BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    COMPACT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    PORTABLE X-RAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    GENERATOR, PULSE, DEMAND, MODEL 5996

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ITREL 3

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·May 5, 2014

    CONSULTA CRT-D

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NIK·October 15, 2012

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURING FACILITY·Product code KDJ·August 10, 2010

    SLEEVE F/SEGM-TRANSP F/MEF

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·November 26, 2018