BEUDAMED
    8 results · 19ms · 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.

    RAREX & OPTEX X-RAY SCREENS

    FDA 510(k)
    FDA Class 1 ·Radiology

    OMEGA

    FDA UDI
    Stryker GmbH·07613154482429·Lid

    IDENTEVENT, VERSION 1.0G

    FDA 510(k)
    FDA Class 2 ·Neurology

    ECAT PET SCANNER, MODELS ECAT EXACT AND ECAT EXACT HR+ AND ECAT ART

    FDA 510(k)
    FDA Class 2 ·Radiology

    CLEARCANNULA-THREADED 8.5MMX75MM 5PK -ST

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEA·December 19, 2019

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·June 30, 2014

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 10, 2010

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·November 27, 2012