View Ceraver on TEKEN44The product page for the REVISION HERMES POSTERO-STABILIZED mentions the following standards: - NF ISO 5832-4 - NF ISO 5834-2 - NF ISO 5832-3 These standards pertain to the materials used in the femoral component, tibial insert, and tibial baseplate, respectively.
A tricompartimental knee implant designed for revision surgeries, featuring a femoral component made of CoCrMo alloy, a tibial insert of Ultra High Molecular Weight Polyethylene (UHMWPE), and a tibial baseplate of Titanium alloy TiAl₆V₄. It offers cylindrical and centered postero-stabilization, rotating mobility, and compatibility with HiFit PS 1st intention.
ISO 5832-3
Implants for surgery — Metallic materials — Part 3: Wrought titanium 6-aluminium 4-vanadium alloy
ISO 5832-4
Implants for surgery — Metallic materials Part 4: Cobalt-chromium-molybdenum casting alloy
ISO 5834-2
Implants for surgery — Ultra-high-molecular-weight polyethylene Part 2: Moulded forms
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