14 - 17 May 2024 OTWorld

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

Product Finder - Biological Assessment of Medical Products: Find out quick & easy which tests are relevant for your product.

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Mr. Dr. Timo Hammer
CEO Hohenstein Laboratories GmbH & Co. KG
Ms. Dr. Anja Gerhardts
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Hohenstein Laboratories GmbH & Co. KG

Schloßsteige 1
74357 Bönnigheim

Tel.: +49 7143 271-898
Fax: +49 7143 271-51

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