BEUDAMED
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    Filters Status: Malfunction ×

    VITROS SALI SLIDES

    FDA Adverse Event
    Malfunction ·JOHNSON &JOHNSON CLINICAL DIAGNOSTICS·Product code DKJ·August 30, 1996

    VITROS CHEMISTRY PRODUCTS SALICYLATE SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code DKJ·October 8, 2008

    VITROS CHEMISTRY PRODUCTS SALICYLATE SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code DKJ·October 8, 2008

    VITROS CHEMISTRY PRODUCTS SALICYLATE SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code DKJ·October 8, 2008

    VITROS CHEMISTRY PRODUCTS SALICYLATE SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code DKJ·October 8, 2008

    VITROS CHEMISTRY PRODUCTS SALICYLATE SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code DKJ·October 8, 2008

    DIMENSION VISTA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code DKJ·June 29, 2020

    UNICEL® DXC 800 PRO SYNCHRON® CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code DKJ·March 16, 2011

    ANALYTICAL P MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code DKJ·July 22, 2009

    DIMENSION® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DKJ·November 30, 2011

    DIMENSION® CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DKJ·August 1, 2012

    VITROS SALI CHEMISTRY SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code DKJ·May 31, 2007

    LIGHTTRAIL REUSABLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEX·May 3, 2018

    LIGHTTRAIL REUSABLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEX·May 3, 2018

    DONJOY

    FDA Adverse Event
    Malfunction ·D.J. ORTHOPEDICS LLC·Product code IOY·December 18, 2002

    MATRIXMND 1.8 DB J-LATCH 03.503.045/.047

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code DZI·September 15, 2022

    MATRIXMND 1.5 DB J-LATCH 03.503.045/.047

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code DZI·February 8, 2024

    MATRIXMND 1.5 DB J-LATCH 03.503.045/.047

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code DZI·April 7, 2023

    MATRIXMND 1.5 DB J-LATCH 03.503.045/.047

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code DZI·December 4, 2023

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·February 28, 2022