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dnaSRPS EN ISO 10993-17:2024/prA1:2024

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

General information

50.20     Aug 7, 2025

50.60    Oct 1, 2025

ISS

Z076

European Norm

11.100.20  

English  

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

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

Life cycle

NOW

PROJECT
dnaSRPS EN ISO 10993-17:2024/prA1:2024
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Aug 7, 2025

Related project

Adopted from EN ISO 10993-17:2023/FprA1 IDENTICAL

Adopted from ISO 10993-17:2023/FDAmd 1 IDENTICAL

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