Medical device licence · 14049 · Class 2
VERTIX
No longer licensed: cancelled
Licence status Cancelled; first licensed November 5, 1999; ended June 2, 2017. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 14049
- Licence holder
- Siemens AgMuenchen, Germany
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Family
- First licensed
- November 5, 1999
- Ended
- June 2, 2017
- Devices covered
- 9
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- AXIOM VERTIX MD TRAUMA
- VERTIX
- VERTIX 3D-III
- VERTIX BRS
- VERTIX FD
- VERTIX PRO
- VERTIX SOLITAIRE
- VERTIX TOP
- VERTIX UM
Recalls and safety alerts that mention it
Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “vertix”. A notice may cover another product or only some lots: read it to see what it covers.
- AXIOM Vertix and AXIOM MultixJune 14, 2024 · Radiology · Performance · Type II
- Axiom Vertix MD Trauma (2014-03-05)April 4, 2014 · Medical devices · Medical devices · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.