BEUDAMED
    6 results · 34ms · 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.

    THE EXPERIMENTAL

    FDA 510(k)
    FDA Class 1 ·Dental

    CDC ANAEROBE BLOOD AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MONOXYCHLOROSENE WAREXIN

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

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·October 6, 2010

    COBAS INTEGRA 400 PLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MZV·December 10, 2012

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 23, 2015