BEUDAMED
    7 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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

    ZEPHIR ANTERIOR CERVICAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·June 11, 2009

    CELL-DYN DILUENT/SHEATH

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

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Death ·RICE CREEK MFG·Product code DTB·March 6, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Product code KDJ·February 15, 2011

    SELECTSECURE

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·August 8, 2014