Medical device licence · 37912 · Class 2
AXIOM ARISTOS
No longer licensed: cancelled
Licence status Cancelled; first licensed May 6, 2002; ended June 2, 2017. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 37912
- Licence holder
- Siemens AgMuenchen, Germany
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Family
- First licensed
- May 6, 2002
- Ended
- June 2, 2017
- Devices covered
- 18
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- AXIOM ARISTOS DX - FD DETECTOR
- AXIOM ARISTOS FX
- AXIOM ARISTOS FX - CEILING RAILS
- AXIOM ARISTOS FX - CEILING SUPPORT
- AXIOM ARISTOS FX - COLLIMATOR
- AXIOM ARISTOS FX - COMPONENT RADIS
- AXIOM ARISTOS FX - GENERATOR
- AXIOM ARISTOS FX - KEYBOARD
- AXIOM ARISTOS FX - SYSTEM PARTS
- AXIOM ARISTOS FX - SYSTEM SOFTWARE
- AXIOM ARISTOS FX - SYSTEM STAND
- AXIOM ARISTOS FX - TABLE
- AXIOM ARISTOS FX - X-RAY TUBE
- AXIOM ARISTOS FX - X-RAY TUBE PARTS INCL. GRID
- AXIOM ARISTOS FX PLUS
- AXIOM ARISTOS MX
- AXIOM ARISTOS TX
- AXIOM ARISTOS VX
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.