Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

Available format(s)

Hardcopy

Language(s)

English

Published date

01-11-2023

Publisher

Norwegian Standards (Norges Standardiseringsforbund)

This document specifies the process and requirements for the toxicological risk assessment of medical device constituents.

Committee	ISO/TC 194
DocumentType	Standard
Pages	84
PublisherName	Norwegian Standards (Norges Standardiseringsforbund)
Status	Current
Supersedes	NS EN ISO 10993-17 : 2009

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NS-EN ISO 10993-17:2023