BEUDAMED
    100 results · 51ms · Sources: EU EUDAMED, US FDA

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    PERI-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code MFX·December 6, 1997

    DURA-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code GXQ·December 19, 1997

    DURA-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code GXQ·September 22, 1997

    DURA-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code GXQ·September 22, 1997

    VASCU-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code DXZ·March 30, 1998

    DURA-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code GXQ·September 22, 1997

    VASCU-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code DXZ·January 29, 1999

    BIOGRAFT

    FDA Adverse Event
    Malfunction ·BIO-VASCULAR, INC.·Product code LXA·December 31, 1998

    4 X 5 SUTURABLE DURAGEN

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORP.·Product code GXQ·September 30, 2005

    BIOGRAFT

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code LXA·March 11, 1998

    BIOGRAFT

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code LXA·February 27, 1998

    DURA-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code GXQ·January 14, 2004

    DURAGUARD

    FDA Adverse Event
    Death ·BIO-VASCULAR, INC.·Product code GXQ·August 29, 1996

    DARDIK BIOGRAFT

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC·Product code FZC·September 26, 1996

    BIO-GUARD BOVINE PERICARDIUM FOR DURA REPLACEMENT

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code GXQ·September 9, 1996

    BIOGRAFT

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC·Product code LXA·February 18, 2002

    DURA-GUARD

    FDA Adverse Event
    Other ·BIO-VASCULAR, INC.·Product code GXQ·January 11, 2002

    VASCU-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code DXZ·February 27, 2002

    BIOGRAFT

    FDA Adverse Event
    Malfunction ·BIO-VASCULAR, INC.·Product code LXA·February 27, 2002

    OCU-GUARD

    FDA Adverse Event
    Injury ·BIO-VASCULAR, INC.·Product code MTZ·August 31, 2000