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 ×

    AXIOM TOTAL KNEE SYST/ACL RETAIN TIBIAL TRAY/INSER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LASERPHOTONICS ML300 STONELASER ALEXANDRITE LITH.

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

    BARTELS HERPES SIMPLEX VIRUS 1 IGM EIA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZF·June 17, 2014

    PERIGEE SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·January 16, 2013

    CAPSURE Z NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010