BEUDAMED
    9 results · 19ms · 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.
    Filters Status: Death ×

    NI

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code KPE·August 12, 2015

    JEVITY

    FDA Adverse Event
    Death ·ABBOTT-ROSS·Product code KPE·January 4, 2002

    NI

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code KPE·September 30, 2015

    PLASTIC BAG AND TUBING FOR TPN

    FDA Adverse Event
    Death ·MCGAW, INC.·Product code KPE·March 1, 1994

    INTRAVIA EMPTY CONTAINER (250ML) GAMMA STERILIZED

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORP.·Product code KPE·December 21, 2007

    VIAFLEX EMPTY CONTAINER (3000) W/CONNECTOR

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORP.·Product code KPE·December 21, 2007

    DUMVETINVIAFLEX

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - JAYUYA·Product code KPE·May 13, 2011

    GLUCERNA

    FDA Adverse Event
    Death ·Product code KPE·December 7, 2011

    ACL 2000/ANTI-THROMBIN III

    FDA Adverse Event
    Death ·INSTRUMENTATION LABORATORIES·Product code JPE·March 4, 1996