BEUDAMED
    13 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code LXH·October 25, 2019

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT: NAIL

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code LXH·October 25, 2019

    SUREFIT DUAL DISPERSIVE ELECTRODE

    FDA Adverse Event
    Other ·CONMED CORPORATION·Product code DRX·July 13, 2010

    VITALITY

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·August 14, 2008

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·February 16, 2011

    PIC

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code MKJ·February 14, 2008

    BD PHASEAL CONNECTOR LUER LOCK (C35)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·October 9, 2020