BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

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    KODAK AUTOMATIC FILM FEEDER, MODEL 11

    FDA 510(k)
    FDA Class 2 ·Radiology

    FEM. MODULAR HEAD - M Ø36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code LZO·December 14, 2018

    Comarch e-Care Platform

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    QUANTA LITE OMP PLUS ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NVY·January 13, 2014

    QUADROX D

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·October 6, 2010

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·November 14, 2012