BEUDAMED
    941 results · 62ms · Sources: EU EUDAMED, US FDA

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    CENTER HEALTH INC.

    FDA registration
    CENTER HEALTH INC.·1 product·🇺🇸 United States

    CARESTREAM HEALTH, INC., GLOBAL R&D CENTER

    FDA registration
    CARESTREAM HEALTH, INC., GLOBAL R&D CENTER·8 products·🇨🇳 China

    ADVIA 2120I WITH DUAL ASPIRATE AUTOSAMPLER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·July 15, 2016

    ADVIA 2120 WITH DUAL ASPIRATE AUTOSAMPLER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·February 25, 2016

    EVIS EXERA II COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·July 13, 2022

    EVIS EXERA III COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·July 13, 2022

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·July 15, 2022

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·July 15, 2022

    EVIS EXERA III DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDT·July 15, 2022

    ADVIA 2120 HEMATOLOGY SYSTEM WITH DUAL ASPIRATE AUTOSAMPLER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·June 23, 2017

    ADVIA 2120I WITH SINGLE ASPIRATE AUTOSAMPLER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·October 30, 2015

    ADVIA 2120I WITH SINGLE ASPIRATE AUTOSAMPLER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·June 9, 2017

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·November 13, 2008

    HOMEPUMP C-SERIES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL - IRVINE·Product code MEB·May 28, 2020

    OMNICELL I.V. STATION ONCO

    FDA Adverse Event
    Malfunction ·OMNICELL, INC.·Product code NEP·March 23, 2021

    ZENITH I

    FDA Adverse Event
    Death ·GF HEALTH PRODUCTS INC.·Product code FNL·September 4, 2020

    MIC GJ FEED TUBE KIT-ENDOSCOPIC/RADIOLOGIC PLACEMENT-22 FR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 8, 2026

    MIC GJ FEED TUBE KIT-ENDOSCOPIC/RADIOLOGIC PLACEMENT-22 FR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 8, 2026

    ADVIA 2120I WITH SINGLE ASPIRATE AUTOSAMPLER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·June 22, 2016

    ADVIA 2120I WITH DUAL ASPIRATE AUTOSAMPLER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·January 13, 2016