CEN - EN ISO 10993-1
Biological Evaluation of Medical Devices - Part 1: Evaluation and Testing
inactive
Organization: | CEN |
Publication Date: | 1 December 1997 |
Status: | inactive |
Page Count: | 22 |
ICS Code (Medical sciences and health care facilities in general): | 11.020 |
ICS Code (Pharmaceutics): | 11.120 |
Document History
December 1, 2020
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
This document specifies:
— the general principles governing the biological evaluation of medical devices within a risk management process;
— the general categorization of medical devices based on...
October 1, 2009
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
This part of ISO 10993 describes:
— the general principles governing the biological evaluation of medical devices within a risk management process;
— the general categorization of devices based on...
June 1, 2009
Biological evaluation of medical devices - Part 1: Evaluation and testing
This part of ISO 10993 describes
a) the general principles governing the biological evaluation of medical devices;
b) the categorization of devices based on the nature and duration of their contact...
August 1, 2003
Biological evaluation of medical devices Part 1: Evaluation and testing
A description is not available for this item.
EN ISO 10993-1
December 1, 1997
Biological Evaluation of Medical Devices - Part 1: Evaluation and Testing
A description is not available for this item.