BEUDAMED
    4 results · 24ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    BLADE 120MM

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code GAD·January 21, 2015

    INSIGNIA

    FDA Adverse Event
    Malfunction ·GUIDANT PUERTO RICO BV·Product code NVZ·July 23, 2011

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code OUT·June 17, 2013

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 25, 2008