• I.S. 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    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 - PART 5: PERFORMANCE OF INFRA-RED EAR THERMOMETERS (WITH MAXIMUM DEVICE)

    Available format(s):  Hardcopy, PDF

    Superseded date:  24-10-2012

    Language(s):  English

    Published date:  01-01-2003

    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.

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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)

    Gives 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)

    Document Type Standard
    Publisher National Standards Authority of Ireland
    Status Superseded
    Superseded By

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

    ISO 2859-2:1985 Sampling procedures for inspection by attributes — Part 2: Sampling plans indexed by limiting quality (LQ) for isolated lot inspection
    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
    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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