Medical device licence · 10077 · Class 3
ALLOFIT CUP SYSTEM
No longer licensed: cancelled
Licence status Cancelled; first licensed September 1, 1999; ended June 18, 2020. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 10077
- Licence holder
- Zimmer Inc.Winterthur, SZ, Switzerland
- Risk class
- Class III (moderate to high risk)
- Licence type
- System
- First licensed
- September 1, 1999
- Ended
- June 18, 2020
- Devices covered
- 10
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- ALLOFIT CUP SYSTEM - ALLOFIT ALLOCLASSIC PLUGS
- ALLOFIT CUP SYSTEM - ALLOFIT HOODED PE INSERT
- ALLOFIT CUP SYSTEM - ALLOFIT STANDARD PE INSERT
- ALLOFIT CUP SYSTEM - ALLOFIT TITANIUM SHELL
- ALLOFIT CUP SYSTEM - ALLOFIT-S TITANIUM SHELL
- ALLOFIT CUP SYSTEM - ALLOFIT-S+
- ALLOFIT CUP SYSTEM - ALPHA DURASUL HOODED INSERT
- ALLOFIT CUP SYSTEM - ALPHA DURASUL STANDARD INSERT
- ALLOFIT CUP SYSTEM - ALPHA HOODED INSERT WITH METASUL INLAY
- ALLOFIT CUP SYSTEM - ALPHA INSERT WITH METASUL INLAY
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 “allofit”. A notice may cover another product or only some lots: read it to see what it covers.
- CUSTOM TRILOGY STYLE ALLOFIT IT INSERTER (2015-11-24)January 14, 2016 · Medical devices · Health products · Type III
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.