BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ACCU-CHEK COMPACT

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code NBW·November 12, 2008

    CAPSURE Z NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 31, 2011

    PRINEO SKIN CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OMD·July 16, 2013

    ALINITY M HR HPV AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·February 26, 2024

    ENDO GIA

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·May 24, 2023

    SIGNIA

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·May 4, 2023

    ENDO GIA ULTRA

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·December 18, 2023