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

Available format(s)

Hardcopy

Language(s)

German - English

Published date

15-02-2024

Publisher

Osterreichisches Normungsinstitut/Austrian Standards

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

DocumentType	Standard
Pages	86
PublisherName	Osterreichisches Normungsinstitut/Austrian Standards
Status	Current
Supersedes	ONORM EN ISO 10993-17 : 2009

$747.88

Including GST where applicable

Product format

I agree to the DRM document license rules apply against the PDF selection made.

Please confirm that you agree to the document license rules for this document.

I agree to the document license rules .

Please confirm that you agree to the document license rules for this document.

Access your standards online with a subscription

Features

ÖNORM EN ISO 10993-17:2024 02 15