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 - 16082 - prosthesis, internal, bone, cap - composed of tial6v4. designed with the mutars cylindrical fit and serration (36 teeth) connection for attachment to the mutars humerus extension piece, humerus reducer piece or humerus connecting part to achieve a functional length adjustment to the stump terminus. it has a sand blasted surface finish and the cap provides a silver coating. a component of the mutars system intended to be used in rare cases of bone tumors and bone metastases in which no full extremity preserving surgery can be carried out to prosthetically preserve a terminal humeral stump. 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 - 58084 - diaphysis prosthesis - composed of tial6v4 with silver coating. it consists of 2 parts: the humerus connecting part distal & connecting part proximal. the two parts connect with the humerus screw for connecting part. the stem is straight & has a hexagonal cross section for rotational stability. one cross hole ?4 mm for optional cortical screw for extra stability. uses cylindrical fit connection to attach to humeral stems or extension pieces. 2 retention rings for securing pet mesh soft tissue attachment tube. a component of the mutars system intended for bridging bone defects in the humeral diaphyseal area. 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. intended to be used with bone cement. 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 - 48067 - knee wedge - composed of tial6v4 with silver coating on outer contour. connected to the distal part of the condyles of the mutars genux femur cemented using femoral spacer screws. spacers are available for left lateral/right medial & right lateral/left medial applications. can only be used with a cemented femoral component of the same size. surfaces of spacers are sandblasted & 0.7 mm deep cement pockets provided to augment cement fixation. bore holes are provided for the 6.5 mm spacer attachment screws. a component of the mutars system intended to be used for bridging bone defects on the distal medial and lateral aspects of the distal femur. 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 - 40124 - hinged total elbow prosthesis - composed of tial6v4 with silver coating. consists of 3 parts: the distal humerus component, cocrmo distal humerus bushing and axle. the bushings are laterally pressed into the distal humerus and the bushings serve as the articulating component for the hinge mechanism (axle). the distal humerus is an all extraosseous part. uses cylindrical fit and serration connection for attachment to various components. has a retention ring for securing a pet mesh soft tissue attachment tube component. a component of the mutars system intended to replace the distal part of the humerus. 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 - 58085 - knee arthrodesis prosthesis - composed of tial6v4 coated with silver to prevent infection. a part of the mutars (modular universal tumor and revision) system. connects with a mutars femoral stem and tibial stem for complete replacement of the knee joint with a rigid connection. may also interconnect with mutars extension piece/s and connecting part depending on the size of the resection. a fused (non-articulating) replacement for the knee joint intended to be implanted after failed primary knee arthroplasty and which functions as a bridge between the resected metaphyses of the femur and tibia. arthrodesis implants are indicated, in the case of - massive bone loss with insufficient skin and soft tissue coverage because of tumors, revisions, fractures or morbus gorham. - a deficit extensor mechanism. 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 - 44362 - constrained polyethylene acetabular liner - crosslinked uhmwpe insert for use with the rs and lumic cups. the liners are available with a 15? lateral lip version (0mm and 4mm offset) to provide greater coverage of the femoral head to help prevent dislocation in cases at greater risk of dislocation, such as hip dysplasia. the pe inserts with 4mm allow for an adjustment of the rotation center after implantation. a polyethylene cup insert used with cementless acetabular reconstruction cup as part of a revision or oncological procedure. implant is used with the mutars rs cup and lumic cup. 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, arthrosis, and large cavitary or segmental acetabular defects.

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

life healthcare pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - mobile bearing symmetric tibial component used for the left as well as for the right tibia. cocrmo?casting alloy with tin coating.features cement pockets on the bone facing implant surface for fixation with bone cement.the posterior notch allows the preservation of the posterior cruciate ligament.the relatively short stem & a small pronounced fin design allow for a high degree of preservation of the tibial bone stock. the component features a conical portion for acceptance of the pe?insert. a cemented tibial component of the acs knee system for use in knee arthroplasty. the acs knee system is indicated, if - severe joint destruction with significant impairment where other therapeutic measures are not more promising. - severe joint pain due to degenerative or rheumatoid arthritis, joint fractures or bone necrosis. - post-operative conditions after previous surgery with or without the use of implants.

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

life healthcare pty ltd - 58228 - bicompartmental knee prosthesis - composed of tial6v4. connection piece for the use of tibial stem extensions. tibially, it is possible to apply an offset, whereas the offset is freely adjustable within 360? in each case. the adapters feature a single female cone design and the fixation of the offset position is achieved by pressing the cones between the stem and the tibial component. height 48mm. a single taper adapter component of the acs knee system. the acs knee system is indicated, if - severe joint destruction with significant impairment where other therapeutic measures are not more promising. - severe joint pain due to degenerative or rheumatoid arthritis, joint fractures or bone necrosis. - post-operative conditions after previous surgery with or without the use of implants.

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

life healthcare pty ltd - 46585 - prosthesis, knee, internal, insert component - composed of uhmw-pe. the symmetric acs fb pe-inserts are fixed to the tibial component via a snap-fit mechanism. the fb pe-insert ultra features a highly congruent articulation between femoral component and pe-insert. thereby an increased stability is provided in flexion and extension. a pe insert component of the acs knee system. the acs knee system is indicated, if - severe joint destruction with significant impairment where other therapeutic measures are not more promising. - severe joint pain due to degenerative or rheumatoid arthritis, joint fractures or bone necrosis. - post-operative conditions after previous surgery with or without the use of implants.