BEUDAMED
    12 results · 29ms · Sources: EU EUDAMED, US FDA

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    GEMORE TRUE SINE INTERFERENTIAL STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971390·

    AUTOSTAT II ANTI-B-2 GLYCOPROTEIN-I IGM ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    CORELEADER HEMO-PAD MODEL CPII 02030

    FDA 510(k)
    FDA Unclassified ·Unknown

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·May 21, 2013

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·June 10, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    INSPIRE HVR DUAL

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTN·November 12, 2024

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 18, 2023

    INSPIRE HVR DUAL HARDSHELL VENOUS/CARDIOTOMY RESERVOIR

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·November 18, 2022

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 7, 2023

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·November 14, 2023