Medical device licence · 21204 · Class 3
CENTERING SLEEVE - PMMA
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed June 8, 2000; ended October 30, 2019. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 21204
- Licence holder
- Biomet Orthopedics, Ata Biomet Sports Medicine, Ata Biomet Biologics, Ata Biomet TraumaWarsaw, IN, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Family
- First licensed
- June 8, 2000
- Ended
- October 30, 2019
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- FEMORAL CENTERING SLEEVE
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 “centering”. A notice may cover another product or only some lots: read it to see what it covers.
- Compress Device Centering Sleeve, Compress Device and Compress Device Short Anti-Rotation Spindle, Anti-Rotation Elliptical Spindle, and Compress Instrument Drill for Anti-Rotation Pin (2018-12-13)January 9, 2019 · Medical devices · Medical devices · Type III
- Compress Device Centering Sleeve, Anti-Rotation Spindle, Anti-Rotation Elliptical Spindle, and Compress Instrument Drill for Anti-Rotation Pin (2018-10-22)November 2, 2018 · Medical devices · Medical devices · Type III
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.