BEUDAMED
    6 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT IRELAND VASCULAR DIVISION REG NO: 9616695·Product code NIM·April 27, 2007

    UNKNOWN LAG SCREW

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code HWC·September 16, 2022

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 13, 2014

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 5, 2012

    FREESTYLE

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC., USA·Product code FMK·September 14, 2007

    UNKNOWN LAG SCREW

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·June 30, 2022