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

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    WIRE, GUIDE - MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TROJAN SUPRA LUBRICATED POLYURETHANE MALE CONDOM

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

    O-RING Condom

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

    BD LEUCOCOUNT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·May 28, 2021

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·November 21, 2012

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code LZH·March 21, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 28, 2010