BEUDAMED
    6 results · 14ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AP & CO. KG·Product code GEI·March 27, 2015

    CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    CAIMAN DISP.INSR.ARTICULAT.D:12 / 240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG& CO. KG·Product code GEI·April 15, 2015

    CAIMAN DISP INSTR ARTICULAT D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 16, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 16, 2014

    CAIMAN DISP. INSTR. ARTICULAT. D.: 12/440MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·July 28, 2014