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

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    IOI COCR UNIPOLAR PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEFIBRILLATOR ANALYZER MODEL QED-5

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PHACOTRON PLUS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    V18 CONTROL WIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP·Product code DQX·March 16, 2007

    V18 CONTROL WIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·May 23, 2007

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014

    BARD URETERAL STENT

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC.·Product code FAD·December 8, 2010