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

helix pharmaceuticals pty ltd - meloxicam, quantity: 7.5 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; povidone; magnesium stearate; sodium citrate dihydrate; colloidal anhydrous silica; crospovidone; microcrystalline cellulose - meloxicam is indicated for symptomatic treatment of osteoarthritis and rheumatoid arthritis.

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

helix pharmaceuticals pty ltd - meloxicam, quantity: 15 mg - tablet, uncoated - excipient ingredients: lactose monohydrate; microcrystalline cellulose; magnesium stearate; colloidal anhydrous silica; sodium citrate dihydrate; povidone; crospovidone - meloxicam is indicated for symptomatic treatment of osteoarthritis and rheumatoid arthritis.

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

johnson & johnson medical pty ltd t/a depuy synthes - 32835 - prosthesis, internal, joint, shoulder, humeral component - the global advantage long humeral stem is uncoated and is made of titanium. implantation is intended to be performed with either bone cement, impacting bone grafting or press-fit. it is designed to provide fixation within the proximal humerus and a site of attachment for a humeral head prosthesis as part of a shoulder joint replacement. long stem humeral components are available for revisions or fractures of the humeral shaft the global advantage long humeral stem is the humeral component of a shoulder joint replacement. it is intended for treatment of patients with osteoarthritis, traumatic arthritis or rheumatoid arthritis. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, ununited humeral head fractures, avascular necrosis of the humeral head.

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

johnson & johnson medical pty ltd t/a depuy synthes - 48088 - humeral head prosthesis - the global ap cta humeral head is made out of cocr and may be cemented or press-fit. the global ap cta humeral head incorporates a taper connection designed to be used with global ap anatomic stems. the global ap cta humeral head is indicated only for hemi-shoulder replacement for the treatment of: - rotator cuff tear arthropathy. - a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis; - fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon?s experience indicates that alternative methods of treatment are unsatisfactory; - other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). - ununited humeral head fractures; - avascular necrosis of the humeral head.

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

johnson & johnson medical pty ltd t/a depuy synthes - 34197 - uncoated shoulder humeral stem prosthesis - the global ap long humeral stem is made of titanium, is uncoated and implantation is intended to be performed with bone cement, press fit or impaction bone grafting. the global ap long humeral stem is designed to provide fixation within the proximal humerus and a site of attachment for a humeral head prosthesis. the global ap long humeral stem is part of the global ap shoulder system and indicated for use in total or hemi-shoulder replacement for the treatment of: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis; 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon?s experience indicates that alternative methods of treatment are unsatisfactory; 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). the global ap long humeral stems are also in

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

johnson & johnson medical pty ltd t/a depuy synthes - 34197 - uncoated shoulder humeral stem prosthesis - the global ap standard humeral stem is made of titanium, is uncoated and implantation is intended to be performed with bone cement, press fit or impaction bone grafting. the global ap standard humeral stem is designed to provide fixation within the proximal humerus and a site of attachment for a humeral head prosthesis. the global ap standard humeral stem is part of the global ap shoulder system and indicated for use in total or hemi-shoulder replacement for the treatment of: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis; 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon?s experience indicates that alternative methods of treatment are unsatisfactory; 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). the global ap standard humeral stems are also indicated for hemi-shoulder replacement for the treatment of: 1. ununited humeral head fractures; 2. avascular necrosis of the humeral head. 3. rotator cuff repairs

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

johnson & johnson medical pty ltd t/a depuy synthes - 39702 - coated shoulder humeral stem prosthesis - the global advantage porocoat humeral stem is made of titanium and is coated with porocoat. porocoat porous?coated humeral stem prostheses are indicated for cemented or cementless use with fixation provided by biological tissue in?growth into the porous coating. the global advantage porocoat stem is designed to provide fixation within the proximal humerus and a site of attachment for a humeral head prosthesis. the global advantage porocoat humeral stem is the humeral stem component of total or hemi shoulder joint replacement. total shoulder or hemi-shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon?s experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resectio

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

johnson & johnson medical pty ltd t/a depuy synthes - 39702 - coated shoulder humeral stem prosthesis - the global unite anatomic proximal body (epiphyseal) is made from titanium and has a porocoat coating for press-fit or cemented applications. the global unite anatomic proximal body is a modular component that connects to both the global unite stem and global unite humeral head. available in multiple neck shaft angles to allow a surgeon the flexibility to adjust the implant construct to match a patient?s native anatomy. the global unite anatomic proximal body (epiphyseal)is one component of the global unite shoulder system and is intended for cemented or uncemented total shoulder or hemi-shoulder replacement in treatment of the following: 1.a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2.fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon?s experience indicates that alternative methods of treatment are unsatisfactory. 3.other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component) hemi-shoulder replacement is also indicated for: 1.ununited humeral head fractures 2.avascular necrosis of the humeral head 3.deformity and/or limited motion

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

johnson & johnson medical pty ltd t/a depuy synthes - 48090 - press-fit shoulder humeral stem prosthesis - the global ap ball taper assembly is made from cocr and is impacted onto the humeral stem. the selected head is then placed onto the impacted ball taper assembly. the ball taper assembly allows for variable geometry of the humeral head (+15? inclination and version) for optimal patient anatomical match. the global ap ball taper assembly is one component of the global ap shoulder system which is intended for total or hemi shoulder arthroplasty. total shoulder or hemi-shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon?s experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). hemi-shoulder replacement is also indicated for: 1. ununited humeral head fractures. 2. avascular necrosis of the humeral head. 3. rotator cuff tear arthropathy. 4. deformity and/or limited motion.

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

johnson & johnson medical pty ltd t/a depuy synthes - 48090 - press-fit shoulder humeral stem prosthesis - the global ap 135 degree taper assembly is made from titanium and is impacted onto the humeral stem. the selected head is then placed onto the impacted 135 degree taper. the 135 degree taper enables the assembled prosthesis to achieve a fixed 135 degree angle. the global ap 135 taper assembly is one component of the global ap shoulder system which is intended for total or hemi shoulder arthroplasty. total shoulder or hemi-shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon?s experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). hemi-shoulder replacement is also indicated for: 1. ununited humeral head fractures. 2. avascular necrosis of the humeral head. 3. rotator cuff tear arthropathy. 4. deformity and/or limited motion.