Identification and quantification of potential degradation products in accordance with the ISO 10993 set
Anaïs DECAUX
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Home • Our services • Expertise • Laboratory biocompatibility tests in accordance with ISO 10993 • Study of degradation products in your medical devices according to ISO 10993-15 • Identification and quantification of potential degradation products in accordance with the ISO 10993 set
The ISO 10993-9 standard specifies the general principles for the conception and examination of a study into potential degradations of materials used in Medical Devices.
The data collected during these studies could be useful when evaluating the toxicological risks of Medical Devices (resorbable or non-resorbable materials)
Three complementary standards allow for degradation products to be identified and quantified:
The implementation of degradation analysis depends on collaboration and information exchanges between characterization specialists, analytical specialists and toxicologists.
For over ten years, the FILAB laboratory has been developing a wide skillset in analytical chemistry and material characterization and has been collaborating with toxicology experts when conducting biodegradation analysis on your biomaterials:
In the context of an examination of the quality and security of your Medical Devices, the FILAB laboratory can offer complementary analytical services with high added value:
Discover the analytical techniques we use at FILAB here
To know more about the analytical services offered at FILAB click here
For more information, feel free to contact us via email at contact@filab.fr or over the phone by calling +33 (0)3 80 52 32 05