09/30168887 DC : 0

FOREWORD
INTRODUCTION
201.1 Scope, object and related standards
201.2 Normative references
201.3 Terminology 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
       201.8.5.5.1 * Defibrillation protection
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
       201.12.1 Accuracy of controls and instruments
       201.12.4 Protection against hazardous output
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
202 Medical electrical equipment - Part 1-2: General
    requirements for safety - Collateral standard:
    Electromagnetic compatibility - Requirements and
    tests
    202.6.1 EMISSIONS
203 Medical electrical equipment - Part 1: General
    requirements for safety - 3 Collateral standard:
    General requirements for radiation protection in
    diagnostic X-ray equipment
206 Medical electrical equipment - Part 1-6: General
    requirements for safety - Collateral standard: Usability
208 Medical electrical equipment - Part 1-8: General
    requirements for safety - Collateral Standard: General
    requirements, tests and guidance for alarm systems
    in medical electrical equipment and medical electrical
    systems
209 Medical electrical equipment - Part 1-9: Medical
    electrical equipment - Part 1-9: General requirements
    for basic safety and essential performance - Collateral
    Standard: Requirements for the reduction of environmental
    impacts
210 Medical electrical equipment - Part 1-10: Medical
    electrical equipment - Part 1-10: General requirements
    for basic safety and essential performance - Collateral
    Standard: Process requirements for the development
    of therapeutic closed-loop controllers
Annex AA (informative) - Particular guidance and rationale
Annex BB (informative) - ELECTRODES, their positions,
         identifications and colour codes
Annex CC (informative) - LEADS, their identification and colour
         codes (other than those specified in 201.12.4.102)
Annex DD (informative) - Polarity of PATIENT LEADS (other
         than those specified in 201.12.4.102)
Annex EE (informative) - Additional marking of ELECTRODES
Annex FF (informative) - NOISE
Annex GG (informative) - Definitions and rules for the
         measurement of ELECTROCARDIOGRAMS
Annex HH (informative) - Calibration and test data sets
Annex II (informative) - CTS test atlas
   II.4 Wave duration tables adapted for different amplituden
        quantization
        II.4.1 CALECG Wave On-/Offsets, Sample Rate = 1000 S/s
        II.4.2 CALECG Interval Durations, Sample Rate = 1000 S/s
        II.4.3 CALECG Wave On-/Offsets, Sample Rate = 500 S/s
        II.4.4 CALECG Interval Durations, Sample Rate = 500 S/s
Bibliography
Index of defined terms used in this particular standard