BEUDAMED
    70 results · 53ms · Sources: EU EUDAMED, US FDA

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    Rhinomanometer

    FDA UDI
    GM INSTRUMENTS LIMITED·05060485270034·An electronic device designed to calculate nasa...

    Acoustic Rhinometer

    FDA UDI
    GM INSTRUMENTS LIMITED·05060485270027·A line powered (AC- powered), or powered via a ...

    ALIQUOT PROBE

    FDA Adverse Event
    Injury ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·February 7, 2013

    EPLEX BLOOD CULTURE IDENTIFICATION GRAM NEGATIVE (BCID-GN) PANEL

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code PEN·April 14, 2025

    EPLEX BLOOD CULTURE IDENTIFICATION PANEL - GRAM POSITIVE (BCID-GP) PANEL

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code PAM·November 14, 2024

    EPLEX BLOOD CULTURE IDENTIFICATION PANEL - GRAM POSITIVE (BCID-GP) PANEL

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code PAM·April 8, 2025

    EPLEX BLOOD CULTURE IDENTIFICATION PANEL - GRAM POSITIVE (BCID-GP) PANEL

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code PAM·April 8, 2025

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·September 12, 2016

    SYNCHRON

    FDA Adverse Event
    Death ·BECKMAN INSTRUMENTS, INC.·Product code JJC·March 31, 1997

    UNKNOWN OXFORD BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·May 23, 2018

    UNKNOWN OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·May 23, 2018

    UNKNOWN TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·May 23, 2018

    UNKNOWN OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·May 23, 2018

    GM EPLEX RESP PATHOGEN 2 PANEL EUA

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code QJR·May 14, 2025

    GM EPLEX RESP PATHOGEN 2 PANEL EUA

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code QJR·March 26, 2025

    GM EPLEX RESP PATHOGEN 2 PANEL EUA

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code QJR·March 26, 2025

    GM EPLEX RESP PATHOGEN 2 PANEL EUA

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code QJR·March 25, 2025

    GM EPLEX RESP PATHOGEN 2 PANEL EUA

    FDA Adverse Event
    Malfunction ·GENMARK DIAGNOSTICS, INC.·Product code QJR·March 24, 2025

    SFX SPI PDS+ UNI VIO 12IN 2-0 S/A CT-1

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code NEW·August 25, 2023

    SFX SYM PDS+ UNI VIO 18IN 0 S/A CT-1

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code NEW·July 1, 2022