Your needs: characterize a PAH powder according to ISO 13779-6
What does ISO 13779-6 provide?
ISO 13779-6 specifies the requirements for hydroxyapatite powders used as raw material for the manufacture of surgical implants or the coating of surgical implants.
Our solutions: PAH powder analysis techniques according to ISO 13779-6
Analysis according to ISO 13779-6
With an analytical park of 2100m², the FILAB laboratory analysis and characterizes your hydroxyapatite powders (HAP) according to the ISO 13779-6 standard thanks to the following services
- Customised chemical analysis: for the composition of PAH powders
- Determination of the Ca/P ratio by XRD: to determine the foreign phases and the proportion of correctly crystallised apatite phases.
- Particle size analysis of PAH powders by laser granulometry
- Validation of cleaning processes
- Analysis of cleaning residues (TOC/HCT) and leachates
Why choose FILAB for PAH powders test according to ISO 13779-6?
The FILAB laboratory has a team of engineers and doctoral students who are highly qualified in the medical device sector. They provide you with their knowledge for a tailor-made analysis of PAH powders in your surgical implants.
In addition, our laboratory is COFRAC ISO 17025 accredited and Research Tax Credit (RTC) approved to offer you the best conditions for the analysis of your medical devices. Our 2100m² of analytical equipment enables us to offer you reliable, fast services at very competitive rates.
