Nový Zéland - angličtina - Ministry for Primary Industries

boehringer ingelheim animal health new zealand limited - abamectin; praziquantel - abamectin 4 g/litre; praziquantel 50 g/litre - endoparasiticide

Nový Zéland - angličtina - Ministry for Primary Industries

boehringer ingelheim animal health new zealand limited - abamectin - abamectin 1 g/litre - endoparasiticide

Nový Zéland - angličtina - Ministry for Primary Industries

boehringer ingelheim animal health new zealand limited - abamectin; praziquantel - abamectin 1 g/litre; praziquantel 18.8 g/litre - endoparasiticide

Nový Zéland - angličtina - Ministry for Primary Industries

boehringer ingelheim animal health new zealand limited - hydroxocobalamin; abamectin - hydroxocobalamin 2 g/litre; abamectin 10 g/litre - parenteral nutrient/electrolyte

Nový Zéland - angličtina - Ministry for Primary Industries

boehringer ingelheim animal health new zealand limited - closantel as the sodium salt; abamectin - closantel as the sodium salt 50 g/litre; abamectin 1 g/litre - endoparasiticide

Nový Zéland - angličtina - Ministry for Primary Industries

boehringer ingelheim animal health new zealand limited - triclabendazole; abamectin - triclabendazole 300 g/litre; abamectin 5 g/litre - endoparasiticide

Nový Zéland - angličtina - Ministry for Primary Industries

boehringer ingelheim animal health new zealand limited - abamectin; cobalt; selenium present as sodium selenate; closantel as the sodium salt - abamectin 1 g/litre; cobalt 15.71 g/litre; selenium present as sodium selenate 0.5 g/litre; closantel as the sodium salt 50 g/litre - endoparasiticide

Nový Zéland - angličtina - Ministry for Primary Industries

boehringer ingelheim animal health new zealand limited - vitamin b12; selenium present as sodium selenate; abamectin - vitamin b12 2 g/litre; selenium present as sodium selenate 4 g/litre; abamectin 10 g/litre - endoparasiticide

Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

smith & nephew pty ltd - 33745 - coated knee femur prosthesis - a cocr femoral component with open box design to replace the femoral condyles during knee joint replacement. the device articulates with a posterior stabilised (ps) tibial insert and, if required, patellar prosthetic components of the knee joint. the internal surface of the femoral component has a sintered cocr bead and hydroxyapatite coating. flex-lok pegs or finned lugs may be added for stability and increased pullout strength. it is intended to be used without bone cement the genesis ii ha coated porous posterior stabilised femoral is a cobalt-chrome alloy component of the genesis ii total knee system, intended for uncemented use. indications for use include rheumatoid arthritis; post-traumatic arthritis, osteoarthritis, or degenerative arthritis; failed osteotomies, unicompartmental replacement or total knee replacement. posterior stabilised knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact.

Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

smith & nephew pty ltd - 34198 - coated knee tibia prosthesis - a sterile implantable device to replace tibial condyles of the knee joint. the titanium tibial base is designed to hold an insert which articulates with a cruciate retaining, posterior stabilised, or constrained femoral, dependent on the insert choice. the porous baseplate incorporates fins, spikes, and screws for increased fixation. the porous surface of the tibial tray has a sintered bead coating and a coating of non-animal derived ha. it is intended to be used without cement. a porous ha coated titanium alloy tibial baseplate component used in conjunction with the genesis ii total knee system. indications for use include rheumatoid arthritis; post-traumatic arthritis, osteoarthritis, or degenerative arthritis; failed osteotomies, unicompartmental replacement or total knee replacement. posterior stabilised knee systems are designed for use in patients in primary and revision surgery, where the anterior and posterior cruciate ligaments are incompetent and the collateral ligaments remain intact.