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

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    AMPLIGREFFE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NON-STERILE POWDERED GREEN COLORED POWDERED LATEX PATIENT EXAMINATION GLOVES WITH & WITHOUT SOUR/APPLE/PEPPERMINT SCENTS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CODA™ Anterior Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ILS·May 23, 2014

    2.0MM IMF SCREW SELF-DRILLING 12MM

    FDA Adverse Event
    Malfunction ·Product code HWC·November 14, 2012

    ATLAS PLUS DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018