BEUDAMED
    6 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.
    Filters Regulation: Us FDA ×

    PRIMADRY PRODUCT LINE

    FDA 510(k)
    FDA Class 2 ·Dental

    PROPHYPEARLS

    FDA 510(k)
    FDA Class 1 ·Dental

    Electric Wheelchair (Robooter E40), Model name: BBR-E40-01

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 20, 2014

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·December 10, 2010

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·January 28, 2013