Contains requirements concerning basic safety and essential performance that are generally applicable to medical electrical equipment. For certain types of medical electrical equipment, these requirements are either supplemented or modified by the special requirements of a collateral or particular standard. Where particular standards exist, this standard should not be used alone.
The contents of the corrigenda of December 2006, of July 2007, the interpretation sheet 1 of April 2008, the interpretation sheet 2 of January 2009 and the interpretation sheet 2 of May 2013 have been included in this copy.
Legislation related to this standard
Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC
WITHDRAWN
EN 60601-1:1990/A2:1995
WITHDRAWN
EN 60601-1-1:2001
WITHDRAWN
EN 60601-1-4:1996
WITHDRAWN
EN 60601-1:1990
WITHDRAWN
EN 60601-1:1990/A1:1993
WITHDRAWN
EN 60601-1-4:1996/A1:1999
WITHDRAWN
EN 60601-1:1990/A1:1993/corrigendum Jul. 1994
WITHDRAWN
EN 60601-1:1990/A13:1996
PUBLISHED
EN 60601-1:2006
60.60
Standard published
Oct 20, 2006
PUBLISHED
EN 60601-1:2006/A1:2013
WITHDRAWN
EN 60601-1:2006/A11:2011
PUBLISHED
EN 60601-1:2006/A12:2014
PUBLISHED
EN 60601-1:2006/A2:2021
PUBLISHED
EN 60601-1:2006/A13:2024
WITHDRAWN
EN 60601-1:2006/AC:2014
PUBLISHED
EN 60601-1:2006/corrigendum Mar. 2010
PUBLISHED
EN 60601-1:2006/AC:2022-12
IN_DEVELOPMENT
prEN IEC 60601-1