BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TDX FPIA ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·December 28, 2007

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    LATEX FOLEY CATHETER, 16F

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, INC.·Product code NWR·July 15, 2014

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 7, 2011

    TDX FPIA ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·January 2, 2008

    2.0MM THREADED DRILL GUIDE WITH DEPTH GAUGE

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FZX·May 23, 2019

    TDX FPIA ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJQ·April 27, 2009

    ECHELON ENDOPATH STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 1, 2022

    LASERSCOPE

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·December 30, 2011