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09/30172484 DC : 0

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

BS EN 60601-2-23 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-23: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF TRANSCUTANEOUS PARTIAL PRESSURE MONITORING EQUIPMENT

Available format(s)

Hardcopy , PDF

Superseded date

30-11-2015

Language(s)

English

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
       201.4.101 Additional ESENTIAL PERFORMANCE requirements
       201.4.7 SINGLE FAULT CONDITION for ME EQUIPMENT
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
       201.8.101 * TRANSDUCERS and cables
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
       201.11.8 * Interruption of power supply/SUPPLY
                MAINS to ME EQUIPMENT
201.12 Accuracy of controls and instruments and
       protection against hazardous outputs
       201.12.1 Accuracy of controls and instruments
       201.12.3 Alarm systems
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 Electromagnetic compatibility - Requirements
    and tests
    202.6 Electromagnetic compatibility
          202.6.1 EMISSIONS
          202.6.2 * IMMUNITY
                   202.6.2.3.1 Requirements
                   202.6.2.6.2 Tests
203 Radiation protection in diagnostic X-ray equipment
206 Usability
208 General requirements, tests and guidance
    for alarm systems in medical electrical
    equipment and medical electrical systems
    208.3 Terms and Definitions
    208.6 ALARM SYSTEMS
          208.6.1.2 * ALARM CONDITION priority
          208.6.6 ALARM LIMIT
          208.6.8 ALARM SIGNAL inactivation states
          208.6.9 * ALARM RESET
          208.6.10 * NON-LATCHING and LATCHING ALARM
                   SIGNALS
          208.6.11 Distributed alarm system
                   208.6.11.2.2 * Failure of remote
                                communication of ALARM
                                CONDITIONS
209 Requirements for the reduction of environmental impacts
210 Process requirements for the development of therapeutic
    closed-loop controllers
Annex AA (informative) - Particular guidance and rationale
Annex BB (informative) - Alarm diagrams of clause
         208/IEC 60601-1-8:2006
Index of defined terms used in this particular standard

BS EN 60601-2-23

Committee
CH/62/4
DocumentType
Draft
Pages
47
PublisherName
British Standards Institution
Status
Superseded
SupersededBy

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