Menu

0

EN ISO 10993-17:2023/A1:2025

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

Publication date:   Feb 17, 2026

General information

60.60   Standard published   Dec 24, 2025

CEN

CEN/TC 206 Biological and clinical evaluation of medical devices

European Norm

11.100.20   Biological evaluation of medical devices

Buying

  Published

PDF - €27.43

  English  



Buy

Related legislation

Legislation related to this standard

2017/745

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

Legislation 2017/745

Life cycle

PREVIOUSLY

PUBLISHED
EN ISO 10993-17:2023

NOW

PUBLISHED
EN ISO 10993-17:2023/A1:2025
60.60 Standard published
Dec 24, 2025