BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    1213809-2018-00490

    FDA Adverse Event
    Malfunction ·August 6, 2018

    2520274-2013-02362

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·May 3, 2013

    ACCU-CHEK ® COMPACT PLUS TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 16, 2014

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP·Product code DTQ·May 2, 2011

    AMISTEM H, HA COATED STEM SIZE 2 STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·February 3, 2017

    MULTIPLE-SEE ATTACHED

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code OAD·March 24, 2009