Link femoral component intracondylar with patellar flange cementable MEGASYSTEM-C - Uncoated knee femur prosthesis أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

link femoral component intracondylar with patellar flange cementable megasystem-c - uncoated knee femur prosthesis

link orthopaedics australia pty ltd - 32831 - uncoated knee femur prosthesis - the link femoral component intracondylar replacement megasystem c articulates with the tibial component of the modular bone and joint revision system megasystem-c. the component is made from cocrmo and uhmwpe, containing a patellar flange, and is equipped with an anti-luxation device. it contains an inner 12/14 female taper and is cementable the femoral component of the modular bone and joint revision system indicated for use in tumor and revision surgery intended to be used for mobility-limiting diseases, fractures or defects of the hip joint, the proximal and distal femur through the proximal tibia (only in combination with endo-model rotational and hinge knee sl or modular) which cannot be treated by conservative or osteosynthetic procedures. ? revision arthroplasty due to juxta-articular bone defects ? revision of loosened femoral prosthesis components involving extensive bone resorption of the proximal femur and widening of the medullary cavity ? revision of loosened femoral prosthesis components by peri-/subprosthetic fracture ? deformed proximal femur due to fractures or osteotomies ? correction of bone deficiencies, e.g. due to tumors ? large post-revision and post-trauma segmental bone defects oncological and revision surgery from tibial to hip area (in conjunction with rotational and hinge knee prostheses)

Link Femoral component Condylar Replacement Megasystem C - Uncoated knee femur prosthesis أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

link femoral component condylar replacement megasystem c - uncoated knee femur prosthesis

link orthopaedics australia pty ltd - 32831 - uncoated knee femur prosthesis - the link femoral component condylar replacement megasystem c articulates with the tibial component of the modular bone and joint revision system megasystem-c. the component is made from cocrmo and uhmwpe, with patella flange and is equipped with an anti-luxation device. it contains a 12/14 inner female taper and cocr screws are used for fixation the femoral component of the modular bone and joint revision system indicated for use in tumor and revision surgery intended to be used for mobility-limiting diseases, fractures or defects of the hip joint, the proximal and distal femur through the proximal tibia (only in combination with endo-model rotational and hinge knee sl or modular) which cannot be treated by conservative or osteosynthetic procedures. ? revision arthroplasty due to juxta-articular bone defects ? revision of loosened femoral prosthesis components involving extensive bone resorption of the proximal femur and widening of the medullary cavity ? revision of loosened femoral prosthesis components by peri-/subprosthetic fracture ? deformed proximal femur due to fractures or osteotomies ? correction of bone deficiencies, e.g. due to tumors ? large post-revision and post-trauma segmental bone defects oncological and revision surgery from tibial to hip area (in conjunction with rotational and hinge knee prostheses)

Link Hip Stem Standard Stem C Cementless, Ti6A14V + HA - Coated hip femur prosthesis, modular أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

link hip stem standard stem c cementless, ti6a14v + ha - coated hip femur prosthesis, modular

link orthopaedics australia pty ltd - 33581 - coated hip femur prosthesis, modular - standard c cementless implant follows concept of straight stem with flattened lateral shoulder. straight profile and rectangular cross section of implant gives proximal stability. hydroxyapatite coating ensures rapid integration into the bone. stem is made from ti6al4v alloy. 12/14 taper is designed for use with link? modular ceramic or metal prosthesis heads of different lengths and diameters. flattened tapered neck to increase range of motion between stem and acetabular cup component straight, cementless femoral stem is a component of hip prosthesis and is for the a total or partial hip prosthesis in osteoarthritis, posttraumatic osteoarthritis, rheumatoid arthritis, necrosis of the femoral head and fracture of the femoral neck

LINK BiMobile Cup Liner, UHMWPE - Constrained polyethylene acetabular liner أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

link bimobile cup liner, uhmwpe - constrained polyethylene acetabular liner

link orthopaedics australia pty ltd - 44362 - constrained polyethylene acetabular liner - self-centering polyethylene acetabular liner promotes even wear patterns and enhances dislocation resistance and are suitable for use with cocrmo heads polyethylene acetabular liner of the link bimobile cup dual mobility system for the treatment of mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures ? primary and secondary coxarthrosis ? osteoarthritis ? necrosis of the femoral head ? femoral neck fractures ? revision after implant loosening ? acetabular dysplasia

LINK BiMobile Cup C, Shell, cemented, CoCrMo alloy, uncoated - Acetabular shell أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

link bimobile cup c, shell, cemented, cocrmo alloy, uncoated - acetabular shell

link orthopaedics australia pty ltd - 43167 - acetabular shell - metal acetabular shell component of an acetabular replacement system used for cement fixation in the acetabulum in hip arthroplasty; made from biocompatible and resilient cocrmo material with a mirror polished on the inner surface to minimize wear with satin finish metal acetabular shell cemented component of the link bimobile cup dual mobility system for the treatment of mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures ? primary and secondary coxarthrosis ? osteoarthritis ? necrosis of the femoral head ? femoral neck fractures ? revision after implant loosening ? acetabular dysplasia

LINK BiMobile Cup CL TiCap Shell, cementless, CoCrMo alloy, TiCaP Double Coating - Acetabular shell أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

link bimobile cup cl ticap shell, cementless, cocrmo alloy, ticap double coating - acetabular shell

link orthopaedics australia pty ltd - 43167 - acetabular shell - metal acetabular shell component of an acetabular replacement system used for cementless fixation in the acetabulum in hip arthroplasty; made from biocompatible and resilient cocrmo material with a mirror polished on the inner surface to minimize wear; double coated with highly porous surface to achieve primary fixation and an osteoconductive calcium phosphate coating, to ensure optimal primary and secondary implant stability. metal acetabular shell cementless component of the link bimobile cup dual mobility system for the treatment of mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures ? primary and secondary coxarthrosis ? osteoarthritis ? necrosis of the femoral head ? femoral neck fractures ? revision after implant loosening ? acetabular dysplasia

ALLMERCAP mercaptopurine monohydrate 20mg/mL oral liquid suspension bottle أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

allmercap mercaptopurine monohydrate 20mg/ml oral liquid suspension bottle

link medical products pty ltd t/a link pharmaceuticals - mercaptopurine monohydrate, quantity: 20 mg/ml - oral liquid, suspension - excipient ingredients: xanthan gum; aspartame; rubus idaeus; sodium methyl hydroxybenzoate; sodium ethyl hydroxybenzoate; potassium sorbate; sodium hydroxide; purified water - allmercap oral liquid suspension is indicated for: treatment of acute lymphoblastic leukaemia (all) in paediatric patients.

RELISTOR methylnaltrexone bromide 12 mg/0.6 mL solution for injection vial أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

relistor methylnaltrexone bromide 12 mg/0.6 ml solution for injection vial

link medical products pty ltd t/a link pharmaceuticals - methylnaltrexone bromide, quantity: 12 mg - injection, solution - excipient ingredients: hydrochloric acid; sodium hydroxide; sodium calcium edetate; glycine hydrochloride; water for injections; sodium chloride - relistor is indicated for the treatment of opioid-induced constipation in patients with advanced illness who are receiving palliative care when response to laxative therapy has not been sufficient.

Tepadina نيوزيلاندا - الإنجليزية - Medsafe (Medicines Safety Authority)

tepadina

link pharmaceuticals ltd - thiotepa 100mg - powder for injection - 100 mg - active: thiotepa 100mg - indicated, in combination with other chemotherapy medicinal products: - with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;