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

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    Filters FDA Adverse Event ×

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·December 17, 2010

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 10

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·January 29, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 15, 2014

    PURGE CASSETTE, STERILE, NON-QSK

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·September 2, 2025