BEUDAMED
    13 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013

    VISIONAIRE GII FEMOR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·July 13, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Death ·CORDIS DE MEXICO·Product code NIQ·September 12, 2008

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·December 28, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·November 18, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·November 21, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·November 21, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·November 21, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·November 21, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·December 28, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·November 21, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·November 21, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·ACUMED, LLC·Product code HRS·November 21, 2025