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

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    Filters Status: Injury ×

    VITEK®2 AST-N351 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code LON·November 17, 2017

    VITEK®2 AST-N351 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code LON·November 17, 2017

    VITEK®2 AST-N351 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code LON·November 17, 2017

    VITEK®2 AST-N351 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code LON·November 17, 2017

    VITEK®2 AST-N351 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code LON·November 17, 2017

    VITEK®2 AST-N351 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code LON·November 17, 2017

    VITEK®2 AST-N351 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code LON·November 17, 2017

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEURMODULATION·Product code GZB·June 27, 2014

    VITEK® 2 AST-GP75 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC·Product code LON·December 6, 2017

    VITEK® 2 GN ID TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code LQM·May 24, 2019

    VITEK® 2 GN ID TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code LQM·May 24, 2019

    VITEK® 2 GN ID TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code LQM·May 24, 2019