BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    FBCC Night Guard

    FDA 510(k)
    FDA Unclassified ·Unknown

    CAPTURE-R READY INDICATOR CELLS

    FDA Adverse Event
    Malfunction ·IMMUCOR·Product code KSZ·July 2, 2009

    NEURODYN RUBY MUSCLE STIMULATOR, NEURODYN AUSSIE MUSCLE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    AVA (Augmented Vascular Analysis)

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPTURE-R READY-SCREEN (POOLED CELLS)

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·August 16, 2019

    VISTA BRITE TIP GUIDING CATHETERS

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DQY·August 24, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 3, 2014

    4000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·July 1, 2013

    COBAS® MPX - 96T

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QHO·September 26, 2025