New Zealand - English - Ministry for Primary Industries

zoetis new zealand limited - canine parvovirus (attenuated); canine parainfluenza virus (attenuated); canine adenovirus type 2 (attenuated); canine distemper virus (attenuated) - canine parvovirus (attenuated) 0 vaccine; canine parainfluenza virus (attenuated) 0 vaccine; canine adenovirus type 2 (attenuated) 0 vaccine; canine distemper virus (attenuated) 0 vaccine - vaccine

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - direct compression moulded uhmwpe arcom posterior stabilised tibial bearing size 59. allows 15 degrees internal/external rotation and no varus/valgus constraint. deep anterior relief to accommodate patella tendon during high flexion direct compression moulded uhmwpe arcom posterior stabilised tibial bearing component of vanguard ssk 360 revision knee system. indications for use: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus, or post-traumatic deformity; correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

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

zimmer biomet pty ltd - 32831 - uncoated knee femur prosthesis - cobalt chrome femoral component with five design features: rounded sagittal profile; deeper/swept back trochlear groove; extended trochlear groove; wider proximal trochlear groove; ten femoral sizes. extended cam for increased resistance to dislocation in deep flexion. femoral component accepts a variety of stem options and offset adapters. packaged with ti alloy screw; for cemented use. cobalt chrome alloy femoral component of vanguard ssk 360/da 360 revision knee system. indications for use: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus, or post-traumatic deformity; correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - direct compression moulded uhmwpe arcom posterior stabilised constrained tibial bearing size 59. allows for 0.5 degrees of internal/external rotation and 1 degree of varus/valgus lift off. large swept back tibial post to provide stability and continued constraint in deep flexion. large tibial post maintains increased post/box contact. at 90 degrees of flexion, 17 mm of the post remains in the box. direct compression moulded uhmwpe arcom posterior stabilised constrained tibial bearing component of vanguard ssk 360 revision knee system. indications for use: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus, or post-traumatic deformity; correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure

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

zimmer biomet pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - cobalt chrome tibial component with finned stem for enhanced rotational stability, and highly polished surface finish to reduce the risk of undersurface wear. designed for use as a component of a rotating platform total knee prosthesis; titanium end cap may be removed to facilitate use with modular stem options. trays increase medio-laterally in 4mm increments. lnterlok finish designed for cemented use cobalt chrome and titanium alloy tibial component of the vanguard rocc rotating platform total knee prosthesis. indications for use: osteoarthritis, rheumatoid arthritis and bone necrosis affecting two knee compartments; correction of genu varus, genu valgus or post-traumatic deformities; sequelae of prior procedures. the device is intended for cemented fixation.

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - the tibial bearing is constructed of e1 antioxidant infused direct compression moulded uhmwpe and articulates with the femoral and tibial tray components. the posterior stabilised standard bearing does not constrain the femur in rotation or varus/valgus lift-off. the vanguard e1 posterior stabilised uhmwpe tibial bearing is intended for use in conjunction with biomet tibial trays in both primary and revision applications, with or without bone cement. the indications for use: 1. painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis and/or 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.

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - the tibial bearing is constructed of e1 antioxidant infused direct compression moulded uhmwpe and articulates with the femoral and tibial tray components. the bearing provides for 15 degrees internal/external rotation, no varus/valgus constraint and includes an enhanced posterior lip. the vanguard e1 cruciate retaining lipped uhmwpe tibial bearing is intended for use in conjunction with biomet tibial trays in both primary and revision applications, with or without bone cement. the indications for use: 1. painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis and/or 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.

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - e1 antioxidant infused uhmwpe tibial bearing. tibial/femoral coronal conformity ratio 1.25:1. medial and lateral bearings designed independently, allowing acl/pcl interaction to drive knee motion. the vanguard xp-xp tibial bearing is intended for use as part of the vanguard xp knee system, for use with vanguard xp-xp or xp-cr tibial tray. indications for use include: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus or post-traumatic deformity; correction of revision of unsuccessful osteotomy, arthrodesis or failure of previous joint replacement procedure. made of e1 antioxidant infused uhmwpe.

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - e1 antioxidant infused uhmwpe tibial bearing, used for an intact, partially functioning pcl. tibial/femoral coronal conformity ratio 1:1. symmetric medial and lateral articulations. the vanguard xp-as tibial bearing right medial/left lateral is intended for use as part of the vanguard xp knee system, for use with vanguard xp-xp or xp-cr tibial tray. indications for use include: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus or post-traumatic deformity; correction of revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. made of e1 antioxidant infused uhmwpe.

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - e1 antioxidant infused uhmwpe tibial bearing, for use with intact, partially functioning pcl. tibial/femoral coronal conformity ratio 1:1. symmetric medial and lateral articulations. the vanguard xp anterior stabilised (as) tibial bearing left medial/right lateral is intended for use as part of the vanguard xp knee system, for use with vanguard xp-xp or xp-cr tibial tray. indications for use include: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus or post-traumatic deformity; correction of revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. made of e1 antioxidant infused uhmwpe.