BEUDAMED
    7 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 ×

    MAGNETIC RESON DIAG DEVICE MAGNETOM PROJECT 016

    FDA 510(k)
    FDA Class 2 ·Radiology

    Sloan Medical

    FDA registration
    Sloan Medical·7 products·🇺🇸 United States

    WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SIMDA abutment

    FDA 510(k)
    FDA Class 2 ·Dental

    ONE TOUCH ULTRA STRP BLUE 100

    FDA Adverse Event
    Malfunction ·LIFESCAN·Product code NBW·January 21, 2013

    INTEGRATED APD SET W/CASSETTE3 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 17, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 14, 2014