BEUDAMED
    6 results · 18ms · 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 ×

    OROSPHERE PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    EDWARDS AQUARIUS SYSTEM, MODEL GE-F098-00

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

    Explorer Mini

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·June 24, 2014

    KLEENSPEC 590 SERIES DISP. VAGINAL SPECULA

    FDA Adverse Event
    Malfunction ·WELCH ALLYN·Product code HIB·November 1, 2010

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·December 21, 2012