Hitachi EUP-V73W User manual

0123
TransvaginalProbe
EUP‐V73W
INSTRUCTIONMANUAL
Notesforoperatorsandresponsiblemaintenancepersonnel
★PleasereadthroughthisInstructionManualcarefullypriortouse.
★KeepthisInstructionManualtogetherwiththesystemwithcareto
makeitavailableanytime.
Tokyo,Japan
Q1E‐EP1430‐5
©Hitachi,Ltd.2013,2017.Allrightsreserved.

(1)Q1E‐EP1430
Manufacturer:
Hitachi,Ltd.
2‐16‐1,Higashi‐Ueno,Taito‐ku,Tokyo,110‐0015,Japan
+81‐3‐6284‐3668
http://www.hitachi.com/businesses/healthcare/index.html
European
Representative:
HitachiMedicalSystemsGmbH
Otto‐von‐Guericke‐Ring3D‐65205Wiesbaden,Germany
EUImporter:HitachiMedicalSystemsEuropeHoldingAG
Address:Sumpfstrasse13CH‐6300Zug,Switzerland
LocalDistributor:

(2)Q1E‐EP1430
Aboutthismanual
Thisinstructionmanualcontainssafetyprecautions,theinspection,theoperation
procedureandthereprocessingprocedureofEUP‐V73W.
Pleasereadthismanualthoroughlytoensurethesafetyoperation.
Ifyouhaveanyquestionsconcerningtheoperationoftheprobe,pleasecontactaservice
support.
Thefollowingconventionsareusedthroughoutthemanualtodenoteinformationof
specialemphasis.
WARNING:“Warning”indicatesthepresenceofahazardwhichmayresultinsevere
personalinjury,substantialpropertydamage,ordeathifthewarningis
ignored.
CAUTION:“Caution”indicatesthepresenceofahazardwhichwillorcancauseminor
personalinjuryorpropertydamageifthecautionisignored.
NOTICE:“Notice”indicatesinformationofinstallation,operation,ormaintenance,
whichisimportant,butnothazardrelated.

(3)Q1E‐EP1430
GraphicalSymbolsforUseinLabelingofHitachiUltrasoundProbes
SomegraphicalsymbolsthatareusedinlabelingofHitachiUltrasoundProbesare
compliantwithEN980:2008standard.Refertothefollowingtableaboutthemeaningsof
them.
ExplanationofSymbol SymbolDescriptiveContent
ManufacturerCompany
NameandAddress
Hitachi,Ltd
2‐16‐1,Higashi‐Ueno,taito‐ku,
Tokyo,110‐0015,Japan
Authorized
RepresentativeinThe
EuropeanCommunity
HitachiMedicalSystemsGmbH
Otto‐von‐Guericke‐Ring3D‐65205Wiesbaden,
Germany
Keepawayfrom
Sunlight
Storetheprobeinacool,dustproofanddark,
dryenvironmenttoavoidhightemperature,
humidityanddirectsunlight.
Containsorpresenceof
naturalrubberlatexContainsorpresenceofnaturalrubberlatex
Donotre‐sterilizeDonotre‐sterilize
DonotreuseDonotreuse

(4)Q1E‐EP1430
Definitionofsymbol
ThefollowingsymbolisalsousedforHITACHIUltrasoundProbes.
LocationSymbolDefinition
Probe
connector
ThisinstrumentcomplieswithDirective93/42/EECrelatingto
MedicalDeviceandDirective2011/65/EUrelatingtoRoHS
Probe
connectorIPX7IPX7mark
Seesection1.6.
Probe
connectorTypeBFAPPLIEDPART
Probe
connectorGeneralwarningsign
Probe
connectorWarning;dangerousvoltage
Probe
connectorCaution;Biohazard
Probe
connector
Followtheinstructionmanualtooperatethisinstrument.Ifnot
avoided,mayresultininjury,propertydamage,orthe
equipmenttrouble.
Probe
connector
STERRADsterilizationcompatibilitymark
Probe
connector
UpperLimitofTemperature;
TheprobesthatareapplicabletoEthyleneOxideGas
Sterilizationusesymbolof“UpperLimitofTemperature:55
degrees”.
Probe
connector
Donotwastetheinstrumentasgeneralwaste.Complywitha
localregulation.
Probe
connectorRxOnly Byprescriptiononly.U.S.FederalLawrestrictsthisdevicetosale
onorderofaphysicianonly.

(5)Q1E‐EP1430
CONTENTSPage
1Introduction∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙1
1.1 Features∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙1
1.2 Principlesofoperation∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙1
1.3 IntendedUse∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙1
1.4 Components∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙2
1.5 Accessories(Option)∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙2
1.6 Externalview∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙3
2InspectionbeforeUse∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙4
2.1 InspectionforAppropriateConnection∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙4
2.2 InspectionforMaterialSurface∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙4
3OperationProcedure∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙5
3.1 ConnectionandSettings∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙5
3.2 HowtoattachtheSterilePunctureAdapter(EZU‐PA7V)∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙7
3.3 DisplayofNeedleGuideLine∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙8
4OptionofEUP‐V73W∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙10
4.1 MagneticsensorEZU‐RV2S∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙10
4.2 MagneticsensorEZU‐RV3S∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙13
5ReprocessingProcedure∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙16
5.1 Pointofuse(Pre‐cleaning)∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙18
5.2 Containmentandtransportation∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙18
5.3 ManualCleaninganddisinfection∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙18
5.4 Drying∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙21
5.5 Inspection∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙21
5.6 Packaging∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙21
5.7 Sterilization∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙22
5.8 Storage∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙24
6MaintenanceandSafetyInspection∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙25
6.1 DailyInspection∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙25
7SafetyPrecautions∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙26
8Specifications∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙28
8.1 Probe∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙28
8.2 SterilePunctureAdapterEZU‐PA7V∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙29
8.3 SuppliersList∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙30
9Disposaloftheprobe∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙30

‐1‐ Q1E‐EP1430
WARNING
1Introduction
1.1 Features
ThetransvaginalprobeEUP‐V73WisConvexArrayelectronicscanning.
Theacousticoutputofthisprobewhenconnectedtoultrasoundscannerwasmeasured
accordingtotheIEC60601‐2‐37standard.Thetableofmeasuredacousticoutputdatais
containedintheoperationalmanualofeachultrasoundscanner.Thisprobeiscategorized
inclassIIaaccordingtoDirective93/42/EEC.
AccordingtoIEC60601‐1theprobeisclassifiedastypeBF.
1.2 Principlesofoperation
Thisprobeandtheultrasounddiagnosticscannerenableimagediagnosisusingultrasonic
waves.Thissystemoperatesundertheprinciplesdescribedbelow.
1) Whenanelectricpulsesignalisappliedfromthetransmittertothetransducerofthe
probe,thetransducerconvertselectricsignalsintomechanicalvibrationenergyfor
emittingpulse‐shapedultrasonicwavesintothebodypart,liquidorothermedium
contactingthetransducer.
2) Theemittedultrasonicwavesarereflectedbyboundarieswithdifferentacoustic
characteristics(acousticimpedance)withinthebody.
3) Thetransducerisalsousedtoreceivereflectedultrasonicwaves.Thetransducer
vibratesmechanicallyduetothereceivedultrasonicwavesandconvertsmechanical
vibrationsintoelectricenergy.Electricsignalsareconvertedtoshadesofbrightnessby
brightnessmodulationtoobtainanimage.
1.3 IntendedUse
TheTransvaginalProbeEUP‐V73Wisdesignedforobservationanddiagnosisofthe
followingregionsmainlybyconnectingwiththeHITACHIultrasounddiagnosticscanner.
GeneralOB/GYNorgans
Biopsy(withaSterilePunctureAdapter)
Transrectal
Neverusetheprobeforfollowingregions.
1) Theheart(Donotcontactdirectly.)
2) Theeyeball

‐2‐ Q1E‐EP1430
CAUTION
CAUTION
1.4 Components
ComponentsofEUP‐V73Wareasfollows:
1) Probe∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 1piece
2) InstructionManual∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 1copy
Theprobeisnotsterilizedwhendelivered.Priortouse,besuretoclean,disinfectandif
necessarysterilizeit.
1.5 Accessories(Option)
1.5.1 SterilePunctureAdapterEZU‐PA7V(Disposable)
EZU‐PA7Vistheattachmentforultrasoundguidedtransvaginalortransrectal
biopsyandaspirationoforgans,cystandtumor.Thesizeofneedlesavailableis16
to19G.Biopsyapplicationrequiresspecialcare.24piecesofSterilePuncture
AdapterEZU‐PA7Varepackagedinonesetasfollows:
ComponentModelQty
SterilePunctureAdapterEZU‐PA7V 24pcs
NOTE:IfyouneedSterilePunctureAdapters,pleasecontactyourlocalHITACHI
distributor.
Onlyawell‐trainedphysicianshouldperformabiopsy.
1.5.2 CondomorProtectionSleeveforSingleUse(Disposable)
Toprotecttheprobeagainstcontamination,useonlylubricationfreecondomordry
typeprotectivetubesleeve.
Lubricationmaycauseadeteriorationoftheprobesurface.Useofnon‐allergic
condomorsleeveisstronglyrecommendedtoavoidallergicreactionsduetolatex
rubber.
Discardtheusedcondomorprotectionsleevecarefully.
1.5.3 MagneticSensorAttachment
MagneticSensorAttachmentisneededforReal‐timeVirtualSonography(RVS).Itisused
tofixthemagneticsensortotheprobe.

‐3‐ Q1E‐EP1430
CAUTION
1.5.4 SpacerforEZU‐RV2S
SpacerforEZU‐RV2SisthespacerneededtofixtheEZU‐RV2StotheMagneticSensor
Attachment.
TheMagneticSensorAttachmentandtheSpacerforEZU‐RV2Sarenotsterilizedwhen
deliveredfromthefactory.Priortouse,besuretoclean,disinfectandifnecessarysterilize
them.
1.6 Externalview
TheexternalviewofEUP‐V73WisshowninFig.1.
Cable
Connector
Un‐immersible
part
Immersiblepart(IPX7)
Magneticsensor
attachment(Option)
Spacerfor
EZU‐RV2S
(Option)
Appliedpart
Immersiblepart:Thispartcanbeimmersedindisinfectantsolution
andalsocanbecleanedbywater.
Un‐immersiblepart:Thispartshouldnotbeimmersedindisinfectant
solutionandalsocannotbecleanedbywater.
Fig.1Externalview

‐4‐ Q1E‐EP1430
CAUTION
2InspectionbeforeUse
Priortouse,theprobeandaccessoriesmustbecarefullyinspectedforappropriateuse.If
youfindanydamage,donotusethemandcontactaservicesupportimmediately.
2.1 InspectionforAppropriateConnection
1) Confirmthattheultrasounddiagnosticscanneriscorrectlyoperating.Pleasereferto
theinstructionmanualofthescannerfortheoperation.
2) Confirmthatanyunauthorizeddevice/instrumentsuchasanunauthorizedbiopsy
attachmentisnotattachedorconnectedtotheprobe.
3) ConfirmthattheSterilePunctureAdapterandsettingsofthescannerareappropriate
fortheprobe.AttachtheSterilePunctureAdaptertotheprobeaccordingto“3.
OperationProcedure”.Displaythe“Needleguideline”onthemonitor.(Refertothe
operationmanualoftheultrasounddiagnosticscanner.)Keeptheprobeheadunder
sterilewaterandinsertapunctureneedleintheSterilePunctureAdapter,then
confirmthattheneedleisinsertedsmoothlyandtheechooftheneedleisdisplayedon
the“Needleguideline”(dotline)onthemonitor.
2.2 InspectionforMaterialSurface
1) Visuallyinspectthesurfaceoftheprobehead,housingandcableforanycrack,scratch
ordenaturalization.
2) VisuallyinspecttheenvelopeoftheSterilePunctureAdapterforanybreak,
deformation,crackordenaturalization.Ifyoufindanydamage,donotusetheSterile
PunctureAdapter.
3) VisuallyinspecttheMagneticsensorattachmentandtheSpacerforEZU‐RV2Sforany
crack,deformationordenaturalization.
BewarenottolosetheSpacerforEZU‐RV2Ssinceitissosmall.

‐5‐ Q1E‐EP1430
3OperationProcedure
3.1 ConnectionandSettings
1) Confirmthattheprobe,theMagneticSensor
AttachmentandtheSpacerforEZU‐RV2Sare
cleaned,disinfectedandifnecessarysterilized.
TheMagneticSensorAttachmentandtheSpacer
forEZU‐RV2SareneededforReal‐timeVirtual
Sonography(RVS).Regardingtheoptionfor
RVS,pleasereferto“4.OptionofEUP‐V73W”.
2) Itisrecommendedtouseadisposableprobecover
forpreventingapatientfrominfectionandthe
probecovershouldbeallergyfreematerialto
avoidallergicreaction.
3) Connecttheprobetotheultrasounddiagnostic
scannerandoperatethescannerandadjustthe
imageaccordingtotheinstructionsgiveninthe
operationmanualoftheultrasounddiagnostic
scanner.Therelationshipbetweenthedirectionof
theprobeandtheright‐leftorientationmarkonthe
imageisshowninFig.2.
4) Putproperquantityofsterilizedacousticjellyontheprobeheadasacouplant.(See
Fig.3)
Fig.2Relationshipbetween
thedirectionoftheprobeand
theRight‐leftOrientation
MarkDirection
Orientation
mark
Sterilizedacousticjelly
Fig.3
J
ellyasacouplant

‐6‐ Q1E‐EP1430
WARNING
5) Putaprobecoverontheprobeanddrawtheprobecoveruntiltheendoftheprobe
shaft.Ifairbubblesremaininjelly,removeairbubblesbypushingjellywithfinger.
(SeeFig.4)
Specialattentionshouldbepaidforaprobecovermadeoutoflatex.Latexmay
causeallergicreactionssuchasitching,rubor,urticaria,swelling,fever,anhelation,
wheezing,depressionofbloodpressure,andshock.
Ifyourpatientshowsanyoftheabovementionedsymptomsduringtheoperation,
stoptheuseofthelatexprotectivesleeveimmediatelyandtakeanappropriate
treatmenttothepatient.
6) FixtheprobecoverwithsterileadhesivetapeasshowninFig.5.Visuallyinspectthe
probecoverforanyholeortears.
7) Inserttheprobegentryandadjusttheprobe’spositionforaclearviewofthedesired
image.Iftheimageisnotclearenough,usesterilesalinesolutiontohaveabetter
image.
8) Afterusingtheprobe,clean,disinfectandsterilizetheprobeimmediately.IfRVSis
carriedout,clean,disinfectandsterilizetheMagneticSensorAttachmentaswellas
theSpacerforEZU‐RV2S.
Probecover
Airbubble
Sterilized
acousticjelly
Fig.4Removalofbubblesinjelly
Sterilizedtape
Fig.5Fixbysterileadhesivetape

‐7‐ Q1E‐EP1430
CAUTION
9) Storetheprobe,theMagneticSensorAttachmentandtheSpacerforEZU‐RV2Sunder
theconditionswrittenin“6.MaintenanceandSafetyInspection”and
“8.Specification”.
Donotusetheprobeiftheimageandthefrequencydonotmatchtheprobe.An
incorrectacousticoutputcanresultinburnsorotherinjuriestothepatient.
Scanfortheminimumlengthoftimenecessaryforthediagnosisandatthelowest
possibleoutput.Thereisthepossibilitythatthepatient’stissuescouldbeaffected.For
detailsabouttheacousticoutput,pleaserefertotheoperationmanualofthe
ultrasounddiagnosticinstrument.
3.2 HowtoattachtheSterilePunctureAdapter(EZU‐PA7V)
HowtoattachtheSterilePunctureAdapter(EZU‐PA7V)totheprobeisinstructedbelow.
1) PutthepicksoftheSterilePunctureAdaptertotheprojectionontheprobe.(Seethe
topofFig.6)
2) PushtheotherendoftheSterilePunctureAdapteruntilthedentsoftheSterile
PunctureAdapterarefixedatthegroovesoftheprobe.(SeethebottomofFig.6)
3) Visuallyinspecttheprobecoverforanyholeortears.
SterilePunctureAdapter
(EZU‐PA7V)
Probecover
Fig.6HowtoattachtheAdapter

‐8‐ Q1E‐EP1430
CAUTION
3.3 DisplayofNeedleGuideLine
Theneedleguidelineindotmarkscanbedisplayedonthemonitorforbiopsy.
Regardingtheneedleguideline,refertotheoperationmanualoftheultrasounddiagnostic
scanner.
NOTE:Theneedleguidelineisintendedtoprovideavisualguidetothedirectionofthe
punctureneedlepathway.Besuretochecktheactualneedlepositiononthe
ultrasoundimagewhenperformingthepunctureoperation.
Theneedleguidelinecanbedisplayedforthisprobe,butiftheimageisdisplayedatsome
angle(seethefiguresbelow),theimagedisplayedmaynotbeappropriateforbiopsy.
Confirmthattheimagedisplayedisappropriatepriortobiopsy.
ProbePunctureadapter
Needle
guideline
Artifactof
punctureadapter
(Guidelineiseffectivelydisplayed.)
(Guidelineisnotdisplayed.)
Needleguideline
Locationofobservation
FOVoftheprobeImagedisplay
Artifactofpunctureadaptermay
appearwhiletheguidelineis
displayedonlyatthevicinity.

‐9‐ Q1E‐EP1430
WARNING
1) Specialattentionshouldbepaidforaprobecovermadeoflatex.Latexmaycause
allergicreactionssuchasitching,rubor,urticaria,swelling,fever,anhelation,
wheezing,depressionofbloodpressure,andshock.
Forthepatientssuspectedoflatexallergy,donotusethelatex‐containingmedical
devices.Ifyourpatientshowsanyofabovementionedsymptomsduringthe
operation,stoptheuseofthelatex‐containingmedicaldevicesimmediatelyandtake
anappropriatetreatmenttothepatient.
2) ThepunctureadapterEZU‐PA7Vandtherecommendedprobecoversaredisposable
andmustnotbereused.
3) Clean,disinfectandsterilizetheprobeandthepunctureadapterwhentheprobecover
istorn.
4) Becarefulabouttheuseofaneedlecannulawiththepunctureadapter.Ifthe
insulationcoatingoftheneedlecannulaisdamaged,itmaycauseaburntotissue.
5) Useaneedlewhosesizeisappropriateforthepunctureadapter,otherwiselooseness
ortightnessoftheneedlecouldresultinbiopsyatanunintendedpartandinjuryto
thepatient.
6) Displaytheneedleguidelineduringbiopsy.Regardingtheneedleguideline,referto
theoperationmanualoftheultrasounddiagnosticscanner.

‐10‐ Q1E‐EP1430
4OptionofEUP‐V73W
RVS(Real‐timeVirtualSonography)isavailablebyusingEUP‐V73Wwithoptions.The
optionsneededforRVSaretheMagneticSensorAttachmentandthemagneticsensor.The
magneticsensorsavailableareEZU‐RV2SandEZU‐RV3SshowninFig.7andFig.12
respectively.
4.1 MagneticsensorEZU‐RV2S
EZU‐RV2SasshowninFig.7isthemagneticsensorforEUP‐V73W.
Fig.7EZU‐RV2S
Magneticsensor(black)
Projectedpart

‐11‐ Q1E‐EP1430
CAUTION
4.1.1 HowtoattachEZU‐RV2S
TheprocedureofattachingthemagneticsensorEZU‐RV2Sisasfollow.
1) ConfirmthatthemagneticsensorattachmentandtheSpacerforEZU‐RV2Sare
cleaned,disinfectedandsterilized.
2) AttachtheSpacerforEZU‐RV2StothemagneticsensorasshowninthetopofFig.8.
3) InsertthemagneticsensorintotheMagneticSensorAttachmentinthecorrect
directionasshowninthebottomofFig.8.
1) Neverattachthemagneticsensorattachmenttotheprobeinthewrongdirection,
otherwiseitmayresultinfalsediagnosis.
2) NeverforgettoattachtheSpacerforEZU‐RV2StoEZU‐RV2S,otherwiseitmayresult
infalsediagnosis.
Projectedpart
Fig.8HowtoattachtheMagneticsensor
Projectedpart
Magneticsensor
attachment
Spacer
Magneticsensor
(EZU‐RV2S:Black)
Spacerfor
EZU‐RV2S

‐12‐ Q1E‐EP1430
CAUTION
4) AttachtheMagneticSensorAttachmenttotheprobeasshowninFig.9.
DonotputyourfingersbetweentheMagneticSensorAttachmentandtheProbewhen
attachingtheMagneticSensorAttachmenttotheprobe.
Fig.9HowtoattachtheMagneticsensorattachment

‐13‐ Q1E‐EP1430
CAUTION
4.1.2 HowtoreleaseEZU‐RV2S
TheprocedureofreleasingthemagneticsensorEZU‐RV2Sisasfollow.
1) DetachtheMagneticSensorAttachmentfromtheprobeasshownFig.10.
2) DetachthemagneticsensorandtheSpacerforEZU‐RV2SfromtheMagneticSensor
AttachmentasshownFig.11.
Clean,disinfectandsterilizetheMagneticSensorAttachmentandtheSpacerfor
EZU‐RV2Spriortothefirstuseastheyarenotsterilizedwhendelivered.
4.2 MagneticsensorEZU‐RV3S
EZU‐RV3SasshowninFig.12isthemagneticsensorforEUP‐V73W.
Fig.10HowtoreleasetheMagnetic
sensorattachmentfromtheprobe
Fig.11Howtoreleasemagneticsensor
fromtheMagneticSensorAttachment
Directionmark
MagneticSensor
(EZU‐RV3S:white)
Fig.12Magneticsensor(EZU‐RV3S)

‐14‐ Q1E‐EP1430
CAUTION
CAUTION
4.2.1 HowtoattachEZU‐RV3S
TheprocedureofattachingthemagneticsensorEZU‐RV3Sisasfollow.
1) ConfirmthattheMagneticSensorAttachmentiscleaned,disinfectedandsterilized.
2) InsertMagneticsensorintotheMagneticsensorattachmentinthecorrectdirectionas
showninFig.13.
NeverattachtheMagneticSensorAttachmenttotheprobeinthewrongdirection,
otherwiseitmayresultinfalsediagnosis.
3) AttachtheMagneticSensorAttachmenttotheprobeasshowninFig.14.
DonotputyourfingersbetweentheMagneticsensorattachmentandtheprobewhen
attachingtheMagneticSensorAttachmenttotheprobe.
Fig.13HowtoattachtheMagneticsensor
Directionmark
ofEZU‐RV3S
Magneticsensorattachment
Magneticsensor
(EZU‐RV3S)
Fig.14Howtoattachthe
MagneticSensorAttachment
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