BEUDAMED
    2,193 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    (COC/AMP/EDDP100/MOP/BZO)MULTI-DRUG ONE STEP 5 DRUG SCREEN TEST PANEL (URINE)

    FDA Adverse Event
    Malfunction ·Product code DIO·December 10, 2015

    AZO

    FDA Adverse Event
    Malfunction ·AMERIFIT·Product code JJW·July 30, 2007

    AZO

    FDA Adverse Event
    Other ·SIEMENS DIAGNOSTICS, INC.·Product code CEN·July 12, 2012

    CLINITEK STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code KQO·April 22, 2013

    CLINITEK STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code KQO·June 19, 2013

    AXONICS

    FDA Adverse Event
    Injury ·AXONICS MODULATION TECHNOLOGIES, INC.·Product code EZW·July 15, 2025

    CLINITEK STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code KQO·July 1, 2013

    QUIDEL TRIAGE TOX DRUG SCREEN, 94600

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code JXO·October 3, 2019

    TOX/SEE DRUG SCREEN

    FDA Adverse Event
    Death ·BIO-RAD LABORATORIES INC·Product code DIO·January 17, 2014

    CLINITEK STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code KQO·May 17, 2013

    CLINITEX STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code KQO·April 8, 2013

    CLINITEK STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code KQO·March 13, 2013

    CLINITEK STATUS

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code KQO·August 15, 2014

    CLINITEK STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code KQO·July 1, 2013

    CLINITEK STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code KQO·June 20, 2013

    CLINITEK STATUS

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code KQO·April 3, 2013

    ALERE ISCREEN 6 PANEL TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DIO·September 13, 2017

    AZO TEST STRIPS

    FDA Adverse Event
    Other ·SIEMENS DIAGNOSTICS, INC.·Product code CEN·July 12, 2012

    AZO TEST STRUOS

    FDA Adverse Event
    Malfunction ·SIEMENS DIAGNOSTICS·Product code CEN·July 12, 2012

    AZO TEST STRIPS

    FDA Adverse Event
    Injury ·TECO DIAGNOSTICS·Product code JMT·June 19, 2018