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 ×

    RHEUMAJET CRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756372183·PROCEDURE PACK

    ACCUTRAC

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

    KTJ-20C BLOOD PRESSURE CUFF, MODEL KTJ-20C

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN CSF SHUNT

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·November 22, 2010

    UNKNOWN STRYKER RIGHT HIP

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·January 8, 2013

    3.5MM LOCKING SCREW SLF-TPNG W/STARDRIVE RECESS 32MM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·July 2, 2014