BEUDAMED
    7 results · 45ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NUCLEUS 22

    FDA Adverse Event
    Injury ·COCHLEAR LIMITED·Product code MCM·May 18, 2025

    THORATEC VENTRICULAR ASSIST DEVICE (VAD) SYSTEM

    FDA Adverse Event
    Malfunction ·THORATEC LABORATORIES CORP.·Product code DSQ·December 30, 1996

    TLC-II PORTABLE VAD DRIVER

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·May 31, 2002

    TLC-II PORTABLE VAD DRIVER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·November 1, 2001

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 24, 2014

    VITROS CHEMISTRY PRODUCTS PHYT SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code DIP·November 3, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012