• BS EN 12470-5:2003

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    Clinical thermometers Performance of infra-red ear thermometers (with maximum device)

    Available format(s):  Hardcopy, PDF

    Superseded date:  31-12-2012

    Language(s):  English

    Published date:  25-04-2003

    Publisher:  British Standards Institution

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

    Foreword
    1 Scope
    2 Normative References
    3 Terms and definitions
    4 Unit
    5 Types of thermometers
    6 Requirements
       6.1 General
       6.2 Range of displayed temperature
       6.3 Maximum permissible error
       6.4 Environmental requirements
       6.5 Indicating unit
       6.6 Construction
    7 Test Methods
       7.1 General
       7.2 Sampling
       7.3 Testing for compliance of the range of displayed
            temperature
       7.4 Testing for compliance of the maximum permissible error
            within ambient operating range
       7.5 Testing for compliance of maximum permissible error under
            extended operating conditions
       7.6 Testing for compliance of maximum permissible error under
            changing environmental conditions
       7.7 Testing for compliance with maximum permissible clinical
            repeatability - Procedure
       7.8 Testing for compliance with the effect of storage and long
            term stability
       7.9 Method of test for mechanical shock
       7.10 Testing for compliance with the variation of the supply
            voltage
       7.11 Testing for compliance with cleaning and disinfection
    8 Information supplied by the manufacturer
       8.1 General
       8.2 Marking
       8.3 Instruction for use
    Annex A (informative) Clinical trial to determine clinical accuracy
       A.1 Introduction
       A.2 Clinical accuracy
       A.3 Clinical trial procedure
       A.4 Clinical bias and its standard deviation
       A.5 Clinical repeatability
    Annex B (informative) Suggested types of testing for the requirements
            of this standard
    Annex C (informative) Example for a suitable design of a black body
            radiator
    Annex D (informative) Alternative approaches to prove compliance
            with 6.3
       D.1 General
       D.2 Separation of the maximum permissible error for the instrument
            and for the probe covers
       D.3 Calculation of the error using error propagation analysis
    Annex ZA (informative) Clauses of this European Standard addressing
            essential requirements or other provision of EU Directives
    Bibliography

    Abstract - (Show below) - (Hide below)

    Defines the metrological and technical requirements for clinical infra-red (IR) ear thermometers with maximum device for intermittent determination of human body temperature.

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

    Committee LBI/1/2
    Development Note Supersedes 00/121313 DC. (04/2003)
    Document Type Standard
    Publisher British Standards Institution
    Status Superseded
    Superseded By
    Supersedes

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

    IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
    ISO 2859-2:1985 Sampling procedures for inspection by attributes — Part 2: Sampling plans indexed by limiting quality (LQ) for isolated lot inspection
    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
    EN 1041:2008+A1:2013 Information supplied by the manufacturer of medical devices
    ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
    IEC 60068-2-14:2009 Environmental testing - Part 2-14: Tests - Test N: Change of temperature
    EN 980:2008 Symbols for use in the labelling of medical devices
    EN 60068-2-14:2009 Environmental testing - Part 2-14: Tests - Test N: Change of temperature
    EN ISO 10993-1:2009/AC:2010 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010)
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