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

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    WELCH ALLYN HI - LUX ILLUMINATOR

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

    FORTADERM ANTIMICROBIAL WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    Uberlube

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

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·February 9, 2013

    SWEET PICOTIP

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 6, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014

    VIDAS ESTRADIOL II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code CHP·January 21, 2021

    VIDAS® ESTRADIOL II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code CHP·September 16, 2021