12/30246621 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Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 60601-2-68 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-68: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY BASED IMAGE GUIDED RADIOTHERAPY EQUIPMENT FOR USE WITH ELECTRON ACCELERATORS, LIGHT ION BEAM THERAPY EQUIPMENT AND RADIONUCLIDE BEAM THERAPY EQUIPMENT
Hardcopy , PDF
30-06-2015
English
FOREWORD
INTRODUCTION
201.1 Scope, object and related standards
201.2 Normative references
201.3 Terms and definitions
201.4 General requirements
201.5 General requirements for testing of ME EQUIPMENT
201.7 ME EQUIPMENT identification, marking and documents
201.8 Protection against electrical HAZARDS from
ME EQUIPMENT
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
201.14 PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS (PEMS)
201.16 ME SYSTEMS
201.17 Electromagnetic compatibility of ME EQUIPMENT and
ME SYSTEMS
201.101 Reference data for X-IGRT
201.102 X-IGRT IMAGING
201.103 IGRT Analysis and correction
203 IEC 60601-1-3:2008 General requirements for basic safety
and essential performance - collateral standard:
Radiation protection in diagnostic X-ray equipment
203.4 General requirements
203.6 RADIATION management
203.8 Limitation of the extent of the X-RAY BEAM and
relationship between X-RAY FIELD and IMAGE RECEPTION AREA
203.10 ATTENUATION of the X-RAY BEAM between the PATIENT
and the X-RAY IMAGE RECEPTOR
203.11 Protection against RESIDUAL RADIATION
203.13 Protection against STRAY RADIATION
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 - General requirements, tests
and guidance for alarm systems in medical electrical
equipment and medical electrical systems
209 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: General
requirements for basic safety and essential performance
- Collateral Standard: Process requirements for the
development of therapeutic closed-loop controllers
Annexes
Annex A (Informative) - General guidance and rational
Annex B (informative) - Sequence of testing
Annex I (informative) - ME SYSTEMS aspects
Annex DD (informative) - Measuring CTDI
Bibliography
Index of defined terms
BS EN 60601-2-68.
Committee |
CH/62/3
|
DocumentType |
Draft
|
Pages |
56
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy |
IEC 60336:2005 | Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots |
IEC 60364-7-710:2002 | Electrical installations of buildings - Part 7-710: Requirements for special installations or locations - Medical locations |
IEC 60522:1999 | Determination of the permanent filtration of X-ray tube assemblies |
IEC TR 60788:2004 | Medical electrical equipment - Glossary of defined terms |
IEC 60976:2007 | Medical electrical equipment - Medical electron accelerators - Functional performance characteristics |
IEC 62366:2007+AMD1:2014 CSV | Medical devices - Application of usability engineering to medical devices |
IEC TR 60977:2008 | Medical electrical equipment - Medical electron accelerators - Guidelines for functional performance characteristics |
IEC 62563-1:2009+AMD1:2016 CSV | Medical electrical equipment - Medical image display systems - Part1: Evaluation methods |
IEC 62220-1:2003 | Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1: Determination of the detective quantum efficiency |
IEC 61217:2011 | Radiotherapy equipment - Coordinates, movements and scales |
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