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 It is in Health Canada’s archive of licences no longer in force.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.