ISO 10993-1

Biological Evaluation of Medical Devices - Part 1: Guidance on Selection of Tests; (Corrigendum 1-1992) (CEN EN 30993-1: 1994)

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Organization: ISO
Publication Date: 1 January 1992
Status: inactive
Page Count: 21
ICS Code (Laboratory medicine): 11.100

Document History

August 1, 2018
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...
August 1, 2018
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...
June 15, 2010
Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process TECHNICAL CORRIGENDUM 1
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...
October 15, 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...
August 1, 2003
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...
December 15, 1997
Biological Evaluation of Medical Devices - Part 1: Evaluation and Testing
A description is not available for this item.
ISO 10993-1
January 1, 1992
Biological Evaluation of Medical Devices - Part 1: Guidance on Selection of Tests; (Corrigendum 1-1992) (CEN EN 30993-1: 1994)
A description is not available for this item.
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