BEUDAMED
    5 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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·May 5, 2026

    REGENCY SR+

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

    VISUM LED II SURGICAL LIGHT

    FDA Adverse Event
    Malfunction ·STRYKER COMMUNICATIONS·Product code FSY·October 19, 2012

    SPECTRUM INFUSION PUMP

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