BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    PANTEX DIRECT DHEA-S COATED TUBE RADIOIMMUNOASSAY

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209123803·

    FiberLocker Implant ; FiberLocker Instrument ; FiberLocker PowerUnit

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

    PAREMA K BAND NON-STERILE

    FDA 510(k)
    FDA Unclassified ·Unknown

    PWRGRSHNG CATH 5F BASICTRAY SL 45CM

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD)·Product code LJS·April 16, 2014

    UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·December 3, 2012

    REPAIR CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·September 7, 2010