BEUDAMED
    155 results · 43ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    VITEK 2 GP TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code LON·May 13, 2010

    VITEK 2 GRAM-POSITIVE IDENTIFICATION TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC·Product code LQL·July 21, 2015

    VITEK® 2 AST-GP67 TEST KIT

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code LON·November 21, 2016

    BACT/ALERT BLOOD COLLECTION ADAPTER CAP AND INSERT

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code FMI·January 20, 2012

    BACT/ALERT SN REAGENT BOTTLE

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code MDB·January 2, 2012

    BACT/ALERT PF BOTTLE

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code JTA·February 23, 2004

    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

    SIMPLASTIN HTF

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code GJS·January 16, 2002

    BACT/ALERT FN CULTURE BOTTLE

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code MDB·February 7, 2002

    VITEK® 2 GRAM-NEGATIVE SUSCEPTIBILITY TEST KIT AST-N263

    FDA Adverse Event
    Injury ·BIOMÉRIEUX, INC.·Product code LON·November 3, 2017

    VITEK® 2 AST-GP75 TEST KIT

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

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Injury ·BIOMERIEUX INC.·Product code MDB·December 21, 2017

    VITEK®2 AST-N351 TEST KIT

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

    BAC T/ALERT BLOOD COLLECTION ADAPTER

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code MDB·December 18, 2003

    MDA

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code GKP·December 4, 2003

    BACT/ALERT MEDIA CULTURE BOTTLE

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code JTA·November 18, 2003

    BACT/ALERT MP BOTTLE

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code JTA·August 14, 2003

    BACT/ ALERT PF BOTTLE

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code MDB·September 10, 2003

    BACT/ALERT SUBCULTURE UNITS

    FDA Adverse Event
    Injury ·BIOMERIEUX, INC.·Product code JTA·September 10, 2003