GENESIS ULTRA INJECTION BROAD SPECTRUM ANTIPARASITIC FOR CATTLE Austrálie - angličtina - APVMA (Australian Pesticides and Veterinary Medicines Authority)

genesis ultra injection broad spectrum antiparasitic for cattle

boehringer ingelheim animal health australia pty. ltd. - clorsulon; ivermectin - parenteral liquid/solution/suspension - clorsulon ungrouped active 100.0 mg/ml; ivermectin anthelmintic active 10.0 mg/ml - parasiticides - cattle - beef | bovine | bullocks | bulls | calves | cows | feedlot cattle | growers | heifer speyed | heifers (meat only) | pod - barber's pole worm - haemonchus spp. | cattle biting louse | cattle tick | eyeworm - thelazia spp. | hookworm - bunostomum phlebotomum | intestinal hair worm - t. colubriformis | intestinal threadworm - s. papillosus | large bowel worm - oesophagostomum spp. | liver fluke | longnosed cattle louse | lungworm - dictyocaulus viviparus | mange mite - s. scabiei var. bovis | screw worm fly - chrysomya bezziana | shortnosed cattle louse | small brown stomach worm - o. ostertagi | small intestinal worm - cooperia spp. | stomach hair worm | thin necked intestinal worm | tubercle-bearing louse | whipworm - trichuris spp. | black scour worm | cattlebiting louse | damalinia bovis (old name) | including inhibited stages | large lungworm | little blue sucking louse | long-nosed sucking louse | pole worm | screw worm fly - larval stages | short nosed sucking louse

GENESIS DRENCH ORAL ANTIPARASITIC FOR SHEEP Austrálie - angličtina - APVMA (Australian Pesticides and Veterinary Medicines Authority)

genesis drench oral antiparasitic for sheep

boehringer ingelheim animal health australia pty. ltd. - ivermectin - oral paste - ivermectin anthelmintic active 1.0 g/l - parasiticides - sheep | ewe | hogget | lamb | ovine | ram | weaner | wether - barber's pole worm - haemonchus placei | black scour worm - trichostrongylus spp. | intestinal threadworm - s. papillosus | large bowel worm - o. venulosum | large mouthed bowel worm | lungworm | nasal bot - parasitic larval stage | nodule worm - oesophagostomum spp. | sheep itch mite | small brown stomach worm-ostertagia spp. | small intestinal worm - cooperia spp. | stomach hair worm | thin necked intestinal worm-n. spathiger | whipworm - trichuris vulpis | hair worm | intestinal hair worm | psorobia ovis | sheep nasal bot fly | small hair worm | teladorsagia | thin necked intestinal worm-ad

GENESIS XTRA DRENCH ORAL BROAD SPECTRUM ANTIPARASITIC FOR SHEEP WITH BARBERS POLE LONG ACTION Austrálie - angličtina - APVMA (Australian Pesticides and Veterinary Medicines Authority)

genesis xtra drench oral broad spectrum antiparasitic for sheep with barbers pole long action

boehringer ingelheim animal health australia pty. ltd. - abamectin; closantel - oral solution/suspension - abamectin anthelmintic active 1.0 g/l; closantel anthelmintic active 50.0 g/l - parasiticides - sheep | ewe | hogget | lamb | ovine | ram | weaner | wether - black scour worm - trichostrongylus spp. | intestinal threadworm - s. papillosus | large bowel worm - o. venulosum | large lungworm - dictyocaulus filaria | large mouthed bowel worm | liver fluke | nasal bot | nodule worm - o. columbianum | ostertagia circumcincta | sheep itch mite | small intestinal worm - cooperia spp. | stomach hair worm | thin necked intestinal worm | whipworm - trichuris ovis | hair worm | intestinal hair worm | psorobia ovis | sheep nasal bot fly | small brown stomach worm | small hair worm

GENESIS II HA Coated Porous Posterior Stabilized Femoral - Coated knee femur prosthesis Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

genesis ii ha coated porous posterior stabilized femoral - coated knee femur prosthesis

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.

Genesis II HA Porous Tibial Base - Coated knee tibia prosthesis Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

genesis ii ha porous tibial base - coated knee tibia prosthesis

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.

Genesis II Cruciate Retaining HA Porous Femoral Component - Coated knee femur prosthesis Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

genesis ii cruciate retaining ha porous femoral component - coated knee femur prosthesis

smith & nephew pty ltd - 33745 - coated knee femur prosthesis - a sterile implantable device designed to replace the femoral condyles during knee joint replacement. the device articulates with cruciate retaining tibial inserts and, if required, patellar prosthetic components of the knee joint. the internal surface of the femoral component has a sintered cocr bead coating and a coating of non-animal derived hydroxyapatite. flex-lok pegs or finned lugs are added for stability and increased pullout strength. it is intended to be used without cement. an uncemented co-cr-mo alloy porous ha cruciate retaining femoral 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.

Genesis II Cruciate Retaining All Polyethylene Tibial Base - Uncoated knee tibia prosthesis, polyethylene Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

genesis ii cruciate retaining all polyethylene tibial base - uncoated knee tibia prosthesis, polyethylene

smith & nephew pty ltd - 33580 - uncoated knee tibia prosthesis, polyethylene - a sterile implantable device to replace tibial condyles of the knee joint. it is a one-piece contoured ultra-high molecular weight polyethylene tibial base designed to articulate with a cruciate retaining femoral component during knee joint replacement. it features structural posterior fins for additional rotational stability, an anatomically placed stem, and a dovetail waffle groove for cement interdigitation. it is intended for cemented use only. a cruciate retaining all polyethylene tibial baseplate component used in conjunction with the genesis ii total knee system. indications for total knee replacement include: 1. rheumatoid arthritis. 2. post-traumatic arthritis, osteoarthritis, or degenerative arthritis. 3. failed osteotomies, unicompartmental replacement, or total knee replacement.

Genesis II Posterior Stabilised Porous Femoral Component - Coated knee femur prosthesis Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

genesis ii posterior stabilised porous femoral component - coated knee femur prosthesis

smith & nephew pty ltd - 33745 - coated knee femur prosthesis - a sterile implantable device designed 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 coating. flex-lok pegs or finned lugs are added for stability and increased pullout strength. it is intended to be used without bone cement. an uncemented porous co-cr-mo alloy posterior stabilised femoral 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.

Genesis II Cruciate Retaining Porous Femoral Component - Coated knee femur prosthesis Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

genesis ii cruciate retaining porous femoral component - coated knee femur prosthesis

smith & nephew pty ltd - 33745 - coated knee femur prosthesis - a sterile implantable device designed to replace the femoral condyles during knee joint replacement. the device articulates with tibial cruciate retaining components and, if required, patellar prosthetic components of the knee joint replacement. the internal surface of the femoral component has a sintered cocr bead coating. flex-lok pegs or finned lugs are added for stability and increased pullout strength. it is intended to be used without cement. an uncemented porous co-cr-mo alloy cruciate retaining femoral 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.

GENESIS II Resurfacing Patella - Polyethylene patella prosthesis Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

genesis ii resurfacing patella - polyethylene patella prosthesis

smith & nephew pty ltd - 34199 - polyethylene patella prosthesis - a polyethylene patellar implant designed to be cemented onto a reamed patella. the patella is measured and cut using the dedicated saw guides and resurfacing technique of choice. fixation holes are drilled and the trial is fitted onto the patella. bone cement is applied to the patellar implant and the implant is clamped onto the reamed patella using a patellar cement clamp. excess cement should be removed following initial fixation. a sterile patellar component of a total knee system. genesis ii resurfacing patellar components are indicated for the following conditions: rheumatoid arthritis; post-traumatic arthritis, osteoarthritis, or degenerative arthritis; failed osteotomies, unicompartmental replacement, or total knee replacement.