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  • ONORM EN ISO 7886-3 : 2010

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    Withdrawn A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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    STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION

    Available format(s): 

    Withdrawn date:  09-10-2020

    Language(s): 

    Published date:  12-01-2013

    Publisher:  Osterreichisches Normungsinstitut/Austrian Standards

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

    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
    4 Nomenclature
    5 Cleanliness
    6 Limits for acidity or alkalinity
    7 Limits for extractable metals
    8 Lubricant
    9 Tolerance on nominal capacity
    10 Graduated scale
    11 Barrel
    12 Piston/plunger assembly
    13 Needle
    14 Performance
    15 Packaging
    16 Labelling
    Annex A (normative) Method for preparation of extracts
    Annex B (informative) Test method for forces required to
                           operate plunger
    Annex C (normative) Test method for testing auto-disable
                           feature
    Annex ZA (informative) Relationship between this European
                           Standard and the Essential
                           Requirements of EU Directive
                           93/42 EEC
    Bibliography

    Abstract - (Show below) - (Hide below)

    Specifies the properties and performance of sterile single-use hypodermic syringes with or without needle, made of plastic materials and stainless steel and intended for the aspiration of vaccines or for the injection of vaccines immediately after filling.

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    Document Type Standard
    Publisher Osterreichisches Normungsinstitut/Austrian Standards
    Status Withdrawn
    Superseded By

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

    ISO 9626:2016 Stainless steel needle tubing for the manufacture of medical devices — Requirements and test methods
    View more information

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