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

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    Filters Regulation: Us FDA ×

    SC Medica FFX

    FDA 510(k)
    FDA Unclassified ·Unknown

    SUTURTEK FASTCLOSE STERNUM CLOSURE DEVICE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MRSA/SA ELITE MGB, ELITE MGB SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·September 27, 2023

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 8, 2018

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·August 25, 2011

    MX40 2.4 GHZ SMART HOPPING

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DSI·September 17, 2014

    BREG POST-OP SHOE

    FDA Adverse Event
    Malfunction ·BREG, INC.·Product code IQI·July 18, 2013