BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    KAPLAN-SIMPSON INFUSASLEEVE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SpiritMB

    FDA UDI
    ORMCO CORPORATION·00889989007411·ID W - Twin - Lower-Universal 1st Bicuspid - Pink

    AMPLATZER DUCT OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MAE·June 7, 2018

    Vaginal Moisturizing Gel

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

    STRYKER NAVIGATION SYSTEM - CT-BASED HIP MODULE, MODEL 6007-621-000

    FDA 510(k)
    FDA Class 2 ·Neurology

    HUDSON AQUAPAK 340 SW, 340 ML W/040 ADAPTOR

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTT·June 5, 2014

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·February 8, 2013

    IKARIA

    FDA Adverse Event
    Malfunction ·IKARIA·Product code MRN·December 28, 2010