BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    DIRECTIGEN 1-2-3(TM) GROUP A STREP TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ENSEAL TISSUE SEALING DEVICE

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

    EnsoETM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 27, 2014

    COLLEAGUE SINGLE CHANNEL VOLUMETRIC PUMP CE FRENCH

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 18, 2010

    NELLCOR OXIMAX N-65

    FDA Adverse Event
    Malfunction ·SANMINA-SCI SYSTEMS·Product code DQA·December 11, 2012