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BSI - BS EN ISO 10993-14

Biological evaluation of medical devices Part 14: Identification and quantification of degradation products from ceramics

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Organization: BSI
Publication Date: 30 June 2009
Status: active
Page Count: 22
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

BS EN ISO 10993-14
June 30, 2009
Biological evaluation of medical devices Part 14: Identification and quantification of degradation products from ceramics
A description is not available for this item.
BS EN ISO 10993-14
December 14, 2001
Biological Evaluation of Medical Devices - Part 14: Identification and Quantification of Degradation Products from Ceramics
A description is not available for this item.
BS EN ISO 10993-14
December 14, 2001
Biological Evaluation of Medical Devices - Part 14: Identification and Quantification of Degradation Products from Ceramics
A description is not available for this item.

References

This document references:
BS EN ISO 10993-9 - Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products
Published by BSI on June 30, 2010
A description is not available for this item.
This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document references:
C92 - Standard Test Methods for Sieve Analysis and Water Content of Refractory Materials
October 10, 1995
These test methods cover a wet and a dry method for sieve analysis of refractory materials. Wet Sieve Analysis—Water promotes the slaking of clays and helps to separate fine particles, washing them...
This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document references:
D4780 - Standard Test Method for Determination of Low Surface Area of Catalysts and Catalyst Carriers by Multipoint Krypton Adsorption
October 15, 2023
This test method covers the determination of the specific surface area of catalysts and catalyst carriers in the range from 0.05 m2/g to 10 m2/g. A volumetric measuring system is used to obtain at...
This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
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 the...
This document references:
BS EN ISO 10993-9 - Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products
Published by BSI on June 30, 2010
A description is not available for this item.
This document references:
BS EN ISO 10993-9 - Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products
Published by BSI on June 30, 2010
A description is not available for this item.
This document is referenced by:
BS EN ISO 22442-1 - Medical devices utilizing animal tissues and their derivatives Part 1: Application of risk management
Published by BSI on December 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 16061 - Instruments for use in association with non-active surgical implants — General requirements
Published by BSI on April 30, 2021
A description is not available for this item.
This document is referenced by:
BS EN ISO 22803 - Dentistry - Membrane materials for guided tissue regeneration in oral and maxillofacial surgery - Contents of a technical file
Published by BSI on January 13, 2006
A description is not available for this item.
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