BEUDAMED
    7 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MARGRON STEM (K032641)

    FDA Adverse Event
    Injury ·PORTLAND ORTHOPAEDICS PTY LTD·Product code KWY·May 31, 2005

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    CONSMA·Product code ITJ·April 2, 2013

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·February 24, 2011

    ECHO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·April 22, 2008

    GRAFTMASTER RX CORONARY STENT GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code MAF·July 9, 2020

    GRAFTMASTER RX CORONARY STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MAF·July 9, 2020

    PERCLOSE PROSTYLE SUTURE-MEDIATED CLOSURE AND REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·July 18, 2023