BEUDAMED
    10 results · 38ms · Sources: EU EUDAMED, US FDA

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    ADVANTA V12,COVERED STENT SYS,9X59X80

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·April 7, 2026

    THUNDERBEAT

    FDA Adverse Event
    Malfunction ·OLYMPUS AMERICA, INC,·Product code GEI·May 10, 2013

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·May 26, 2011

    VITROS 5,1 FS CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·August 14, 2008

    ADVANTA V12 COVERED STENT SYSTEM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code NIO·August 13, 2025

    SYRINGE 30ML LL S/C 56

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·April 16, 2024

    ADVANTA V12 COVERED STENT

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·September 10, 2025

    S.M.A.R.T. NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·January 28, 2016

    ADVANTA V12,COVERED STENTSYS, 9X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026

    ADVANTAV12,COVERED STENTSYS, 6X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026