If re operation is required in case of fracture of the ceramic femoral head make sure that the ceramic femoral head is substituted by a revision ceramic or a metallic femoral head never use another ceramic head on an existing stem make sure all ceramic particles have been removed and replace the polyethylene cup liner even if it seems to be in good condition and well fixed.
Biolox delta ceramic femoral head mri safety.
Biolox delta ceramic femoral head.
What mri safety information does the labeling contain.
Biolox delta ceramic femoral head 32mm dia 1 12 14 taper close.
Biolox delta ceramic femoral head 0 36mm dia 11 13 taper close.
Labeling does not contain mri safety information device required to be labeled as containing natural rubber latex or dry natural rubber 21 cfr 801 437.
The titanium adapters have an internal 12 14 taper that mates with the femoral stem while the option heads have a taper designed to mate with the adapters.
The need for a low wear ceramic bearing in revision arthroplasty was not available in the past.
Biolox delta ceramic v40 femoral head.
Biolox delta is the only ceramic with 15 years of successful clinical experience and with more than 8 million sold components.
Ceramic femoral head prosthesis a sterile implantable artificial substitute for a diseased or injured femoral head that has an outer surface made of ceramic e g.
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The option is comprised of two components.
Accessgudid biolox delta modular head 36mm long 4 0mm 12 14 eurocone taper 05055196964396 biolox delta ceramic head.
Labeling does not contain mri safety information.
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What mri safety information does the labeling contain.
The biolox delta component is a traditional one piece ceramic head indicated for primary hip arthroplasty only.
Biolox delta ceramic femoral head s ΓΈ 40 3 5 taper 12 14 close.
What mri safety information does the labeling contain.
Labeling does not contain mri safety information device required to be labeled as containing natural rubber latex or dry natural rubber 21 cfr 801 437.
Labeling does not contain mri safety information device required to be labeled as containing natural rubber latex or dry natural rubber 21 cfr 801 437.
Labeling does not contain mri safety information device required to be labeled as containing natural rubber latex or dry natural rubber 21 cfr 801 437.