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

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    Filters FDA Adverse Event ×

    SMR HUMERAL HEAD Ø44 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWT·May 23, 2022

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·May 8, 2014

    STERNAL LOCK-PL 2.4 STRAIG 20HO TI

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·October 22, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 28, 2007

    SMR HUMERAL HEAD Ø44 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWT·May 17, 2023