refer to Section 10.1 for Troubleshooting guidelines.

Boost IndicatorLightswhentheBoostModehasbeenactivated.

Blue Zone IndicatorLightswhenthePowerLevelControlispositionedintheBlueZoneofthepowerscale.

Idealforeffectivesubgingivaldebridementandgreaterpatientcomfort.

Rinse IndicatorLightswhenthePowerLevelControlisturnedfullycounterclockwise.Rinsemodeprovideslavagetoflushtheproceduralareawithnegligibletipmovement.

Purge ControlLightswhenthePurgefunctionisactivated.ToactivatePurge,removeinsertfromthehandpiece,andpressthePurgebutton.Waterwillpurgethroughsystemfor2minutes.Foroptimalefficiency,turnthehandpiecelavagecontroltomaximumwaterflow.Todeactivatemodeduringthe2minutecycle,pressPurgebuttonagainorpressfootcontrol.

ThePurgeControlisalsousedduringtheFootControlSynchronizationprocess.SeeSection6.8.

7.3 handpiece / Cable

7.4 Cavitron 30K ultrasonic InsertsThemanystylesofCavitronandCavitronBellissima30KUltrasonicInsertsareeasilyinterchangeableforvariousproceduresandapplications.Seeenclosedliteratureforspecificinformation.

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Steri-Mate®

Handpiece

O-Ring Provides seal for handpiece coolant. O-ring should be replaced when worn.

Connecting BodyTransfers and amplifies mechanical motion of stack to insert tip.

Magnetostrictive StackConverts energy provided by the handpiece into mechanical oscillations used to activate the insert tip.

Insert MarkingManufacturer, Date (YYMM), Frequency, Type, Tip Lot Number (if applicable)

Finger GripInsert TipShape and size of tip determines access and adaptation. Preheated Lavage directed to tip.

Lavage ControlTurntheLavageControltoselectflowrateduringsystemoperation.Clockwiseincreasesflowatinserttip,counterclockwisedecreasesflow.Theflowratethroughthehandpiecealsodeterminesthetemperatureofthelavage.Lowerflowratesproducewarmerlavage.Higherflowratesproducecoolerlavage.Ifthehandpiecebecomeswarm,increasetheflowrate.Withexperience,theDentalHealthcareProfessionalwillbeabletodeterminethebestflowratesettingforoptimumoperatingefficiencyandpatientcomfort.

Swivel FeatureReducescabledragashandpiecerotatesduringprocedures.

Steri-Mate Grip Accessory (not shown)TheSteri-MateGripprovidesanergonomicandcomfortablegraspofthehandpiece.ThegripissterilizableandisavailableinseveraldifferentcolorsasanaccessoryforyourSteri-MateHandpiece.Seeinstallationinstructionsprovidedwiththegrip.

Pressinganywhereonthetopofthefootcontrolactivatesthesystem.

7.6 Accessories and user replaceable part

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7.6.1 Accessories

1. ACPowerCord 2. DualPositionFootControl(Wireless) 3. AuxiliaryFootControlCable 4. Cavitron30KUltrasonicInserts 5. CavitronDualSelectDispensingsystem 6. CavitronSteri-MateSterilizableHandpiece 7. CavitronSteri-MateGrip(Availableinavariety ofcolors)7.6.2 user replaceable part Kits 1. CavitronInsertReplacementO-ring12/Packs PN:62351(black)forplasticandBellissimainserts PN:62605(green)formetalgripsandprophy 2. Steri-MateHandpieceCableO-ring,PN:79357 3. Lavage(Water)Filter,10/Pack,PN:90158

Fordetailedinformation,contactyourlocalDENTSPLYProfessionalRepresentativeorauthorizedDENTSPLYProfessionalDistributor.

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7.5 wireless Foot Control Information and Operation

Thefootcontrolisatwo-positionedmomentaryswitch.Thefirstpositionactivatesboththeultrasonicenergyandlavageattheinserttip.ThesecondpositionactivatestheBoostMode.TheBoostMode(fullydepressedfootcontrol)increasestheultrasonicpowerlevelforquick,efficientremovaloftenaciousdepositswithouttouchingthesystembase.TodeactivateBoostMode,releasefootcontroltofirstposition.

NON-DEPRESSED DEPRESSED 1st POSITION

DEPRESSED 2nd POSITION

SECTION 8: System Setup, Operation and Techniques for use8.1 handpiece Setup

ConnecttheHandpiecetotheCableAssemblyby aligningtheelectricalconnections.IfCableAssembly doesnotseatintothehandpiece,gentlyrotatethe handpieceuntilcontactsalign,thenfullyinserthandpiece.

Holdemptyhandpieceinanuprightpositionovera sinkordrain.ActivatetheFootControluntilwaterexits tobleedanyairbubblesthatmightbetrappedinsidethe handpiece.

LubricatetheO-ringontheinsertwithwaterbefore placingitintothehandpiece.Fullyseatinsertwitha gentlepush-twistmotion.DONOTFORCE.

TurntheLavageControltoselectflowrateduring systemoperation.Clockwiseincreasesflowatinserttip, counterclockwisedecreasesflow.Theflowratethrough thehandpiecealsodeterminesthetemperatureof thelavage.Lowerflowratesproducewarmer lavage.Higherflowratesproducecoolerlavage.If thehandpiecebecomeswarm,increasetheflowrate. WithexperiencetheDentalHealthcareProfessionalwill beabletodeterminethebestflowratesettingfor optimumoperatingefficiencyandpatientcomfort.

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8.2 patient positioning

Foroptimalaccesstoboththeupperandlowerarches,thebackrestofthechairshouldbeadjustedasforotherdentalprocedures.Thisassurespatientcomfortandclinicianvisibility.

Havethepatientturnhis/herheadtotherightorleft.Alsopositionchinupordowndependinguponthequadrantandsurfacebeingtreated.EvacuateirrigantusingeitherasalivaejectororHighVolumeEvacuator(HVE).

8.3 performing ultrasonic Scaling procedures

Note: Refer to the Infection Control Information booklet supplied with your system and Section 9 of this manual for general procedures to be followed at the beginning of each day and between patients.

TheedgesofCavitronUltrasonicInsertsareintentionally roundedsothereisminimaldangeroftissuelaceration withproperultrasonicscalingtechnique.Wheneverthe inserttipisplacedinthepatient’smouth,thelips, cheekandtongueshouldberetractedtoprevent accidental(prolonged)contactwiththeactivatedtip.

TurnPowerLevelControltoselectultrasonicpowerlevel foroperation.Clockwiseincreasessystempower. Powerlevelwillincreasethroughoutthefullrangeofthe control.Holdthehandpieceoverasinkordrain. Pressthefootcontroltoactivatethesystem.Check spraytoverifyfluidisreachingtheworkingendofthe inserttip.AdjusttheLavageControltoensureadequate flowfortheselectedpowersetting.Greaterflowsettings providecoolerirrigation.

Itmaybenecessarytoadjustlavagewiththesystemin“Boost”mode(FootControlfullydepressed)soadequatefluidwillbeavailabletocooltiptotoothinterface.

Ingeneral,itissuggestedthata“feather-light-touch”be usedforultrasonicscaling.Themotionoftheactivated tipandacousticeffectsoftheirrigatingfluid,inmost cases,areadequatetoremoveeventhemosttenacious calculus.

PeriodicallychecktheCavitronUltrasonicInsertforwear withtheCavitronInsertEfficiencyIndicator.

TheuseofasalivaejectororHighVolumeEvacuator (HVE)isrecommendedduringallprocedures.

Setthesystem’sPowerLevelControltothelowest efficientpowersettingfortheapplicationandthe selectedinsert.

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8.4 patient Comfort Considerations

Reasons for sensitivity

Incorrecttipplacement.Thepointshouldneverbe directedtowardtoothrootsurfaces.

Notkeepingtipinmotionontooth.Donotallowthe inserttoremaininastaticpositiononanyoneareaof thetooth.Changetheinsert’spathofmotion.

Applyingexcessivepressure.Useaverylightgrasp andpressure,withasofttissuefulcrumwhenever possible,especiallyonexposedcementum.

Ifsensitivitypersists,decreasepowersettingand/or movefromthesensitivetoothtoanotherandthenreturn.

SECTION 9: System CareItisrecommendedthatyouperformthefollowingmaintenanceprocedures to help maximize water quality and to be incompliancewithCDCguidelinesforinfectioncontrol.

9.1 daily maintenance

START-UP .PROCEDURES .AT .THE .BEGInnInG .OF .THE .DAy:

1. Openthemanualshut-offvalveonthedentaloffice watersupplysystem. 2. InstallasterilizedSteri-Matehandpieceonthe handpiececable. 3. TurnMainPowerSwitchtotheON(I)position.Verify theON/OFFindicatorlightislit. 4. SetthePowerLevelControltotheminimumsetting (notrinse). 5. SettheLavageControlonthehandpiececableto maximum. 6. HoldtheHandpiece(withoutaninsertinstalled) uprightoverasinkordrain.ActivatethePurge Controlbutton. • ThePurgebuttonwilllightfortwominutes indicatingactivationofthepurgefunction. • IfthePurgebuttonisactivatedwithaninsert presentinthehandpiece,thebuttonwillblinkfor 3secondsanddisable.Removetheinsertfrom thehandpieceandpressthePurgebuttonagain. • ThePurgefunctioncanbeinterruptedatanytime bypressingthePurgebuttonagainorby pressingthefootcontrol. 7. Aftercompletingthepurgecycle,placeasterilized insertintotheHandpieceandsettheUltrasonic PowerLevelControlandLavageControltoyour preferredoperatingposition.

•

•

•

•

BETWEEn .PATIEnTS:

1. Removeultrasonicinsertused.Cleanandsterilize theultrasonicinsert(s)followingtheprocedures outlinedintheCavitronUltrasonicInsertInfection ControlDirectionforUseenclosedwitheveryinsert. 2. Holdthehandpieceoverasinkordrainandactivate PurgefunctionasdescribedinStep6ofStart-Up Procedures.

3. Afterthepurgecycleiscomplete,turnthesystemOFF,(O)position.

4. RemovetheSteri-Matehandpiece.Cleanandsterilizethehandpiecefollowingtheprocedureoutlinedinthebookletenclosedwithyourunit.

5. Disinfectthesurfacesofthecabinet,PowerCord,HandpieceCable,WaterSupplyLine,FootControlandAuxillaryCable(ifapplicable)byapplyinganapprovednon-immersiontypedisinfectantsolution*carefullyfollowingtheinstructionsprovidedbythedisinfectantsolutionmanufacturer.TocleanSystem,generouslyspraydisinfectantsolutiononacleantowelandwipeallsurfaces.Discardusedtowel.Drywithacleancloth.Todisinfectsystem,generouslyspraydisinfectantonacleantowelandwipeallsurfaces.Allowdisinfectantsolutiontoairdry.Neverspraydisinfectantsolutiondirectlyonthesystem.

6. Inspectthehandpiececableforanybreaksortears. 7. IfusingaclosedwatersupplyorDualSelect Dispensingsystem,checkforadequatefluidvolume forthenextpatient.

8. Whenreadyforuse,placeasterilizedSteri-Matehandpieceonthehandpiececableandasterilizedinsertintothehandpieceandadjustsystemcontrolstopreferredoperatorpositions.

SHUT-DOWn .PROCEDURES .AT . .THE .EnD .OF .THE .DAy:Followthe“BetweenPatients”maintenanceprocedures,Steps1through6.Inaddition,itisrecommendedtoclosethemanualshut-offvalveonthedentalwatersupplysystem.

*NOTE: Water-based disinfection solutions are preferred. Some alcohol-based disinfectant solutions may be harmful and may discolor plastic materials.

9.2 weekly maintenance

Itisstronglyrecommendedthatthissystembedisinfectedbychemicallyflushingthewaterlineswitha1:10SodiumHypochloritesolution(NaOC1)attheendofeachweek.ThiscanbeaccomplishedbyconnectingthisdevicetotheCavitronDualSelectDispensingSystemoranumberofotherdevicesavailablefromyourlocaldistributors.WherethisdeviceisconnectedtotheCavitronDualSelectDispensingSystem,pleasefollowtheDualSelectsystem’sDirectionsfor

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Usemanual.Ifconnectedtoanotherdevice,pleasefollowthosedirectionsforuse,keepinginmindthatachemicalflushshouldbeperformedatmaximumwaterflowforatleast30seconds.Thesystemshouldbeleftundisturbedfor10minutesbutnomorethan30minutestoallowthesodiumhypochloritesolutiontosoakinthelines.Asasuggestion,itisrecommendedthatasignbeplacedonthesystemstatingthattheSYSTEMISBEINGDISINFECTEDWITHASTRONGDISINFECTANTANDSHOULDNOTBEUSED.Whenready,flushsystemwithcleanwaterforatleast30secondsoruntilsodiumhypochloriteodordisappears.ALLCHEMICALSMUSTBEFLUSHEDFROMTHESYSTEMBEFOREITISREADYFORPATIENTUSE.

9.3 water Line Filter maintenance

Whenthewaterlinefilterbecomesdiscolored,thefiltershouldbereplacedtopreventreducedwaterflowtotheCavitronPlusUltrasonicScaler.A10-packofreplacementfiltersisavailablebyorderingPartNumber90158fromyourlocalauthorizedDENTSPLYDistributor.

1. VerifysystemisturnedOFF. 2. Disconnectthewatersupplyhosefromthewater source.Ifaquick-disconnectconnectorisattached totheendofthehose,relievethewaterpressureby pressingthetipoftheconnectorinanappropriate containertodrainthewater. 3. Graspthefittingoneithersideofthefilterdiskand twistcounterclockwise.Removethefiltersection fromeithersideofthewaterhose. 4. Installthereplacementfilterontothewaterhose fittings.Thefiltershouldbepositionedtomatchup withthecorrecthosefitting. 5. Handtightenthetwohosefittingsinaclockwise direction.Reconnectthewatersupplyhose,operate theunittobleedtheairandtestforleaks.

SECTION 10: TroubleshootingAlthoughserviceandrepairoftheCavitronPlusUltrasonicScalershouldbeperformedbyDENTSPLYpersonnel,thefollowingaresomebasictroubleshootingproceduresthatwillhelpavoidunnecessaryservicecalls.Generally,checkalllinesandconnectionstoandfromtheSystem,alooseplugorconnectionwilloftencreateproblems.CheckthesettingsontheSystem’scontrols.

10.1 Troubleshooting guide

Symptom: System will not operate: No Power ON indicator

1. CheckthattheMainPowerSwitchisintheON(l) position,andthatthedetachablePowerCordisfully seatedinthereceptacleonbackofSystem.

2. Checkthatthesystem’spowercordplugisfullyseated inanapprovedACwalloutlet. 3. Checkthatthewalloutletisfunctional.

Symptom:System will not operate: Power ON Indicator is illuminated

1. Iftheofficehasmorethanonefootcontrol,testeachtoensurethattheproperfootcontrolisbeingused.Withahandpieceandinsertinstalled,depressthefootcontroltothefirstposition.Thesystemshoulddispensewater.Ifnoneofthefootcontrolsoperatethesystem,continuetothenextstep.

2. Resynchronizeonefootcontroltothesystem(seeSection6.8FootControlSynchronization).

Symptom:System operates: No water flow to insert tip

1. Assurethathandpiecelavagecontrolisproperly adjusted. 2. Checkforcloggedinsert. 3. Checkthatdentalofficewatersupplyvalvesareopen. 4. IfthesystemisconnectedtoDualSelectDispensing System,checkthatfluidlevelintheselectedbottleis sufficient.Makesurevalvesareopenwhenusing externalwatersource. 5. Checkthatthewaterlinefilterisclean.Replacefilter ifneeded.

Symptom: System operates: No insert cavitation

1. CheckthatthePowerLevelControlisnotinRinseMode.

2. Checktheinsertfordamageandthatitisproperly installedinthehandpiece. 3. Checkthatthehandpieceisproperlyinstalledtothe cableassembly. 4. IfSteri-Mategripisusedonthehandpiece,verifythat thegripisflushwiththehardplasticoftheinsertport. 5. Turnthesystem’sMainPowerSwitchtotheOFF(0) position.Wait5secondsandturnthesystembackON. 6. Ifproblemstillexists,replaceboth“AA”batteriesin footcontrolwithnew“AA”batteries(RefertoSection 6.7)orconnectauxiliaryfootcontrolcable.

Symptom:System operates: Purge Mode will not function – icon flashing

1. Checkthatthereisnoinsertinthehandpiece. 2. Checkthathandpieceisproperlyinstalledtothecable assembly.

Symptom:System operates: Service Indicator blinking

• Slow Blinking (1 blink per second) Thesystemisnotoperatingwithinfactory specifications. 1.Removeinsert. 2.TurnMainPowerSwitchOFF,(O)position.Waitfive seconds.TurnunitON,(I)position. 3.OperatePurgefunction. 4.Ifserviceindicatorstillblinks,refertoSection10.2 TechnicalSupportandRepairstohaveunit servicedassoonaspossible. • Fast Blinking (3 blinks per second) –Indicatesimproperset-up 1. Ifinsertisinthehandpiece,remove.Verifythe handpieceisproperlyseatedanddepressthefoot controlfor2seconds.Ifblinkingstops,thesystem isreadyforuse.Ifblinkingremains,continuetothe nextstep. 2.AttachaNEWhandpieceanddepressfootcontrol for2seconds.Ifblinkingstops,thesystemis readyforuse.Discardtheoldhandpieceorreturnif withinwarranty.Ifblinkingremains,continuetothe nextstep. 3.Installandfullyseataninsertintohandpiece. Depressfootcontrolfor2seconds.Ifblinking stops,unitisreadyforuse.Ifblinkingremains, continuetothenextstep.

4.InstallandfullyseataNEWinsertinhandpieceanddepressfootcontrolfor2seconds.Ifblinkingstops,systemisreadyforuse.Discardoldinsertorreturnifwithinwarranty.Ifblinkingremains,refertoSection10.2TechnicalSupportandRepairstohaveunitservicedassoonaspossible.

Symptom:System operates: Service Indicator illuminated

1. Ensurethatthebaseunithasadequateventilationand isnotnearaheatsource(i.e.radiator,heatlamp, sunlightorotherheatproducingoperatoryequipment). 2. TurnMainPowerSwitchtotheOFF(O)position.Allow systemtocoolfor10minutesandturnsystemON,(I) position.Verifylightisnotilluminated. 3. Iflightisstillilluminated,refertoSection10.2 TechnicalSupportandRepairstohaveunitservicedas soonaspossible.

10.2 Technical Support and repairs

FortechnicalsupportandrepairassistancecallDENTSPLYProfessionalCavitronCareSMFactoryCertifiedServiceat1-800-989-8826MondaythroughFriday,8:00A.M.to5:00P.M.(EasternTime).ForareasoutsidetheU.S.,contactyourlocalDENTSPLYProfessionalrepresentative.

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SECTION 11: warranty periodTheCavitronPlusUltrasonicScaleriswarrantedforTWOYEARSfromdateofpurchase.TheSteri-MateHandpieceenclosedwithyoursystemiswarrantedforSIXMONTHSfromdateofpurchase.RefertotheWarrantyStatementSheetfurnishedwithyoursystemforfullWarrantyStatementandTerms.

SECTION 12: SpecificationsElectricalVoltage Continuous(100-240VAC)

Current 1.0Amperes,Maximum

Phase Single

Frequency 50/60Hertz

WaterPressure 20to40psig(138to275kPa)

WaterFlowRate MinimumSetting(CCW)<15ml/min MaximumSetting(CW)>55ml/min

Weight 3.3lbs(1.5Kg)

Dimensions Height:5in(12,7cm) Width:9.5in(24,13cm) Depth:8in(20,32cm) HandpieceCablelength:6.5ft.(2.0M) AuxillaryFootControlCablelength:8ft.(2.4M) WaterSupplyLinelength:8ft.(2.4M)

FootControl ProtectionClassIPX1.Notforoperatingtheatres.

RemoteCommunication Frequency: 2405to2480MHz Power: <1mW Channels: 16

OperatingEnvironment Temperature:15to40Deg.Celsius(59to104Deg.Fahrenheit) RelativeHumidity:30%to75%(non-condensing)

TransportandStorageConditions Temperature:-40to70Deg.Celsius(-40to158Deg.Fahrenheit) RelativeHumidity:10%to100%(non-condensing) AtmosphericPressure:500to1060hPa

SECTION 13: Classifications

•Typeofprotectionagainstelectricshock: Class1•Degreeofprotectionagainstelectricshock: TypeB•Degreeofprotectionagainsttheharmfulingressofwater: Ordinary•Modeofoperation: Continuous•Degreeofsafetyofapplicationinthepresenceofaflammableanaestheticmixturewithairorwithoxygenornitrousoxide: Equipmentnotsuitableforuseinthepresenceof flammableanaestheticoroxygen.IIA(rule9) (ISO/IEC60601)

SECTION 14: disposal of unit•Accordancewithlocalandstatelaws.

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Rinse Boost

Low Batt.Service

On/Off

PURGE

BlueZone

CAvITrON pLuS uLTrASONIC SCALEr QuICK rEFErENCE guIdE

diagnostic displayON/OFFIlluminateswhentheMainPowerOn/Offswitchisinthe“ON”position.

BLuE ZONEIlluminateswhentheultrasonicpowercontrolispositionedintheBlueZoneofthepowerscale.TheBlueZoneextendedlow-powerrangeiseffectiveforsubgingivaldebridementandgreaterpatientcomfortduringdefinitivetherapy.

rINSEIlluminateswhentheultrasonicpowerlevelcontrolisturnedfullycounterclockwise.Withaninsertinthehandpiece,activatetheFootControlandlavagewilloccurwithnegligibletipmovement.

BOOSTIlluminateswhentheBoostModeisactivatedbytheFootControl.Toactivate,fullydepressFootControltothesecondposition.TodeactivateBoostMode,releaseFootControltofirstposition.

purgE BuTTONIlluminateswhenthePurgefunctionisactivated.ToactivatePurge,removeinsertfromthehandpiece,pressthePurgebuttonontheDiagnosticDisplayandwaterwillpurgethroughsystemlinesfortwominutes.Foroptimalefficiency,turntheHandpieceLavageControltomaximumwaterflow.Todeactivateduringthetwominutecycle,pressPurgebuttonagainorpressFootControl.

SErvICELightswhenthesystemisnotfunctioningproperly.Thisdisplayhasthreedistinctmodes:

Slowblink(1blinkpersecond)meansthesystemisnotoperatingwithinfactoryspecifications.Fastblink(3blinkspersecond)indicatesanimproperset-up.Steadylightindicatesthesystemisoverheating.

RefertoTroubleshootingguidelinesonreverseside.

LOw BATTErYIlluminateswhentheFootControlbatterypowerisapproachingendoflife.ReplacebatteriesasinstructedintheDirectionsforUse.

Power ControlpOwEr LEvEL CONTrOL Turnknobtoselectultrasonicpowerlevelforoperation.Turningtheknobclockwiseincreasesthedistancetheinserttipmoves(stroke)withoutchangingthefrequency;turningtheknobcounterclockwisedecreasesthedistancetheinserttipmoves(stroke)withoutchangingthefrequency.

rINSERinsemodeisusedduringanultrasonicscalingprocedurewhenlavageisrequiredtoflushtheproceduralarea.Toactivate,turnPowerLevelControlfullycounterclockwiseuntila“click”isheard.

BLuE ZONEProvidesanextendedlow-powerrangeforeffectivesubgingivaldebridementandgreaterpatientcomfortduringdefinitivetherapy.

•••

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RINSE

RINSE POWER

ACTION TAKEN1. CheckthattheMainPowerSwitchisintheON(I)position,andthatthedetachablepowercord isfullyseatedinthereceptacleonbackofsystem.2. Checkthatthesystem’spowercordplugisfullyseatedinanappropriateACwalloutlet.3. Checkthatthewalloutletisfunctional.

1. Iftheofficehasmorethanonefootcontrol,testeachtoensurethattheproperfootcontrolisbeingused.Withahandpieceandinsertinstalled,depressthefootcontroltothefirstposition.Thesystemshoulddispensewater.Ifnoneofthefootcontrolsoperatethesystem,continuetothenextstep.

2. Resynchronizeonefootcontroltothesystem(seeDirectionsforUseSection6.8FootControlSynchronization).

1. Assurethathandpiecelavagecontrolisproperlyadjusted.2. Checkforcloggedinsert;Replaceinsertifnecessary.3. Checkthatdentalofficewatersupplyvalvesareopen.4. IfthesystemisconnectedtoDualSelectDispensingSystem,checkthatfluidlevelintheselected bottleissufficient.Makesurevalvesareopenwhenusingexternalwatersource.5. Checkthatthewaterlinefilterisclean;Replacefilter,ifneeded.

1. CheckthatthePowerLevelControlisnotinRinseMode.2. ChecktheinsertfordamageandthatitisproperlyinstalledintheHandpiece.3. Checkthatthehandpieceisproperlyinstalledtothecableassembly.4. Verifythatthehandpiece’ssoftgripisflushwiththehardplasticoftheinsertport.(Skipthisstep ifnotusingSoftGripAccessory)5. Turnthesystem’sMainPowerSwitchOFF,(O)position.Wait5secondsandturnthesystembackON.6. Ifproblemstillexists,replaceboth“AA”batteriesinfootcontrolwithnew“AA”batteries,or connectAuxiliaryFootControlCable.

1. Slowblinking(1blinkpersecond)-Thesystemisnotoperatingwithinfactoryspecifications. A. Removeinsert. B. TurnMainPowerSwitchOFF,(O)position.Waitfiveseconds.TurnswitchON,(I)position. C. OperatePurgefunction. D. Ifserviceindicatorstillblinks,refertoTechnicalSupportandRepairstohaveunitserviced assoonaspossible.2. Fastblinking(3blinkspersecond)–Indicatesimproperset-up A. Ifinsertisinthehandpiece,remove.Verifythehandpieceisproperlyseatedanddepress thefootcontrolfor2seconds.Ifblinkingstops,thesystemisreadyforuse.Ifblinking remains,continuetothenextstep. B. AttachaNEWhandpieceanddepressfootcontrolfor2seconds.Ifblinkingstops,the systemisreadyforuse.Discardtheoldhandpieceorreturnifwithinwarranty.Ifblinking remains,continuetothenextstep. C. Installandfullyseataninsertintohandpiece.Depressfootcontrolfor2seconds.If blinkingstops,unitisreadyforoperation.Ifblinkingremains,continuetothenextstep. D. IInstallandfullyseataNEWinsertinhandpieceanddepressfootcontrolfor2seconds.If blinkingstops,systemisreadyforuse.Discardoldinsertorreturnifwithinwarranty. Ifblinkingremains,refertoTechnicalSupport

1. Ensurethatthebaseunithasadequateventilationandisnotnearaheatsource(i.e.radiator, heatlamp,sunlightorotherheatproducingoperatoryequipment).2. TurnMainPowerSwitchOFF,(O)position.Allowsystemtocoolfor10minutesandturnsystem ON,(I)position.Verifylightisnotilluminated.3. Iflightisstillilluminated,refertoTechnicalSupportandRepairstohaveunitservicedassoonas possible

1. Checkthatthereisnoinsertinthehandpiece.2. Checkthathandpieceisproperlyinstalledtothecableassembly.

QuICK rEFErENCE guIdE TrOuBLEShOOTINgSYmpTOm

System will not operate:

No Power ON Indicator

System will not operate:

Power ON Indicator is illuminated

System operates: No water flow to

insert tip

System operates: No insert cavitation

Serviceindicatorblinking

System operates: Service indicator

illuminated

System operates: Purge mode will

not function --icon flashing