Medical device licence · 26018 · Class 3
LACTOSORB ARTHRORIVET SYSTEMS
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed December 1, 2000; ended October 31, 2019. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 26018
- Licence holder
- Biomet Sports MedicineRedding, CA, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Group Family
- First licensed
- December 1, 2000
- Ended
- October 31, 2019
- Devices covered
- 6
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- ARTHRORIVET LACTOSORB RESORBABLE COPOLYMER
- CANNULATED RESORBABLE ARTHRORIVET
- CANNULATED RESORBABLE RC ARTHRORIVET
- POP RIVET LACTOSORB RESORBABLE COPOLYMER
- RC ARTHRORIVET
- RC POP RIVET
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 “lactosorb”. A notice may cover another product or only some lots: read it to see what it covers.
- Various LactoSorb System Implants (2020-10-30)December 11, 2020 · 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.