BEUDAMED
    10,000 results · 133ms · Sources: EU EUDAMED, US FDA

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    Sample Container

    FDA UDI
    Scivita Medical Technology Co., Ltd.·06971381257588·Bronchus Sampler is composed of the sampler con...

    Dimension® Small Sample Container (SSC)

    FDA UDI
    Siemens Healthcare Diagnostics Inc.·00842768005909·Small Sample Container (SSC) - Dimension® - 100...

    Dimension Vista® Small Sample Container (SSC)

    FDA UDI
    Siemens Healthcare Diagnostics Inc.·00842768028915·Small Sample Container (SSC), 1000 Pieces

    FINESSE ULTRA BIOPSY PROBE

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·July 28, 2015

    MPA

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 14, 2009

    GALILEO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·June 2, 2016

    2517506-2017-00411

    FDA Adverse Event
    Malfunction ·April 20, 2017

    EMIT 2000 GENTAMICIN PLUS ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code LCD·April 19, 2017

    0.8% SURGISCREEN

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·December 29, 2005

    BD VACUTAINER® URINE COMPLETE CUP KIT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JSM·October 4, 2022

    MTS ANTI-IGG CARD

    FDA Adverse Event
    Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·February 10, 2009

    Atellica Solution IM1300 Analyzer, Siemens Material Number 11066001, UDI # 00630414007960

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JJE·May 7, 2020

    Atellica Solution IM1600 Analyzer, Siemens Material Number 11066000, UDI # 00630414002026

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JJE·May 7, 2020

    ADVIA 1800

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·June 27, 2016

    0.8% SELECTOGEN

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·June 18, 2004

    0.8% SURGISCREEN

    FDA Adverse Event
    Other ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·October 31, 2005

    SELECTOGEN

    FDA Adverse Event
    Other ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·September 8, 2005

    DRB1*15 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 9, 2013

    0.8% SELECTOGEN

    FDA Adverse Event
    Other ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·November 11, 2005

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·June 18, 2004