
Contents
2
|
EN
LM
T
68
65
1c
0
2/
20
22
Contents
1.1 Intended use .................................................... 3
1.2 Description of function ..................................... 3
1.3 User qualification ............................................. 3
1.4 Indications ........................................................ 4
1.5 Contraindications ............................................. 4
1.6 Side effects ...................................................... 4
2.1 Safety information ............................................ 4
2.2 General information ......................................... 5
2.3 Safety information in these instructions
for use .............................................................6
3.1 Overview .......................................................... 7
3.2 Control panel in display .................................... 8
3.3 Symbols in display ............................................ 9
3.4 Accessories (optional) ....................................... 9
3.5 Operating states ............................................. 10
3.6 Batteries ......................................................... 10
3.7 Trolley 2.0 ...................................................... 10
3.8 Data management/compatibility ..................... 11
4.1 Setting up and connecting device ................... 12
4.2 Connecting circuit .......................................... 12
4.3 Before first use ............................................... 14
4.4 Switch device on and off / Start and end
therapy ..........................................................14
4.5 Performing circuit test .................................... 14
4.6 Calibrating FiO
cell ........................................ 14
4.7 Pairing device with LUISA app ........................ 15
5.1 Navigating in the menu ................................. 16
5.2 Patient menu structure .................................. 16
6 Hygiene treatment and servicing
6.1 Hygiene treatment ........................................ 18
6.2 Function check .............................................. 19
6.3 Checking alarms ............................................ 20
6.4 Servicing ....................................................... 20
6.5 Disposal ........................................................ 21
7.1 Sequence in which alarms are displayed ........ 22
7.2 Muting alarms ............................................... 22
7.3 Configuring physiological alarms ................... 22
7.4 Technical alarms ............................................ 24
7.5 Nurse call and remote alarm .......................... 28
10.1 Pneumatic diagram ....................................... 33
10.2 System resistances ......................................... 34
10.3 Emission of electromagnetic interference ....... 35
10.4 Electromagnetic interference immunity .......... 35
10.5 Markings and symbols ................................... 36
10.6 Scope of delivery ........................................... 36
10.7 Accessories .................................................... 37
10.8 Removable parts ............................................ 37
10.9 Warranty ....................................................... 38
10.10 Declaration of Conformity ........................... 38