Medical device licence · 69222 · Class 4
PRO SPACE DBM (PUTTY OR GEL)
No longer licensed: cancelled
Licence status Cancelled; first licensed September 9, 2005; ended December 6, 2017. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 69222
- Licence holder
- Aesculap Implant Systems, LlcCenter Valley, PA, United States
- Risk class
- Class IV (highest risk)
- Licence type
- Device Family
- First licensed
- September 9, 2005
- Ended
- December 6, 2017
- Devices covered
- 2
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- PROSPACE DBM GEL
- PROSPACE DBM PUTTY
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.