BEUDAMED
    826 results · 63ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Death ×

    PUREWICK INCONTENANCE PRODUCT

    FDA Adverse Event
    Death ·C. R. BARD, INC.·Product code NZU·January 2, 2025

    MESH SOFRADIM - UGYTEX¿

    FDA Adverse Event
    Death ·SOFRADIM PRODUCTION SAS·Product code FTL·June 25, 2018

    GORE DUALEMESH BIOMATERIAL

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES, INC.·Product code FTL·April 24, 2008

    BARD

    FDA Adverse Event
    Death ·C.R. BARD INC.·Product code DKT·February 17, 2004

    BARD BIPOLAR PACING ELECTRODE CATHETER

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code LDF·May 14, 2010

    DIGNICARE STOOL MANAGEMENT SYSTEM

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code KNT·April 23, 2010

    FCHOON MULTIPURPOSE 7FR

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code DQO·September 3, 1996

    9 FRENCH BALLOON CATHETER 30CC

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code DSP·May 7, 1996

    BARD NASOGASTRIC TUBE

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code KNT·November 23, 2010

    BARD

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code MSD·February 18, 2003

    PONSKY NON-BALLOON REPLACEMENT GASTROSTOMY TUBE

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code KNT·October 20, 1994

    BARD CPS SYSTEM

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code DTZ·November 1, 1994

    *

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code DSP·April 25, 1997

    FEMORAL RECOVERY FILTER FEMORAL SYSTEM

    FDA Adverse Event
    Death ·C.R. BARD INC.·Product code DTK·July 30, 2004

    BARD NASOGASTRIC SUMP TUBE

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code FEG·December 7, 2006

    PORT, CATHETER, IMPLANTED

    FDA Adverse Event
    Death ·C.R. BARD INC.·Product code LJT·January 19, 2017

    BARD NASOGASTRIC SUMP TUBE

    FDA Adverse Event
    Death ·C.R. BARD, INC·Product code KNT·July 23, 2002

    RECOVERY FILTER

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code DTK·June 4, 2004

    BARD MINNESOTA FOUR LUMEN ESOPHAGOGASTRIC TUBE

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code KNT·June 5, 2003

    BARD

    FDA Adverse Event
    Death ·C.R. BARD INC.·Product code DTK·February 4, 2005