EUROLAB laboratory provides testing and compliance services within the scope of ISO 5832-11 standard. ISO 5832-11 specifies the properties and corresponding test methods of the wrought titanium alloy known as titanium 6-aluminum 7-niobium alloy (Ti-6-Al 7-Nb) for use in the manufacture of surgical implants.
No known surgical implant material has been shown to be completely free of adverse reactions in the human body. However, long-term clinical experience with the use of the material referred to in this part of ISO 5832 has shown that an acceptable level of biological response can be expected when the material is used in appropriate applications.
If any of the pieces do not meet the specified requirements or go outside the size limits, two more test pieces representing the same lot will be tested in the same way. The alloy will be considered suitable only if both additional test pieces meet the specified requirements.
EUROLAB assists manufacturers with ISO 5832-11 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.
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EUROLABreporting and certification activities, United Accreditation Foundation (UAF), Turkish Accreditation Agency (TÜRKAK) ve Enterprise Accreditation Foundation (EAF) based on the accreditation provided by the accreditation body. The Enterprise Accreditation Foundation (EAF) accreditation body is also a signatory of the United Nations (UN GLOBAL COMPACT) organization.
