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

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    MODIFICATION TO:NESS L300

    FDA 510(k)
    FDA Class 2 ·Neurology

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014605159·MAQUET/SIEMENS 1130 3" SOFTCARE

    ITOTAL IDENTITY SMALL KEEL PUNCH

    FDA UDI
    Conformis, Inc.·00810933030650·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450180327·

    SYRINGE 50ML LL TIP 1ML

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·June 26, 2024

    SYRINGE 50ML LL TIP 1ML

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·October 7, 2024

    RPI SKIN OR AIR TEMPERATURE PROBE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CHALLENGER DIRECT COMPOSITE

    FDA 510(k)
    FDA Class 2 ·Dental

    SYRINGE 50ML LL TIP 1ML

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·July 15, 2024

    BD 50ML LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY·Product code FMF·November 12, 2024

    SYRINGE 50ML LL TIP 1ML

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·November 15, 2024

    TRIAGE PROFILER SOB PANEL 25T

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·July 19, 2017

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Injury ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·December 13, 2019

    TRIAGE PROFILER SOB PANEL 25T

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHX·August 29, 2017

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·March 4, 2021

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·August 3, 2018

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·January 25, 2017

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 23, 2019

    FORTIFY VR, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·April 26, 2013

    ADVANCE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·April 6, 2011