BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Trex_HD

    FDA 510(k)
    FDA Class 2 ·Neurology

    BI-METRIC HEAD/NECK HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304223196·

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 1, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 29, 2021

    COFLEX-F

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDISTIM VERIQC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 14, 2011

    QUADRA H FEMORAL STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 5, 2013