BEUDAMED
    6 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·May 6, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 16, 2010

    SROM*STM ST,30+4L NK,16X11X150

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code JDI·January 7, 2013

    SMR SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·January 29, 2026

    SMR REVERSE HUMERAL BODY

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code KWS·November 23, 2020

    SMR GLENOID PEG TT SMALL-R #L

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 5, 2020