EN 60601-2-4:2011
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators
19-08-2011
31-07-2020
FOREWORD
201.1 Scope, object and related standards
201.2 Normative references
201.3 Terms and definitions
201.4 General requirements
201.5 General requirements for testing of ME
EQUIPMENT
201.6 Classification of ME EQUIPMENT and ME
SYSTEMS
201.7 ME EQUIPMENT identification, marking
and documents
201.8 Protection against electrical HAZARDS from
ME EQUIPMENT
201.9 Protection against MECHANICAL HAZARDS
of ME EQUIPMENT and ME SYSTEMS
201.10 Protection against unwanted and excessive
radiation HAZARDS
201.11 Protection against excessive temperatures
and other HAZARDS
201.12 Accuracy of controls and instruments and
protection against hazardous outputs
201.13 HAZARDOUS SITUATIONS and fault conditions
201.14 PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS
(PEMS)
201.15 Construction of ME EQUIPMENT
201.16 ME SYSTEMS
201.17 Electromagnetic compatibility of ME EQUIPMENT
and ME SYSTEMS
201.101 Charging time
201.102 INTERNAL ELECTRICAL POWER SOURCE
201.103 Endurance
201.104 SYNCHRONIZER
201.105 Recovery of the MONITOR and/or ECG input
after defibrillation
201.106 Disturbance to the MONITOR from charging
or internal discharging
201.107 Requirements for RHYTHM RECOGNITION
DETECTOR
201.108 DEFIBRILLATOR ELECTRODES
201.109 External pacing (U.S.)
202 Electromagnetic compatibility - Requirements
and tests
Annexes
Annex C (informative) - Guide to marking and
labelling requirements for ME EQUIPMENT
and ME SYSTEMS
Annex AA (informative) - Particular guidance and
rationale
Annex BB (informative) - Mapping between the
elements of the second edition of
IEC 60601-2-4 and IEC 60601-2-4:2010
Bibliography
Index of defined terms used in this particular standard
Annex ZA (normative) - Normative references to
international publications with their
corresponding European publications
Annex ZZ (informative) - Coverage of Essential
Requirements of EC Directives
IEC 60601-2-4:2010 establishes particular basic safety and essential performance requirements for cardiac defibrillators. This third edition cancels and replaces the second edition published in 2002. This edition constitutes a technical revision, revised to structurally align it with IEC 60601-1:2005 and to implement the decision of IEC SC 62A that the clause numbering structure of particular standards written to IEC 60601-1:2005 would adhere to the form specified in ISO/IEC Directives, Part 2:2004. The aim of this third edition is to bring this particular standard up to date with reference to the third edition of the general standard through reformatting and technical changes.
| Committee |
CLC/TC 62
|
| DevelopmentNote |
Supersedes HD 395.2.4. (03/2003) Supersedes UNE EN 60601-2-4. (02/2014) CHILD IS AVAILABLE NOW
|
| DocumentType |
Standard
|
| ProductNote |
CHILD IS AVAILABLE NOW
|
| PublisherName |
European Committee for Standards - Electrical
|
| Status |
Superseded
|
| Supersedes |
| Standards | Relationship |
| NBN EN 60601 2-4 : 2011 | Identical |
| IEC 60601-2-4:2010 | Identical |
| DIN EN 60601-2-4 : 2012 | Identical |
| I.S. EN 60601-2-4:2011 | Identical |
| NF EN 60601-2-4 : 2012 | Identical |
| BS EN 60601-2-4:2011 | Identical |
| NEN EN IEC 60601-2-4 : 2011 | Identical |
| VDE 0750-2-4 : 2012 | Identical |
| CEI EN 60601-2-4 : 2012 | Identical |
| UNE-EN 60601-2-4:2004 | Identical |
| IEC 60601-2-4:2010+AMD1:2018 CSV | Identical |
| UNE-EN 60601-2-4:2011 | Identical |