
Biological Evaluation Of Medical Devices - Part 12: Sample Preparation And Reference Materials
出版:Standardiserings-Kommissionen I Sverige

专家解读视频
Describes requirements and gives guidance on the procedures to be followed in the preparation of samples and the selection of reference materials for medical device testing in biological systems in accordance with one or more parts of the ISO 10993 series.
ISO 10993-12:2007 - Identical
NF EN ISO 10993-12:2005 - Identical
I.S. EN ISO 10993-12:2004 - Identical
NBN EN ISO 10993-12:2005 - Identical
ONORM EN ISO 10993-12:2005 - Identical
DIN EN ISO 10993-12 (2005-03) - Identical
BS EN ISO 10993-12:2007 - Identical
NEN EN ISO 10993-12:2004 - Identical
DIN EN ISO 10993-12 (2008-02) - Identical
UNE EN ISO 10993-12:2008 - Identical
NF EN ISO 10993-12:2008 - Identical
NBN EN ISO 10993-12:2008 - Identical
SN EN ISO 10993-12:2005 - Identical
NEN EN ISO 10993-12:2007 - Identical
NS EN ISO 10993-12 Ed. 3 (2007) - Identical
ONORM EN ISO 10993-12:2008 - Identical
UNI EN ISO 10993-12:2008 - Identical
SN EN ISO 10993-12:2008 - Identical
UNI EN ISO 10993-12:2005 - Identical
NS EN ISO 10993-12 Ed. 2 (2005) - Identical
UNE EN ISO 10993-12:2005 - Identical