SS-EN-ISO-10993-11 › Historical Revision Information
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10 993-11:1993)
Document Center Inc. is an authorized dealer of SIS standards.
The following bibliographic material is provided to assist you with your purchasing decision:
The following bibliographic material is provided to assist you with your purchasing decision:
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
This document comes with our free Notification Service, good for the life of the document.
This document is available in either Paper or PDF format.
Designation Name
SS-EN ISO 10993-11:2009
Revision Level
2009 EDITION
Status
Superseded
Publication Date
May 8, 2009
Language(s)
English
Page Count
44
International Equivalent
EN ISO 10993-11:2009(IDT); ISO 10993-11:2006(IDT)