BEUDAMED
    7 results · 21ms · 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 ×

    Rapid Therapy System

    FDA 510(k)
    FDA Class 2 ·Neurology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707012276·CALIBRA 1ST MOL BANDS W/G8025-03 n.UL 31

    MODIFICATION TO ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRESTIGE 24I; BIOLIS 24I; MGC 240

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DLC HEX SCRDRVR SHAFT CARDAN

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·October 6, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 3, 2013

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·June 2, 2011