ISO 13779-3 Implants for Surgery, Hydroxyapatite, Part 3: Chemical Analysis and Characterization of Crystallinity and Phase Purity

Medical Tests

ISO 13779-3 Implants for Surgery, Hydroxyapatite, Part 3: Chemical Analysis and Characterization of Crystallinity and Phase Purity

EUROLAB laboratory provides testing and compliance services within the scope of ISO 13779-3 standard. This standard specifies test methods for chemical analysis, evaluation of crystallinity and phase composition of hydroxyapatite-based materials such as powders, coatings or bulk products.

ISO 13779-3 Implants for Surgery, Hydroxyapatite, Part 3: Chemical Analysis and Characterization of Crystallinity and Phase Purity

These tests aim to identify the properties of the material and communicate them between organizations. Although these tests can be used in this way, they are not written to replace a company's internal operational and evaluation tests.

No known surgical implant material has been shown to cause absolutely any adverse reaction in the human body. However, long-term clinical experience with the use of material referred to in this part of ISO 13779 has shown that a viable level of biological response can be expected if the material is used in appropriate applications.

The biological response to the coating of hydroxyapatite ceramic has been proven by clinical use history and laboratory studies.

EUROLAB assists manufacturers with ISO 13779-3 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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