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

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    SUBCUTANEOUS TISSUE EXPANDER

    FDA 510(k)
    FDA Unclassified ·Unknown

    Comus Locking Plate systems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GEOMEDIC ANAMETRIC TOTAL KNEE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·May 5, 2014

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·October 15, 2012

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·August 6, 2010

    Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487, 100047194; CD3211-36Q/100004091, 100004093,100019784, 100035620, 100042486, 100047054; CD3215-36/100006995, 100010246, 100010247, 100010249, 100010250, 100012569, 100012570, 100034981, 100046577, 100046802, 60019065; CD3215-36Q/100004059, 100004060, 100004061, 100023304, 100030590, 100033678, 100042492, 100046803, 100046906

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