BEUDAMED
    32 results · 40ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 – >=16 µg/mL

    FDA 510(k)
    FDA Class 2 ·Microbiology

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971390·

    CORELEADER HEMO-PAD MODEL CPII 02030

    FDA 510(k)
    FDA Unclassified ·Unknown

    QUANTA LITE CCP3.1 IGG/IGA ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·October 17, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 9, 2018

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·January 11, 2019

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 21, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·December 21, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    ATLANTIS? SR PRO²

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code DQO·June 17, 2013

    PULSAR MAX II

    FDA Adverse Event
    Malfunction ·GUIDANT CLONMEL IRELAND·Product code NVZ·July 23, 2011

    BD LOGIC BLOOD GLUCOSE MONITOR

    FDA Adverse Event
    Malfunction ·NOVA BIOMEDICAL CORP·Product code NBW·September 19, 2008

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 3, 2018