EN 60522:1999
(pr=7491) Determination of the permanent filtration of X-ray tube assemblies |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60580:2000
(pr=12235) Medical electrical equipment - Dose area product meters |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-1:2006
(pr=15126) Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
6060
|
90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices |
PUB
|
C 22/01 |
M/432 |
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
EN 60601-1:2006/A1:201X
(pr=23401) Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
5091
|
90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices |
NEW
|
|
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
EN 60601-1:2006/A11:2011
(pr=23800) Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices |
OFF
|
|
EN 60601-1-2:2007
(pr=20576) Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
FprEN 60601-1-2:2012
(pr=24111) Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic disturbances - Requirements and tests |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-1-3:2008
(pr=20988) Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-1-3:2008/A1:2013
(pr=24481) Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-1-6:2010
(pr=22408) Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
6060
|
90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices |
PUB
|
C 22/01 |
M/432 |
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
EN 60601-1-6:2010/FprA1:2012
(pr=24231) Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
5060
|
90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices |
NEW
|
|
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
EN 60601-1-8:2007
(pr=20488) Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-1-8:2007/A1:2013
(pr=23611) Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
BT
|
|
|
EN 60601-1-9:2008
(pr=20739) Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
|
EN 60601-1-9:2008/FprA1:2013
(pr=24462) Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
|
EN 60601-1-10:2008
(pr=20906) Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-1-10:2008/FprA1:2012
(pr=24464) Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-1-11:2010
(pr=22366) Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
FprEN 60601-1-12:2013
(pr=23973) Medical electrical equipment - Part 1-12: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment |
5020
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-1:1998
(pr=4226) Medical electrical equipment - Part 2-1: Particular requirements for the safety of electron accelerators in the range of 1 MeV to 50 MeV |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-1:1998/A1:2002
(pr=14390) Medical electrical equipment - Part 2-1: Particular requirements for the safety of electron accelerators in the range of 1 MeV to 50 MeV |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-2:2009
(pr=21601) Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-2:2009/A11:2011
(pr=23801) Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-3:1993
(pr=4266) Medical electrical equipment - Part 2: Particular requirements for the safety of short-wave therapy equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-3:1993/A1:1998
(pr=7356) Medical electrical equipment - Part 2: Particular requirements for the safety of short-wave therapy equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-3:201X
(pr=23125) Medical electrical equipment - Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipment |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-4:2003
(pr=5723) Medical electrical equipment - Part 2-4: Particular requirements for the safety of cardiac defibrillators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-4:2011
(pr=22219) Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
M/432 |
EN 60601-2-5:2000
(pr=5698) Medical electrical equipment - Part 2-5: Particular requirements for the safety of ultrasonic physiotherapy equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-6:201X
(pr=23126) Medical electrical equipment - Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-8:1997
(pr=8530) Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray equipment operating in the range 10 kV to 1 MV |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-8:1997/A1:1997
(pr=5895) Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray equipment operating in the range 10 kV to 1 MV |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-8:201X
(pr=22435) Medical electrical equipment - Part 2-8: Particular requirements for the basic safety and essential performance of therapeutic X-ray equipment operating in the range 10 kV to 1 MV |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-10:2000
(pr=13401) Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-10:2000/A1:2001
(pr=13403) Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-10:201X
(pr=23127) Medical electrical equipment - Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-11:1997
(pr=7099) Medical electrical equipment - Part 2-11: Particular requirements for the safety of gamma beam therapy equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-11:1997/A1:2004
(pr=15468) Medical electrical equipment - Part 2-11: Particular requirements for the safety of gamma beam therapy equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-11:201X
(pr=22963) Medical electrical equipment - Part 2-11: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-12:2006
(pr=17023) Medical electrical equipment - Part 2-12: Particular requirements for the safety of lung ventilators - Critical care ventilators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-13:2006
(pr=17024) Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-13:2006/A1:2007
(pr=20601) Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-16:1998
(pr=5728) Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
FprEN 60601-2-16:2008
(pr=20652) Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-16:201X
(pr=23248) Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-17:2004
(pr=15469) Medical electrical equipment - Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
FprEN 60601-2-17:201X
(pr=22894) Medical electrical equipment - Part 2-17: Particular requirements for basic safety and essential performance of automatically-controlled brachytherapy afterloading equipment |
3090
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-18:1996
(pr=5724) Medical electrical equipment - Part 2: Particular requirements for the safety of endoscopic equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-18:1996/A1:2000
(pr=13125) Medical electrical equipment - Part 2: Particular requirements for the safety of endoscopic equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-19:2009
(pr=21300) Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-19:2009/A11:2011
(pr=23802) Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-20:2009
(pr=21336) Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-20:2009/A11:2011
(pr=23803) Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-21:2009
(pr=21184) Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-21:2009/A11:2011
(pr=23804) Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-23:2000
(pr=13388) Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-24:1998
(pr=4263) Medical electrical equipment - Part 2-24: Particular requirements for the safety of infusion pumps and controllers |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
FprEN 60601-2-24:2012
(pr=22587) Medical electrical equipment - Part 2-24: Particular requirements for basic safety and essential performance of infusion pumps and controllers |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-25:1995
(pr=4239) Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-25:1995/A1:1999
(pr=7612) Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-26:2003
(pr=7613) Medical electrical equipment - Part 2-26: Particular requirements for the safety of electroencephalographs |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-26:201X
(pr=22410) Medical electrical equipment - Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-27:2006
(pr=15939) Medical electrical equipment - Part 2-27: Particular requirements for the safety, including essential performance, of electrocardiographic monitoring equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-27:201X
(pr=22194) Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment |
5099
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-28:2010
(pr=22081) Medical electrical equipment - Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-29:2008
(pr=21124) Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-29:2008/A11:2011
(pr=23805) Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-30:2000
(pr=7615) Medical electrical equipment - Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-31:2008
(pr=21207) Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
M/432 |
EN 60601-2-31:2008/A1:2011
(pr=22895) Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
M/432 |
EN 60601-2-33:2002
(pr=14260) Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-33:2002/A1:2005
(pr=16323) Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-33:2002/A2:2008
(pr=20705) Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-33:2010
(pr=21927) Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
M/432 |
EN 60601-2-33:2010/A1:201X
(pr=24301) Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |
5099
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-33:2010/A11:2011
(pr=23806) Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
|
EN 60601-2-34:2000
(pr=7362) Medical electrical equipment - Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-34:201X
(pr=22292) Medical electrical equipment - Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-36:1997
(pr=5752) Medical electrical equipment - Part 2: Particular requirements for the safety of equipment for extracorporeally induced lithotripsy |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
FprEN 60601-2-36:2012
(pr=24442) Medical electrical equipment - Part 2-36: Particular requirements for the basic safety and essential performance of extracorporeally induced lithotripsy |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-37:2008
(pr=20719) Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-37:2008/FprA1:2012
(pr=24465) Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-37:2008/A11:2011
(pr=23808) Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-39:2008
(pr=20657) Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-39:2008/A11:2011
(pr=23809) Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-40:1998
(pr=5729) Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-41:2009
(pr=21567) Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-41:2009/FprA1:2011
(pr=23618) Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-41:2009/A11:2011
(pr=23810) Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-43:2010
(pr=21942) Medical electrical equipment - Part 2-43: Particular requirements for basic safety and essential performance of X-ray equipment for interventional procedures |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-44:2009
(pr=21573) Medical electrical equipment - Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipment for computed tomography |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-44:2009/A1:2012
(pr=23378) Medical electrical equipment - Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipment for computed tomography |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-44:2009/A11:2011
(pr=23811) Medical electrical equipment - Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipment for computed tomography |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-45:2001
(pr=13404) Medical electrical equipment - Part 2-45: Particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-45:2011
(pr=22703) Medical electrical equipment - Part 2-45: Particular requirements for the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
M/432 |
EN 60601-2-46:1998
(pr=11993) Medical electrical equipment - Part 2-46: Particular requirements for the safety of operating tables |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-46:2011
(pr=22193) Medical electrical equipment - Part 2-46: Particular requirements for the basic safety and essential performance of operating tables |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
M/432 |
EN 60601-2-47:2001
(pr=7365) Medical electrical equipment - Part 2-47: Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/023, M/432 |
EN 60601-2-47:201X
(pr=22367) Medical electrical equipment - Part 2-47: Particular requirements for the basic safety and essential performance of ambulatory electrocardiographic systems |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
M/432 |
EN 60601-2-49:2001
(pr=13682) Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-50:2009
(pr=21398) Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-50:2009/A11:2011
(pr=23812) Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 60601-2-51:2003
(pr=14389) Medical electrical equipment - Part 2-51: Particular requirements for safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 60601-2-52:2010
(pr=16043) Medical electrical equipment - Part 2-52: Particular requirements for basic safety and essential performance of medical beds |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/295, M/432 |
EN 60601-2-52:2010/FprA1:2013
(pr=24365) Medical electrical equipment - Part 2-52: Particular requirements for basic safety and essential performance of medical beds |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
FprEN 60601-2-62:2013
(pr=23954) Medical electrical equipment - Part 2-62: Particular requirements for the basic safety and essential performance of high intensity therapeutic ultrasound (HITU) equipment |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-63:201X
(pr=23427) Medical electrical equipment - Part 2-63: Particular requirements for basic safety and essential performance of dental extra-oral x-ray equipment |
5099
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
FprEN 60601-2-64:2013
(pr=24562) Medical electrical equipment - Part 2-64: Particular requirements for the basic safety and essential performance of light ion beam medical equipment |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60601-2-65:2013
(pr=23428) Medical electrical equipment - Part 2-65: Particular requirements for the basic safety and essential performance of dental intra-oral X-ray equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
|
FprEN 60601-2-68:2012
(pr=24313) Particular requirements for basic safety and essential performance of X-ray based image guided radiotherapy equipment for use with electron accelerators, light ion beam therapy systems and radionuclide beam therapy systems |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 60627:2001
(pr=13344) Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter grids |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
FprEN 60627:2013
(pr=23735) Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter grids |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 61217:1996
(pr=4738) Radiotherapy equipment - Coordinates, movements and scales |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 61217:1996/A1:2001
(pr=13345) Radiotherapy equipment - Coordinates, movements and scales |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 61217:1996/A2:2008
(pr=21021) Radiotherapy equipment - Coordinates, movements and scales |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 61217:2012
(pr=22904) Radiotherapy equipment - Coordinates, movements and scales |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 61223-3-4:2000
(pr=12943) Evaluation and routine testing in medical imaging departments - Part 3-4: Acceptance tests - Imaging performance of dental X-ray equipment |
9500
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
WTH
|
C 173/2 |
|
EN 61223-3-5:2004
(pr=15782) Evaluation and routine testing in medical imaging departments - Part 3-5: Acceptance tests - Imaging performance of computed tomography X-ray equipment |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NOJ
|
|
|
EN 61676:2002
(pr=14230) Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 61676:2002/A1:2009
(pr=21845) Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 62083:2009
(pr=21813) Medical electrical equipment - Requirements for the safety of radiotherapy treatment planning systems |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
|
EN 62220-1:2004
(pr=15458) Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1: Determination of the detective quantum efficiency |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/295, M/432 |
FprEN 62220-1-1:2013
(pr=24759) Medical electrical equipment - Characteristics of digital x-ray imaging devices - Part 1-1: Determination of the detective quantum efficiency - Detectors used in radiographic imaging |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 62220-1-2:2007
(pr=16995) Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-2: Determination of the detective quantum efficiency - Detectors used in mammography |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 62220-1-3:2008
(pr=21057) Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-3: Determination of the detective quantum efficiency - Detectors used in dynamic imaging |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 62304:2006
(pr=16632) Medical device software - Software life-cycle processes |
6060
|
98/79/EC
Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices |
PUB
|
C 22/03 |
M/432 |
90/385/EEC
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices |
PUB
|
C 22/01 |
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
EN 62366:2008
(pr=20763) Medical devices - Application of usability engineering to medical devices |
6060
|
98/79/EC
Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices |
PUB
|
C 22/03 |
M/432 |
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
EN 62366:2008/FprA1:2012
(pr=24463) Medical devices - Application of usability engineering to medical devices |
5060
|
2006/95/EC
Council Directive 2006/95/EC of 12 December 2006 on the harmonization of the laws of Member States relating to electrical equipment designed for use within certain voltage limits |
NEW
|
|
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
FprEN 62570:2009
(pr=22680) Magnetic resonance equipment for medical imaging - Instructions for marking items within the controlled access area |
5060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 80601-2-30:2010
(pr=21531) Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PEN
|
|
|
EN 80601-2-30:2010/FprA1:2013
(pr=24008) Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers |
5020
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 80601-2-35:2009
(pr=21913) Medical electrical equipment - Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads and mattresses and intended for heating in medical use |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
|
EN 80601-2-35:2009/A11:2011
(pr=23807) Medical electrical equipment - Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads and mattresses and intended for heating in medical use |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
EN 80601-2-58:2009
(pr=21530) Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
M/432 |
EN 80601-2-58:2009/A11:2011
(pr=23813) Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
OFF
|
|
|
FprEN 80601-2-58:2013
(pr=24527) Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery - Proposed Horizontal Standards |
5020
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|
EN 80601-2-59:2009
(pr=21362) Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening |
6060
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
PUB
|
C 22/02 |
|
EN 80601-2-60:201X
(pr=23009) Medical electrical equipment - Part 2-60: Particular requirements for basic safety and essential performance of dental equipment |
5091
|
93/42/EEC
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices |
NEW
|
|
|