Medical device licence · 91330 · Class 2
FLEXOR VUE DEFLECTING ENDOSCOPIC SYSTEM
No longer licensed: cancelled
Licence status Cancelled; first licensed May 15, 2013; ended December 10, 2020. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 91330
- Licence holder
- Cook, IncorporatedBloomington, IN, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- System
- First licensed
- May 15, 2013
- Ended
- December 10, 2020
- Devices covered
- 3
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- FLEXOR 180 DEFLECTING URETERAL ACCESS SHEATH
- FLEXOR VUE DEFLECTING ENDOSCOPIC SYSTEM
- VUEOPTIC VISUALIZATION SOURCE
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 “flexor”. A notice may cover another product or only some lots: read it to see what it covers.
- Flexor® Check-Flo Introducer and Rösch-Uchida Transjugular Liver Access SetsDecember 3, 2025 · Cardiovascular - General and plastic surgery · Performance · Type II
- FLEXOR TOUHY-BORST SIDE-ARM INTRODUCER (SHUTTLE SEECT) & FLEXOR CHECK-FLO INTRODUCER (2020-11-25)December 24, 2020 · Medical devices · Medical devices · Type II
- FLEXOR CHECK-FLO INTRODUCER (2017-09-08)October 6, 2017 · Medical devices · Medical devices · Type III
- Holmium Laser Fiber, Flexor Vue Deflecting Endoscopic System, and Vueoptic Visulation Source (2017-04-24)June 7, 2017 · Medical devices · Medical devices · Type II
- Flexor RTPS Guiding Sheath (2015-06-09)July 8, 2015 · Medical devices · Health products · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.