BEUDAMED
    5 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SUMMIT BASIC CEMENTED SZ 2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD. 3006356043·Product code JDI·June 25, 2014

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·January 3, 2013

    ADVIA 2400

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JGS·November 5, 2010

    ALARIS PUMP MODULE SET NON-VENTED BLOOD SET

    FDA Adverse Event
    Malfunction ·Product code FPA·June 29, 2021

    BD ALARIS¿ LVP BLD180M 15D SS

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 30, 2020