EUROLAB laboratory provides testing and compliance services within the scope of ISO 5832-7 standard. ISO 5832-7 specifies the properties and corresponding test methods of a malleable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy for use in the manufacture of surgical implants.
The mechanical properties of a sample from a finished product made of this particular material need not exactly comply with those specified in this standard.
No known surgical implant material has been shown to be completely free from adverse reactions in the human body. However, long-term clinical experience with the use of the material referenced in this document has shown that an acceptable biological response can be expected at the tabular level when the material is used.
EUROLAB assists manufacturers with ISO 5832-7 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.
