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

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    Filters FDA Adverse Event ×

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 4, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·February 28, 2011

    TORONTO STENTLESS PORCINE VALVE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL CANADA, INC.·Product code LWR·February 27, 2008

    PHENOM CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code QJP·May 19, 2026

    AUTOSOFTÂ XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 21, 2024

    AUTOSOFTÂ XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 21, 2024

    AUTOSOFTÂ XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 21, 2024