BEUDAMED
    7 results · 27ms · 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.

    HEMOPHRON

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

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0106120·Trial, 26 x 12mm, 8 Degree, Tapered, Straight

    FM20

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    VECTORVISION KNEE

    FDA 510(k)
    FDA Class 2 ·Neurology

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, NEUROMODULATION·Product code GZB·May 6, 2014

    RELIA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NVZ·October 31, 2012

    1644487-2008-00540

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 29, 2008