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    I.S. EN 12470-2:2000

    Withdrawn A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

    CLINICAL THERMOMETERS - PART 2: PHASE CHANGE TYPE (DOT MATRIX) THERMOMETERS

    Available format(s):  Hardcopy, PDF

    Withdrawn date:  19-08-2009

    Language(s):  English

    Published date:  02-02-2001

    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 Type of thermometers
    6 Requirements
    7 Test methods
    8 Information supplied by the manufacturer
    Annex A (informative) - Suggested types of testing for the
                            requirements of this standard
    Annex ZA (informative) - Relationship between this European
                             Standard and the Essential
                             Requirements of EU Directive
                             93/42/EEC
    Bibliography

    Abstract - (Show below) - (Hide below)

    Describes performance requirements and test methods for phase change-type (dot matrix) thermometers for measuring temperature in body cavities.

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

    Development Note 2001 Edition Re-Issued in August 2009 & incorporates AMD 1 2009. (08/2009)
    Document Type Standard
    Publisher National Standards Authority of Ireland
    Status Withdrawn

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

    EN 556:1994 + A1:1998 STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR TERMINALLY-STERILIZED MEDICAL DEVICES TO BE LABELLED "STERILE"
    ISO/IEC Guide 98:1993 Guide to the expression of uncertainty in measurement (GUM)
    ISO 2859-2:1985 Sampling procedures for inspection by attributes — Part 2: Sampling plans indexed by limiting quality (LQ) for isolated lot inspection
    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
    EN 980:2008 Symbols for use in the labelling of medical devices
    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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