BS ISO 5832-14:2007 Implants for surgery. Metallic materials. Wrought titanium 15-molybdenum 5-zirconium 3-aluminium alloy
No known surgical implant material has ever been shown to cause absolutely no adverse reactions in the human body. However, long-term clinical experience of the use of the material referred to in this part of BS ISO 5832 has shown that an acceptable level of biological response can be expected, when the material is used in appropriate applications.
BS ISO 5832 consists of the following parts, under the general title Implants for surgery:
Metallic materials:
Part 1: Wrought stainless steel
Part 2: Unalloyed titanium
Part 3: Wrought titanium 6-aluminium 4-vanadium alloy
Part 4: Cobalt-chromium-molybdenum casting alloy
Part 5: Wrought cobalt-chromium-tungsten-nickel alloy
Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy
Part 7: Forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy
Part 8: Wrought cobalt-nickel-chromium-molybdenum-tungsten-iron alloy
Part 9: Wrought high nitrogen stainless steel
Part 11: Wrought titanium 6-aluminium 7-niobium alloy
Part 12: Wrought cobalt-chromium-molybdenum alloy
Part 14: Wrought titanium 15-molybdenum 5-zirconium 3-aluminium alloy
BS ISO 5832-14 specifies the characteristics of, and corresponding test methods for, the wrought titanium 15-molybdenum 5-zirconium 3-aluminium alloy for use in the manufacture of surgical implants.
BS ISO 5832-14 applies to materials in bar form up to a maximum diameter of 100 mm.
The following referenced documents are indispensable for the application of this document.
BS EN ISO 643:2003 Steels. Micrographic determination of the apparent grain size
ISO 6892 Metallic materials. Tensile testing at ambient temperature