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EVS-EN ISO 10993-12:2021/A1:2025

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials - Amendment 1 (ISO 10993 12:2021/Amd 1:2025)

General information

Valid from 01.10.2025
Base Documents
ISO 10993-12:2021/Amd 1:2025; EN ISO 10993-12:2021/A1:2025
Directives or regulations
None

Standard history

Status
Date
Type
Name
01.10.2025
Amendment
01.10.2025
Main + amendment
01.07.2021
Main
Amendment to EN ISO 10993-12:2021

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EVS-EN ISO 15223-1:2021/A1:2025

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Amendment

EVS-EN ISO 10993-5:2009/A11:2025

Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity
Valid from 15.05.2025
Amendment

EVS-EN ISO 10993-4 V2:2017/A1:2025

Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2017/Amd 1:2025, Corrected version 2025-04)
Valid from 17.03.2025