Medical device licence · 14962 · Class 4
INTERSTIM SYSTEM
Yes: licensed in Canada
Licence status Issued (active); first licensed December 2, 1999. It is in Health Canada’s list of active licences.
- Licence number
- 14962
- Licence holder
- Medtronic Inc.Minneapolis, MN, United States
- Risk class
- Class IV (highest risk)
- Licence type
- System
- First licensed
- December 2, 1999
- Devices covered
- 9
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- INTERSTIM SYSTEM - ANTENNA
- INTERSTIM SYSTEM - ICON PATIENT PROGRAMMER
- INTERSTIM SYSTEM - INTERSTIM IMPLANTABLE STIMULATOR
- INTERSTIM SYSTEM - MEMORY MODULE SOFTWARE
- INTERSTIM SYSTEM - PATIENT PROGRAMMER
- INTERSTIM SYSTEM - TEMPORARY PERIPHERAL NERVE EVALUATION KIT
- INTERSTIM SYSTEM - TEMPORARY TEST STIMULATION LEAD
- TEST STIMULATION LEAD
- TEST STIMULATION LEAD KIT
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 “interstim”. A notice may cover another product or only some lots: read it to see what it covers.
- InterStim™ SystemsSeptember 24, 2026 · Gastroenterology and urology · Device compatibility · Type II
- Interstim Percutaneous ExtensionJanuary 24, 2022 · Gastroenterology and urology · Increased risk or new adverse events · Type II
- INTERSTIM SYSTEM - TEMPORARY PERIPHERAL NERVE EVALUATION KIT (2016-02-19)March 29, 2016 · Medical devices · Medical devices · Type III
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.