BEUDAMED
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    Filters Status: Malfunction ×

    C.R. BARD INC.

    FDA Adverse Event
    Malfunction ·BARD UROLOGICAL DIVISION·Product code EYJ·January 10, 1995

    C.R. BARD, INC.

    FDA Adverse Event
    Malfunction ·BARD UROLOGICAL DIVISION·Product code EYJ·January 10, 1995

    C.R. BARD, INC.

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC.·Product code KOD·January 25, 2007

    C.R. BARD, INC.

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC.·Product code KOD·September 16, 1999

    C.R. BARD INC.

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC.·Product code KOD·February 23, 1999

    C.R. BARD, INC.

    FDA Adverse Event
    Malfunction ·USCI·Product code GBA·January 12, 1993

    BARDPORT (C.R. BARD INC.)

    FDA Adverse Event
    Malfunction ·BARD·Product code LJT·December 9, 1997

    BARD® URETHRAL CATHETERIZATION TRAY WITH RED RUBBER CATHETER

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC.·Product code KOD·August 16, 2018

    LEG BAG WITH FLIP-FLO VALVE, FABRIC LEG STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·August 8, 2018

    LEG BAG WITH FLIP-FLO VALVE, FABRIC LEG STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·February 26, 2020

    COMPOSIX KUGEL

    FDA Adverse Event
    Malfunction ·DAVOL, INC.·Product code FTL·July 2, 2007

    BARD MAGIC 3 GO COUDE

    FDA Adverse Event
    Malfunction ·BARD / C.R. BARD, INC.·Product code EZD·July 14, 2023

    BARD MAGIC 3 GO COUDE

    FDA Adverse Event
    Malfunction ·BARD / C.R. BARD, INC.·Product code EZD·July 14, 2023

    BARD MAGIC 3 GO COUDE

    FDA Adverse Event
    Malfunction ·BARD / C.R. BARD, INC.·Product code EZD·July 14, 2023

    BARD MAGIC 3 GO COUDE

    FDA Adverse Event
    Malfunction ·BARD / C.R. BARD, INC.·Product code EZD·July 14, 2023

    BARD® TOUCHLESS® URETHRAL CATHETER KIT WITH RED RUBBER CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FCM·July 28, 2017

    BARDEX® LUBRI-SIL® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·February 20, 2020

    BARDEX® LUBRI-SIL® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·February 14, 2020

    BARDEX® LUBRI-SIL® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·April 2, 2018

    BARDIA® FOLEY CATHETER SILICONE COATED

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·July 1, 2019