BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LATERAL STRAIGHT STEM 15.0 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·March 28, 2012

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 22, 2013

    ASR UNI FEMORAL IMPL SIZE 46

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

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 9, 2014

    SULOX-HD 32 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·April 23, 2019

    SULOX, HEAD, M¸ 32/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·August 3, 2018

    SULOX-HEAD 28 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·April 4, 2019