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

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    QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    STOCKERTIR PURGE CONTROL (APC) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GNR TRAFFIC LIGHT PNA FISH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 29, 2026

    SINGLE USE ASPIRATION NEEDLE NA-U401SX

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FCG·August 3, 2023

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·June 17, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 4, 2014

    SINGLE USE ASPIRATION NEEDLE NA-U401SX

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FCG·August 3, 2023