BEUDAMED
    5,577 results · 76ms · Sources: EU EUDAMED, US FDA

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    BD PROBETEC ET INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code KHO·July 24, 2003

    BD DIAGNOSTIC SYSTEMS PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 22, 2021

    BBL MGIT MYCOBACTERIA GROWTH INDICATOR TUBE

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code MDB·March 13, 2012

    BD BACTEC 12B MYCOBACTERIA CULTURE VIALS MIDD

    FDA Adverse Event
    Other ·BD DIAGNOSTIC SYSTEMS·Product code JTA·March 19, 2010

    BD BACTEC FX - TOP UNIT

    FDA Adverse Event
    Other ·BD DIAGNOSTIC SYSTEMS·Product code JTA·February 26, 2010

    BBL THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITA

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code JSG·October 31, 2012

    PHOENIX PMIC/ID-62 PANEL

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code LON·February 23, 2012

    BBL THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITA

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code JSG·October 31, 2012

    BBL CRYSTAL ENTERIC/NONFERMENTER ID KIT

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code JSS·March 8, 2013

    BD INNOVA PLATE STREAKER

    FDA Adverse Event
    Malfunction ·BD DIAGNOSTIC SYSTEMS·Product code MKZ·March 8, 2013

    BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMP

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code MKZ·March 8, 2013

    BD BACTEC FX - TOP UNIT

    FDA Adverse Event
    Malfunction ·BD DIAGNOSTIC SYSTEMS·Product code JTA·November 2, 2009

    BD MAX INSTRUMENT

    FDA Adverse Event
    Malfunction ·BD DIAGNOSTIC SYSTEMS·Product code OOI·January 6, 2014

    BD PROBETEC CHLAMYDIA TRACHOMATIC (CT) QX

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code MKZ·January 13, 2014

    BBL MGIT MYCOBACTERIA GROWTH INDICATOR TUBE

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code MDB·August 10, 2011

    BD SERO-FUGE 2002 CENTRIFUGE

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code LXG·June 4, 2013

    BD SERO-FUGE 2001 CENTRIFUGE

    FDA Adverse Event
    Injury ·BD DIAGNOSTIC SYSTEMS·Product code LXG·May 22, 2013

    DIFCO DESOXYCHOLATE AGAR

    FDA Adverse Event
    Other ·BD DIAGNOSTIC SYSTEMS·Product code JSG·November 24, 2010

    BD PHOENIX PANEL NMIC/ID-123

    FDA Adverse Event
    Malfunction ·BD DIAGNOSTIC SYSTEMS·Product code LON·March 1, 2011

    BBL GRAM IODINE

    FDA Adverse Event
    Other ·BD DIAGNOSTIC SYSTEMS·Product code KPA·February 6, 2006