Medical device licence · 101333 · Class 2
MYOTECH DRY NEEDLES
No longer licensed: suspended: invalid quality-system certificate
Licence status Suspended: invalid quality-system certificate; first licensed June 29, 2018; ended November 30, 2020. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 101333
- Licence holder
- Suzhou Fanhao Medical Instrument Co., Ltd.Suzhou, 100, China
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Family
- First licensed
- June 29, 2018
- Ended
- November 30, 2020
- Devices covered
- 10
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- MYOTECH DRY NEEDLES
- MYOTECH DRY NEEDLES - 2.0
- MYOTECH DRY NEEDLES - HIGH VIS
- MYOTECH DRY NEEDLES - SIX SERIES
- MYOTECH ECO DRY NEEDLES
- RED CORAL PREMIUM DRY NEEDLES - MYOTECH DRY NEEDLES
- RED CORAL PREMIUM DRY NEEDLES - MYOTECH DRY NEEDLES 2.0
- RED CORAL PREMIUM DRY NEEDLES - MYOTECH DRY NEEDLES HIGH VIS
- RED CORAL PREMIUM DRY NEEDLES - MYOTECH DRY NEEDLES SIX SERIES
- RED CORAL PREMIUM DRY NEEDLES - MYOTECH ECO DRY NEEDLES
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.