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This document is purchased as a PDF (Portable Document Format) and accessed via CSA OnDemand™, where you can view, navigate, and print it, or download it for offline use with Adobe Acrobat Viewer. This PDF contains Digital Rights Management protection and is intended for individual use. Please see Terms of Use for CSA’s copyright license and more information.
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This document is purchased as a PDF (Portable Document Format) and accessed via CSA OnDemand™, where you can view, navigate, and print it, or download it for offline use with Adobe Acrobat Viewer. This PDF contains Digital Rights Management protection and is intended for individual use. Please see Terms of Use for CSA’s copyright license and more information.
This part of ISO 10993 specifies methodologies for the evaluation of the systemic toxicity potential of medical devices which release constituents into the body. In addition, it includes pyrogenicity testing.
The test methods cited in this part of ISO 10993 are from International Standards, national standards, directives and regulations. This part of ISO 10993 is concerned with either the actual product or its leachables. It is intended that tests for extracts or leachables be conducted by choosing appropriate extraction vehicles to yield a maximum extraction of leachable materials, in order to conduct biological testing.
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