BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    AliveCor Heart Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·October 23, 2023

    ORTHO SOLUTIONS - STERILE, DRILLS, TAPS, GUIDE PINS & WIRES

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

    SAME/VARIOUS DISTRIBUTORS/WE MAY PRIVATE LABEL

    FDA 510(k)
    FDA Class 1 ·General Hospital

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 24, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 20, 2011

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·August 27, 2008

    VARIABLE SELF-DRILLING SCREW DIAM. 4X14MM (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·October 4, 2017