• AAMI ISO 14708-5 : 2010

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 5: CIRCULATORY SUPPORT DEVICES

    Available format(s):  Hardcopy, PDF

    Superseded date:  08-05-2020

    Language(s):  English

    Published date:  01-01-2010

    Publisher:  Association for the Advancement of Medical Instrumentation

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

    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
    4 Symbols and abbreviated terms
    5 General requirements for non-implantable parts
    6 Requirements for particular active implantable medical
       devices
    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 packaging
    12 Construction of the non-reusable packaging
    13 Markings on the active implantable medical device
    14 Protection from unintentional biological effects 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
       damage caused by temperature changes
    27 Protection of the active implantable medical device from
       electromagnetic non-ionizing radiation
    28 Accompanying documentation
    Annex AA (informative) - Relationship between the fundamental
                             principles in ISO/TR and the clauses
                             of this part of ISO 14708
    Annex BB (informative) - Relationship between the clauses of
                             this part of ISO 14708 and the
                             fundamental principles listed in
                             Annex AA
    Annex CC (informative) - Rationale
    Annex DD (informative) - In vitro test
    Bibliography

    Abstract - (Show below) - (Hide below)

    Describes requirements for safety and performance of active implantable circulatory support devices.

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

    Committee WG 6
    Development Note Supersedes AAMI TIR26. (04/2010)
    Document Type Standard
    Publisher Association for the Advancement of Medical Instrumentation
    Status Superseded
    Superseded By
    Supersedes

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

    IEC 60068-1:2013 Environmental testing - Part 1: General and guidance
    IEC 60068-2-27:2008 Environmental testing - Part 2-27: Tests - Test Ea and guidance: Shock
    ISO 5840:2005 Cardiovascular implants Cardiac valve prostheses
    ISO 7198:2016 Cardiovascular implants and extracorporeal systems — Vascular prostheses — Tubular vascular grafts and vascular patches
    IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
    IEC 60601-1-8:2006+AMD1:2012 CSV Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems
    IEC 60068-2-64:2008 Environmental testing - Part 2-64: Tests - Test Fh: Vibration, broadband random and guidance
    IEC 62366:2007+AMD1:2014 CSV Medical devices - Application of usability engineering to medical devices
    IEC 60601-1-2:2014 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
    ISO/TR 14283:2004 Implants for surgery Fundamental principles
    ISO/IEC Guide 51:2014 Safety aspects Guidelines for their inclusion in standards
    IEC 62304:2006+AMD1:2015 CSV Medical device software - Software life cycle processes
    ISO 14708-1:2014 Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
    ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
    CFR 21(PTS1-99) : 0 FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 1-99
    ISO 14155:2011 Clinical investigation of medical devices for human subjects Good clinical practice
    ISO 5198:1987 Centrifugal, mixed flow and axial pumps Code for hydraulic performance tests Precision grade
    ISO 14971:2007 Medical devices Application of risk management to medical devices
    ISO Guide 31:2015 Reference materials — Contents of certificates, labels and accompanying documentation
    IEC 60601-1-1:2000 Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems
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