Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 48088 - humeral head prosthesis - constructed of tial6v4 with tin coating. the modular humerus caps are available in three different sizes and allow an optimal glenoid contact. connects to a humerus head component as part of the modular universal tumor and revision system (mutars) and articulates with the glenoid. humerus cap component of the mutars system used as part of a humeral 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.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 33711 - reverse shoulder prosthesis - constructed of uhmw-pe. locks onto the outer locking rim of the glenoid implant and articulates with the humerus inverse cap as part of the modular universal tumor and revision system (mutars) inverse humeral replacement. glenosphere component of the mutars system used as part of an inverse humeral replacement in case of rotator cuff insufficiencies. 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.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 46585 - prosthesis, knee, internal, insert component - constructed of uhmw-pe. pe insert component used as part of the modular universal tumour and revision system (mutars) in various knee replacement configurations. the inlay is inserted from behind, moved forward towards the anterior locking rim and pushed down at the posterior part until it is securely locked into the tibial component. connects to various tibial components. a pe insert component of the mutars system used as part of a 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.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 32831 - uncoated knee femur prosthesis - constructed of cocrmo with titanium nitride coating. kri ? knee reconstruction implant is a constrained revision knee implant that replaces the distal femoral condyles. connects with various stems and extension pieces as part of the modular universal tumour and revision system (mutars) connects to the tibial plateau using the locking mechanism m-o-m. a femoral condyle replacement component of the mutars system used 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.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - composed of titanium tial6v4 alloy. modular proximal tibial component of the mutars (modular universal tumor and revision system) system. includes locking mechanism m-o-m and screws for connection to the corresponding genux femoral component, distal femur or kri. uses mutars pe-inlay x-small and connects to various connecting parts and extension pieces depending on the length of reconstruction required. proximal tibial replacement component indicated for tumours in the area of the proximal tibia with a constrained femoral resurfacing knee joint 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.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 43167 - acetabular shell - composed of tial6v4. the mutars (modular universal tumor & revision system) lumic system is a modular acetabular reconstruction system, which relieves patients from pain and limited mobility after massive acetabular bone loss or severe acetabular defects. connects to various lumic stems and inserts, the lumic cup can be rotated in 5 degree increments in order to prevent luxation. in order to adjust the rotation for optimal stability, first the proximal femur replacement should be performed. an acetabular component of the mutars lumic system used in partial pelvic reconstruction replacement for the hip joint after many or complicated revisions or after major bone defects of the acetabulum. primary indication for the use of the mutars lumic system is after bone resection because of a tumour (peri acetabular tumours). further indications for the use of the mutars lumic system 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.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 34190 - uncoated hip femur prosthesis, modular - tial6v4 alloy with sand blasted surface. on the lateral surface a porous structure is provided for better bone ingrowth. trochanter major-like curvature for attachment of trochanteric bone and/or soft tissue with various lateral and medial suture holes. connects with other mutars components through a precise female cylindrical connection with serrated teeth (72) to provide rotational stability and allow for intra-operative adjustment of the femoral antetorsion angle in 5 degree increments. a hip joint replacement component of the mutars system that replaces the proximal part of the 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.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 58085 - knee arthrodesis prosthesis - composed of tial6v4 with silver coating. tibial part of a two part arthrodesis for bridging the knee joint. to be combined with the mutars rs arthrodesis implant femoral component via two screws & 2 boreholes (diam. 8.5 mm). 50 mm in ml, 37 mm in ap with height of 52.5 mm. utilizes the female mutars taper connection design for attachment to the rs stem. a component of the mutars system intended to serve as part of 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.

Australija - engleski - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 58085 - knee arthrodesis prosthesis - composed of tial6v4 with silver coating. femoral part of a two part arthrodesis for bridging the knee joint. to be combined with the mutars rs arthrodesis implant tibial component via two screws & 2 boreholes (diam. 8.5 mm). 50 mm in ml, 37 mm in ap with height of 53.4 mm. utilizes the female mutars taper connection design for attachment to the rs stem. the component incorporates angle of 7 degrees between the rotation and femoral axis to match the anatomical femoral-tibial angle. a component of the mutars system intended to serve as part of 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.

Australija - engleski - 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.