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

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    BLADE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LUPUS(LE)-LATEX TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SOLARSHIELD CLIPS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    S-ROM M HEAD 36MM +6

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 13, 2013

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 13, 2013

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·February 6, 2013

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·December 30, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·July 21, 2014