イスラエル - 英語 - Ministry of Health

bioavenir ltd, israel - remifentanil as hydrochloride - powder for solution for injection - remifentanil as hydrochloride 1 mg - remifentanil - remifentanil bioavenir is indicated as an analgesic agent for use during induction and/or maintenance of general anaesthesia under close supervision .remifentanil bioavenir is indicated for provision of analgesia and sedation in mechanically ventilated intensive care patients 18 years of age and over.

イスラエル - 英語 - Ministry of Health

bioavenir ltd, israel - remifentanil as hydrochloride - powder for solution for injection - remifentanil as hydrochloride 2 mg/vial - remifentanil - remifentanil bioavenir is indicated as an analgesic agent for use during induction and/or maintenance of general anaesthesia under close supervision .remifentanil bioavenir is indicated for provision of analgesia and sedation in mechanically ventilated intensive care patients 18 years of age and over.

イスラエル - 英語 - Ministry of Health

bioavenir ltd, israel - remifentanil as hydrochloride - powder for solution for injection - remifentanil as hydrochloride 5 mg - remifentanil - remifentanil bioavenir is indicated as an analgesic agent for use during induction and/or maintenance of general anaesthesia under close supervision .remifentanil bioavenir is indicated for provision of analgesia and sedation in mechanically ventilated intensive care patients 18 years of age and over.

オーストラリア - 英語 - Department of Health (Therapeutic Goods Administration)

smith & nephew pty ltd - 38155 - press-fit femoral stem prosthesis - the redapt sleeved monolithic stem is a tapered, distally fixed femoral stem that is manufactured from forged titanium alloy (ti-6al-4v) and has a grit blast finish. the redapt sleeved monolithic stem features a non-modular, fixed neck; the stem utilizes modular sleeves, where the surgeon can elect to use a sleeved stem in cases where there is proximal/distal mismatch. it has a 12/14 neck taper design. hip components are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or noninflammatory degenerative joint disease (nidjd) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. hip components are also indicated for inflammatory degenerative joint disease including rheumatoid arthritis, arthritis secondary to a variety of diseases and anomalies, and congenital dysplasia; treatments of nonunion, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement that are unmanageable using other techniques; endoprosthesis, femoral osteotomy, or girdlestone resection; fracture-dislocation of the hip; and correction of deformity. the redapt? revision femoral hip system is intended to be used without cement. the redapt revision hip system is indicated for revision surgery only.

オーストラリア - 英語 - Department of Health (Therapeutic Goods Administration)

stryker australia pty ltd - 33178 - revision uncoated hip femur prosthesis - the femoral link shaft is available as 165 and 225mm curved titanium link shafts with male fittings at both ends.the system also allows the conversion of the mets proximal and mets distal femoral systems into a total femur using the link shaft. at the distal end of the link shaft the male fitting has a shroud that is intended to be inserted into the principle shaft. the femoral link shaft is a component of the mets modular total femur, which is designed as a modular system that can be used to replace diseased or deficient bone in the femur. the mets? modular total femur is intended for the replacement of the total femoral bone. ? limb salvage procedures where radical resection and replacement of the bone is required ? painful and disabled joint resulting from avascular necrosis osteoarthritis, rheumatoid arthritis or traumatic arthritis ? correction of varus, valgus or post traumatic deformity ? correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement ? ligament deficiencies ? tumor resections ? revision of previously failed total joint arthroplasty ? trauma ? treatment of non-unions, femoral neck and trochanteric fracture of the proximal femur with head involvement, unmanageable using other techniques

オーストラリア - 英語 - Department of Health (Therapeutic Goods Administration)

link orthopaedics australia pty ltd - 33178 - revision uncoated hip femur prosthesis - 'the cocrmo coupling component with an inner 12/14 taper is part of a modular system that is part of the proximal femur replacement. the neck is then attached to the coupling. it is made from cocrmo and uhmwpe for cementless application the modular stem segment component of the modular bone and joint revision system indicated for tumor and revision surgery for coupling proximal femur replacement mobility limiting diseases, fractures or defects of the hip joint, the proximal femur through the proximal tibia (only in combination with endo-model rotational and hinge knee sl or modular) which cannot be treated by conservative or osteosynthetic procedures.

オーストラリア - 英語 - Department of Health (Therapeutic Goods Administration)

coopervision australia pty ltd - 47842 - soft corrective contact lens, daily-wear - contact lenses for vision correction

オーストラリア - 英語 - Department of Health (Therapeutic Goods Administration)

coopervision australia pty ltd - 47841 - soft corrective contact lens, daily-disposable - contact lenses for vision correction

オーストラリア - 英語 - Department of Health (Therapeutic Goods Administration)

coopervision australia pty ltd - 16581 - contact lens case - used for the storage of contact lenses.

オーストラリア - 英語 - Department of Health (Therapeutic Goods Administration)

contact lens centre australia ltd - 37581 - contact lens, vision corrective, single use - vision correction.