BEUDAMED
    6 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·August 23, 2016

    NUCLEUS 22

    FDA Adverse Event
    Injury ·COCHLEAR LIMITED·Product code MCM·May 18, 2025

    SYSLOC MINI AVF 15G X 1" BE 30CM /CLAMP

    FDA Adverse Event
    Injury ·JMS SINGAPORE PTE LTD·Product code FIE·May 30, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·November 20, 2012

    LEAD MODEL UNK

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 15, 2010

    SULOX HEAD, M, A, 28/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·September 8, 2017