• PREN 45502-2-2 : DRAFT 1998

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-2: PARTICULAR REQUIREMENTS FOR ACTIVE IMPLANTABLE MEDICAL DEVICES INTENDED TO TREAT TACHYARRHYTHMIA (INCLUDES IMPLANTABLE DEFIBRILLATORS)

    Available format(s): 

    Superseded date:  01-03-2008

    Language(s): 

    Published date:  12-01-2013

    Publisher:  Comite Europeen de Normalisation

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

    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Definitions
    4 Symbols and abbreviations (optional)
    5 General requirements for non-implantable parts
    6 Measurement of implantable pulse generator and lead
       characteristics
    7 General arrangement of the packaging
    8 General markings for active implantable medical devices
    9 Markings on the sales packaging
    10 Construction of the sales packaging
    11 Markings on the sterile pack
    12 Construction of the non-reusable pack
    13 Markings on the active implantable medical device
    14 Protection from unintended biological effects being caused
       by the active implantable medical device
    15 Protection from harm to the patient or user caused by
       external physical features of the active implantable medical
       device
    16 Protection from harm to the patient caused by electricity
    17 Protection from harm to the patient caused by heat
    18 Protection from ionizing radiation released or emitted
       from the active implantable medical device
    19 Protection from unintended effects caused by the device
    20 Protection of the device from damage caused by external
       defibrillators
    21 Protection of the device from changes caused by high
       power electrical fields applied directly to the patient
    22 Protection of the active implantable medical device
       from changes caused by miscellaneous medical treatments
    23 Protection of the active implantable medical device from
       mechanical forces
    24 Protection of the active implantable medical device from
       damage caused by electrostatic discharge
    25 Protection of the active implantable medical device from
       damage caused by atmospheric pressure changes
    26 Protection of the active implantable medical device from
       changes caused by temperature changes
    27 Protection of the active implantable medical device from
       electromagnetic non-ionizing radiation
    28 Accompanying documentation
    ANNEX AA (Informative) Table of cross-references from 90/385/EEC
                           and prEN 45502-1
    ANNEX BB (Informative) Relationship between the clauses of this
                           standard and the essential requirements
                           (90/385/EEC) listed in Annex AA
    ANNEX CC (Informative) Notes on EN 45502-3
    ANNEX DD (Informative) Code for Describing Modes of the
                           implantable pulse generator
    ANNEX EE (Informative) Interface Circuits
    ANNEX FF (Informative) Selection of capacitor C[x]

    Abstract - (Show below) - (Hide below)

    Specifies requirements that are applicable to IMPLANTABLE CARDIOVERTER DEFIBRILLATORS and the functions of ACTIVE IMPLANTABLE MEDICAL DEVICES intended to treat tachyarrhythmia.

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

    Comment Closes On
    Document Type Draft
    Publisher Comite Europeen de Normalisation
    Status Superseded
    Superseded By

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

    IEC 60068-2-27:2008 Environmental testing - Part 2-27: Tests - Test Ea and guidance: Shock
    EN 60068-2-27:2009 Environmental testing - Part 2-27: Tests - Test Ea and guidance: Shock
    IEC TR 60878:2015 Graphical symbols for electrical equipment in medical practice
    EN 60068-2-6:2008 Environmental testing - Part 2-6: Tests - Test Fc: Vibration (sinusoidal)
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