Medical device licence · 91264 · Class 2
DUOFLEX COIL SUITE
No longer licensed: suspended: invalid quality-system certificate
Licence status Suspended: invalid quality-system certificate; first licensed May 6, 2013; ended July 29, 2019. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 91264
- Licence holder
- Mr Instruments, Inc.Minnetonka, MN, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Group Family
- First licensed
- May 6, 2013
- Ended
- July 29, 2019
- Devices covered
- 2
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- DUOFLEX INTERVENTIONAL SUITE
- DUOFLEX SUITE
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.