DSF/PREN ISO 10993-11
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2015)
pending
| Organization: | DS |
| Status: | pending |
| Page Count: | 42 |
| ICS Code (Biological evaluation of medical devices): | 11.100.20 |
scope:
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.
Document History
June 6, 2018
Biological evaluation of medical devices – Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
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.
June 15, 2009
Biological evaluation of medical devices – Part 11: Tests for systemic toxicity
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.
October 13, 2006
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
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.
November 28, 1995
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
This part of the Standard specifies methodologies for the evaluation of the systemic toxicity potential of medical devices which release constituents into the body. In addition, it includes...
Biological evaluation of medical devices – Part 11: Tests for systemic toxicity (ISO/FDIS 10993-11:2017)
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.
DSF/PREN ISO 10993-11
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2015)
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.
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 adverse systemic reactions.