BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    QUANTUM II SYSTEM

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·October 21, 2011

    AMBIENT SUPER TURBOVAC 90 WITH FINGER SWITCH

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·October 21, 2011

    AMBIENT SUPER TURBOVAC 90 WITH FINGER SWITCH

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·October 21, 2011

    DIAMOND NEEDLE WITH THREADED CANNULA

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code KIH·March 30, 2007

    FLOW CONTROL VALVE UNIT CABLE

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·December 6, 2011

    FLOW CONTROL VALVE UNIT

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·December 6, 2011

    STAMMBERGER SINU-FOAM NASAL DRESSING

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code LYA·October 12, 2011

    STAMMBERGER SINU-FOAM NASAL DRESSING

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code LYA·October 12, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014

    STAMMBERGER SINU-FOAM NASAL DRESSING

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code LYA·October 21, 2011

    STAMMBERGER SINU-FOAM NASAL DRESSING

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code LYA·October 21, 2011