Defines requirements for the information for supplying by a manufacturer for different categories of medical devices as required by the relevant EU Directives. Does not define the language to be used for such information. Meant to complement the specified requirements of the EU Directives on medical devices in the context of defining means where certain requirements may be met.

UNI CEI EN 1041:2013

UNI CEI EN 1041:2009

NBN EN 1041:1998 - Identical

ONORM EN 1041:1998 - Identical

DIN EN 1041 (1998-04) - Identical

BS EN 1041:1998 - Identical

I.S. EN 1041:2008 - Identical

BS EN 1041:2008 - Identical

CEI UNI EN 1041 Ed. 3 (2013) - Identical

CEI UNI EN 1041 Ed. 4 (2014) - Identical

NBN EN 1041:2008 - Identical

DIN EN 1041 (2013-12) - Identical

ONORM EN 1041:2013 - Identical

BS EN 1041:2008+A1:2013 - Identical

CEI UNI EN 1041 Ed. 2 (2010) - Identical

UNE EN 1041:2009 - Identical

NS EN 1041 Ed. 2 (2008) - Identical

SN EN 1041:2008 - Identical

ONORM EN 1041:2008 - Identical

DIN EN 1041 (2008-11) - Identical

SS EN 1041 Ed. 2 (2008) - Identical

NEN EN 1041:2008 - Identical

NF EN 1041:2008 - Identical

SN EN 1041:1998 - Identical

NEN EN 1041:1998 - Identical

NF EN 1041:1998 - Identical

I.S. EN 1041:1998 - Identical

NS EN 1041 Ed. 1 (1998) - Identical

SS EN 1041 Ed. 1 (1998) - Identical

UNE EN 1041:1998 - Identical