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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.
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