BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNI LFIT MEDIAL FEMORAL COMP.

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code HRY·April 15, 2013

    BD ALARIS¿ SMARTSITE¿ GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 9, 2023

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·January 11, 2013

    JOSTENT GRAFTMASTER

    FDA Adverse Event
    Injury ·AV-RANGENDINGEN·Product code MAF·November 30, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 2, 2014

    BD GEM V/NV 20D 0.2 FLTR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·July 28, 2022

    GEM V/NV NTG 20DP 20PK

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 10, 2020

    BD ALARIS¿ SMARTSITE¿ GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·January 20, 2023