BEUDAMED
    37 results · 66ms · Sources: EU EUDAMED, US FDA

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    RADI

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS, INC.·Product code MGB·November 20, 2003

    FEMOSTOP GOLD

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS AB·Product code DXC·February 9, 2010

    PRESSUREWIRE CERTUS

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code DXO·May 28, 2010

    PRESSURE WIRE SENSOR

    FDA Adverse Event
    Death ·RADI MEDICAL SYSTEMS AB·Product code DQX·February 27, 2004

    RADI PRESSUREWIRE 4

    FDA Adverse Event
    Death ·RADI MEDICAL SYSTEMS AB·Product code NQH·March 1, 2004

    PRESSURE WIRE SENSOR

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code DQX·December 18, 2003

    PRESSUREWIRE SENSOR

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS AB·Product code DQX·August 14, 2003

    FEMOSTOP GOLD

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code DXC·November 3, 2009

    FEMOSTOP GOLD

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code DXC·December 7, 2009

    PRESSURE WIRE SENSOR

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code DQX·February 21, 2003

    PRESSURE WIRE SENSOR

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code DQX·February 26, 2003

    PRESSURE WIRE SENSOR

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code DQX·March 21, 2003

    BONOPTY BIOPSY SYSTEM

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS AB·Product code GAA·May 13, 2009

    PRESSUREWIRE CERTUS

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS AB·Product code DQX·June 10, 2009

    BONOPTY BIOPSY SET

    FDA Adverse Event
    Other ·RADI MEDICAL SYSTEMS AB·Product code KNW·July 2, 2004

    FEMOSTOP PLUS

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code MGB·January 9, 2006

    PRESSUREWIRE (R) SENSOR

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS AB·Product code DQX·December 14, 2006

    PRESSUREWIRE 5

    FDA Adverse Event
    Malfunction ·RADI MEDICAL SYSTEMS AB·Product code DQX·December 4, 2006

    CR BARD

    FDA Adverse Event
    Death ·RADI MEDICAL SYSTEMS AB·Product code DXC·July 22, 2002

    PRESSUREWIRE SENSOR

    FDA Adverse Event
    Injury ·RADI MEDICAL SYSTEMS AB·Product code DQX·June 29, 2006