BEUDAMED
    10,000 results · 44ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    BARDEX® LUBRICATH® FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·May 20, 2025

    UNKNOWN LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·June 17, 2025

    BARDEX® LUBRICATH® FOLEY CATHETER

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

    BARDEX® LUBRICATH® FOLEY CATHETER

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

    BARDEX® LUBRICATH® FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·June 2, 2025

    BARDEX® LUBRICATH® FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·April 10, 2025

    BARDEX® LUBRICATH® FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·May 6, 2025

    BARDEX® LUBRICATH® FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·April 9, 2025

    BARDEX® LUBRICATH® FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·June 26, 2025

    UNKNOWN LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·June 17, 2025

    BARDEX® LUBRICATH® FOLEY CATHETER COUDE TIP

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·May 9, 2025

    UNKNOWN LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·June 17, 2025

    BARDEX® LUBRICATH® FOLEY CATHETER COUNCILL MODEL

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·April 15, 2025

    UNKNOWN LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·June 11, 2025

    BARDEX® LUBRICATH® FOLEY CATHETER TIEMANN MODEL COUDE

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·April 22, 2025

    UNKNOWN LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZC·May 9, 2025

    UNKNOWN LATEX TEMP-SENSING CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·May 23, 2025

    BARDIA® FOLEY CATHETER SILICONE COATED

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·May 21, 2025

    BARDIA® FOLEY CATHETER SILICONE COATED

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

    UNKNOWN LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·April 4, 2025