EN ISO 10993-17 标准查询与下载

DIN EN ISO 10993-17:2009 医疗器械的生物学评定.第17部分:可浸出物质容许限值的确定(ISO 10993-17-2002);德文版本EN ISO 10993-17-2009

This part of ISO 10993 specifies a method for the determination of allowable limits for substances leachable from medical devices. It is intended

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002); English version of DIN EN ISO 10993-17:2009-08

EN ISO 10993-17:2002 医疗器械的生物评定.第17部分:可浸出物质容许限值的确定ISO 10993-17-2002

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances ISO 10993-17: 2002

EN ISO 10993-17:2023 医疗器械的生物学评价 第 17 部分：医疗器械成分的毒理学风险评估 (ISO 10993-17:2023)

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

DIN EN ISO 10993-17:2003 医疗器械生物学评价 第17部分：可滤出物质允许限值的建立（ISO 10993-17:2002）

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

DIN EN ISO 10993-17:2024 医疗器械生物学评价 第17部分：医疗器械成分的毒理学风险评估（ISO 10993-17:2023）

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

UNE-EN ISO 10993-17:2009 医疗器械的生物学评价 第17部分：确定可浸出物质的允许限度（ISO 10993-17:2002）

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

EN ISO 10993-17:2009 医疗器械的生物评定.第17部分:可浸出物质容许限值的确定

This part of ISO 10993 specifies a method for the determination of allowable limits for substances leachable from medical devices. It is intended

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances

NS-EN ISO 10993-17:2002 医疗器械的生物学评价 第17部分：可浸出物质允许限值的建立（ISO 10993-17:2002）

  Full Description This part of ISO 10993 specifies a method for the determination of allowable limits for substances leachable

Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

UNE-EN ISO 10993-17:2003 医疗器械的生物学评价 第17部分：可浸出物质允许限值的建立 (ISO 10993-17:2002)

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

NS-EN ISO 10993-17:2009 医疗器械的生物学评价 第17部分：可浸出物质允许限值的建立 (ISO 10993-17:2002)

  Full Description ADOPTED_FROM:EN ISO 10993-17:2009 ISO 10993-17:2002 specifies the determination of allowable limits

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

DIN EN ISO 10993-17 E:2021 医疗器械生物学评价 第17部分：医疗器械成分的毒理学风险评估 (ISO/DIS 10993-17:2021) 草案

Draft Document – 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

NF EN ISO 10993-17:2009 医疗器械生物学评价第17部分：浸出物允许限量的制定

Évaluation biologique des dispositifs médicaux - Partie 17 : établissement des limites admissibles des substances relargables

AENOR UNE-EN ISO 10993-17:2009 医疗器械的生物学评价 第17部分：可浸出物质允许限值的建立 (ISO 10993-17:2002)

  Full Description ENGLISH * SAME AS ISO 10993-17

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

BS EN ISO 10993-17:2009 医疗器械的生物学评价 制定可浸出物质的允许限值

Biological evaluation of medical devices. Establishment of allowable limits for leachable substances

BS EN ISO 10993-17:2023 医疗器械生物学评价-医疗器械成分毒理学风险评估

This document specifies the process and requirements for the toxicological risk assessment of medical device constituents. The methods and criteria

Biological evaluation of medical devices - Toxicological risk assessment of medical device constituents