BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    SONICATOR 710 (MODEL ME710)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    LBI EMBOLECTOMY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Low Dose CT Lung Cancer Screening Option

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 30, 2014

    ADJ. X-CONN. LARGE 55.5-81.0MM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE·Product code NKB·October 4, 2010

    TI MATRIX LOCKING CAP

    FDA Adverse Event
    Death ·SYNTHES BRANDYWINE·Product code NKB·December 20, 2012