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

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    Filters FDA Adverse Event ×

    IMPL-HOLDER F/SYNFIX-LR

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·March 8, 2013

    QUICKSET TPRD HEX SCDR U-JOINT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·August 8, 2014

    SYBRONPRO TL

    FDA Adverse Event
    Injury ·EBI INC.·Product code DZE·February 16, 2011

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·July 14, 2016

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·November 23, 2015