Australia - English - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 33745 - coated knee femur prosthesis - replaces femoral articular surface of knee joint. rounded sagittal profile; deeper, swept-back trochlear groove; longer trochlear groove; wide proximal trochlear groove; variables improve lateral release rates, extensor moment arm, patella alignment, patella tracking; reduce patella tendon irritation potential. removable lugs for posterior, distal augment options; articulates with one of 3 cr pe tibial inserts and if required, patella component. porous ha finish for cementless application chrome/cobalt/molybdenum alloy cruciate retaining femoral component, with porous and hydroxyapetite coating, for use in knee joint replacement due to: osteoarthritis, rheumatoid arthritis or traumatic arthritis; failure of a previous joint replacement procedure; correction of varus, valgus or post-traumatic deformity; correction or revision of unsuccessful osteotomy or arthrodesis. porous coated devices are indicated for non-cemented use.

Australia - English - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 32831 - uncoated knee femur prosthesis - posterior stabilised interlok finish femoral component for use in total knee arthroplasty. accommodates distal and posterior augment options, with closed box design this component must be used with a tibial tray component and one of 2 posterior stabilized bearing options. chrome/cobalt/molybdenum alloy interlok finish closed box femoral component for use in knee joint replacement due to 1) painful, and disabled joint resulting from avascular necrosis, arthritis (all types) where one or more compartments are involved 2) correction of varus, valgus, or posttraumatic deformity 3) correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. the posterior stabilised femoral component is designed for use where the posterior cruciate ligament requires substitution. the interlok finish is designed for use with bone cement.

Australia - English - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 32831 - uncoated knee femur prosthesis - posterior stabilised interlok finish femoral component for use in total knee arthroplasty. accommodates distal and posterior augment options. open box design allows for additional preservation of distal bone. this component must be used with a tibial tray component and one of 2 posterior stabilized bearing options. chrome/cobalt/molybdenum alloy interlok finish open box femoral component for use in knee joint replacement due to 1) painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved 2) correction of varus, valgus, or posttraumatic deformity 3) correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure the posterior stabilised femoral component is designed for use where the posterior cruciate ligament requires substitution. the interlok finish is designed for use with bone cement.

Australia - English - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 33745 - coated knee femur prosthesis - posterior stabilised porous coated femoral component for use in total knee arthroplasty. accommodates distal and posterior augment options. open box design allows for additional preservation of distal bone. this component must be used with a tibial tray component and one of 2 posterior stabilised bearing options. chrome/cobalt/molybdenum alloy open box femoral component for use in knee joint replacement due to 1) painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved 2) correction of varus, valgus, or posttraumatic deformity 3) correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure the posterior stabilised femoral component is designed for use where the posterior cruciate ligament requires substitution. the porous finish is designed for cementless use.

Australia - English - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 33745 - coated knee femur prosthesis - cruciate retaining porous coated femoral component for use in total knee arthroplasty. the cr femoral component has removable lugs to allow for posterior and distal augment options. this component must be used with a tibial tray component and one of 3 cruciate retaining bearing options. chrome/cobalt/molybdenum alloy cruciate retaining femoral component for use in knee joint replacement due to 1) painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved 2) correction of varus, valgus, or posttraumatic deformity 3) correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure the porous coated device is intended for uncemented use.

Australia - English - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 32831 - uncoated knee femur prosthesis - cruciate retaining interlok finish femoral component for use in total knee arthroplasty. the cr femoral component has removable lugs to allow for posterior and distal augment options. this component must be used with a tibial tray component and one of 3 cruciate retaining bearing options. chrome/cobalt/molybdenum alloy cruciate retaining femoral component for use in knee joint replacement due to 1) painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved 2) correction of varus, valgus, or posttraumatic deformity 3) correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure the interlok finish is designed for use with bone cement.

Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

conquest crop protection pty ltd - cypermethrin; triadimenol - suspension concentrates for seed treatment (fs) - cypermethrin pyrethroid active 4.0 g/l; triadimenol triazole active 150.0 g/l - mixed function seed treat - barley | oats | wheat - bunt | covered smut (bunt) - tilletia spp. | flag smut on cereal | granary weevil | indian meal moth | leaf scald - suppression | lesser grain borer | loose smut - ustilago avenae | powdery mildew | powdery mildew - suppression | rice weevil | rust-red flour beetle | sawtoothed grain beetle | speckled leaf blotch - suppression | stripe rust - suppression | tropical warehouse moth | bunt | common bunt | grain borer | seedborne flag smut | seedling infections | soilborne flag smut | trilletia tritici | ustilago nuda (tritici)

Singapore - English - HSA (Health Sciences Authority)

zimmer pte. ltd. - orthopaedics - 1. painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved. 2. correction of varus, valgus, or posttraumatic deformity. 3. correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. the regenerex femoral augments are indicated for use with the vanguard total knee system. the regenerex tibial augments are indicated for use with standard and offset biomet tibial trays. femoral components and tibial tray components with porous coatings are indicated for cemented and uncemented biological fixation application. non-coated (interlok) femoral components, tibial tray components and all polyethylene patellar components are indicate-d for cemented application only. regenerex and osseoti components are intended only for uncemented biologic fixation application.

Germany - English - HMA (Heads of Medicines Agencies)

vita (europe) limited - thymol 12.5 g - gel - bees - thymol