SN EN ISO 10993-17:2003被替代
Biological Evaluation Of Medical Devices - Part 17: Establishment Of Allowable Limits For Leachable Substances
出版：Swiss Standards
專家解讀視頻
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.
Supersedes SN 119800. (06/2006)
DIN EN ISO 10993-17 (2003-06) - Identical
BS EN ISO 10993-17:2002 - Identical
NF EN ISO 10993-17:2009 - Identical
NEN EN ISO 10993-17:2009 - Identical
NS EN ISO 10993-17:2009 - Identical
SS EN ISO 10993-17 Ed. 2 (2009) - Identical
UNI EN ISO 10993-17:2009 - Identical
ISO 10993-17:2002 - Identical
ONORM EN ISO 10993-17:2003 - Identical
SS EN ISO 10993-17 Ed. 1 (2003) - Identical
UNE EN ISO 10993-17:2003 - Identical
NF EN ISO 10993-17:2003 - Identical
NBN EN ISO 10993-17:2003 - Identical
NS EN ISO 10993-17 Ed. 1 (2003) - Identical
EN ISO 10993-17:2009 - Identical
I.S. EN ISO 10993-17:2003 - Identical
UNI EN ISO 10993-17:2004 - Identical
NEN EN ISO 10993-17:2003 - Identical
