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

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    EPISCOPE, MODEL 47300

    FDA 510(k)
    FDA Class 1 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123052·K-WIRE - DOUBLE TROCAR 1.0mm DIA x 75mm

    REST ASSURED GENERATION III DENTAL PROTECTOR

    FDA 510(k)
    FDA Unclassified ·Unknown

    PRISMAFLO

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

    WALLFLEX ¿ DUODENAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code MUM·January 17, 2013

    EMG REINFORCED ENDOTRACHEAL TUBE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·December 3, 2010

    COREVALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 8, 2014

    G7 OSSEOTI MULTIHOLE 74MM J

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 21, 2023

    G7 SCREW 6.5MM X 25MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·August 21, 2023