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

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    TBAN

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ATB ADVANCED PTA DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mammomat Fusion with Stereotactic Biopsy

    FDA 510(k)
    FDA Class 2 ·Radiology

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 19, 2014

    UNIDENTIFIED KNEE IMPLANT OR INSTRUMENT

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 15, 2013

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 19, 2011