BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    60 MICRO VOLUME EXTENSION SET W/.22 MICRON FILTER, 21 EXTENSION SET W/1.2 MIVTON GILYRT, INJ. SITE, CLAMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Bladeless Optical Obturators

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

    INO THERAPEUTICS INOBLENDER, MODEL 10004

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HALO XP ELECTROPHYSIOLOGY CATHETER WITH AUTO ID

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·June 13, 2012

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    LUMAX 340 DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code MRM·January 3, 2011

    LARGE SUTURECUT NEEDLE DRIVERINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 23, 2014