Medical device licence · 738 · Class 4
VENTAK MINI AICD
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed January 18, 1999; ended October 26, 2021. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 738
- Licence holder
- Boston Scientific CorporationWatertown, MA, United States
- Risk class
- Class IV (highest risk)
- Licence type
- Single Device
- First licensed
- January 18, 1999
- Ended
- October 26, 2021
- Devices covered
- 9
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- DF-1 PLUG
- SOFTWARE APPLICATION MODEL 2840 VERSION 3.2
- SOFTWARE APPLICATION MODEL 2840 VERSION 4.0
- VENTAK MINI HE AICD - IMPLANTABLE CARDIOVERTOR DEFIBRILLATOR
- VENTAK MINI III AICD - IMPLANTABLE CARDIOVERTOR DEFIBRILLATOR
- VENTAK MINI III HE - IMPLANTABLE CARDIOVERTOR DEFIBRILLATOR
- VENTAK MINI IV - IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
- VENTAK MINI+ AICD -IMPLANTABLE CARDIOVERTOR DEFIBRILLATOR
- VENTAK MINIAICD SOFTWARE
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.