BEUDAMED
    6 results · 20ms · 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 ×

    RSVP RF-2000

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MEDRAD FLUOROVISION HR 2000, HIGH RESOLUTION IMAGE

    FDA 510(k)
    FDA Class 2 ·Radiology

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 28, 2014

    OPTI-FREE REPLENISH

    FDA Adverse Event
    Injury ·ALCON - FORTH WORTH / ALCON LABORATORIES, INC.·Product code LPN·November 19, 2010

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·January 9, 2013