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

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    Visera Hysterovideoscope Olympus HYF Type V

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BD BBL™ Martin-Lewis Agar

    FDA UDI
    BECTON, DICKINSON AND COMPANY·10382902215575·Plate Martin-Lewis Agar 20 Ea

    WONDFO CANNABINOIDS URINE TEST WONDFO PROPOXYPHENE URINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SPECTRUM SILICONE CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    XPERT SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR SWITZERLAND·Product code FGE·November 5, 2008

    COMPOUNDERS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - BUFFALO GROVE·Product code NEP·August 24, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·July 3, 2013

    BD BBL¿ MARTIN-LEWIS AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTY·August 11, 2021

    BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. Catalog Number: 221557

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·April 14, 2021

    BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. Catalog Number: 221557

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JTY·March 17, 2021

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025