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

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    BLACK OVAL-TOP TORP/PORP

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ANGIOPLASTY INFLATION DEVICE & CARTR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Solar™ Anorectal Manometry Catheter (Model Number: K1210AC-L-2212)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RELIAVAC CLOSED WOUND SUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC.·Product code GCY·December 8, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014

    SIMPLEX P-US TOBRA FD 10-PK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·December 19, 2012

    CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026