• ISO 18113-1:2022

    Current The latest, up-to-date edition.

    In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements

    Available format(s):  Hardcopy, PDF, PDF 3 Users, PDF 5 Users, PDF 9 Users

    Language(s):  English, French

    Published date:  06-10-2022

    Publisher:  International Organization for Standardization

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    Abstract - (Show below) - (Hide below)

    This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

    This document does not address language requirements since that is the domain of national laws and regulations.

    This document does not apply to:

    a) IVD medical devices for performance evaluation (e.g. for investigational use only);

    b) shipping documents;

    c) material safety data sheets / Safety Data Sheets;

    d) marketing information (consistent with applicable legal requirements).

    .

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

    Document Type Standard
    Publisher International Organization for Standardization
    Status Current
    Supersedes

    Standards Referenced By This Book - (Show below) - (Hide below)

    CLSI EP34:2018(R2023) Establishing and Verifying an Extended Measuring Interval Through Specimen Dilution and Spiking
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