EUROLAB laboratory provides testing and compliance services within the scope of ISO 13779-1 standard. ISO 13779-1 specifies requirements for ceramic hydroxyapatite intended for use as surgical implants.
ISO 13779-1 does not apply to hydroxyapatite coatings, hydroxyapatite powder or nanoparticle type and calcium phosphate ceramics that are not primarily composed of crystalline hydroxyapatite.
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 material referred to in ISO 13779 has shown that an acceptable level of biological response can be expected if the material is used in appropriate applications.
The biological response to hydroxyapatite ceramic has been demonstrated by clinical use history and laboratory studies.
EUROLAB assists manufacturers with ISO 13779-1 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.
