Australien - engelsk - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 35217 - cement, orthopaedic, bone - indicated for the use of fixation of prosthesis to living bone arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk. the bone cement should be used with an appropriate prosthesis. indicated for the use of fixation of prosthesis to living bone arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk. the bone cement should be used with an appropriate prosthesis.

Australien - engelsk - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 45062 - soft-tissue anchor, non-bioabsorbable - the mitek fastin rc threaded titanium alloy anchor is preloaded on a disposable inserter assembly, with orthocord partially-absorbable sutures, supplied with or without needles - shoulder: rotator cuff repair, biceps tenodesis, acromio-clavicular separation repair and slap repair - foot/ankle: lateral stabilisation, medial stabilisation, achilles tendon repair - knee: medial collateral ligament repair, patellar tendon repair, posterior oblique ligament repair, iliotibial band tenodesis - elbow: biceps tendon reattachment, tennis elbow, ulnar or radial collateral ligament reconstruction

Australien - engelsk - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 45062 - soft-tissue anchor, non-bioabsorbable - the mitek fastin rc threaded titanium alloy anchor is preloaded on a disposable inserter assembly, with panacryl absorbable sutures, supplied with or without needles - shoulder: rotator cuff repair, biceps tenodesis, acromio-clavicular separation repair and slap repair - foot/ankle: lateral stabilisation, medial stabilisation, achilles tendon repair - knee: medial collateral ligament repair, patellar tendon repair, posterior oblique ligament repair, iliotibial band tenodesis - elbow: biceps tendon reattachment, tennis elbow, ulnar or radial collateral ligament reconstruction

Australien - engelsk - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 46059 - orthopaedic cement, medicated - self-curing, radiopaque, polymethyl methacrylate based cements, containing antibiotic, used for securing a metal or polymeric prosthesis to living bone in arthroplasty procedures. the device relies on close mechanical interlock between irregular bone surface and the prosthesis. it is supplied as a two-component system, consisting of separate, sterile liquid and powder components, which are mixed together at the point of use to produce the cement. indicated for the fixation of prostheses to living bone in arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk.

Australien - engelsk - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 46059 - orthopaedic cement, medicated - self-curing, radiopaque, polymethyl methacrylate based cements, containing antibiotic, used for securing a metal or polymeric prosthesis to living bone in arthroplasty procedures. the device relies on close mechanical interlock between irregular bone surface and the prosthesis. it is supplied as a two-component system, consisting of separate, sterile liquid and powder components, which are mixed together at the point of use to produce the cement. indicated for the fixation of prostheses to living bone in arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk.

Australien - engelsk - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 46059 - orthopaedic cement, medicated - self-curing, radiopaque, polymethyl methacrylate based cements, containing antibiotic, used for securing a metal or polymeric prosthesis to living bone in arthroplasty procedures. the device relies on close mechanical interlock between irregular bone surface and the prosthesis. it is supplied as a two-component system, consisting of separate, sterile liquid and powder components, which are mixed together at the point of use to produce the cement. indicated for the fixation of prostheses to living bone in arthroplasty procedures of joints in which infection by gentamicin sensitive organisms is a potential risk.

Singapore - engelsk - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients.

Singapore - engelsk - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - the uhmwpe cement restrictor is intended for use in cemented total and hemiarthroplasty procedures to restrict distal flow of bone cement in the femoral medullary cavity.

Singapore - engelsk - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - 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. 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.

Singapore - engelsk - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - 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 arthropathy. global c.a.p.tm is indicated for intact or repairable rotator cuff. 4. deformity and/or limited motion