Biomet Orthopedics Hip Joint Replacement Prostheses System Singapur - angielski - HSA (Health Sciences Authority)

biomet orthopedics hip joint replacement prostheses system

zimmer pte. ltd. - orthopaedics - intended for (1) noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis, (2) rheumatoid arthritis, (3) correction of functional deformity, (4) treatment of non-union, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable using other techniques, (5) revision of previously failed total hip arthroplasty

Biomet Orthopedics Ringloc+ Quick Connect Drill Bit Singapur - angielski - HSA (Health Sciences Authority)

biomet orthopedics ringloc+ quick connect drill bit

zimmer pte. ltd. - orthopaedics - disposable drill bits used during the implantation of medical devices to create round holes in bone.

Biomet Persona Partial Knee System Singapur - angielski - HSA (Health Sciences Authority)

biomet persona partial knee system

zimmer pte. ltd. - orthopaedics - the persona partial knee system is limited to the medial tibiofemoral compartment of the knee intended for patients with painful and/or disabling knee joints due to the following indications: - noninflammatory degenerative joint disease (nidjd), e.g., osteoarthritis, avascular necrosis; - traumatic arthritis; - previous tibial condyle or plateau fractures with loss of anatomy or function; - varus deformities; and - revision of the articular surface of a previously implanted persona partial knee system providing that the tibial plate locking mechanism is not compromised and the femoral and tibial plate components remain well fixed and undamaged. the persona partial knee system is a single use implant intended for implantation with bone cement.

Biomet Phoenix Ankle Nail System Singapur - angielski - HSA (Health Sciences Authority)

biomet phoenix ankle nail system

zimmer pte. ltd. - orthopaedics - the phoenix ankle nail system is indicated for tibiotalocalcaneal arthrodesis (fusion). specific indications include: 1. avascular necrosis of the talus 2. failed total ankle arthroplasty 3. trauma (malunited tibial pilon fracture) 4. severe deformity or instability as a result of talipes equinovarus, cerebral vascular accident, paralysis or other neuromuscular disease 5. revision ankle arthrodesis 6. neuroarthropathy 7. rheumatoid arthritis 8. osteoarthritis 9. pseudoarthrosis 10. post-traumatic arthrosis 11. previously infected arthrosis 12. charcot foot 13. severe endstage degenerative arthritis 14. severe defects after tumor resection 15. pantalar arthrodesis

Biomet Refobacin Bone Cement R Singapur - angielski - HSA (Health Sciences Authority)

biomet refobacin bone cement r

zimmer pte. ltd. - orthopaedics - intended for use as a bone cement for stable anchoring of suitable joint prostheses in primary operations, with added protection against infection and also in revision operations resulting from aseptic loosening of prosthesis and infection of the prosthesis by gentamicin sensitive strains. radiopaque bone cement with gentamicin.

Biomet Refobacin Plus Bone Cement Singapur - angielski - HSA (Health Sciences Authority)

biomet refobacin plus bone cement

zimmer pte. ltd. - orthopaedics - refobacin plus bone cement is used for stable anchoring of suitable joint prostheses in primary operations, with added protection against infection also in revision operations resulting from aseptic loosening of the prosthesis and infection of the prosthesis by gentamicin sensitive strains.

Biomet Refobacin Revision Bone Cement Singapur - angielski - HSA (Health Sciences Authority)

biomet refobacin revision bone cement

zimmer pte. ltd. - orthopaedics - for stable fixation of arthroplastic joint replacements to bone where cemented implantation is indicated and an elevated risk of infection is very likely. genta clinda cement is indicated particularly for exchange arthroplasties in septically loosened joint replacements.

Biomet StageOne™ Hip Cement Spacer Mold with Reinforcement Singapur - angielski - HSA (Health Sciences Authority)

biomet stageone™ hip cement spacer mold with reinforcement

zimmer pte. ltd. - orthopaedics - indicated for use to mold a temporary hemi-hip replacement for skeletally mature patients undergoing a two-stage revision procedure due to a septic process. the temporary prosthesis is inserted into the femoral medullary canal and acetabular cavity following removal of the existing femoral and acetabular implants and debridement. the device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). the hemi-hip femoral prosthesis is not intended for use more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion, etc.) because of inherent mechanical limitations of the device material (polymethylmethacrylate/gentamicin), the molded temporary prosthesis is only indicated for compliant patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers) throughout the implant period.

Biomet StageOne™ Select Hip Spacer Molds Singapur - angielski - HSA (Health Sciences Authority)

biomet stageone™ select hip spacer molds

zimmer pte. ltd. - orthopaedics - indicated for use to mold a temporary hemi-hip replacement for skeletally mature patients undergoing a 2-stage revision procedure due to septic process. the temporary prosthesis is molded using polymethylmethacrylate/gentamicin bone cement, assembled and inserted into the femoral medullary canal and acetabular cavity following removal of existing femoral and acetabular implants and debridement. the device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). the hemi-hip prosthesis made from the stageone select cement molds is not intended for use more than 180 days, at which time it must be explanted and permanent devices implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion) due to the inherent mechanical limitations of the hemi-hip prosthesis material (polymethylmethacrylate/gentamicin), the temporary hemi-hip prosthesis is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers) throughout the implant period.

Biomet Suture Manipulation Instruments Singapur - angielski - HSA (Health Sciences Authority)

biomet suture manipulation instruments

zimmer pte. ltd. - orthopaedics - sterile single-use arthroscopic instrument utilized in conjunction with a nitinol wire or nylon monofilament to aid in passing suture through soft tissue.