09/30172488 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Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 60601-2-26 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-26: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROENCEPHALOGRAPHS
Hardcopy , PDF
30-06-2015
English
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201.1 Scope, object and related standards
201.1.1 Scope
201.1.2 Object
201.1.3 Collateral standards
201.1.4 Particular standards
201.2 Normative references
201.3 Terminology and definitions
201.4 General requirements
201.5 General requirements for testing of ME EQUIPMENT
201.5.4 Other conditions
201.5.8 Sequence of tests
201.6 Classification of ME EQUIPMENT and ME SYSTEMS
201.6.2 Protection against electric shock
201.6.6 Mode of operation
201.7 ME EQUIPMENT identification, marking
and documents
201.8 Protection against electrical HAZARDS form ME EQUIPMENT
201.8.1 Fundamental rule of protection against electrical
shock
201.8.101 Multipurpose channel(s)
201.8.3 Classification of APPLIED PARTS
201.8.7 LEAKAGE CURRENTS and PATIENT AUXILIARY CURRENTS
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
202 Medical electrical equipment - Part 1-2: General
requirements for safety - Collateral standard:
Electromagnetic compatibility - Requirements and tests
202.6.1 EMISSIONS
202.6.2 IMMUNITY
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
AA.1 Use with defibrillator
AA.2 Rationale for defibrillator test voltages
AA.3 Guidance and rationale for particular clauses
Index of defined terms used in this particular standard
BS EN 60601-2-26
| Committee |
CH/62/4
|
| DocumentType |
Draft
|
| Pages |
31
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy |
| IEC 60601-2-25:2011 | Medical electrical equipment - Part 2-25: Particular requirements for the basic safety and essential performance of electrocardiographs |
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