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

life healthcare pty ltd - 61006 - humeral stem extension prosthesis - composed of tial6v4 with silver coating. combines the mutars humerus connection part with the mutars humerus extension piece or mutars humerus head with the mutars distal humerus. the reducer utilizes the mutars cylindrical fit and serration connection design for attachment to the mutars humerus head, humerus extension piece, humerus connecting part, humerus stem, distal humerus, proximal ulna. a component of the mutars system intended to provide extraosseous length adjustment in cases of a total humerus replacement. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis. the silver coated surface builds a long term prophylaxis against the colonisation of human pathogenic bacteria such as staphylococcus aureus and epidermis, exclusive enterobacteriae and should not be considered as acute treatment.

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

life healthcare pty ltd - 61561 - body femoral/tibial extension stem, uncoated - composed of tial6v4 with silver anti-infective coating. consists of two parts: the mutars connecting part distal & mutars connecting part proximal. the two parts are connected to each other with the mutars screw for connecting part. utilizes the mutars cylindrical fit & serration connection design for attachment to the distal femur or modular proximal tibia component and a femoral or tibial stem. the connecting part has 1 retention ring for securing a pet mesh soft tissue attachment tube. a component of the mutars system intended to be sued as an extraosseous length adjustment in the area of the distal femur or proximal tibia for the bridging of bone defects. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis. the silver coated surface builds a long term prophylaxis against the colonisation of human pathogenic bacteria such as staphylococcus aureus and epidermis, exclusive enterobacteriae and should not be considered as acute treatment.

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

life healthcare pty ltd - 32831 - uncoated knee femur prosthesis - composed of tial6v4 alloy. connection of mutars kri with mutars rs stems and mutars intramedullary connecting module. a screw component of the mutars system used to lock the mutars kri m-o-m in place. primary indication for the use of the mutars system is after bone resection because of tumour.further indications for the use of the mutars system are massive bone loss,such as morbus gorham or for revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis.

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

life healthcare pty ltd - 33692 - rotating hinged total knee prosthesis - composed of cocrmo with tinbn coating. the mutars genux mk coupling connects the mutars femoral components with the mutars tibial components and creates therefore a rotating hinge knee system. it restrains the movement in the knee joint and replaces the removed ligament. the coupling consists of three components: the spherical cap, the locking bolt, and the connecting pin. the mutars genux mk coupling can only be combined with the mutars genux mk tibia. a locking mechanism for the coupling of knee joint components used in the mutars system as part of a total knee replacement. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis.

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

life healthcare pty ltd - 61561 - body femoral/tibial extension stem, uncoated - composed of tial6v4 with silver coating on outer circumference. combines the mutars connection part with the mutars extension piece or proximal femur. the surface is sandblasted & utilizes the mutars cylindrical fit & serration connection design for attachment to the proximal femur replacement component & connecting part. the surface is sandblasted and provides one retention ring for securing a pet mesh soft tissue attachment tube component. a component of the mutars system intended for the extraosseous length adjustment in cases of a total femur replacement. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or forthe revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis. the silver coated surface builds a long term prophylaxis against the colonisation of human pathogenic bacteria such as staphylococcus aureus and epidermis, exclusive enterobacteriae and should not be considered as acute treatment.

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

life healthcare pty ltd - 48088 - humeral head prosthesis - composed of tial6v4. an all extraosseous part that has a sand blasted surface & provides a silver coating applied circumferentially. uses the cylindrical fit & serration connection for attachment to the connecting part, extension piece & a femoral stem. six holes at the proximal part of the head are used for securing a pet mesh soft tissue attachment tube. the thread at the proximal part serves for connecting with the mutars humerus cap and mutars humerus cap inverse respectively. a component of the mutars system intended to replace the humeral head as part of a proximal or total humerus reconstruction. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis. the silver coated surface builds a long term prophylaxis against the colonisation of human pathogenic bacteria such as staphylococcus aureus and epidermis, exclusive enterobacteriae and should not be considered as acute treatment.

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

life healthcare pty ltd - 33714 - body femoral extension - composed of tial6v4 alloy. mutars screw for connection of various mutars system components. a connecting screw component of the mutars system.primary indication for the use of the mutars system is after bone resection because of tumour.further indications for the use of the mutars system are massive bone loss,such as morbus gorham or for revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis.

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

life healthcare pty ltd - 48066 - knee stem - serves as a connection between the mutars genux mk stems and the mutars genux mk tibia and femur respectively that allow an adjustment of the tibial or femoral offset. made of tial6v4 alloy with sandblasted surface. it has a symmetric female double taper with an angle of 3 degrees 1? 18? and a length of 17 mm. the diameter at the top is 9.14 mm. the offset adapter has an additional fit (diameter 12 mm g6). the overall length is 57.74 mm and it includes a bilateral extraction thread (m8). an adaptor component of the mutars system intended to offset the alignment of the femoral or tibial stem connection as part of a knee replacement prosthesis. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis

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

life healthcare pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - tibial component of a coupled total knee replacement. constructed from cocrmo alloy with silver coating. m-o-m components are coupled by the metal-on-metal connecting mechanism. it is recommended to use the m-o-m components in case of an extra-articular resection. connects to various tibial stems & spacers as part of a modular universal tumour and revision system (mutars). a component of the mutars system intended to replace the tibial articulating surfaces of the knee. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis.

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

life healthcare pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - tibial component of a coupled total knee replacement. constructed from cocrmo alloy with titanium nitride coating to prevent allergic reactions. m-o-m components are coupled by the metal-on-metal connecting mechanism. it is recommended to use the m-o-m components in case of an extra-articular resection.connects to various tibial stems & spacers as part of a modular universal tumour and revision system (mutars). a component of the mutars system intended to replace the tibial articulating surfaces of the knee. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis.