BEUDAMED
    6 results · 17ms · 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.

    MUELLER HINTON AGAR & MUELLER HINTON AGAR W/5% SHE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SLIMMANAGER, MODEL SM-X, SM-E

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD MAX CT/GC/TV, BD MAX INSTRUMENT

    FDA 510(k)
    FDA Class 2 ·Immunology

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·June 5, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 29, 2012

    *

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·September 23, 2010