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

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    SYSMEX CA-6000

    FDA 510(k)
    FDA Class 2 ·Hematology

    RANFAC CUT BIOPSY NEEDLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SINGLE LUMEN CATHETER KITS

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

    CDS/R/4K DILUENT/SHEATH, 20L

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·April 12, 2007

    CD SAPPHIRE, CD 4000 SYSTEMS DILUENT/SHEATH

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·December 8, 2006

    CELL-DYN DILUENT/SHEATH

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKL·January 5, 2007

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·February 15, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·December 21, 2010

    RESTORIS PST/TFS TOTAL HIP SYS

    FDA Adverse Event
    Injury ·MAKO SURGICAL·Product code OQG·July 11, 2014