ApprovalTrail

Medical device licence · 8258 · Class 2

GUIDE WIRES

No longer licensed: cancelled

Licence status Cancelled; first licensed July 19, 1999; ended June 11, 2021. It is in Health Canada’s archive of licences no longer in force.
Licence number
8258
Licence holder
Angiomed Gmbh & Co. Medizintechnik KgKarlsruhe, 08, Germany
Risk class
Class II (low to moderate risk)
Licence type
Device Group Family
First licensed
July 19, 1999
Ended
June 11, 2021
Devices covered
3

Devices on this licence

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

  • GUIDEWIRE, TEFLON COATED
  • INTERVENTIONAL GUIDE WIRE
  • PORTA CAVAL INTRODUCER SET

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