BS EN 13795-2:2019 specifies information to be supplied to users and third party verifiers in addition to the
usual labelling of medical devices (see EN 1041 and EN ISO 15223-1), concerning manufacturing and
processing 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. | File Size : | 1
file
, 800 KB |
| ISBN(s) : | 9780580980848 |
| Note : | This product is unavailable in Ukraine, Russia, Belarus |
| Number of Pages : | 32 |
| Product Code(s) : | 30358662, 30358662, 30358662 |
| Published : | 04/12/2019 |