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

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    TORQUE DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFIED PEEL-AWAY INTRODUCER SET LINE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CODMAN COLLINS RADIOPARENT STERNAL BLADES

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

    2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 19, 2014

    DLP SINGLE STAGE VENOUS CANNULA

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DWF·February 15, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·January 19, 2011