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NEN EN ISO 10993-17:2003被替代

Biological Evaluation Of Medical Devices - Part 17: Establishment Of Allowable Limits For Leachable Substances

出版：Nederlands Normalisatie Instituut

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基本信息
標(biāo)準(zhǔn)編號(hào)： NEN EN ISO 10993-17:2003
發(fā)布時(shí)間：2003/2/1 0:00:00
標(biāo)準(zhǔn)類別：Standard
出版單位：Nederlands Normalisatie Instituut
標(biāo)準(zhǔn)頁(yè)數(shù)：25
標(biāo)準(zhǔn)簡(jiǎn)介

Describes a method for the determination of allowable limits for substances leachable from medical devices. It is intended for use in deriving standards and estimating appropriate limits where standards do not exist. It describes a systematic process through which identified risks arising from toxicologically hazardous substances present in medical devices can be quantified.

替代本標(biāo)準(zhǔn)的新標(biāo)準(zhǔn)

NEN EN ISO 10993-17:2009

等同采用的國(guó)際標(biāo)準(zhǔn)

ISO 10993-17:2002 - Identical

NF EN ISO 10993-17:2003 - Identical

NBN EN ISO 10993-17:2003 - Identical

DIN EN ISO 10993-17 (2003-06) - Identical

BS EN ISO 10993-17:2002 - Identical

SN EN ISO 10993-17:2003 - Identical

I.S. EN ISO 10993-17:2003 - Identical

UNI EN ISO 10993-17:2004 - Identical

NS EN ISO 10993-17 Ed. 1 (2003) - Identical

UNE EN ISO 10993-17:2003 - Identical

SS EN ISO 10993-17 Ed. 1 (2003) - Identical

ONORM EN ISO 10993-17:2003 - Identical