Сінгапур - англійська - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - when used with compatible femoral components, the knee system is indicated for cemented use in cases of osteoarthritis and rheumatoid arthritis. the porous coated keeled and non keeled m.b.t.™ (mobile bearing tibial) tray configurations of the lcs total knee system are indicated for non-cemented use in skeletally mature individuals undergoing primary surgery for reconstructing knees damaged as a result of noninflammatory degenerative joint disease (nidjd) or either of its composite diagnoses of osteoarthritis and post-traumatic arthritis pathologies. the rotating platform device configuration is indicated for use in knees whose anterior and posterior cruciate ligaments are absent or are in such condition as to justify their sacrifice. the p.f.c. sigma rp curved bearings when used with the p.f.c. sigma cruciate retaining femoral component can be used in posterior cruciate ligament retaining procedures.

Сінгапур - англійська - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - total or unicompartmental knee arthroplasty is intended to provide patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components.

Австралія - англійська - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 38156 - ceramic femoral head prosthesis - a delta taper sleeve (ts) ceramic head hip prosthesis is composed of a packaged biolox delta ceramic femoral head with metal tapered sleeve adapters. the delta ts ceramic head hip prosthesis is intended to allow assembly with depuy femoral hip stem tapers, either in a primary hip replacement surgery, or in revision hip replacement surgery with well-fixed femoral stems. the depuy delta ts ceramic femoral head is intended for use in total hip arthroplasty applications to replace the articular surface of the femoral head in primary hip surgery and for the salvage of a failed previous hip surgery.

Австралія - англійська - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 36259 - prosthesis, internal, joint, shoulder, glenoid component - global steptech apg replaces the glenoid portion of the humero-glenoid shoulder joint. it is made from highly cross-linked polyethylene and features a central peg for bone graft, three peripheral pegs for cemented fixation and a front face designed to articulate with a humeral head. three "step" options of polyethylene on the backside surface are designed to compensate for a high degree of scapular bone loss and restore glenoid retroversion. global steptech apg is a glenoid component intended for use in total shoulder arthroplasty in combination with a depuy synthes humeral head. global steptech apg is indicated for use as a replacement of glenoid surfaces disabled by osteoarthritis and traumatic arthritis (when used with all total shoulder systems); rheumatoid arthritis and fracture/dislocations of the humeral head (when used with the global shoulder system and global unite); avascular necrosis (when used with global cap (from the global shoulder system) and global unite); deformity and/or limited motion (when used with global cap (from the global shoulder system)); and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable e.g. revision of a failed primary component (when used with the global shoulder system (except global cap) and global unite).

Австралія - англійська - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 45253 - orthopaedic cement preparation/delivery kit - vac-mix is a vacuum mixing system syringe system pre-packed with bone cement powder and liquid. the device is single use only and reduces the exposure to monomer fumes during the preperation of bone cement that 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. a single use system supplied with bone cement and a collection of surgical instruments used for cement delivery such as injectors, delivery tubes, and mixing devices.

Австралія - англійська - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 45253 - orthopaedic cement preparation/delivery kit - a vacuum mixing system with syringe pre-packed with bone cement powder and liquid. the device is single use only and reduces the exposure to monomer fumes during the preperation of bone cement that 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. a single use system supplied with bone cement and a collection of surgical instruments used for cement delivery such as injectors, delivery tubes, and mixing devices.

Сінгапур - англійська - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - indicated for joint replacement, for severe arthropathy due to advanced rheumatoid or osteo-arthritis where conservative therapy or alternative treatments have failed or are considered unsuitable, arthropathy due to degenerative disease, acute trauma, and a previous failed joint replacement. the patient’s joint must be anatomically and structurally suited to receive the selected implant(s)

Сінгапур - англійська - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - ha-coated stems of the corail hip system are intended for use in total hip arthroplasty and are intended for uncemented use. total hip arthroplasty is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. total hip replacement is indicated in the following conditions: 1. a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. avascular necrosis of the femoral head. 3. acute traumatic fracture of the femoral head or neck. 4. failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement. 5. certain cases of ankylosis. ha-coated stems of the corail hip system are indicated for cementless use only.

Сінгапур - англійська - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - duraloc constrained acetabular liner system is intended to use as components of a total hip prosthesis to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components.

Сінгапур - англійська - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - indicated for total or unicompartmental knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post traumatic arthritis, rheumatoid arthritis, or a failed previous implant. in candidates for unicompartmental knee arthroplasty, only one side of the joint (the medial or lateral compartment) is affected.