Medical device licence · 67714 · Class 3
PS DE REVISION
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed March 10, 2005; ended December 9, 2025. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 67714
- Licence holder
- Lok Qualit Inc.Laval, QC, Canada
- Risk class
- Class III (moderate to high risk)
- Licence type
- System
- First licensed
- March 10, 2005
- Ended
- December 9, 2025
- Devices covered
- 28
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- BOUTON ROTULIEN MONOBLOC CIMENTE
- EMBASE TIBIALE CIMENTEE
- EVOLUTION SYSTEME DE GENOU - PLATEAUX TIBIAUX PS - UHMWPE
- EXTENSION TIBIALE
- HERMES EVOLUTION SYSTEME DE GENOU - BOUTON ROTULIEN MONOBLOC - UHMWPE
- HERMES EVOLUTION SYSTEME DE GENOU - CALES FEMORALES DISTALES
- HERMES EVOLUTION SYSTEME DE GENOU - CALES FEMORALES POSTERIEURES
- HERMES EVOLUTION SYSTEME DE GENOU - COMPOSANTS FEMORAUX DE REPRISE
- HERMES EVOLUTION SYSTEME DE GENOU - EMBASES TIBIALES POSTERO-STABILISEES
- HERMES EVOLUTION SYSTEME DE GENOU - PLATEAUX TIBIAUX PS - UHMWPE
- HERMES EVOLUTION SYSTEME DE GENOU - RALLONGE TIBIALE - TIAL6V4
- HERMES EVOLUTION SYSTEME DE GENOU - TIGES FEMORALES DISTALES
- HERMES EVOLUTION SYSTEME DE GENOU - VIS POUR FIXATION DES PLATEAUX TIBIAUX
- HERMES EVOLUTION SYSTEME DE GENOU - VIS POUR FIXATION RALLONGE TIBIALE
- HERMES PS DE REVISION - CALE FEMORALE DISTALE
- HERMES PS DE REVISION - CALE FEMORALE POSTERIEURE
- HERMES PS DE REVISION - COMPOSANT FEMORAL CIMENTE
- HERMES PS DE REVISION - EXTENSION FEMORALE
- HIFIT/HERMES - EMBASE TIBIALE CIMENTEE
- HIFIT/HERMES - VIS POUR RALLONGE TIBIALE
- HIFIT/HERMES/CERAGYR - BOUTON ROTULIEN MONOBLOC CIMENTE
- HIFIT/HERMES/CERAGYR - EXTENSION TIBALE
- PS DE REVISION - CALE FEMORALE DISTALE
- PS DE REVISION - CALE FEMORALE POSTERIEURE
- PS DE REVISION - COMPOSANT FEMORAL CIMENTE
- PS DE REVISION - EXTENSION FEMORALE
- VIS POUR FIXATION DES CALES FEMORALES
- VIS POUR RALLONGE TIBIALE
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.