09/30168887 DC : 0
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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BS EN 60601-2-25 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-25: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROCARDIOGRAPHS
Hardcopy , PDF
30-11-2015
English
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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
BS EN 60601-2-25
| Committee |
CH/62/4
|
| DocumentType |
Draft
|
| Pages |
127
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy |
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