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BSI - BS EN ISO 10993-16

Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables

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Organization: BSI
Publication Date: 31 January 2018
Status: active
Page Count: 28
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

BS EN ISO 10993-16
January 31, 2018
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
BS EN ISO 10993-16
January 31, 2018
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
BS EN ISO 10993-16
January 31, 2018
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
BS EN ISO 10993-16
March 31, 2010
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
BS EN ISO 10993-16
July 31, 2009
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
BS EN ISO 10993-16
November 15, 1997
Biological Evaluation of Medical Devices Part 16: Toxicokinetic Study Design for Degradation Products and Leachables
A description is not available for this item.
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References

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:
BS EN ISO 10993-18 - Biological evaluation of medical devices Part 18: Chemical characterization of medical device materials within a risk management process
Published by BSI on June 30, 2020
A description is not available for this item.
This document references:
BS EN ISO 10993-12 - Biological evaluation of medical devices Part 12: Sample preparation and reference materials
Published by BSI on October 31, 2012
A description is not available for this item.
This document references:
BS EN ISO 10993-17 - Biological evaluation of medical devices Part 17: Toxicological risk assessment of medical device constituents
Published by BSI on November 30, 2023
A description is not available for this item.
This document references:
BS EN ISO 10993-2 - Biological evaluation of medical devices Part 2: Animal welfare requirements
Published by BSI on November 30, 2022
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 is referenced by:
BS EN ISO 10993-6 - Biological evaluation of medical devices Part 6: Tests for local effects after implantation
Published by BSI on December 31, 2016
A description is not available for this item.
This document is referenced by:
BS EN ISO 7405 - Dentistry - Evaluation of biocompatibility of medical devices used in dentistry
Published by BSI on November 30, 2018
A description is not available for this item.
This document is referenced by:
BS EN ISO 10993-13 - Biological evaluation of medical devices Part 13: Identification and quantification of degradation products from polymeric medical devices
Published by BSI on October 31, 2010
A description is not available for this item.
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