BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    OSTEONICS CEMENT RESTRICTOR

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

    CURE LP

    FDA UDI
    MEDITECH SPINE, LLC·B167900462000·

    CURE LP

    FDA UDI
    SpineArt SA·07640332475232·AWL SHEATH - VARIABLE

    URINE PHENCYCLIDINE (PCP) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF 94A

    FDA 510(k)
    FDA Unclassified ·Unknown

    BRILLIANCE DUAL ENERGY OPTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·December 21, 2020

    CARPENTIER-EDWARDS S.A.V. BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 27, 2014

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·Product code FKX·January 7, 2013

    ANEURX AAADVANTAGE STENT GRAFT SYSTEM -HYDRO

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·October 28, 2010