Anthos A7 Plus User manual
A7 Plus
SMART TOUCH
EN
97050644
Rev.006
2017.03
33EN
A7 Plus
- OPERATING INSTRUCTION
TABLE OF CONTENTS
1. Safety guidelines ........................................................... 4
1.1. Symboldenition ............................................................. 4
1.2. Intendeduse.................................................................... 4
1.2.1. Classicationandreferencestandards ........................... 4
1.2.2. Environmentalconditions ................................................ 5
1.2.2.1. Transportandpackagingconditions................................ 5
1.2.3. Warranty .......................................................................... 5
1.2.4. Disposingtheequipmentwhennolongerused............... 5
1.3. Safetyrules...................................................................... 6
1.4. Cleaninganddisinfecting ................................................ 7
2. Description of the equipment....................................... 8
2.1. Nameplate ....................................................................... 8
2.2. Dentalunits...................................................................... 8
2.3. Dentalchair ..................................................................... 9
3. Turning on the dental operatory................................... 9
4. Dental chair operation .................................................. 10
4.1. Safetydevices ............................................................... 10
4.2. Emergencydevices ....................................................... 10
4.3. Adjustableheadrest........................................................11
4.4. Adjustablearmrest(optional)..........................................11
5. Instrument board operation........................................ 12
5.1. Doctor’scontrolconsole ................................................ 14
5.1.1. Userinterface ................................................................ 16
5.1.1.1. Operatorselection ......................................................... 17
5.1.1.2. Generalsettings ............................................................ 17
5.1.1.2.1. Hygienesystemsettings............................................... 18
5.1.1.2.1.1.BIOSTERdisinfectioncyclesetting .............................. 18
5.1.1.2.1.2.FlushingCYCLESETTING........................................... 19
5.1.1.2.1.3.W.H.E.systemtankemptying ...................................... 19
5.1.1.2.2. Hydrounitsettings......................................................... 20
5.1.1.2.2.1.Bowlwaterdeliverysetting ........................................... 20
5.1.1.2.2.2.Cupwaterdeliverysetting............................................. 21
5.1.1.2.2.3.Automaticbowlmovementsetting ................................ 21
5.1.1.2.3. Footcontroladjustment................................................ 22
5.1.1.2.4. Operatinglampadjustment .......................................... 22
5.1.1.2.5. OtherSettings................................................................ 23
5.1.1.2.6. Timeanddatesetting ................................................... 23
5.1.1.2.7. Chronometer................................................................. 24
5.1.1.2.8. Personalizationoffavouritekeys................................... 24
5.1.1.2.9. Operatordataentry ...................................................... 25
5.1.1.2.10.LANGUAGEselection ................................................... 25
5.1.1.2.11.APEXLOCATORsetting ............................................... 25
5.1.3. ProgrammingthechairpositionsA,B,CandD ........... 26
5.1.4. Emergencystopbutton.................................................. 26
5.1.5. SMARTTOUCHscreendisablebutton. ........................ 26
5.2. Footcontrol.................................................................... 27
5.2.1. "Multifunction”footcontrol ............................................. 27
5.2.2. "Push-pedal”footcontrol ............................................... 28
5.2.3. "PowerPedal"footcontrol............................................. 30
5.2.4. Wirelessfootcontrol...................................................... 32
5.3. Syringe .......................................................................... 34
5.4. Turbine .......................................................................... 35
5.5. Micromotor..................................................................... 37
5.5.1. RESTORATIVEoperatingmode ................................... 40
5.5.2. ENDODONTICoperatingmode .................................... 40
5.5.3. IMPLANToperatingmode............................................. 42
5.5.4. Reductionratiosettingmenu......................................... 43
5.5.5. RECIPROCATINGoperatingmode............................... 44
5.6. Scaler ............................................................................ 45
5.7. TLEDcuringlight.......................................................... 48
5.8 C-U2dentalcamera ...................................................... 51
5.9. ZEN-Xiintegratedsensor ............................................. 55
5.10. Peristalticpump............................................................. 56
5.11. ElectronicAPEXLOCATOR ......................................... 57
6. Assistant’s board operation ....................................... 59
6.1. Assistant’stouchpad...................................................... 59
6.2. Syringeonassistant’sboard ......................................... 60
6.3. Curinglamponassistant’sboard .................................. 60
6.4. Intraoralcameraonassistant’sboard ........................... 60
6.5. Suctiontubes................................................................. 61
6.6. Instrumenttray............................................................... 62
6.7. Hydraulicsalivaejector................................................. 62
7. Hydrogroup operation................................................. 63
7.1. Fillcupandbowl............................................................ 63
7.2 S.H.S.system................................................................ 65
7.3. W.H.E.(WaterHygienizationEquipment)system ........ 66
7.4. BIOSTERautomaticdisinfectionsystem....................... 67
7.5. AutomaticinstrumentFLUSHINGCYCLE(FLUSHING) 69
7.6. ACVSsystem(AutomaticCleaningVacuumSystem)... 70
7.7. Opening/closingthesidehydrogroupcover .................. 71
8. Accessories ................................................................. 72
8.1. Operatinglamp............................................................. 72
8.2. Monitoronlamppole..................................................... 72
8.3. Negatoscopeforpanoramas ......................................... 72
8.4. Air/water/230Vquick-connectcouplers ......................... 72
9. Maintenance ................................................................ 73
9.1. Instrumentmaintenance................................................ 73
9.2. Drainingcondensate...................................................... 73
9.3. Cleaningthesurgicalsuctionlter................................. 73
9.4. Surgicalsuction ............................................................. 74
9.5. CATTANIsurgicalseparator .......................................... 75
9.6 Cleaningtheturbinereturnairlter ............................... 76
9.7. CATTANI amalgamgravityseparator .......................... 76
9.8. METASYSamalgamseparator...................................... 76
9.9. DÜRRamalgamseparator ............................................ 76
9.10. Dentalchair ................................................................... 76
10. Fault messages............................................................ 77
11. Specications .............................................................. 78
11.1. Overalldimensions:A7PlusCONTINENTAL............... 79
11.2. Overalldimensions:A7PlusINTERNATIONAL ........... 80
12. Dental operatory maintenance plan....................................... 81
4
4
EN
A7 Plus
- OPERATING INSTRUCTION
1. Safety guidelines
• These instructions explain how to correctly use the following dental units:
A7 Plus CONTINENTAL, A7 Plus INTERNATIONAL
Carefully read and become familiar with the content of this manual before using the equipment.
•ThedentalunitsdescribedinthismanualaremanufacturedbyCEFLAs.c.-viaSeliceProv.le23/A-40026Imola(BO)Italy,amanufacturer
complyingwiththeEuropeanDirectiveondevices.
• Theseinstructionsdescribealltheversionsoftheoperatingunitswiththemaximumpossibleaccessories,thereforenotalltheparagraphsare
applicabletotheunityouhavepurchased.
•Nopartofthismanualistobereproduced,storedinaretrievalsystemortransmittedinanyformorbyanymeans,i.e.electronic,mechanical,
photocopying,translationorotherwise,withoutthepriorwrittenpermissionofCEFLAs.c.
•Theinformation,specicationsandillustrationscontainedinthispublicationarenotbinding.
CEFLAs.c.reservestherighttomaketechnicalimprovementsandchangeswithoutmodifyingtheinstructionscontainedherein.
•Themanufacturerhasacompanypolicyofcontinualdevelopment.Althougheveryeortismadetokeeptechnicaldocumentationup-to-dateatall
timesthemanualmaynotcorrespondexactlytocurrentspecications.Themanufacturerreservestherighttomakechangeswithoutpriornotice.
•TheoriginalversionofthismanualiswritteninItalian.
•Thisequipmentisequippedwithadevicethatpreventsliquidbackup
•Themanufacturer’swebsitecontainsalistofauthorisedagentsofthevariouscountries.
Listofsymbolsusedinthisdocumenttodenotecertainconditions:
1) Typeofprotectionagainstdirectandindirectcontact:ClassI.
Typeofprotectionagainstdirectandindirectcontact:TypeB.
2) WARNING!
Failuretoobservemayresultinequipmentdamageorinjurytothe
userand/orpatient.
3) "Consulttheinstructionmanual".
Meansthatit is advisable to consult the instruction manual before
usingthatpartofthedevice.
4) NOTE:
Identiesinformationthatisespeciallyimportantfortheuserand/or
assistant.
5) Earthground.Functionalearthconnection.
6) Alternatingcurrent.
7) Partsterilisedinasteamautoclaveupto135°C.
8) ON/OFFbutton.
9) "Refertotheinstructionmanual".
Meansthatforreasonsofsafetyyouneedtoconsulttheinstruction
manualbeforeusingthedevice.
10) Open(apartoftheunit).
11) Closed(apartoftheunit).
12) EquipmentinaccordancewithessentialrequirementsofdirectiveEEC
93/42andsubsequentchanges(ClassIIaequipment).
Notiedbody:IMQspa.
13) Equipment in accordance with essential requirements of directive
EEC93/42andsubsequentchanges(ClassImedicalequipmentfor
ordinaryuse).
14)WastedisposalsymbolinaccordancewithDirective2012/19/EU.
15) “Warningbiologicalhazard”.
Itprovidesinformationaboutpossiblerisksofcontaminationderiving
fromcontactwithuids,storageofinfectedbiologicalwaste.
16) Manufacturer.
17) Monthandyearofconstructions.
18) Apparatusserialnumber.
19) DVGWmark(qualityassurancekitemarkregardingsupplyofdrinking
water).
20) Product/equipmentidenticationcode.
21)Donotpush.
22)Footcrushinghazard.
23)DeviceequivalenttoClass2lightsource.
24) Ukrainiannationalsymbolofconformity.
1.2. Intended use
•TheA7PLUSseriesofoperatoriesaremedicaldevicesintendedfordentaltreatment.
•Theinstrumentboardmayholdupto6instruments.
•Theassistant’sboardcanhold2suctiontubesand3instruments.
•Thisequipmentmustbeusedonlybyadequatelytrainedpersonnel(doctorsandparamedics).
•Thedeviceisintendedfornon-continuous operation(seetheoperatingtimesoftheindividualpartsinthededicatedsections).
•Thedeviceisclassiedaspollutiondegree2.
•Overvoltageclass:II.
• MEDICALDEVICESclassication
ClassicationofthedentalunitinaccordancewiththeindicationsgiveninannexIXofdirective93/42/EECandsubsequentchanges:Class IIa.
• ELECTRICALMEDICALEQUIPMENTclassication
ClassicationofthedentalunitinaccordancewithstandardI.E.C.60601-1forsafetyofmedicalequipment:Class I - Type B.
• Referencestandards
A7PLUSseriesoperatoryunitsaredesignedandconstructedincompliancewithIEC60601-13.aEd.-2007,IEC60601-1-63.aEd.-2010,IEC
623661.aEd.-2007,IEC80601-2-601.aEd.-2012,IEC60601-1-23.aEd.,ISO68753.aEd.-2011,ISO7494-12.aEd.-2011andEN1717(typeAA
andAB)standardsasfarasthewatermainssafetydevicesareconcerned.
• ClassicationofRADIODEVICESANDCOMMUNICATIONTERMINALS(onlywhentheWIRELESSfootcontrolispresent)
EquipmentclassicationaccordingtoDirective99/05/ECArt.12:Class I.
55
EN
A7 Plus
- OPERATING INSTRUCTION
1.2.2. Environmental conditions
Theequipmentistobeinstalledinroomsthatsatisfythefollowingrequirements:
•temperaturebetween10and40°C.
•relativehumiditybetween30and75%.
•atmosphericpressurerangingfrom700to1060hPa.
•altitude≤3000m;
•airpressureenteringequipmentrangingfrom6to8bar.
•waterhardnessenteringequipmentnotover60mg/l.
•waterhardnessattheequipmentinletmustnotbeabove25°f(Frenchdegrees)or14°d(Germandegrees)foruntreateddrinkingwater.Forwater
withahigherhardnessdegree,itisrecommendedtosoftenwateruntilitreachesahardnessdegreebetween15and25°f(Frenchdegrees)or
between8.4and14°d(Germandegreees);
•waterpressureenteringequipmentrangingfrom3to5bar.
•watertemperatureenteringequipmentnothigherthan25°C.
1.2.2.1. Transport and packaging conditions
•Temperature:from-10to70°C;
•Relativehumidity:from10%to90%;
•Atmosphericpressure:from500to1060hPa.
1.2.3. Warranty
CEFLAs.c.standsbehinditsproductswarrantingsafety,reliabilityandperformance.
Thewarrantyisvalidonlyunderthefollowingterms:
•Theconditionsgivenonthewarrantycerticateareobserved.
•Theequipmentisusedonlyasinstructedinthismanual.
•TheelectricalwiringintheroominwhichtheequipmentisinstalledmustconformtoIEC60364-7-710(standardsforelectricalwiringinmedical
anddentaloces).
•A3x1.5mm2lineprotectedbyabi-polarcut-outthatconformstoapplicablestandards(10A,250V,distancebetweencontactsatleast3mm)must
beusedtofeedtheequipment.
WARNING!
The color of the three wires (POWER, NEUTRAL and EARTH) should satisfy the requirements of current standards.
•Installation,repairsand,ingeneral,anyotheroperationsrequiringthecasingtobeopenedaretobeperformedexclusivelybypersonnelauthorized
by ANTHOS.
1.2.4. Disposing the equipment when no longer used
AssetoutinDirectives2011/65/ECand2012/19/EC,ontherestrictionsoftheuseofcertainhazardoussubstancesinelectricalandelectronic
equipmentalongwithcollection,treatment,recyclinganddisposalofwasteelectricalandelectronicequipmentthelattermustbetreatedasmunici-
palwaste,thereforesortedandcollectedseparately.Whennewequipmentofequivalenttypeispurchasedthewasteequipmentshouldbereturned
tothedistributoronaone-to-onebasisfordisposal.Asfarasreuse,recyclingandotherformsofwasterecoverymentionedaboveareconcerned,
themanufacturerisresponsiblefortheactionsspeciedbyindividuallocallaws.Ecientcollectionofsortedwasteseparatelytorecycleandtreat
wasteelectricalandelectronicequipmentaidsinpreventingnegativeenvironmentalimpactswhileprotectinghumanhealth.Inadditionitfacilitates
recyclingofthematerialsusedtoconstructtheequipment.Illegalwastedisposalcarriesheavynesdenedbylocallaws.
WARNING!
The crossed out wheeled bin placed on the equipment indicates that the waste equipment must be collected separately from other waste.
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