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Norm
ÖNORM EN ISO 10993-11
Issue date: 2018 10 15
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
This document specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse syst...
Valid
Publisher:
Austrian Standards International
Format:
Digital | 46 Pages
Language:
German
| English
| Download GER/ENG
Optionally co-design standards:
ICS
This document 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.
ÖNORM EN ISO 10993-11
2018 10 15
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
Norm
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ÖNORM EN ISO 10993-11
2009 09 15
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)
Norm
ÖNORM EN ISO 10993-11
2006 11 01
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)
Norm
ÖNORM EN ISO 10993-11
1996 01 01
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:1993)
Norm
Norm
Issue date :
2018 08 17
Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process (Corrected version 2018-10)
Norm
Issue date :
2006 07 06
Biological evaluation of medical devices — Part 2: Animal welfare requirements
Norm
Issue date :
2017 09 14
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
