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This document specifies procedures for the generation of medical device extracts for chemical characterization testing to support toxicological risk assessment. It supports the activities of EN ISO 10993-18:2020 that depend on chemical analysis of device extracts for chemical characterization.
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This document specifies procedures for the generation of medical device extracts for chemical characterization testing to support toxicological risk assessment. It supports the activities of EN ISO 10993-18:2020 that depend on chemical analysis of device extracts for chemical characterization.
