Full Description

BS EN 13795-2:2019 specifies information to be supplied to users and third party verifiers in addition to theusual labelling of medical devices (see EN 1041 and EN ISO 15223-1), concerning manufacturing andprocessing requirements.

Cross References:
EN ISO 22612:2005
ISO 9073-10:2003
ISO 22612:2005
EN ISO 139:2005
EN ISO 11737-1:2018
ISO 13938-1:1999
ISO 11737-1:2018
ISO 10993-1:2009
ISO 139:2005
ISO 139:2005/AMD 1:2011
EN ISO 10993-1:2009
EN ISO 9073-10:2004
EN 29073-3:1992
EN ISO 13938-1:1999
ISO 11607-2
ISO 10993-10
ISO 11092
EN ISO 15797
ISO 11607-1
EN ISO 9237
EN ISO 10993-10
EN ISO 10993-5
EN ISO 11607-1
EN 1041
ISO 15797
EN 14065
EN 62366
EN ISO 13485
ISO 13485
ISO 10993-5
EN ISO 15223-1
ISO 15223-1
ISO 9237
EN ISO 11092
EN ISO 11607-2


Replaces BS EN 13795:2011+A1:2013 which remains current

All current amendments available at time of purchase are included with the purchase of this document.

Product Details

Published: 04/12/2019 ISBN(s): 9780580980848 Number of Pages: 32 File Size: 1 file , 800 KB Product Code(s): 30358662, 30358662, 30358662 Note: This product is unavailable in United Kingdom