BEUDAMED
    321 results · 40ms · Sources: EU EUDAMED, US FDA

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    GENDEX GX-770

    FDA Adverse Event
    Malfunction ·GENDEX CORP·Product code EHD·January 24, 2014

    GENDEX GX-770

    FDA Adverse Event
    Malfunction ·GENDEX CORP.·Product code EHD·September 15, 2014

    GENDEX GX-770

    FDA Adverse Event
    Malfunction ·GENDEX CORP.·Product code EHD·September 15, 2014

    GENDEX DENTALX-RAY MACHINE

    FDA Adverse Event
    Malfunction ·GENDEX CORP.·Product code EHD·May 18, 1995

    GENDEX

    FDA Adverse Event
    Malfunction ·GENDEX CORP·Product code IZO·December 6, 2001

    A13309A

    FDA Adverse Event
    Malfunction ·GENDEX-DEL MEDICAL IMAGING CORP.·Product code IYB·October 16, 1998

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 30, 2015

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 27, 2015

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 2, 2006

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 30, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 30, 2006

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 26, 2006

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 27, 2007

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 23, 2006

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 31, 2006

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 9, 2014

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 9, 2014

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 21, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 18, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 16, 2006