Medical device licence · 92152 · Class 3
AQUILION TSX-101A_/T
No longer licensed: cancelled
Licence status Cancelled; first licensed October 23, 2013; ended March 11, 2025. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 92152
- Licence holder
- Canon Medical Systems CorporationOtawara-Shi, Japan
- Risk class
- Class III (moderate to high risk)
- Licence type
- System
- First licensed
- October 23, 2013
- Ended
- March 11, 2025
- Devices covered
- 16
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- AQUILION TSX-101A_/T - CONSOLE
- AQUILION TSX-101A_/T - DAS/DETECTOR
- AQUILION TSX-101A_/T - DISPLAY CONSOLE KIT
- AQUILION TSX-101A_/T - FAST IMAGE RECONSTRUCTION SYSTEM
- AQUILION TSX-101A_/T - GANTRY
- AQUILION TSX-101A_/T - INJECTOR SYNCHRONIZATION SYSTEM
- AQUILION TSX-101A_/T - LCD MONITOR FOR SUREFLUORO
- AQUILION TSX-101A_/T - MAIN UNIT
- AQUILION TSX-101A_/T - SOFTWARE
- AQUILION TSX-101A_/T - SOFTWARE OPTIONS
- AQUILION TSX-101A_/T - SURE CARDIO PROSPECTIVE
- AQUILION TSX-101A_/T - SUREFLUORO
- AQUILION TSX-101A_/T - SYSTEM TRANSFORMER
- AQUILION TSX-101A_/T - X-RAY GENERATOR
- AQUILION TSX-101A_/T - X-RAY HIGH VOLTAGE GENERATOR
- AQUILION TSX-101A_/T - X-RAY TUBE
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 “aquilion”. A notice may cover another product or only some lots: read it to see what it covers.
- Aquilion ONE Vision, Aquilion PRIME (2019-02-19)March 8, 2019 · Medical devices · Medical devices · Type II
- AQUILION PRIME MULTISLICE HELICAL CT SCANNEROctober 6, 2016 · Medical devices · Medical devices · Type II
- Aquilion One System (2015-06-11)July 9, 2015 · Medical devices · Health products · Type II
- AQUILION ONE SYSTEM (2015-01-06)April 13, 2015 · Medical devices · Health products · Type II
- Aquilion ONE System - Software (2014-08-12)September 9, 2014 · Medical devices · Medical devices · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.