• I.S. EN 12376:1999

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR STAINING IN BIOLOGY

    Available format(s):  Hardcopy, PDF

    Superseded date:  02-05-2013

    Language(s):  English

    Published date:  01-01-1999

    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
    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
        3.1 Information supplied by the manufacturer
        3.2 Label
        3.3 In vitro diagnostic
        3.4 Staining
        3.5 Dye
        3.6 Stain
             3.6.1 Stock solution of stain
        3.7 Chromogenic reagent
        3.8 Fluorochrome
        3.9 Antibody
             3.9.1 Polyclonal antibody
             3.9.2 Monoclonal antibody
        3.10 Nucleic acid probe
        3.11 Lectin
    4 Requirements for information supplied by the manufacturer
        4.1 General requirements
             4.1.1 Information supplied by the manufacturer
                     with reagents used for staining in biology
             4.1.2 Product name
             4.1.3 Description of reagent
             4.1.4 Intended use
        4.2 Additional requirements for specific kinds of
             reagents
             4.2.1 Fluorochromes
             4.2.2 Metal salts
             4.2.3 Antibodies
             4.2.4 Nucleic acid probes
    Annex A (informative) Examples of information supplied by
                          the manufacturer with reagents commonly
                          used in biological staining procedures
        A.1 Methyl Green-Pyronin Y stain
        A.2 Feulgen-Schiff reaction
        A.3 Immunohistochemical demonstration of oestrogen
             receptors
        A.4 Flow cytometric demonstration of T-cells
    Annex B (informative) Bibliography

    Abstract - (Show below) - (Hide below)

    Defines requirements for information supplied by the manufacturer with reagents used in staining in biology.

    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)

    EN 376 : 2002 INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING
    EN 375 : 2001 INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE
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