Biological Evaluation
Search Results
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AAMI/ISO 1099307E
Biological Evaluation of Medical Devices - Part 7: Ethylene Oxide Sterilization Residuals, Errata (22-Jan-2010)
Amendment by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 01/22/2010.
Languages: English
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AAMI/ISO 10993-10:2010/(R)2014
Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization
standard by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 09/04/2010.
Languages: English
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AAMI/ISO 10993-11:2006/(R)2014 [ Withdrawn ]
This document has been replaced. View the most recent version.
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
standard by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 10/19/2006.
Languages:
Historical Editions: AAMI/ISO 10993-11:2017
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AAMI/ISO 10993-11:2017
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
standard by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 04/27/2020.
Languages: English
Historical Editions: AAMI/ISO 10993-11:2006/(R)2014
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AAMI/ISO 10993-1:2003
This document has been replaced. View the most recent version.
Biological Evaluation of Medical Devices Part 1: Evaluation and Testing
standard by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 12/01/2003.
Languages: English
Historical Editions: AAMI/ISO 10993-1:2018, AAMI/ISO 10993-1:2009/(R)2013
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AAMI/ISO 10993-1:2009 Erratum
Erratum for Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Amendment by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 06/10/2013.
Languages: English
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AAMI/ISO 10993-1:2009/(R)2013 [ Withdrawn ]
This document has been replaced. View the most recent version.
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process; Includes Erratum (2013)
standard by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 09/03/2009.
Languages:
Amendments, rulings, and supplements: AAMI/ISO 10993-1:2009 Erratum
Historical Editions: AAMI/ISO 10993-1:2018, AAMI/ISO 10993-1:2003
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AAMI/ISO 10993-1:2018
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
standard by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 04/27/2020.
Languages: English
Historical Editions: AAMI/ISO 10993-1:2009/(R)2013, AAMI/ISO 10993-1:2003
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AAMI/ISO 10993-12:2002
This document has been replaced. View the most recent version.
Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials
standard by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 03/27/2003.
Languages: English
Historical Editions: AAMI/ISO 10993-12:2012, AAMI/ISO 10993-12:2007
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AAMI/ISO 10993-12:2007
This document has been replaced. View the most recent version.
Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials
standard by Association for the Advancement of Medical Instrumentation/International Org. for Standardization, 11/08/2007.
Languages: English
Historical Editions: AAMI/ISO 10993-12:2012, AAMI/ISO 10993-12:2002