BEUDAMED
    6 results · 24ms · 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 ×

    CONCEPT 4MM CANCELLOUS SCREW WITH EYELET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SIMON BREAST LESION LOCALIZATION NEEDLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MAESTRO SERIES 100/200 CARDIAC SINGLE CHAMBER PACE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·June 18, 2014

    MONARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTN·January 17, 2013

    RESURFACING CUP COUPLING HANDLE

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code JDI·December 10, 2010