NIOX MINO - Default Chapter; Table of Contents

1
Warning! ........................................................... 2
Intended use (Europe) ..................................... 2
Training requirements ..................................... 2
Presentation ..................................................... 3
Installation and set-up .................................... 4
Measurement ................................................... 5
EnterpatientID(optional)................................. 5
Perform FeNO measurement............................ 6
View stored results .......................................... 7
Ambient NO measurement ............................. 7
Demonstration mode ....................................... 7
Change settings ............................................... 8
Timeanddate................................................... 8
Soundvolume................................................... 8
Toplightintensity.............................................. 8
Bluetoothon/off................................................. 8
QCon/off.......................................................... 8
Information menu ............................................ 9
Turn off NIOX MINO
®
....................................... 9
General care ................................................... 10
Preventive inspections.................................... 10
ChangeSensor............................................... 10
ChangeNOscrubber...................................... 10
Disposalofused/expiredproducts.................. 11
Returnshipments........................................... 11
Support........................................................... 11
Limitedwarranty............................................. 11
Troubleshooting ............................................. 11
Alert codes...................................................... 12
Technical data ................................................ 13
Display buttons and symbols.......................... 13
Symbolsexplanation....................................... 15
Backplate........................................................ 15
Baselabel...................................................... 15
Dimensionsandweight................................... 15
Electrical data................................................. 15
Noiselevel(standby)..................................... 15
Shelf-life.......................................................... 15
Operatingconditions....................................... 15
ExhaledNO-performancedata..................... 16
Linearity.......................................................... 16
Precision......................................................... 16
Accuracy......................................................... 16
Method comparison........................................ 16
Inhalation parameters..................................... 16
Exhalation parameters.................................... 16
Memory capacity............................................ 16
Transportandstorage..................................... 16
Patientlter(mouthpiece)............................... 16
Responsiblemanufacturer.............................. 16
NIOX MINO
®
parts
and accessories ............................................. 17
Connect NIOX MINO
®
to a PC using USB .... 18
NIOX
®
Panel .................................................... 18
Special6sFeNOmeasurement...................... 19
Nasal measurement........................................ 19
Cautions ......................................................... 19
Clinical documentation ................................. 20
Vigilance ......................................................... 20
Guidance and manufacturer's declaration .. 21
Electromagneticemissions............................. 21
UsermanualEPM-000110,version09,April2017,
for instruments with software version 20XX,
22XX and 23XX.Xcanbeanynumberbetween0
and9.Theversionnumberforyourinstrumentcan
beseenintheInformationmenu,seepage9.
Information in this document is subject to
change.Amendmentswillbemadeavailableby
CircassiaABastheyoccur.
•NIOXMINOisCE-markedaccordingtoInVitro
DiagnosticDeviceDirective98/79/ECand
approvedforclinicaluseinEECcountries.
•NIOXMINOis510(k)cleared,k101034,byFDA.
•NIOXMINOisRoHScompliant.
•Copyright©2017CircassiaAB,Uppsala,
Sweden.
•NIOXMINOandNIOXareregisteredtrademarks
ofCircassiaAB.
•CircassiaisaregisteredtrademarkofCircassia
Limited.
Table of contents