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

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    Filters Regulation: Us FDA ×

    VYGON DOUBLE LUMEN ENDOTRACHEAL TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    United Urologics Intermittent Catheter

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

    SOMNOFIT

    FDA 510(k)
    FDA Class 2 ·Dental

    HEARTMATE II SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·June 10, 2014

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 30, 2013

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·December 17, 2010