BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013

    ECHELON FLEX 60

    FDA Adverse Event
    Malfunction ·ETHICON ENDOSURGERY LLC·Product code GDW·May 5, 2011

    CONTOUR TEST STRIPS (50)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·July 18, 2008

    M2A-T UNIV 2-HOLE SHELL SZ 41/58

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·May 30, 2013

    CANNULA & CATHETER

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DWF·April 22, 2025

    M2A-38 CUP NON FLARED SZ 58MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 30, 2013