11.100.20 - Biological evaluation of medical devices
Showing 49–64 of 246 results
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ISO 10993-16:2017
Évaluation biologique des dispositifs médicaux — Partie 16: Conception des études toxicocinétiques des produits de…
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ISO 10993-17:2002
Évaluation biologique des dispositifs médicaux — Partie 17: Établissement des limites admissibles des substances relargables…
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ISO 10993-16:2010
Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and…
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ISO 10993-15:2019
Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from…
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ISO 10993-15:2000
Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from…
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ISO 10993-14:2001
Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from…
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ISO 10993-12:2021
Biological evaluation of medical devices — Part 12: Sample preparation and reference materials Published By…
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ISO 10993-13:2010
Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from…
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ISO 10993-12:2012
Biological evaluation of medical devices — Part 12: Sample preparation and reference materials Published By…
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ISO 10993-11:2017
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity Published By Publication…
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ISO 10993-11:2006
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity Published By Publication…
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ISO 10993-10:2021
Biological evaluation of medical devices – Part 10: Tests for skin sensitization Published By Publication…
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ISO 10993-10:2010
Biological evaluation of medical devices — Part 10: Tests for irritation and skin sensitization Published…
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VDI 5701:2018 Edition
Biomaterialien in der Medizin – Klassifikation, Anforderungen und Anwendungen Published By Publication Date Number of…
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VDI 2017:2019 Edition
Medical Grade Plastics (MGP) Published By Publication Date Number of Pages DIN 2019-07 38
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DIN ISO 13022:2014 Edition
Medical products containing viable human cells – Application of risk management and requirements for processing…