BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    HOOD NASAL SEPTAL BUTTON

    FDA 510(k)
    FDA Unclassified ·Unknown

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471155978·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 230mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123045·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 100mm

    BD BACTEC Plus PRIME Aerobic/F Culture Vials

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Shoulder PacemakerTM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER-SILICON VALLEY·Product code GEX·December 9, 2010

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 9, 2014

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 28, 2012

    TPRLC 133 FP TYPE1 PPS HO 17.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·April 6, 2023

    CER BIOLOXD OPTION HD 36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 13, 2023