• I.S. EN 62274:2005

    Current The latest, up-to-date edition.

    MEDICAL ELECTRICAL EQUIPMENT - SAFETY OF RADIOTHERAPY RECORD AND VERIFY SYSTEMS

    Available format(s):  Hardcopy, PDF

    Language(s):  English

    Published date:  01-01-2005

    Publisher:  National Standards Authority of Ireland

    For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
    Only cited Standards give presumption of conformance to New Approach Directives/Regulations.

    Dates of withdrawal of national standards are available from NSAI.

    Add To Cart

    Table of Contents - (Show below) - (Hide below)

    FOREWORD
    INTRODUCTION
    1 Scope and object
       1.1 Scope
       1.2 Object
       1.3 Relationship to other standards
    2 Normative references
    3 Terms and definitions
    4 General requirements for tests
       4.1 Testing during development
       4.2 Testing during installation
    5 ACCOMPANYING DOCUMENTS
    6 Requirements for safety
       6.1 RADIATION quantities
       6.2 Date and time
       6.3 Coordinate systems and scales
       6.4 Protection against unauthorized use
       6.5 Correctness of data transfer
       6.6 Data acceptance
       6.7 Deleting and editing data
       6.8 Backing up data
       6.9 Archiving data
    7 TREATMENT machine set-up verification
       7.1 Prevention of TREATMENT
       7.2 Override
       7.3 Transfer of prescribed TREATMENT data
       7.4 Accompanying information
    8 TREATMENT recording and reporting
    9 Accuracy
    10 Abnormal operation and fault conditions
       10.1 General hardware diagnostics
       10.2 Data and code
    11 Human errors in software design
    12 Change in software versions
    13 Human errors in use
    Annex A (normative) Hardware safety
    Annex ZA (normative) Normative references to international
                         publications with their corresponding
                         European publications
    Bibliography
    Index of defined terms

    Abstract - (Show below) - (Hide below)

    Defines certain specific aspects of the connection of the RVS to a network or to other radiotherapy equipment, and the communication protocol to be used.

    General Product Information - (Show below) - (Hide below)

    Development Note For CENELEC adoptions of IEC publications, please check www.iec.ch to be sure that you have any corrigenda that may apply. (01/2017)
    Document Type Standard
    Publisher National Standards Authority of Ireland
    Status Current

    Standards Referencing This Book - (Show below) - (Hide below)

    IEC 60950-1:2005+AMD1:2009+AMD2:2013 CSV Information technology equipment - Safety - Part 1: General requirements
    EN 61217:2012 Radiotherapy equipment - Coordinates, movements and scales
    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
    • Access your standards online with a subscription

      Features

      • Simple online access to standards, technical information and regulations
      • Critical updates of standards and customisable alerts and notifications
      • Multi - user online standards collection: secure, flexibile and cost effective