DIN EN ISO 10993-17/A1:2009-02
Superseded Draft amendment
Historical

DIN EN ISO 10993-17/A1:2009-02

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
Most recent standard
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Technical characteristics

Publisher Deutsche Institut für Normung e.V. (DIN)
Publication Date 02/01/2009
Page Count 8
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ISBN ---
Weight (in grams) ---
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Previous versions

DIN EN ISO 10993-17/A1:2024-09

DIN EN ISO 10993-17/A1:2024-09

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents - Amendment 1 (ISO 10993-17:2023/DAM 1:2024); German and English version EN ISO 10993-17:2023/prA1:2024
01/09/2024
Active
Most Recent
DIN EN ISO 10993-17:2024-02

DIN EN ISO 10993-17:2024-02

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023); German version EN ISO 10993-17:2023
01/02/2024
Active , Has Draft
Most Recent
DIN EN ISO 10993-17:2021-12

DIN EN ISO 10993-17:2021-12

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
01/12/2021
Superseded
Historical
DIN EN ISO 10993-17:2009-08

DIN EN ISO 10993-17:2009-08

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002); German version EN ISO 10993-17:2009.
01/08/2009
Superseded
Historical
DIN EN ISO 10993-17/A1:2009-02

DIN EN ISO 10993-17/A1:2009-02

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
01/02/2009
Superseded
Historical
DIN EN ISO 10993-17:2003-06

DIN EN ISO 10993-17:2003-06

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002); German version EN ISO 10993-17:2002.
01/06/2003
Superseded
Historical
DIN EN ISO 10993-17:1999-12

DIN EN ISO 10993-17:1999-12

Biological evaluation of medical devices - Part 17: Methods for the establishment of allowable limits for leachable substances using health-based risk assessment (ISO/DIS 10993-17:1999); German version prEN ISO 10993-17:1999
01/12/1999
Superseded
Historical
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