Medical device licence · 25239 · Class 3
DOUBLE LOOP URETERAL STENT
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed November 10, 2000; ended October 20, 2008. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 25239
- Licence holder
- Coloplast Manufacturing France SasLe Plessis-Robinson, France
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Group Family
- First licensed
- November 10, 2000
- Ended
- October 20, 2008
- Devices covered
- 4
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- DOUBLE LOOP STENT IN BIOSOFT - POLYURETHANE
- DOUBLE LOOP STENT IN POLYURETHANE
- DOUBLE LOOP STENT IN SILICONE
- DOUBLE LOOP STENT IN VORTEK
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.