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

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    B-D DRAKE WILLOCK #7000 SERIES ULTRAF

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

    Fixated Asfora BULLET CAGE® (FABC)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ESOPHAGEAL Z-STENT WITH DUA ANTI-REFLUX VALVE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SIZE 5 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 22, 2020

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 15, 2014

    MAXIMO II VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·October 31, 2012

    PULSE GEN MODEL 104

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·June 2, 2015

    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018