BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SERIES 20000 LEGACY

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·January 17, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 5, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·December 9, 2010

    CORAIL2 NON COL HO SIZE 12

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWL·July 14, 2015

    TOTAL ASR ACET IMP SIZE 48

    FDA Adverse Event
    Injury ·DEPUY INTL LTD·Product code KWA·January 31, 2011

    TAPER SLEEVE ADAPTER 12/14 +8

    FDA Adverse Event
    Injury ·DEPUY INTL LTD·Product code KWA·January 31, 2011

    DEPUY ASR XL FEM IMP SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTL LTD·Product code KWA·January 31, 2011

    CORAIL2 NON COL HO SIZE 10

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWY·July 14, 2015

    LARGE MOD HEAD ADAPT 12/14 +5

    FDA Adverse Event
    Malfunction ·DEPUY INTL LTD·Product code KWA·January 31, 2011

    DEPUY ASR XL FEM IMP SIZE 43

    FDA Adverse Event
    Malfunction ·DEPUY INTL LTD·Product code KWA·January 31, 2011

    TOTAL ASR ACET IMP SIZE 48

    FDA Adverse Event
    Malfunction ·DEPUY INTL LTD·Product code KWA·January 31, 2011