Medical device licence · 30048 · Class 3
ALOKA PROBES
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed June 11, 2001; ended November 21, 2023. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 30048
- Licence holder
- Fujifilm Healthcare CorporationKashiwa-Shi, Japan
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Family
- First licensed
- June 11, 2001
- Ended
- November 21, 2023
- Devices covered
- 8
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- COMBINATION TRANDUCERS
- CONVEX TRANSDUCER
- LINEAR TRANSDUCER
- MECHANICAL TRANSDUCER
- PHASED ARRAY TRANSDUCERS
- SINGLE BEAM TRANSDUCER
- TRANSESOPHAGEAL TRANSDUCERS
- VOLUME MODE TRANSDUCERS
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 “aloka”. A notice may cover another product or only some lots: read it to see what it covers.
- ALOKA ARIETTA 850November 19, 2021 · Obstetrics and gynaecology · Inaccurate test or measurement results · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.