Table of contents
Warning! ............................................................ 2
Presentation ....................................................... 3
Measurement ..................................................... 6
Time and date .................................................... 9
Sound volume ................................................... 9
QC on/off .......................................................... 9
®
General care .................................................... 11
Change Sensor ................................................. 11
Support ............................................................ 12
Alert codes ...................................................... 13
Backplate ......................................................... 16
Base label ....................................................... 16
Shelf-life .......................................................... 16
Linearity .......................................................... 17
Precision .......................................................... 17
Accuracy ......................................................... 17
.................................... 10
Cautions ........................................................... 22
Vigilance .......................................................... 23
User manual EPM-000200, version 01, October
2013, for instruments with software version 20XX
and 21XX. X can be any number between 0 and 9.
The version number for your instrument can be seen
in the Information menu, see page 10.
Information in this document is subject to change.
Amendments will be made available by Aerocrine
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 © 2013 Aerocrine AB, Solna, Sweden.
• Aerocrine, NIOX MINO and NIOX are registered
trademarks of Aerocrine AB.
E N G L I S H
1