BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SOLOSITE DERMAL WOUND GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    3I PATIENT-SPECIFIC DENTAL ABUTMENT AND OVERDENTURE BAR

    FDA 510(k)
    FDA Class 2 ·Dental

    AXERA 2 ACCESS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MENTOR SMOOTH ROUND SPECTRUM

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·July 9, 2018

    VERSASTEP PLUS 11MM CANN/DILT W/RADEXPSLV

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GCJ·April 4, 2014

    MONARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTN·January 25, 2013

    PALM CONTROL FOR SURGIGRAPHIC 6000

    FDA Adverse Event
    Malfunction ·STERIS·Product code FQO·December 9, 2010