DIN EN ISO 10993-11
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
active, Most Current
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| Organization: | DIN |
| Publication Date: | 1 September 2018 |
| Status: | active |
| Page Count: | 44 |
| ICS Code (Biological evaluation of medical devices): | 11.100.20 |
scope:
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.
Document History
DIN EN ISO 10993-11
September 1, 2018
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 systemic reactions.
December 1, 2015
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2015); German and English version prEN ISO 10993-11:2015
A description is not available for this item.
August 1, 2009
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)
A description is not available for this item.
February 1, 2009
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006); English version prEN ISO 10993-11:2008, Amendment 1
A description is not available for this item.
November 1, 2006
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)
A description is not available for this item.
December 1, 1995
Biological evaluation of medical devices - Tests for systemic toxicity (ISO 10993-11:1993)
A description is not available for this item.