Your needs: analyze and characterize your HAP (hydroxyapatite) powders
HAP powders and medical devices
Hydroxyapatite, or HAP, is used in the Medical Device sector to manufacture surgical implants as a filling material. This bioactive ceramic is particularly used for its biocompatibility, strong mechanical properties, porous morphology and bioresorbability.
Chemical analysis of medical devices
Chemical analysis assessing the purity of hydroxyapatite (HAP) powders must meet the precise criteria set out in the NF ISO 13779-3 standard (available on the www.boutique.afnor.org website).
To this end, the support of an analytical and testing laboratory enables you to carry out your industrial projects while ensuring the compliance of your products.
In addition, FILAB offers analysis according to ASTM F1854 to study the porosity of an HAP coating on an implant.
Chemical analysis assessing the purity of hydroxyapatite (HAP) powders must meet the precise criteria set out in the NF ISO 13779-3 standard (available on the www.boutique.afnor.org website).
To this end, the support of an analytical and testing laboratory enables you to carry out your industrial projects while ensuring the compliance of your products.
In addition, FILAB offers analysis according to ASTM F1854 to study the porosity of an HAP coating on an implant.
What does ISO 13779-3 say?
The ISO 13779-3:2018 standard, entitled “Implants for surgery — Hydroxyapatite — Part 3: Chemical analysis and characterization of crystallinity ratio and phase purity”, specifies test methods for the chemical analysis, evaluation of the crystallinity ratio and phase composition of hydroxyapatite-based materials, such as powders, coatings or bulk products.
These tests are intended to describe material properties and facilitate communication between different organizations. They are not designed to replace a company’s functional and internal evaluation tests, although they may be used for this purpose.
ISO 13779-3:2018 introduces a new method for measuring the crystallinity ratio of hydroxyapatite and proposes the Rietveld method as an alternative for quantifying the content of foreign phases.
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Our solutions: expert support and various analytical methods to characterize your HAP powders
Why choose FILAB for HAP powder analysis?
The FILAB laboratory is accredited for the analysis of HAp powders used in surgical implants in accordance with ISO 13779-3.
With state-of-the-art analytical equipment and a qualified team of PhD holders and engineers, Filab laboratory analyzes and characterizes your HAP hydroxyapatite powders according to the NF ISO 13779-3 standard, through the following services:
Chemical analysis of the composition of HAP hydroxyapatite powders
Solubility testing of HAP hydroxyapatite powder
Determination of the presence of foreign phases (alpha-TCP, beta-TCP, CaO and TTCP) by XRD
Ca/P ratio measurement
Detection of oxyapatite by FTIR infrared spectroscopy
analysis according to ASTM F1854
To support you under the best possible conditions, the FILAB laboratory is accredited Research Tax Credit (CIR).
Through our three levels of service—analysis, expertise, and R&D support—FILAB assists companies in every sector and of every size in resolving their industrial challenges by providing clients with the expertise and experience of its team.
