BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    STRIP, STERILIZATION INDICATOR; DRY HEAT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FETASONDE MODEL 2108

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

    POINT TO POINT LEVEL

    FDA 510(k)
    FDA Class 2 ·Radiology

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Injury ·AESCULAP INC·Product code KCT·October 12, 2016

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 11, 2014

    NEW LIGASURE 5MM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·November 1, 2010

    ELEVATE PROLAPSE REPAIR SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·December 21, 2012

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code KCT·July 26, 2016