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Healthcare > Laboratory medicine > Medical devices. Biological evaluation

Medical devices. Biological evaluation

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BS EN ISO 10993-23:2021/Amd 1

Biological evaluation of medical devices — Part 23: Tests for irritation - Amendment 1: Biological evaluation of medical devices — Part 23: Tests for irritation — Amendment 1

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18/11/2024

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BS EN ISO 10993-17:2023

Biological evaluation of medical devices. Toxicological risk assessment of medical device constituents

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PD ISO/TS 11796:2023

Biological evaluation of medical devices. Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devices

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BS EN ISO 10993-18:2020+A1:2023

Biological evaluation of medical devices. Chemical characterization of medical device materials within a risk management process

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BS EN ISO 10993-15:2023

Biological evaluation of medical devices. Identification and quantification of degradation products from metals and alloys

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PD ISO/TR 10993-55:2023

Biological evaluation of medical devices. Interlaboratory study on cytotoxicity

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BS EN ISO 10993-10:2023

Biological evaluation of medical devices. - Part 10: Tests for skin sensitization

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BS EN ISO 10993-9:2021

Biological evaluation of medical devices. Framework for identification and quantification of potential degradation products

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BS ISO 17593:2022

Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy

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