DIN EN ISO 10993-1
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10)
active, Most Current
| Organization: | DIN |
| Publication Date: | 1 May 2021 |
| Status: | active |
| Page Count: | 52 |
| ICS Code (Biological evaluation of medical devices): | 11.100.20 |
Document History
DIN EN ISO 10993-1
May 1, 2021
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10)
A description is not available for this item.
April 1, 2017
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO/DIS 10993-1:2017); German and English version prEN ISO 10993-1:2017
A description is not available for this item.
April 1, 2010
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009)
This part of ISO 10993 describes:
This part of ISO 10993 describes: — the general principles governing the biological evaluation of medical devices within a risk management process; — the...
October 1, 2009
Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)
A description is not available for this item.
March 1, 2009
Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003); English version FprEN ISO 10993-1:2009, Amendment 1
A description is not available for this item.
December 1, 2003
Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003)
A description is not available for this item.
June 1, 1998
Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:1997); German version EN ISO 10993-1:1997
A description is not available for this item.