BEUDAMED
    6 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SMR REVERSE HUMERAL BODY SHORT

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·July 5, 2021

    TRSX5/WD86/ADULT/28FB/BH16/1255/U2222C/COM/U240 9153637785

    FDA Adverse Event
    Injury ·DANYANG JUMAO HEALTHCARE EQUIPMENT CO.,LTD.·Product code IOR·October 11, 2016

    L3W0250 - KALTOSTAT

    FDA Adverse Event
    Malfunction ·CONVATEC LTD·Product code NAC·August 8, 2022

    ENDO RETRACT II 10MM INSTRUMENT

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC P·Product code GCJ·March 15, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 21, 2011

    CELL-DYN WBC REAGENT A

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·March 18, 2008