BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    TOUCHLESS II INTERMITTENT CATHETER

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

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756371049·OCULOPLASTIC PACK

    CURE CATHETER

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

    AT HOME DRUG TEST, MODEL 9068 T

    FDA 510(k)
    FDA Unclassified ·Unknown

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 11, 2013

    SEGURA HEMISPHERE STONE RETRIEVAL BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFL·November 30, 2010

    INFUSION PUMP, UNKNOWN

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2014

    MONOCRYL UD 27IN USP2-0

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAN·October 25, 2024

    MONOCRYL UD 27IN USP2-0

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAN·October 25, 2024