BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ELLIPSE DR, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 30, 2014

    MULTI-LINK RX VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-CLONMEL·Product code MAF·November 20, 2010

    UNK

    FDA Adverse Event
    Injury ·UNK·Product code FTL·December 29, 2012

    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

    GMK-REVISION FEMUR REVISION PS SIZE 5 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 18, 2022

    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