BEUDAMED
    8 results · 21ms · 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 ×

    CRYOMINI

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

    NA

    FDA UDI
    STRYKER CORPORATION·07613327056471·Insert, Fundus Grasper

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 5, 2024

    SPEEDYBELL

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

    SOF-PACH REUSABLE NEUROSTIMULATION ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    MAXI 500

    FDA Adverse Event
    Injury ·ARJOHUNTLEIGH MAGOG INC·Product code FSA·April 11, 2013

    SYNCHRON CX5 DELTA

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·May 6, 2011

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·July 23, 2008