BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    BARDIA® COUDE OLIVE TIP URETHRAL CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·November 13, 2025

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·June 2, 2022

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·June 28, 2024

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·June 28, 2024

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·December 13, 2024

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·October 8, 2024

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·May 9, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 19, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·May 26, 2015

    BARDIA® COUDE OLIVE TIP URETHRAL FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·August 27, 2025

    BARDAM COUDE CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·September 16, 2021