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

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    Filters FDA Adverse Event ×

    S4 IMPLANTS

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code KWP·August 29, 2008

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FRN·February 27, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·March 13, 2014

    FEEDING TUBE, MIC*TRANSGASTRIC-JEJUNAL

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK·Product code KNT·February 16, 2011

    BD¿ 5ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·November 15, 2017

    5 ML BD DISCARDIT II¿ SYRINGE W/NEEDLE 24G X 1 IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 13, 2017