BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    980 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·December 14, 2016

    CANTATA 2.9 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·September 14, 2017

    INTELLIVUE MX500 PATIENT MONITOR

    FDA Adverse Event
    Death ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·December 4, 2023

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014

    VERSAPULSE POWERSUITE 100 WATT

    FDA Adverse Event
    Malfunction ·LUMENIS (ISRAEL)·Product code GEX·January 8, 2006

    DIAMOND 3

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·June 16, 2011