BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    LOW PROFILE SCREW,CORTICAL,3.5X16MM,DRP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·June 26, 2019

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 14, 2014

    EPIC II CRITICAL CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·November 15, 2012

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC·Product code NDN·September 22, 2010

    LOW PROFILE SCREW,CORTICAL,3.5X14MM,DRP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·October 6, 2025

    VAL KREULOCK SCREW, TI, 2.4X18

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·October 6, 2025

    LOW PROFILE SCREW,CORTICAL,3.5X14MM,DRP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·October 6, 2025