BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    SMALL TI RIB HOOK CAP/EXTENDED

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MDI·November 10, 2016

    M2A-MAGNUM PF CUP 62ODX56ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 29, 2026

    M2A-MAGNUM MOD HD SZ 56MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 29, 2026

    HA TAPERLOC POR FMRL 15X150

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MEH·April 29, 2026

    M2A TAPER 37/28MM LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 27, 2014

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code KPE·November 14, 2012

    TALENT THORACIC STENT GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·September 3, 2010

    ACCUVUE ADVANCE

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·October 19, 2007