BEUDAMED
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    Filters FDA Adverse Event ×

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·April 15, 2015

    OLYMPUS ESG-100, 100...120 V~,

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code GEI·September 27, 2022

    8.5MM MEDULLARY REAMER HEAD

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HTO·May 4, 2013

    PRESSURE INFUSION BAG

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code KZD·August 21, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER - SILICON VALLEY·Product code GEX·May 3, 2011