Standard

ISO 10993-11:2017

Sep 2017 Current

Note: Now under development: ISO/DIS 10993-11

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Abstract

ISO 10993-11:2017 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.

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Standard from ISO
Published: September 14 2017
Edition: 3
Document type: IS
Pages
ISBN:

Publisher: ISO
Distributor: ISO
ICS: 11.100.20
International TC: ISO/TC 194

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Adopted by: SN EN ISO 10993-11:2018
Adopted by: NF EN ISO 10993-11:2018
Revises: ISO 10993-11:2006
Revised by: ISO/DIS 10993-11

ISO 10993-11:2017

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ISO 10993-11:2017

ISO 10993-11:2006

ISO 10993-11:1993

Abstract

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Version history History (3)

ISO 10993-11:2017

ISO 10993-11:2006

ISO 10993-11:1993

Abstract

Products specifications

Product Relations

Product life cycle