Circassia NIOX VERO User manual

NIOXVERO®UserManualChinese(English)
000925-03(EPM-000187)October2017
NIOX VERO® Airway Inflammation Monitor
User Manual

Remember
Itisimportanttoadheretothefollowingspecifiedconditions:
• Ambienttemperature:+10°Cto+35°C
• Humidity:20%to80%RH(non-condensing)
• Mobilephones,cordlessphonesandgasemittingappliances
mightinterferewiththeinstrumentandshouldthereforebe
keptawayfromtheinstrument.Interferencecouldmakeit
impossibletoperformameasurement.
•Exhaledbreathcontainswatervaporwhichcancondense
insidetheinstrument.Whenexcessivelyusedinashort
period,thereisariskforcondensationofwaterinside
NIOX VERO®.
Normallyamaximumof10exhalations/hourcanbeperformed
withNIOXVERO®duringcontinuoususe.However,itis
possibletoperform20exhalationsinonehourifthe
instrumentispausedforaminimumof30minutespriortothe
nextsessionofexhalations.Exhalationsincludefailedand
successfulmeasurements.
• AvoidspillingwaterorotherfluidsontheinstrumentorSensor.
• Alwaysuseaclosedcaseorbag(NIOXVERO®bag
recommended)fortransportationandstorageofNIOXVERO®.
• Itisrecommended,afterinsertinganewsensor,towaitfor
threehourswiththeinstrumentswitchedonbeforeperforming
ameasurement.
• Operationallife-timeforNIOXVERO®Instrument:Minimum5
yearsattimeofdelivery,or15000measurements.
• Operationallife-timeforNIOXVERO®Sensor:Maximum12
monthsafteropeningpackageandinstalledinNIOXVERO®or
expirationdateasstatedontheSensor,whichevercomesfirst.
WARNING!
Use of substances containing alcohol close to the NIOX VERO®
instrument may cause erroneous measurement results.
DO NOT clean the instrument or handle with alcohol or any
spray or wipe containing alcohol!
Do not use substances containing alcohol on or close to the
NIOX VERO®instrument. This includes any cleaning agents
used to clean the facility, or other equipment in the area, as well
as alcohol wipes or sprays used on patients.
CAUTION!
:DonotuseNIOXVERO
® in the proximity of areas
where volatile substances such as organic fluids or disinfectants
arebeingused.Specialattentionshouldbepaidtoaerosolsand
disinfectionbaths,eitheropenvesselsorultrasonicbaths.

Tableofcontents
NIOXVERO®UserManualChinese(English)
000925-03 1
1Important information ...............................................................3
1.1
Before using NIOX VERO®Airway Inflammation Monitor........ 3
1.2
About this manual .................................................................... 3
1.3
Compliance.............................................................................. 3
1.4
Responsible manufacturer and contacts.................................. 3
1.5
Warnings.................................................................................. 4
1.6
Intended use ............................................................................ 5
2Product description ..................................................................6
2.1
NIOX VERO®accessories and parts ....................................... 6
2.2
Instrument................................................................................ 6
3Installation and set up ..............................................................7
4User interface .......................................................................... 11
4.1
Main and settings view........................................................... 11
4.2
Main View............................................................................... 11
4.3
Settings view.......................................................................... 12
5Using NIOX VERO® ............................................................... 12
5.1
Start the instrument from power save mode.......................... 12
5.2
Register patient ID (optional) ................................................. 12
5.3
Measure FeNO....................................................................... 13
5.4
Demonstration mode.............................................................. 16
5.5
Measure ambient NO............................................................. 17
5.6
Change settings..................................................................... 18
5.7
Turn off the instrument........................................................... 20
6Using NIOX VERO® with NIOX® Panel ...................................21
7Troubleshooting ......................................................................21
7.1
Alert codes and actions ......................................................... 21
8Preventive care ....................................................................... 26
8.1
General care.......................................................................... 26
8.2
Change disposals .................................................................. 26
8.3
Operational life-time............................................................... 28
8.4
Disposal of instrument and accessories ................................ 29
8.5
Return shipments................................................................... 29
9Safety information .................................................................. 30
9.1
Warnings................................................................................ 30
9.2
Cautions................................................................................. 30
9.3
Substances disturbing FeNO measurement.......................... 31
9.4
Electromagnetic immunity...................................................... 31
9.5
Electromagnetic emissions.................................................... 31
9.6
Operating conditions.............................................................. 31
10Reference information ......................................................... 33
10.1
Buttons and descriptions ..................................................... 33
10.2
Symbols and descriptions.................................................... 33
10.3
Symbol explanation ............................................................. 34
11Technical data ...................................................................... 35
11.1
Dimensions and weight........................................................ 35
11.2
Electrical data...................................................................... 35
11.3
Noise level........................................................................... 35
11.4
Exhaled NO - performance data.......................................... 35
11.5
Linearity............................................................................... 35
11.6
Precision.............................................................................. 35
11.7
Accuracy.............................................................................. 35

Tableofcontents
NIOXVERO®UserManualChinese(English)
2000925-03
11.8
Method comparison ............................................................. 36
11.9
Inhalation parameters .......................................................... 36
11.10
Exhalation parameters....................................................... 36
11.11
Essential performance....................................................... 36
11.12
Memory capacity................................................................ 36
11.13
Patient filter........................................................................ 36
11.14
Bluetooth............................................................................ 36
11.15
Rechargeable battery capacity .......................................... 37
11.16
Instructions for transport and storage................................ 37
12NIOX VERO® parts and accessories ...................................38
12.1
Parts included in NIOX VERO®package
(Article No. 12-1100).................................................................... 38
12.2
Accessories.......................................................................... 38
13Vigilance ................................................................................ 39

Chapter1Important information
000925-03NIOXVERO®UserManualChinese(English) 3
1 Important information
1.1 Before using NIOX VERO® Airway Inflammation
Monitor
NIOXVERO
®
mayonlybeoperatedasdirectedinthismanualby
trained healthcare professionals. Trained status is achieved only
aftercarefulreadingofthismanual.Readtheentireinstructionsfor
use and make certain that you fully understand the safety
information.
1.2 About this manual
NIOXVERO®UserManual-English000925(EPM-000187),version
03,October2017,forinstrumentswithsoftwareversion1D1x-xxxx.
Forinstructiononhowtoviewthesoftwareversionnumber
installedintheinstrument,seepage 19.
Information in this document is subject to change. Amendments
willbemadebyCircassiaABastheyoccur.
The User Manual provides instructions on how to operate
NIOX VERO®.It containsnumberedstep-by-stepinstructionswith
screens and illustrations. Choices within steps are displayed with
bulletpoints.
1.3 Compliance
NIOXVERO®isCE-markedaccordingtoInVitroDiagnosticsDevice
Directive98/79/EC.NIOX VERO®isRoHScompliant.
Medical Device Registration Certificate Number: Country
mechanicalinjectioninto20152210902
Productstandardnumber:YZB/SWE0696-2015
1.4 Responsible manufacturer and contacts
Mailingaddress:
CircassiaAB,P.O.Box3006
SE-75003Uppsala,Sweden
Visitingaddress:
Hansellisgatan13
SE-75450Uppsala
Manufacturing site: 110 Oaza-Inoshiri-aza-Nishiueno, Wakimachi,
Mima,Tokushima,779-3603,Japan
Agentandservice:
Companyname:CircassiaABBeijingRepresentativeOffice
Address:Room1008,10F,Building1,No2.ChaoYangMenBeiDajie,
DongchengDistrict,Beijing
Symbol Description
WARNING
Indicatesapotentiallyhazardoussituationthat,
ifnotavoided,canresultinbodilyharmor
injury.
CAUTION
Indicatesapotentiallyhazardoussituationthat,
ifnotavoided,candamageaproductorsystem,
causelossofdataorharmtobusiness.
Note
Alertsthereadertoimportantinformationon
theproperuseoftheproduct,user
expectations,errorsituations,andactions
relatedtothese.

Chapter1Important information
4000925-03NIOXVERO®UserManualChinese(English)
www.circassia.com
www.niox.com
1.5 Warnings
• Donotusesubstancescontainingalcoholonorclosetothe
NIOX VERO®instrument.Thisincludesanycleaningagents
usedtocleanthefacility,orotherequipmentinthearea,as
wellasalcoholwipesorspraysusedonpatients.
• NIOX VERO®shouldonlybeoperatedbyhealthcare
professionals.
• OperateNIOX VERO®asstatedinthismanual.Circassiaaccepts
noresponsibilityfordamagedequipmentorfaultyresults,if
theequipmentisnothandledaccordingtothismanual.
• WhenselectinganaccessoryforyourNIOX VERO®product
keepinmindthatanaccessorynotrecommendedbyCircassia
ABmayresultinlossofperformance,damagetoyour
NIOX VERO®product,fire,electricshock,injuryordamageto
otherproperty.Theproductwarrantydoesnotcoverproduct
failureordamageresultingfromusewithnonapproved
accessories.Circassiatakesnoresponsibilityforhealthand
safetyproblemsorotherproblemscausedbytheuseof
accessoriesnotapprovedbyCircassia.
• NIOXVERO®shouldnotbeusedadjacenttoorstackedwith
otherelectronicequipment.
• Onlyusethepowersupplyprovided.Pulltheplugwhen
disconnectingNIOXVERO®fromthepoweroutlet.
• UseonlythebreathinghandlesuppliedbyCircassia.
• NomodificationofNIOXVERO®instrument,handleorSensor
isallowed.
• Donotdroptheinstrumentorsubjectittostrongimpact.
• DonotuseadamagedNIOXVERO®instrumentordamaged
components.
• KeeptheinstrumentandSensoroutofwater.Ensurethatno
liquidisspilledordroppedontheinstrumentorSensor.
• DonotheatordisposeoftheinstrumentorSensorinfire.Refer
to"Disposalofinstrumentandaccessories"onpage 29.
• NIOXVERO®andtheNOscrubberinthebreathinghandle
containspotassiumpermanganate.Usedorexpired
instrumentsandbreathinghandlesshouldbedisposedofas
hazardouswasteinaccordancewithlocalwastedisposal
regulations.
• Thebreathinghandlemustnotbeusedafterexpirationdate.
• Patientfiltersshouldbeusedimmediatelyafteropening.
• NIOXVERO®Sensorcontainschemicalsthatcouldbeharmful
ifswallowed.
• BecarefulwhenopeningtheSensorcan.Theinsideofthe
openingmayhavesharpedges.
• DonottouchorcleanthewhiteSensormembrane.
• AfterinsertinganewSensoritisrecommendedtowaitfor
threehourswiththeinstrumentswitchedonbeforeperforming
ameasurement.
• Makesuretousethecorrectmeasurementmode,otherwise
incorrectFeNOresultsmightbeobtained.
• UseofsubstancescontainingalcoholclosetotheNIOX VERO®
instrumentmaycauseerroneousmeasurementresults.
• Donotreusepatientfilters.
• DonotuseNIOXVERO®intheproximityofareaswhere

Chapter1Important information
000925-03NIOXVERO®UserManualChinese(English) 5
volatilesubstancessuchasorganicfluidsordisinfectantsare
beingused.Specialattentionshouldbepaidtoaerosolsand
disinfectionbaths,eitheropenvesselsorultrasonicbaths.Do
notusetheinstrumentinthepresenceofflammableanesthetic,
vaporsorliquids.
1.6 Intended use
NIOXVERO®measuresNitricOxideinhumanbreath.
FractionalexhaledNitricOxide(FeNO)isincreasedinsomeairway
inflammatoryprocessessuchasasthmaanddecreasesinresponse
to anti-inflammatory treatment. FeNO measurements with
NIOX VERO® are quantitative, non-invasive, simple and safe and
should be used as part of regular assessment and monitoring of
patientswiththeseconditions.
NIOX VERO® is suitable for patients age 4 and above. As
measurement requires patient cooperation, some children below
theageof7mayrequireadditionalcoachingandencouragement.
NIOXVERO®shouldbeusedasdirectedintheNIOXVERO®User
Manual.
CAUTION!
• NIOXVEROcanbeoperatedwithtwodifferentexhalationtimes,
10secondsand6seconds.The10secondtestisthepreferred
mode.Forchildrenwhoarenotabletoperformthe10second
test,the6secondtestisanalternative.
• The6secondtestshouldbeusedwithcautioninpatientsover
theageof10years.Itshouldnotbeusedinadultpatients.
Incorrectuseofthe6sexhalationmodemayresultinfalselylow
FeNOvalues,whichcanleadtoincorrectclinicaldecisions.

Chapter2Product description
6000925-03NIOXVERO®UserManualChinese(English)
2 Product description
2.1 NIOX VERO® accessories and parts
(A)Breathinghandleandhandlecap,(B)Sensor(supplied
separately), (C) Instrument (including stand), (D) Rechargeable
battery(TypeNoBJ-G510039AA),(E)Patientfilter(supplied
separately),(F)USBcable,(G)Poweradapterandpowercord
Note: OnlyaccessoriesandpartssuppliedbyCircassiamaybe
used.
2.2 Instrument
H)ON/OFFbutton,(I)Poweradapterport,(J)USBport
(K)BatteryLED-litwhenbatteryischarging,(L)StandbyLED-
blinkinginStandby/Sleepmode,(M)TouchpanelDisplay

Chapter3Installation and set up
000925-03NIOXVERO®UserManualChinese(English) 7
(N)Breathinghandleholder,(O)Breathinghandleport
3 Installation and set up
Openthepackagewithcare.Prior to installation, check that the
package contains all the parts (see page 6). A screwdriver is
requiredforopeningthecompartmentlidandinstallationofSensor
andbattery.Removetheplasticfilmfromthedisplay.
1. Carefullyplacetheinstrumentwiththedisplayfacingdownon
aflatandcleansurface,thenunscrewandremovethe
compartmentlid.Thereisataperonthesideofthelidforbetter
gripwhenopening.
2. OpentheSensorcan.

Chapter3Installation and set up
8000925-03NIOXVERO®UserManualChinese(English)
WARNING!OpentheSensorcanwithcare.Theinsideofthe
openingmayhavesharpedges.
3. OpentheSensorpackage.
WARNING!
DonottouchorcleanthewhiteSensormembrane.
CAUTION!
TheSensorshouldonlybestoredinitsoriginal
unopenedpackageorinstalledinaNIOXVERO®instrument.
4. InserttheSensorandturntheswivelclockwiseuntillocked.
5. Openthebatterypackage.
Note: Onlyusethecorrectrechargeablebatterysuppliedby
Circassia.(TypeNoBJ-G510039AA,ArticleNo12-1150)
6. Inserttherechargeablebatteryandreplacethelid.Tightenthe
screwbyusingascrewdriver.
7. Takethebreathinghandletubeandpushtheendofthetube
intothebreathinghandleportslowlyuntilthetriangleisno
longervisible.
ThebreathinghandleandthepatientfilterareAppliedparts
TypeB.

Chapter3Installation and set up
000925-03NIOXVERO®UserManualChinese(English) 9
Note: OnlyattachthebreathinghandlesuppliedbyCircassia.
ArticleNo12-1010
Note: Usecarenottobendthehandletube.
Note: Thetriangleshouldnotbevisiblewhenassembledcorrectly.
8. Attachthepoweradaptertotheinstrumentandthentothe
poweroutlet.Wheninstallingtheunit,eitheruseasocketoutlet
withareadilyaccessiblepowerswitch,orconnecttheACcord
plugtoaneasilyaccessiblesocketoutletneartheequipment.If
afaultshouldoccurduringoperationoftheunit,usethepower
switchtocutthepowersupply,orremovetheACcordplug.
Note: OnlyusethepoweradaptersuppliedbyCircassiawiththe
instrument.ArticleNo12-1120.
9. Positiontheinstrumentwiththestandfoldedout.
10. StarttheinstrumentbyslidingtheON/OFFbuttontoONand
allowtheinstrumenttostartupandperformtheinternalcheck
andmeasurementprocedures.

Chapter3Installation and set up
10 000925-03NIOXVERO®UserManualChinese(English)
CAUTION!
AfterinsertinganewSensoritisrecommendedtowait
forthreehourswiththeinstrumentswitchedonbefore
performingameasurement.
11. Whentheinternalcheckiscompleted,themainmenuappears.
12. SelecttheSettingsbuttononthemainmenu.
13. SelectTimeanddate.
ThisopenstheTimeanddatesettingview.
14. Selectbetween12hUSand24hISOtime
anddateformat.
15. Settimebypressingthebuttonforhour.It
changescolortoblue.Changethevalueto
thecurrenthourbypressingtheincreaseor
decreasebuttons.Repeatthisprocedurefor
minute,year,monthandday.
16. SelectOK toacceptthechangesandreturntothemain
menu.
TheUndobutton closestheviewwithoutsavingany
changes.
17. SelecttheSettingsbuttononthemainmenu.
18. SelecttheBreathinghandlebutton.Thisopensthe
Breathinghandleview.
19. SelecttheResetBreathinghandlebutton.The
breathinghandleinformationviewopenstoconfirm
insertionofthebreathinghandle.
20. SelecttheOKbuttontoconfirminsertionofanew
breathinghandle.Thissetstheremainingmeasurements
to1000andexpirydateoneyearfromthecurrentdate.
TheReturnbuttonreturnstoSettingsviewwithout
registeringchange.

Chapter4User interface
000925-03NIOXVERO®UserManualChinese(English) 11
4 User interface
4.1 Main and settings view
This section describes the main view, settings view, menus and
symbols.Buttonsandsymbolsarefurtherdescribedonpage 33.
4.2 Main View
(A)Statusbar,(B)Instructivedemonstration,(C)PatientID,(D)Main
menu,(E)Startmeasurementbutton
4.2.1 Main menu
(a)Measurementmode10s/6s(onlyshownwhen6sisanoption,
formoreinformationsee“Enable/disable6smeasurement
mode”onpage 20,(b)Demo,(c)PatientIDentry,(d)Settings
4.2.2 Status bar
(e)Batterystatus,(f)Bluetoothenabled(inthispositionaUSB
connectionmaybeindicatedinstead ),(g)Breathinghandlehas
expiredorisabouttoexpire-blinkingsymbol,(h)Instrumenthas
expiredorisabouttoexpire-blinkingsymbol,(i)Sounddisabled,
(j)Sensorstatusandnumberofremainingmeasurements,
(k)Temperatureoutsideofspecification,(l)Humidityoutsideof
specification,(m)Time

Chapter5Using NIOX VERO®
12 000925-03NIOXVERO®UserManualChinese(English)
4.3 Settings view
(A)Modesconfiguration-seepage 20,(B)Volumesettings-see
page 18,(C)Alertlog-seepage 19,(D)Instrument&Sensorinfo
-seepage 19,(E)Timeanddatesettings-seepage 18,
(F)Measurementlog-seepage 18,(G)Ambientmeasurement-
seepage 17,(H)Breathinghandlestatusandsettings-see
page 26,(I)Returntomainview
5 Using NIOX VERO®
5.1 Start the instrument from power save mode
If NIOX VERO®isinstandbyorsleep mode simply touch the
displaytoactivateit.
5.2 Register patient ID (optional)
Note: IfPatientIDisused,itmustbeenteredbeforeeach
measurement,evenifitisthesamepatient.Local
RegulationsonPatientinformationprivacymustbe
consideredwhenusinguniquepatientidentifiers.

Chapter5Using NIOX VERO®
000925-03NIOXVERO®UserManualChinese(English) 13
1. SelecttheRegisterpatientIDbuttonfromthemain
menu.
2. Enterupto12characters(alphaornumeric).
3. SelecttheABC-buttontoactivateakeyboardwiththealphabet.
The123-buttonchangesviewbacktothenumericalkeyboard.
4. SelectOKbuttontoconfirmtheregistration.
UsetheErasebuttontoerase.
UsetheUndobuttontoundoaregistration.
5.3 Measure FeNO
Verifyproperpreparationsbeforeperformingameasurementwith
NIOX VERO®.Abasicpreventiveinspectionisrecommendedbefore
eachuse(seepage 26).
WARNING!
Thepatientfilterisforsingleuseonly.
5.3.1 Preparation for measurement
1. Liftthebreathinghandlefromtheholderandremovethe
handlecap.
2. Obtainanewpatientfilter.Attachthepatientfiltertothe
breathinghandle.Makesuretotwistthepatientfilterinplace
untilitclicksintoplace.
Note: Storethepatientfiltersin
theoriginalboxpriorto
use.
Note: DoNOTusesharpobjects
toopenthepatientfilter
packaging.Donottouch
thefiltermembrane.
Note: Patientfiltersshouldbe
usedimmediatelyafter
opening.
Note: Thereisariskofleakageifthefilterisnotcorrectlyattached
tothebreathinghandleandthismayresultinincorrect
measurementvalues.
Note: DonotswitchOFFtheinstrumentduringmeasurement
procedure.

Chapter5Using NIOX VERO®
14 000925-03NIOXVERO®UserManualChinese(English)
3. Givethebreathinghandletothepatientandguidethepatient
toprovideabreathsampleasdescribedinthenextsection.
5.3.2 Measurement
1. Emptythelungsbybreathingoutthoroughly.
2. Closethelipsaroundthemouthpieceonthepatientfilterso
thatnoairleakageoccurs.
3. Inhaledeeplythroughthepatientfiltertototallungcapacity.
Duringinhalation,thecloudonthedisplaymovesupwards.
Note: Theprocedureisactivatedbyinhalingairfromthehandle
orbypressingthestartmeasurementbutton.

Chapter5Using NIOX VERO®
000925-03NIOXVERO®UserManualChinese(English) 15
4. Exhaleslowlythroughthefilterwhilekeepingthecloudwithin
thelimitsasindicatedonthedisplay(thewhitelines).
5. Theinstrumentdisplayandaudiosignalsguidetheusertothe
correctexhalationpressure.
Acontinuoussoundindicatescorrectpressurewithafrequency
proportionaltothepressure.
Anintermittenthighfrequencysound-toostrongpressure
Anintermittentlowfrequencysound-tooweakpressure
Exhalationwith:
Pressurecorrect Pressuretoostrong Pressuretooweak
6. Exhaleuntilthecloudhaspassedtheflag.
7. Theinstrumentwillanalyzethesampleandgeneratearesultin
approximatelyoneminute.
Note: Donotexhaleorinhalethroughthepatientfilterduringthe
analysisprocess.
8. Theresultisthendisplayed:(A)PatientID-ifapplicable,(B)
FeNOvalueinppb(partsperbillion),(C)Measurementmode
10s/6s,

Chapter5Using NIOX VERO®
16 000925-03NIOXVERO®UserManualChinese(English)
(D)Measurementsequencenumber,(E)OK-returnstomain
view.
5.3.3 Perform 6s NO measurement
CAUTION!
• NIOXVEROcanbeoperatedwithtwodifferentexhalation
times,10secondsand6seconds.The10secondtestisthe
preferredmode.Forchildrenwhoarenotabletoperformthe
10secondtest,the6secondtestisanalternative.
• The6secondtestshouldbeusedwithcautioninpatientsover
theageof10years.Itshouldnotbeusedinadultpatients.
Incorrectuseofthe6sexhalationmodemayresultinfalsely
lowFeNOvalues,whichcanleadtoincorrectclinicaldecisions.
6s measurement mode is not activated by default, refer to
“Enable/disable6smeasurementmode”onpage 20.
1. Changeto6sMeasurementmodebyselectingthe10s
button(greenmansymbol)onthemainmenu.
2. Thebuttonchangesto6smeasurementmode(orange,
smallchildsymbol).
3. The6smeasurementmodeisillustratedwithanorange
startbutton.
4. Performmeasurementasinstructedinthe“5.3.2
Measurement”section.
5. Waitfortheresult.
6. Theresultscreendisplaystheiconfor6smeasurement.
Note: Thedevicewillalwaysreturntothedefault10s
modeaftera6smeasurement.
5.4 Demonstration mode
Tohelpprofessionalsinguidingpatients,theinstrumentcontains
threeanimateddemonstrationswithvisualandaudioguidesofthe
differentstagesofameasurementprocedure.
1. SelecttheAnimationbuttononthemainmenu.
2. Selectwhichanimationtouse(Cloud,DoraorMeter)
3. SelecttheDemobutton.
4. Selecttheforwardbuttontomovetothefollowingsequence.
5. Theundobuttonclosesthedemonstrationandreturnsto
animationselect.

Chapter5Using NIOX VERO®
000925-03NIOXVERO®UserManualChinese(English) 17
6. SelectOKbutton toconfirmthechanges
7. Theundobuttonreturnstothemainmenuwithoutsaving
changes.
5.5 Measure ambient NO
Note: An ambient measurement may be requested by technical support
during troubleshooting.
Note: Anambientmeasurementiscountedasonemeasurement
onNIOX VERO
®
Sensorandtheinstrument.
1. Attachapatientfiltertothebreathinghandleuntilitclicksinto
place.
2. SelecttheSettingsbuttononthemainmenu.
3. SelectAmbientMeasurementbutton.
4. SelecttheStartmeasurementbutton.
a. Inhalation
throughthe
breathing
handle.
b. Exhalation
throughthe
breathing
handlewith
correct
pressure.
c. Exhalation
throughthe
breathing
handlewith
pressuretoo
weak.
d. Exhalation
throughthe
breathing
handlewith
pressuretoo
strong.

Chapter5Using NIOX VERO®
18 000925-03NIOXVERO®UserManualChinese(English)
5. Theprogressbarisvisibleuntilthemeasurementisfinished
andtheresultisdisplayed:Ambientmeasurementvalue(in
ppb),measurementmodeandmeasurementsequence
number.
5.6 Change settings
5.6.1 Change time and date
1. SelecttheSettingsbuttononthemainmenu.
2. SelecttheTimeandDatebutton.
Formoredetailsrefertopage 10.
5.6.2 Change sound volume
1. SelecttheSettingsbuttononthemainmenu.
2. SelecttheSoundbutton.
3. Thesettingsforsoundandvolumeopens.
4. Selectdecrease/increasetoadjustvolume.
5. Thevolumebarindicatesthesetvolume.
6. SelecttheOKbuttontosavesettingsandreturntotheSettings
view.
TheUndobuttonclosestheviewwithoutsavingchanges.
7. Thestatusbarindicatesmutestatuswhenthesound
volumeissettozero.
5.6.3 View measurement logs
Allmeasurementresultsarestoredintheinstrumentandcanbe
viewedatanytime.
1. SelecttheSettingsbuttononthemainmenu.
2. SelectPatientmeasurementslogviewbutton.
3. Theselectedlogwilldisplaythefollowing:
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