BEUDAMED
    8 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M2A-MAGNUM PF CUP 50ODX44ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 24, 2019

    COLLEAGUE SINGLE CHANNEL VOLUMETRIC PUMP CE FRENCH

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 18, 2010

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 13, 2012

    ISTENT TRABECULAR MICRO-BYPASS

    FDA Adverse Event
    Injury ·GLAUKOS CORPORATION·Product code OGO·April 17, 2014

    INTEGRAL/X POR RED PROX 10MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·July 17, 2019

    M2A-MAGNUM TAPER INSRT STD

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·July 17, 2019

    M2A-MAGNUM TAPER INSRT STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 17, 2019

    M2A-MAGNUM MOD HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·July 17, 2019