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

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    PREFORM GUIDEWIRE - SAFARI

    FDA Adverse Event
    Malfunction ·LAKE REGION MFG., INC.·Product code DQX·July 13, 2015

    STARTER GUIDEWIRE

    FDA Adverse Event
    Malfunction ·LAKE REGION MFG, INC.·Product code DQX·November 26, 2003

    ZIPWIRE HYDROPHILLIC GUIDEWIRE

    FDA Adverse Event
    Malfunction ·LAKE REGION MFG., INC.·Product code DQX·July 1, 2015

    GUIDE WIRES

    FDA Adverse Event
    Malfunction ·LAKE REGION MFG, INC.·Product code DQX·August 21, 2003

    GUIDE WIRES

    FDA Adverse Event
    Injury ·LAKE REGION MFG, INC.·Product code DQX·September 16, 2003

    GUIDE WIRE

    FDA Adverse Event
    Death ·LAKE REGION MFG, INC.·Product code DQX·March 6, 2003

    STARTER GUIDEWIRE

    FDA Adverse Event
    Death ·LAKE REGION MFG, INC.·Product code DQX·July 21, 2004

    ZIPWIRE SS GUIDEWIRE

    FDA Adverse Event
    Malfunction ·LAKE REGION MFG, INC.·Product code DQX·May 1, 2006

    MANDREL GUIDEWIRES OR M-WIRES

    FDA Adverse Event
    Injury ·LAKE REGION MFG., INC·Product code DQX·September 1, 2017

    ZIPWIRE HYDROPHILIC GUIDEWIRE

    FDA Adverse Event
    Injury ·LAKE REGION MFG., INC.·Product code DQX·May 27, 2015

    GUIDEWIRE

    FDA Adverse Event
    Injury ·LAKE REGION MFG. CO., INC.·Product code DQX·August 31, 1995

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