BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    ARGYLE DUAL LUMEN UMBILICAL VESSEL CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150720·K-WIRE - SINGLE TROCAR 1.1mm DIA x 100mm

    da Vinci SP Instruments (SP1098)

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

    FS SERIES WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    EXTENSION SET 30IN

    FDA Adverse Event
    Malfunction ·HOSPIRA INC.·Product code FPA·June 3, 2009

    APM/AIM PUMP SET W/C

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·September 28, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·December 8, 2010

    PULSE GEN MODEL 104

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 17, 2014

    HEARTSTART 4000

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 21, 2012