BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL

    FDA 510(k)
    FDA Class 1 ·Microbiology

    CENTRIA FERRITIN RIA

    FDA 510(k)
    FDA Class 2 ·Immunology

    CP100 & 200 12-LEAD RESTING ELECTROCARDIOGRAPHS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® K2 EDTA (K2E) 10.8 MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 22, 2018

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·July 27, 2023

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·February 21, 2013

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·January 26, 2011

    ADVIA 2400

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·July 31, 2014

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·July 27, 2023