SS-EN-ISO-10993-11 › Historical Revision Information
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10 993-11:1993)
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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.
To find similar documents by classification:
11.100.20 (Biological evaluation of medical devices Medical microbiology, see 07.100.10)
Active implantable medical devices. Medical devices
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Designation Name
SS-EN ISO 10993-11:2006
Revision Level
2006 EDITION
Status
Superseded
Publication Date
Aug. 31, 2006
Language(s)
English
Page Count
32