09/30172484 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Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 60601-2-23 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-23: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF TRANSCUTANEOUS PARTIAL PRESSURE MONITORING EQUIPMENT
Hardcopy , PDF
30-11-2015
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
201.4.101 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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