CEI EN 60601-2-4 : 2012

FOREWORD
1 Scope, object and related
    standards
2 Normative references
3 Terms and definitions
4 General requirements
5 General requirements for
    testing of ME EQUIPMENT
6 Classification of ME EQUIPMENT
    and ME SYSTEMS
7 ME EQUIPMENT identification,
    marking and documents
8 Protection against electrical
    HAZARDS from ME EQUIPMENT
9 Protection against MECAHNICAL
    HAZARDS of ME EQUIPMENT and
    ME SYSTEMS
10 Protection against unwanted
    and excessive radiation HAZARDS
11 Protection against excessive
    temperatures and other HAZARDS
12 * Accuracy of controls and
    instruments and protection
    against hazardous outputs
13 HAZARDOUS SITUATIONS and fault
    conditions
14 PROGRAMMABLE ELECTRICAL MEDICAL
    SYSTEMS (PEMS)
15 Construction of ME EQUIPMENT
16 ME SYSTEMS
17 Electromagnetic compatibility
    of ME EQUIPMENT and ME SYSTEMS
101 * Charging time
102 Internal electrical power source
103 * Endurance
104 * Synchronizer
105 * Recovery of the MONITOR and/or
    ECG input after defibrillation
106 * Disturbance to the MONITOR from
    charging or internal discharging
107 * Requirements for RHYTHM
    RECOGNITION DETECTOR
108 DEFIBRILLATOR ELECTRODES
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