BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M2A-MAGNUM 42-50 TAPER INSERT STD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 12, 2013

    MLRY-HD POR FEMORAL 14X175MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·November 12, 2013

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 12, 2013

    STYLE 10 SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·October 15, 2025

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·March 27, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 24, 2011

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 3, 2008

    M2A-MAGNUM MODULAR HEAD SIZE 50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 27, 2013