Medical device licence · 71781 · Class 2
REFA PHYSIOLOGICAL AMPLIFIER
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed June 28, 2006; ended October 28, 2018. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 71781
- Licence holder
- Twente Medical Systems International B.V.Oldenzaal, Netherlands
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Family
- First licensed
- June 28, 2006
- Ended
- October 28, 2018
- Devices covered
- 16
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- B_HOLTER
- CINDI
- MOBI5
- MOBI6
- MOBI8
- NEXUS-10
- NEXUS-10 MARK II
- NEXUS-32F
- NEXUS-4
- NEXUS-XX
- PORTI7
- QUICKAMP-136
- QUICKAMP-40
- QUICKAMP-XX
- REFA8
- REFA_EXT
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.