Vieworks Co. Ltd. FXRD-1012NAW Benutzerhandbuch
Rev.1.0
Page 135 of 151
VW40-152-009
VIVIX-S 1012N User Manual
U.S.A / Canada
Item
IEC 60601-1(ed.2 am1+ am2+ co1) Medical electrical equipment- Part1: General requirements for safety
UL 60601-1(ed.2)
-
CSA-C22.2 No. 601-1-M90 (R2006)
Medical electrical equipment – Part 1: General requirements for safety
(adopted amendment 2:1995 to IEC60601-1)
(adopted amendment 2:1995 to IEC60601-1)
IEC 60601-1-2: 2007 (ed.3)
Medical electrical equipment-Part 1-2: Collateral standard:
Electromagnetic compatibility
Electromagnetic compatibility
IEC 60601-1-4: 2000 (ed.1.1)
Medical electrical equipment- Part 1-4: Collateral Standard:
Programmable electrical medical systems
Programmable electrical medical systems
IEC 62304:2006
Medical device software-software life cycle processes
ISO 14971:2012
Medical Device- Application of risk management to medical devices
European Union
Item
MDD (Medical Device Directive)
93/42/EEC as amended by 2007/47/EC
EN ISO 13485:2012
Medical devices – Quality Management systems – Requirements for
regulatory purposes
regulatory purposes
EN 60601-1: 2007(ed.3)
Medical electrical equipment- Part1: General requirements for safety
IEC 60601-1-2: 2007(ed.3)
Medical electrical equipment-Part 1-2: Collateral Standard :
Electromagnetic compatibility-Requirements and tests
Electromagnetic compatibility-Requirements and tests
IEC 60601-1-4: 2000(ed.1.1)
Medical electrical equipment- Part 1-4: Collateral Standard :
Programmable electrical medical systems
Programmable electrical medical systems
IEC 62304:2006
Medical device software-Software life cycle processes
ISO 14971: 2012
Medical device – Application of risk management to medical devices.