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

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    PARAGON 8500 CARDIO-PULMONARY BED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GentleCath Intermittent Urinary Catheter

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KONTRON PERCUTAEOUS DOUBLE-LUMEN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TBD

    FDA Adverse Event
    Malfunction ·Product code KOD·April 5, 2018

    FORTIFY DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 13, 2014

    ALLURA XPER FD20

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZI·October 5, 2010

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 13, 2012