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>DIN Standards>DIN EN ISO 10993-17 Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023 + Amd 1:2025) (includes Amendment A1:2025)
in stockReleased: 2026-05
DIN EN ISO 10993-17 Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023 + Amd 1:2025) (includes Amendment A1:2025)

DIN EN ISO 10993-17

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023 + Amd 1:2025) (includes Amendment A1:2025)

Biologische Beurteilung von Medizinprodukten - Teil 17: Toxikologische Risikobewertung von Medizinproduktbestandteilen (ISO 10993-17:2023 + Amd 1:2025) (enthält Änderung A1:2025)

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Status:Standard
Released:2026-05
Standard number:DIN EN ISO 10993-17
Name:Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023 + Amd 1:2025) (includes Amendment A1:2025)
Pages:83
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DIN EN ISO 10993-17

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