BEUDAMED
    13 results · 70ms · Sources: EU EUDAMED, US FDA

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    EXPRO ELITE SNARE

    FDA Adverse Event
    Malfunction ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·May 15, 2009

    EXPRO ELITE

    FDA Adverse Event
    Malfunction ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·March 28, 2007

    EXPRO ELITE

    FDA Adverse Event
    Malfunction ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·September 2, 2009

    MICRO ELITE

    FDA Adverse Event
    Malfunction ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code DQY·September 8, 2009

    EXPRO ELITE

    FDA Adverse Event
    Malfunction ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·August 19, 2009

    EXPRO ELITE

    FDA Adverse Event
    Malfunction ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·September 2, 2009

    EXPRO ELITE SNARE

    FDA Adverse Event
    Injury ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·April 15, 2008

    EXPRO ELITE SNARE

    FDA Adverse Event
    Injury ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·August 29, 2008

    EXPRO ELITE SNARE

    FDA Adverse Event
    Injury ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·September 30, 2008

    EXPRO ELITE SNARE

    FDA Adverse Event
    Malfunction ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·August 6, 2012

    EXPRO ELITE

    FDA Adverse Event
    Malfunction ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·August 6, 2012

    EXPRO ELITE SNARE

    FDA Adverse Event
    Injury ·RADIUS MEDICAL TECHNOLOGIES, INC.·Product code MMX·March 5, 2008

    RAYHACK DRILL GUIDE ANGLED, REF 4010-0206, 1 EACH, Rx ONLY, NON-STERILE, Wright Medical EMEA Krijgsman 11, 1186 Amstelveen, The Netherlands, Wright Medical Technology, 4677 Airline Road, Arlington, TN 38002 Intended use: Preparation of the Radius prior to device implantation

    FDA Recall
    Terminated ·Wright Medical Technology Inc·Product code LXH·April 8, 2010