NF EN ISO 14971:2009被替代
Medical Devices - Application Of Risk Management To Medical Devices
出版：Association Francaise de Normalisation
專家解讀視頻
Describes a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic (IVD) medical devices, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls.
Indice de classement: S99-211. (09/2001) PR NF EN ISO 14971 December 2005. (12/2005) PR NF EN ISO 14971 April 2009. (04/2009) 2007 version is still active. (11/2009)
I.S. EN ISO 14971:2009 - Identical
BS EN ISO 14971:2009 - Identical
UNI EN ISO 14971:2008 - Identical
SN EN ISO 14971:2007 - Identical
ONORM EN ISO 14971:2007 - Identical
NS EN ISO 14971:2012 - Identical
UNE EN ISO 14971:2012 - Identical
SN EN ISO 14971:2012 - Identical
SS EN ISO 14971 Ed. 4 (2012) - Identical
NBN EN ISO 14971:2012 - Identical
BS EN ISO 14971:2012 - Identical
I.S. EN ISO 14971:2012 - Identical
SN EN ISO 14971:2010 - Identical
ONORM EN ISO 14971:2009 - Identical
DIN EN ISO 14971 (2009-10) - Identical
NEN EN ISO 14971:2009 - Identical
SS EN ISO 14971 Ed. 3 (2009) - Identical
NS EN ISO 14971:2009 - Identical
NBN EN ISO 14971:2009 - Identical
UNE EN ISO 14971:2009 - Identical
