Nowa Zelandia - angielski - Medsafe (Medicines Safety Authority)

johnson & johnson medical new zealand ltd - gentamicin - bone cement - 1.7%w/w - smartmix cemvac pre-filled with depuy cmw 1 gentamicin bone cement is 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. the cement is indicated for use in children only in the case of limb preservation where no other procedure is likely to give a good chance of successful treatment. the cement should be used with an appropriate prosthesis.

Singapur - angielski - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - is indicated for use with cemented femoral stems to occlude the medullary canal to enable cement containment, to facilitate cement pressurization to achieve cement-bone interdigitation and prevent excessive bone cement usage. it can be used with any cemented femoral stem up to a maximum of 220mm in length.

Singapur - angielski - 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.

Singapur - angielski - HSA (Health Sciences Authority)

johnson & johnson international (singapore) pte ltd - orthopaedics - intended for cemented use in total knee replacement for cases of osteoarthritis and rheumatoid arthritis. the rpf inserts and femoral components are indicated where a higher than normal degree of post-operative flexion is required. the rotating platform prosthesis and modular revision components are indicated for revision of failed knee prosthesis.

Singapur - angielski - HSA (Health Sciences Authority)

johnson & johnson pte ltd - orthopaedics - 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. hemi-hip prostheses are intended to be used for hemi-hip arthroplasty where there is evidence of a satisfactory natural acetabulum and sufficient femoral bone to seat and support the femoral stem.

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

johnson & johnson medical pty ltd t/a depuy synthes - 38156 - ceramic femoral head prosthesis - a biolox delta ts ceramic femoral head is composed of a packaged biolox delta ceramic femoral head with metal tapered sleeve adapters. the biolox delta ts ceramic femoral head is manufactured from biolox delta alumina matrix composite ceramic. the biolox delta ts ceramic head 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 taper sleeve (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. 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.

Nowa Zelandia - angielski - Medsafe (Medicines Safety Authority)

johnson & johnson medical new zealand ltd - gentamicin - bone cement - 1.7%w/w

Nowa Zelandia - angielski - Medsafe (Medicines Safety Authority)

johnson & johnson medical new zealand ltd - gentamicin - bone cement - 1.7%w/w

Australia - angielski - 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

Australia - angielski - 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