NEN-EN-ISO 10993-13
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
inactive
| Organization: | NEN |
| Publication Date: | 1 December 1998 |
| Status: | inactive |
| Page Count: | 28 |
| ICS Code (Biological evaluation of medical devices): | 11.100.20 |
scope:
Provides guidance on general requirements for the design of tests for identifying and quantifying degradation products from finished polymeric medical devices ready for clinical use.
Document History
June 1, 2010
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
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...
May 1, 2009
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
This part of ISO 10993 provides guidance on general requirements for the design of tests for identifying and quantifying degradation products from finished polymeric medical devices ready for...
August 1, 2008
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
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...
NEN-EN-ISO 10993-13
December 1, 1998
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
Provides guidance on general requirements for the design of tests for identifying and quantifying degradation products from finished polymeric medical devices ready for clinical use.
August 1, 1997
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymers
Provides guidance on general requirements for the design of tests for identifying and quantifying degradation products from finished polymeric medical devices ready for clinical use.