ApprovalTrail

Medical device licence · 17003 · Class 4

MEMOTHERM AORTIC STENT

No longer licensed: cancelled

Licence status Cancelled; first licensed February 22, 2000; ended May 25, 2009. It is in Health Canada’s archive of licences no longer in force.
Licence number
17003
Licence holder
Angiomed Gmbh & Co. Medizintechnik KgKarlsruhe, Germany
Risk class
Class IV (highest risk)
Licence type
Single Device
First licensed
February 22, 2000
Ended
May 25, 2009
Devices covered
1

Devices on this licence

By name, as listed. The official record lists model numbers and identifiers.

  • MEMOTHERM AORTIC STENT

Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.