Biocompatibility
The basis for the biological assessment of medical devices is the DIN EN ISO 10993 series of standards. DIN EN ISO 10993-1 specifies which endpoints you must consider in the biological risk assessment of your product.
Hohenstein tests non-animal according to recognised in vitro methods.

For more information: https://www.hohenstein-medical.com/en/our-services/biocompatibility

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