BEUDAMED
    3 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNKNOWN DEPUY ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 8, 2010

    ENDOTRACH TUBE 8229965 5PK 6.5MM EMG FLX

    FDA Adverse Event
    Injury ·XOMED MFG JACKSONVILLE·Product code ETN·January 3, 2013

    32MM -4 LFIT V40 HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·June 25, 2014