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Norm
ÖNORM EN ISO 10993-11
Issue date: 2006 11 01
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)
This part of ISO 10993 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adv...
Withdrawn: 2010 01 01
§ Legal References
Publisher:
Austrian Standards International
Format:
Digital | 32 Pages
Language:
German
| English
Currently valid:
Optionally co-design standards:
ICS
This part of ISO 10993 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
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 :
2009 10 13
Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process
Norm
Issue date :
2006 07 06
Biological evaluation of medical devices — Part 2: Animal welfare requirements
Norm
Issue date :
2007 10 31
Biological evaluation of medical devices — Part 12: Sample preparation and reference materials (Corrected version 2008-02)
Norm
Issue date :
2006 07 06
Biological evaluation of medical devices — Part 2: Animal welfare requirements
Norm
Issue date :
2009 09 15
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)
Norm
Issue date :
2006 08 15
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
