Mobius AIRO Mobile CT System - Index

MI-42-0001 Rev. 19 277
INDEX
INDEX
Numerics
3D Image Controls............................................... 118
60601-9.2 Hazards Associated with Moving Parts............ 31
A
Accessories....................................................... 249
Combining ...................................................... 198
List of ............................................................ 250
Marked and labeled............................................ 250
Add new phantom................................................ 140
AIRO
Medical purpose
................................................... 5
Technical description .......................................... 197
Approved areas for use ......................................... 208
Areas of high occupancy ......................................... 20
Assessing patient risk ............................................ 27
Authorized EU representative ..................................... 2
Axial scan described............................................. 200
B
Battery charge, minimum for operation................. 210, 246
Beam shape (x-ray).............................................. 211
Before scanning................................................... 70
Brakes, system.................................................... 54
Bypass 2D scan........................................... 103, 104
C
Cables, power and network...................................... 42
Calibration
Daily gain calibration
........................................... 152
Instructions (available on request) ........................... 198
Certification labels ............................................... 228
Changing patient information ................................... 131
Circuit diagrams (available on request) ....................... 198
Collisions, risks when moving system .......................... 32
Column
Available User Manual supplements
.......................... 63
Label for updated column ...................................... 64
Rating plate label............................................... 225
Specifications................................................... 207
Types............................................................. 63
Compatible equipment .......................................... 251
Brainlab navigation systems .................................. 250
Combining ...................................................... 198
Limits on medical software.................................... 250
Limits on non-authorized combinations ..................... 250
Compliance
General electromagnetic immunity
........................... 218
Standards ....................................................... 218
Components
Overview
........................................................... 8
Parts lists (available on request) ............................. 198
System subassemblies........................................ 200
Confirm the Ring Rotation ........................................ 91
Connectivity ...................................................... 212
DICOM 3.1...................................................... 212
Ethernet ......................................................... 212
Contact data ......................................................... 2
Contraindications ................................................... 5
Controls ............................................................. 40
Correcting patient information .................................. 131
CTDI
Acronym
........................................................... 21
See X-ray dose.
Current
Statement
....................................................... 209
Tube ............................................................. 211
Customer support................................................... 2
D
Daily inspections ................................................. 169
Detachable pendant
Connecting
...................................................... 271
Connector location............................................. 270
Disconnecting .................................................. 272
Deviation from indications (maximum) ........................ 210
Device description
General
............................................................. 4
Technical........................................................ 199
Diagrams.......................................................... 203
Pendant display (hardwired) .................................... 69
Sample OR setup ................................................ 55
System ............................................................ 68
System in scan mode............................................. 9
System in transport mode........................................ 8
With dimensions ............................................... 203
DICOM ............................................................ 201
Conformance statement......................................... 10
Display. See Pendant.
Displayed scan parameters
..................................... 108
Distributor............................................................ 2
DLP, acronym ...................................................... 21
Documentation
Available guides
.................................................. 12
Cautions format ................................................... 3
Intended audience ............................................... 11
Notes format....................................................... 3