ANSI/AAMI/ISO 10993-13:2010(R2014)
Superseded
View Superseded by
Biological evaluation of medical devices, Part 13: Identification and quantification of degradation products from polymeric devices.
English
10-08-2014
11-04-2023
This part of ISO 10993 provides general requirements for the design of tests in a simulated environment for identifying and quantifying degradation products from finished polymeric medical devices ready for clinical use.
| Committee |
TC 194
|
| DocumentType |
Standard
|
| ISBN |
1570203962
|
| Pages |
28
|
| PublisherName |
Association for the Advancement of Medical Instrumentation
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ISO 10993-13:2010 | Identical |
| AAMI TIR17:2017(R2023) | Compatibility of materials subject to sterilization |
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