BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    ENTRI FLEX FEEDING TUBE

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

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code KNT·June 12, 2024

    NeuroStar Advanced Therapy System (Version 3.8)

    FDA 510(k)
    FDA Class 2 ·Neurology

    NDI PASSIVE SPHERES

    FDA 510(k)
    FDA Class 2 ·Neurology

    ESPIRIT

    FDA Adverse Event
    Malfunction ·PHILIPS RESPIRONICS·Product code CBK·May 21, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 29, 2012

    TALENT THORACIC STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·September 8, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

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