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    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    BS EN ISO 6710 - SINGLE-USE CONTAINERS FOR VENOUS BLOOD SPECIMEN COLLECTION

    Available format(s):  Hardcopy, PDF

    Superseded date:  31-10-2017

    Language(s):  English

    Published date: 

    Publisher:  British Standards Institution

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

    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
    4 Materials
    5 Draw volume
    6 Design
    7 Construction
    8 Sterility and special microbiological states
    9 Additives
    10 Marking and labelling
    11 Container identification
    Annex A (normative) - Draw volume test
            for non-evacuated containers
    Annex B (normative) - Draw volume test for
            evacuated containers
    Annex C (normative) - Test for leakage of
            container
    Annex D (normative) - Test for robustness
            of the container
    Annex E (normative) - Concentrations of additives
            and volume of liquid additive
    Annex F (informative) - Recommended colour code
            for identifying additives and accessories
    Annex ZA (informative) - Relationship between
             this European standard and the essential
             requirements of Directive 98/79/EC
             [OJ L 331] aimed to be covered
    Bibliography

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

    Comment Closes On
    Committee CH/212
    Document Type Draft
    Publisher British Standards Institution
    Status Superseded
    Superseded By

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

    ISO 11137-1:2006 Sterilization of health care products Radiation Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
    EN 556-2:2015 Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE" - Part 2: Requirements for aseptically processed medical devices
    ISO/TS 17665-2:2009 Sterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1
    ISO 15223-1:2016 Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements
    ISO 17665-1:2006 Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
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