Medical electrical equipment. Safety of radiotherapy record and verify systems

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

12-28-2005

Publisher

British Standards Institution

Applies to the design and manufacture and some installation aspects of a record and verify system (RVS) for use in radiotherapy in human medical practice that a) provides, defines, or displays treatment machine set up data; imports data either through input by the operator or directly from other devices, b) may control the ability of that equipment to operate; c) records data of all treatment sessions; and d) is intended to be: 1) for normal use, under the authority of appropriately licensed or qualified persons, by operators having the required skills and training; 2) maintained in accordance with the recommendations given in the instructions for use; and 3) used within the environmental and electrical supply conditions specified in the technical description.

Committee	CH/62/3
DevelopmentNote	Supersedes 03/311952 DC (01/2006)
DocumentType	Standard
Pages	22
PublisherName	British Standards Institution
Status	Current

Standards	Relationship
IEC 62274:2005	Identical
NBN EN 62274 : 2007	Identical
UNE-EN 62274:2005	Identical
I.S. EN 62274:2005	Identical
EN 62274:2005	Identical
NF EN 62274 : 2005	Identical
DIN EN 62274:2007-05	Identical

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EN 61217:2012	Radiotherapy equipment - Coordinates, movements and scales
IEC 61000-2-4:2002	Electromagnetic compatibility (EMC) - Part 2-4: Environment - Compatibility levels in industrial plants for low-frequency conducted disturbances
EN 60601-2-29:2008/A11:2011	MEDICAL ELECTRICAL EQUIPMENT - PART 2-29: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RADIOTHERAPY SIMULATORS
IEC 60601-1:2005+AMD1:2012 CSV	Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
EN 61000-2-4:2002/AC:2014	ELECTROMAGNETIC COMPATIBILITY (EMC) - PART 2-4: ENVIRONMENT - COMPATIBILITY LEVELS IN INDUSTRIAL PLANTS FOR LOW-FREQUENCY CONDUCTED DISTURBANCES
IEC TR 60788:2004	Medical electrical equipment - Glossary of defined terms
IEC 60601-1-6:2010+AMD1:2013 CSV	Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
EN 60950-1:2006/A2:2013	INFORMATION TECHNOLOGY EQUIPMENT - SAFETY - PART 1: GENERAL REQUIREMENTS (IEC 60950-1:2005/A2:2013, MODIFIED)
IEC 62083:2009	Medical electrical equipment - Requirements for the safety of radiotherapy treatment planning systems
IEC 60601-1-2:2014	Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
EN 60601-1-2:2015	Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
IEC 60601-2-17:2013	Medical electrical equipment - Part 2-17: Particular requirements for the basic safety and essential performance of automatically-controlled brachytherapy afterloading equipment
IEC 61217:2011	Radiotherapy equipment - Coordinates, movements and scales
EN 60601-1-4:1996/A1:1999	MEDICAL ELECTRICAL EQUIPMENT - GENERAL REQUIREMENTS FOR SAFETY - COLLATERAL STANDARD: PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS
IEC 60601-2-29:2008	Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators
IEC 60601-1-4:1996+AMD1:1999 CSV	Medical electrical equipment - Part 1-4: General requirements for safety - Collateral Standard: Programmable electrical medical systems
IEC 60601-2-11:2013	Medical electrical equipment - Part 2-11: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment