BEUDAMED
    7 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·June 29, 2017

    2520274-2013-10225

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 11, 2013

    UNKNOWN DEPUY TIBIAL SLEEVE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 28, 2014

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 13, 2011

    BIPLATE SCHAEDLER/SCHAED KV 5% SB 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·June 25, 2021

    BD BBL¿ SCHAEDLER K-V AGAR WITH 5% SHEEP BLOOD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·August 2, 2021

    BIPLATE SCHAEDLER/SCHAED KV 5% SB 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·July 1, 2021