BEUDAMED
    9,275 results · 29ms · Sources: EU EUDAMED, US FDA

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    FSG-Abdruckschaum

    Device
    EU MDR · Eu Md Class 1 ·Formschaum Gronau GmbH·On the market

    Fuse

    FDA UDI
    ENDOCHOICE, INC.·00840253114594·Gastroscope

    Fuse

    FDA UDI
    ENDOCHOICE, INC.·00840253114587·Gastroscope

    ROCHE ACCUCHEK INFORM METERS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code NBW·September 28, 2009

    FULLFIRE SELECT DIFFUSE TIP PROBE

    FDA Adverse Event
    Malfunction ·MONTERIS MEDICAL CORPORATION·Product code GEX·August 5, 2016

    BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 21, 2025

    BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·April 3, 2025

    BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 24, 2025

    PYXIS MEDSTATION ES SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION 303·Product code BRY·January 8, 2025

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·December 2, 2025

    BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 18, 2025

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·August 6, 2025

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·December 31, 2025

    BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·July 14, 2025

    BD PYXIS MEDSTATION ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·December 31, 2024

    ADVANTA V12 COVERED STENT

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code NIO·March 18, 2021

    Klic10 Blood Collection Accessories Set F

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·1 device

    Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model KMBB4OSU2FUS

    FDA Recall
    Terminated ·Arjo, Inc.·Product code FSG·January 5, 2007

    Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model KMBB4MSU2FUS

    FDA Recall
    Terminated ·Arjo, Inc.·Product code FSG·January 5, 2007

    Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model KMBB4OLU2FUS

    FDA Recall
    Terminated ·Arjo, Inc.·Product code FSG·January 5, 2007