Skip to main content
Back

Sorry - this product is no longer available

EN ISO 10993-17:2023/prA1

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents - Amendment 1 (ISO 10993-17:2023/DAmd 1:2024)

General information

Draft
Base Documents
ISO 10993-17:2023/DAmd 1; EN ISO 10993-17:2023/prA1
Directives or regulations
None
You can view draft standards in the Commenting portal🡭.

Standard history

Status
Date
Type
Name
Amendment
EN ISO 10993-17:2023/prA1
01.12.2023
Main
Amendment to EN ISO 10993-17:2023

Required fields are indicated with *

*
*
*
Standard monitoring