BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    A-V RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PYRAMID® +4 Anterior Lumbar Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994286093·PLATE 9873041 3HOLE 41MM

    RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER

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

    3DIEMME RealGUIDE

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 13, 2014

    SCULPTRA

    FDA Adverse Event
    Injury ·SANOFIAVENTIS U.S. LLC·Product code LMH·October 14, 2010

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 13, 2012