Singapore - English - HSA (Health Sciences Authority)

transmedic pte ltd - orthopaedics - tutobone® is used in areas where cancellous bone is required rather than cortical bone. this includes in particular the filling of bone defects and the plastic reconstruction of removed or damaged bony regions, especially in cases of exchange arthroplasty.

Singapore - English - HSA (Health Sciences Authority)

transmedic pte ltd - general hospital - implants for surgical reconstruction of connective tissue defect in patients, e.g. for duraplasty, tympanoplasty, orbital floor recontsruction, hernia or omphalopele repair.

Singapore - English - HSA (Health Sciences Authority)

transmedic pte ltd - general hospital - tutopatch® serves as a replacement in reinforcement of connective tissue structures and as a barrier membrane.

Singapore - English - HSA (Health Sciences Authority)

globus medical singapore pte. ltd. - orthopaedics - intended for posterior pedicle screw fixation (t1-s2/ilium), posterior hook fixation (t1-l5), or anterolateral fixation (t8-l5). indicated for skeletally mature patients and for pediatric patients (creo 4.75 only). indicated as an adjunct to fusion for all of the following indications: ddd, spondylolisthesis, trauma, deformities or curvatures, tumor, stenosis, and failed previous fusion. when used as an adjunct to fusion, intended to be used with autograft and/or allograft. intended for treatment of ss (grd 3 and 4) of the l5-s1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft, having implants attached to the lumbosacral spine and/or ilium with removal of the implants after attainment of a solid fusion. levels of pedicle screw fixation for these patients are l3-sacrum/ilium. when used for posterior non-cervical pedicle screw fixation in pediatric patients, the 4.75 implants are indicated as an adjunct to fusion to treat adolescent idiopathic scoliosis.

Singapore - English - HSA (Health Sciences Authority)

globus medical singapore pte. ltd. - orthopaedics - the intercontinental® plate-spacer system is a stand-alone lateral lumbar interbody fusion device intended for use in patients with degenerative disc disease (ddd) at one or more contiguous levels of the lumbosacral spine (l2-s1). ddd is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. the patients should be skeletally mature and have had at least 6 months of non-operative treatment. the patients may have up to grade 1 spondylolisthesis or retrolisthesis at the involved level(s). the intercontinental® plate-spacer system is to be filled with autogenous bone graft material, and to be used with 2 titanium alloy screws which accompany the implant. the intercontinental® plate system is intended for use in the treatment of thoracolumbar (t1-l5) spine instability as a result of fracture (including dislocation, subluxation), tumor, ddd, scoliosis, kyphosis, lordosis, spinal stenosis, or failed previous spine surgery.

Singapore - English - HSA (Health Sciences Authority)

globus medical singapore pte. ltd. - orthopaedics - revere® stabilization system is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in treatment of instabilities/deformities of the thoracic, lumbar and sacral spine as a posterior pedicle screw system. revere® stabilization system is intended for treatment of severe spondylolisthesis of l5-s1 in skeletally mature patients with autogenous bone graft. levels of pedicle screw fixation are l3-sacrum/ilium; posterior non-pedicle screw fixation (t1-sacrum/ilium); anterolateral screw fixation (t8-l5). revere 4.5 implants are non-cervical spinal fixation devices intended for posterior pedicle screw fixation (t1-s2/ilium), posterior hook fixation (t1-l5), or anterolateral fixation (t8-l5). for posterior non-cervical pedicle screw fixation in pediatric patients, revere® 4.5 implants are indicated as an adjunct to fusion to treat adolescent idiopathic scoliosis and is intended to be used with autograft/allograft.

Singapore - English - HSA (Health Sciences Authority)

globus medical singapore pte. ltd. - orthopaedics - the transition® stabilization system is intended to provide spinal alignment and dynamic stabilization in skeletally mature patients in the thoracic, lumbar and sacral spine. the system is intended to be used for the following indications: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, degenerative spondylolisthesis with objective evidence of neurologic impairment, spondylosis, spinal stenosis, fracture, disclocation, scoliosis, kyphosis, spinal tumor, pseudoarthrosis and failed previous fusion. transition® may also be used as an adjunct to fusion, in conjunction with autogenous bone graft or synthetic bone graft substitutes for the same intended uses.

Ireland - English - HPRA (Health Products Regulatory Authority)

sol s.p.a. - oxygen - medicinal gas, compressed - 100 percent volume/volume - medical gases; oxygen

Singapore - English - HSA (Health Sciences Authority)

globus medical singapore pte. ltd. - orthopaedics - when used as a posterior pedicle screw system, it is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, pseudoarthrosis and failed previous fusion. system is also intended for treatment of severe spondylolisthesis (grades 3 and 4) of the l5-s1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft, having implants attached to the lumbosacral spine and/or ilium with removal of the implants after attainment of a solid fusion. levels of pedicle screw fixation for these patients are l3-sacrum/ilium.

Singapore - English - HSA (Health Sciences Authority)

globus medical singapore pte. ltd. - orthopaedics - the elsa® spacer is a stand-alone lateral lumbar interbody fusion device intended for use in patients with degenerative disc disease (ddd) at one or more contiguous levels of the lumbosacral spine (l2-s1). ddd is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. these patients should be skeletally mature and have had at least six (6) months of non-operative treatment. in addition, these patients may have up to grade 1 spondylolisthesis or retrolisthesis at the involved level(s). the elsa® spacer is to be filled with autogenous bone graft material, and is to be used with two titanium alloy screws which accompany the implant.