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DIN EN ISO 10993-16

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)

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Organization: DIN
Publication Date: 1 February 2018
Status: active
Page Count: 24
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

DIN EN ISO 10993-16
February 1, 2018
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
A description is not available for this item.
April 1, 2016
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO/DIS 10993-16:2016); German and English version prEN ISO 10993-16:2016
A description is not available for this item.
June 1, 2010
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)
A description is not available for this item.
August 1, 2009
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)
A description is not available for this item.
February 1, 2009
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997); English version prEN ISO 10993-16:2008, Amendment 1
A description is not available for this item.
November 1, 1997
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997)
A description is not available for this item.

References

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