
Medical Devices - Quality Management Systems - Requirements For Regulatory Purposes (Iso 13485:2003)
出版:Belgian Standards

专家解读视频
Defines requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.
Supersedes NBN EN 46001. (11/2003) Supersedes NBN EN ISO 13488. (06/2007) Supersedes NBN EN 46003. (11/2009)
ONORM EN ISO 13485:2012 - Identical
UNE EN ISO 13485:2013 - Identical
UNI EN ISO 13485:2004 - Identical
NF EN ISO 13485:2004 - Identical
SN EN ISO 13485:2003 - Identical
DIN EN ISO 13485 (2010-01) - Identical
ONORM EN ISO 13485:2010 - Identical
I.S. EN ISO 13485:2012 - Identical
BS EN ISO 13485:2012 - Identical
NEN EN ISO 13485:2012 - Identical
SS EN ISO 13485 Ed. 3 (2012) - Identical
UNE EN ISO 13485:2012 - Identical
NS EN ISO 13485:2012 - Identical
NF EN ISO 13485:2012 - Identical
SN EN ISO 13485:2012 - Identical
DIN EN ISO 13485 (2012-11) - Identical
BS EN ISO 13485:2016 - Identical
EN ISO 13485:2016 - Identical