BEUDAMED
    9 results · 27ms · 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.

    VARIOUS KITS

    FDA 510(k)
    FDA Not Classified ·Unknown

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517397225·CoRoent XLR-F, 16x34x24mm 12°

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517391407·CoRoent XLR-F, 16x34x24mm 12°

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517191892·Brigade Trial, 16x34x24mm 12°

    SYMBIA

    FDA 510(k)
    FDA Class 2 ·Radiology

    OMNIPRO I'MRT

    FDA 510(k)
    FDA Class 2 ·Radiology

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 28, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code FKX·December 17, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 14, 2014