BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    882.4310

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBE·September 27, 2012

    MAESTRO PERFORATOR CHUCK

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBB·September 30, 2006

    Breckenridge® Intervertebral Body/VBR Fusion System

    FDA UDI
    BIOMET SPINE LLC·00887868211454·

    Breckenridge ACDF System

    FDA UDI
    Highridge Medical, LLC·03662663280341·ACDF PEEK 0° 14x18x10mm

    BRECKENRIDGE INTERVERTEBRAL BODY/VBR FUSION SYSTEM

    FDA UDI
    BIOMET SPINE LLC·00888480570608·

    882.4360

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBB·October 3, 2012

    882.4360

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBE·September 19, 2012

    VACCESS PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·July 24, 2019