DIN EN ISO 10993-17
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
inactive
| Organization: | DIN |
| Publication Date: | 1 June 2003 |
| Status: | inactive |
| Page Count: | 31 |
| ICS Code (Biological evaluation of medical devices): | 11.100.20 |
Document History
February 1, 2024
Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)
A description is not available for this item.
December 1, 2021
Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO/DIS 10993-17:2021); German and English version prEN ISO 10993-17:2021
A description is not available for this item.
August 1, 2009
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
A description is not available for this item.
February 1, 2009
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002); English version prEN ISO 10993-17:2008, Amendment 1
A description is not available for this item.
DIN EN ISO 10993-17
June 1, 2003
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
A description is not available for this item.
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