DIN EN ISO 10993-17:2003-06
Superseded Standard
Historical

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.
Most recent standard

Summary

Biologische Beurteilung von Medizinprodukten - Teil 17: Nachweis zulässiger Grenzwerte für herauslösbare Bestandteile (ISO 10993-17:2002); Deutsche Fassung EN ISO 10993-17:2002 / Achtung: Übergangsfrist, festgelegt durch DIN EN ISO 10993-17 (2009-08), bis 2010-03-21 beachten.

Notes

A transition period, as set out in DIN EN ISO 10993-17 (2009-08), exists until 2010-03-21.

Technical characteristics

Publisher Deutsche Institut für Normung e.V. (DIN)
Publication Date 06/01/2003
Page Count 8
EAN ---
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
Superseded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Superseded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 10993-17:1999-12

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Superseded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
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Superseded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 10993-17:2009-08

DIN EN ISO 10993-17:2009-08

Évaluation biologique des dispositifs médicaux - Partie 17: Établissement des limites admissibles des substances relargables (ISO 10993-17:2002); Version allemande EN ISO 10993-17:2009
01/08/2009
Superseded
Historical
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 10993-17:2024-02

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
Superseded
Historical
DIN EN ISO 10993-17:2026-05

DIN EN ISO 10993-17:2026-05

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023 + Amd 1:2025); German version EN ISO 10993-17:2023 + A1:2025
01/05/2026
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