Medical device licence · 60264 · Class 3
ENTERRA THERAPY SYSTEM
No longer licensed: cancelled
Licence status Cancelled; first licensed August 16, 2002; ended August 5, 2025. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 60264
- Licence holder
- Medtronic Inc.Minneapolis, MN, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- System
- First licensed
- August 16, 2002
- Ended
- August 5, 2025
- Devices covered
- 4
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- ENTERRA II
- ENTERRA THERAPY IMPLANTABLE PULSE GENERATOR (IPG)
- ENTERRA THERAPY PROGRAMMER
- ENTERRA THERAPY PROGRAMMER SOFTWARE
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 “enterra”. A notice may cover another product or only some lots: read it to see what it covers.
- Itrel 3 System and Enterra Therapy Implantable Pulse Generator (IPG), and InterStim system - InterStim Implantable Stimulator (2015-01-08)January 21, 2015 · Medical devices · Health products · Type III
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.