BEUDAMED
    9 results · 38ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CM DRIVE ACQUA IMPLANT 3.5X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 22, 2018

    TRUSTEEL

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 10, 2025

    TRUSTEEL

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 10, 2025

    ADVIA CENTAUR XP CKMB ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code JHX·March 20, 2013

    COREVALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·August 15, 2014

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 9, 2011

    GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 2+ L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 13, 2022

    NAVIEN INTRACRANIAL CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code DQY·April 3, 2017

    NAVIEN INTRACRANIAL CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code DQY·July 20, 2017