BEUDAMED
    696 results · 159ms · Sources: EU EUDAMED, US FDA

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    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·April 13, 2018

    LOFRIC ORIGO

    FDA Adverse Event
    Injury ·WELLSPECT HEALTHCARE·Product code EZD·December 11, 2025

    BARDIA ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·September 9, 2020

    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·December 18, 2018

    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·October 4, 2024

    BARDIA ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·September 9, 2020

    BARDEX® FOLEY CATHETER SILICONE COATED

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·December 23, 2025

    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·February 14, 2024

    BARDEX® LUBRICATH® FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·April 8, 2025

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 27, 2012

    BARDEX ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GBM·April 1, 2021

    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·August 21, 2018

    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·July 23, 2018

    BARDIA® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·August 20, 2018

    BARDEX® I.C. TEMPERATURE SENSING FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·August 11, 2023

    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·August 6, 2018

    BARDEX® I.C. TEMPERATURE SENSING FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·April 24, 2019

    BARDEX® LUBRI-SIL® I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code MJC·July 18, 2024

    UNKNOWN LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·August 5, 2025

    BARDEX® LUBRI-SIL® ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·December 22, 2021