BEUDAMED
    149 results · 64ms · Sources: EU EUDAMED, US FDA

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    SATURNE 41

    FDA Adverse Event
    GENERAL ELECTRIC CO.·Product code IYE·July 19, 1996

    GE CATH LAB X-RAY SYSTEM

    FDA Adverse Event
    GENERAL ELECTRIC CO.·Product code IZI·July 11, 1996

    RADIOGRAPHIC/FLUOROSCOPIC X-RAY UNIT-TABLE

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code KXJ·August 9, 1996

    VIVID E9

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code ITX·May 14, 2014

    12 LEAD ECG MONITOR

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code DXH·June 23, 2021

    VIVID E9

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code IYO·December 3, 2014

    GIRAFFE OMNIBED CARESTATION

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code FMT·June 7, 2022

    CENTERGRAFT SENIX HF MAMMOGRAM MACHINE

    FDA Adverse Event
    GENERAL ELECTRIC CO.·Product code IZH·May 7, 1996

    GE MAC 5000

    FDA Adverse Event
    Injury ·GENERAL ELECTRIC CO.·Product code DPS·September 16, 2003

    DESGIN 50

    FDA Adverse Event
    Injury ·GENERAL ELECTRIC CO.·Product code FTD·March 11, 1994

    SEIKOSHA VIDEO PRINTER

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code JAA·March 24, 1994

    SFX 90-90 TABLE

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code KXJ·March 29, 1994

    GE 450 W MRI SCANNER 1.5 TESLA MAGNET UNK

    FDA Adverse Event
    GENERAL ELECTRIC CO.·Product code LNH·October 16, 2018

    DASH

    FDA Adverse Event
    GENERAL ELECTRIC CO·Product code MHX·April 12, 2013

    GENERAL ELECTRIC PORTABLE X-RAY UNIT

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO·Product code IZL·July 16, 1997

    ANGIOGRAPHY EQUIPMENT

    FDA Adverse Event
    GENERAL ELECTRIC CO.·Product code IZI·December 28, 1994

    FLUOROSCOPE

    FDA Adverse Event
    GENERAL ELECTRIC CO.·Product code JAA·November 9, 1994

    FLUOROSCOPIC X-RAY UNIT

    FDA Adverse Event
    GENERAL ELECTRIC CO.·Product code JAA·October 31, 1994

    LEAD APRON

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code EAJ·August 14, 1997

    PRESTIGE VH FOOT REST

    FDA Adverse Event
    Malfunction ·GENERAL ELECTRIC CO.·Product code KXJ·September 26, 1997