BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    COBALT CHROME FEMORAL HEAD SZ 28 3.5MM 12/14 SHORT NECK

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JDI·December 15, 2016

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·January 11, 2013

    REPLY DR

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA CRM S.R.L.·Product code DXY·December 1, 2010

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    VITEK® 2 AST-N334 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 10, 2018

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018

    VITEK® 2 AST-GN09 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·September 5, 2018