BEUDAMED
    6 results · 26ms · 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.

    STOMAHESIVE POWDER

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    NEXUS PRESSURE RATED EXTENSION SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CapKlenZ

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 2, 2014

    PINNACLE MTL INS NEUT40IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 16, 2012

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2010