NS EN ISO 10993-17 Ed. 1 (2003)被替代
Biological Evaluation Of Medical Devices - Part 17: Establishment Of Allowable Limits For Leachable Substances
出版：Norwegian Standards (Norges Standardiseringsforbund)
专家解读视频
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.
DIN EN ISO 10993-17 (2003-06) - Identical
UNI EN ISO 10993-17:2004 - Identical
NEN EN ISO 10993-17:2003 - Identical
ONORM EN ISO 10993-17:2003 - Identical
ISO 10993-17:2002 - Identical
UNE EN ISO 10993-17:2003 - Identical
SS EN ISO 10993-17 Ed. 1 (2003) - Identical
SN EN ISO 10993-17:2003 - Identical
BS EN ISO 10993-17:2002 - Identical
NBN EN ISO 10993-17:2003 - Identical
NF EN ISO 10993-17:2003 - Identical
I.S. EN ISO 10993-17:2003 - Identical
