• UNI EN ISO 10993-5 : 2009

    Current The latest, up-to-date edition.

    BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 5: TESTS FOR IN VITRO CYTOTOXICITY

    Available format(s): 

    Language(s): 

    Published date:  16-09-2009

    Publisher:  Ente Nazionale Italiano di Unificazione (UNI)

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

    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
    4 Sample and control preparation
       4.1 General
       4.2 Preparation of liquid extracts of material
       4.3 Preparation of material for direct-contact tests
       4.4 Preparation of controls
    5 Cell lines
    6 Culture medium
    7 Preparation of cell stock culture
    8 Test procedures
       8.1 Number of replicates
       8.2 Test on extracts
       8.3 Test by direct contact
       8.4 Test by indirect contact
       8.5 Determination of cytotoxicity
    9 Test report
    10 Assessment of results
    Annex A (informative) - Neutral red uptake (NRU) cytotoxicity
            test
    Annex B (informative) - Colony formation cytotoxicity test
    Annex C (informative) - MTT cytotoxicity test
    Annex D (informative) - XTT cytotoxicity test
    Annex ZA (informative) - Relationship between this
             International Standard and the Essential Requirements
             of EU Directive 93/42/EEC
    Annex ZB (informative) - Relationship between this
             International Standard and the Essential Requirements
             of EU Directive 90/385/EEC
    Bibliography

    Abstract - (Show below) - (Hide below)

    Specifies test methods to assess the in vitro cytotoxicity of medical devices.

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

    Committee CT 44
    Development Note Supersedes UNI EN 30993-5. (04/2001)
    Document Type Standard
    Publisher Ente Nazionale Italiano di Unificazione (UNI)
    Status Current
    Supersedes

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

    UNI 11533 : 2014 MASS-PRODUCED ORTHOPEDIC FOOTWEAR DESIGNED FOR FOOT ORTHOTIC - SAFETY AND PERFORMANCE REQUIREMENTS AND TEST METHODS

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

    ISO 10993-12:2012 Biological evaluation of medical devices Part 12: Sample preparation and reference materials
    ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
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