BEUDAMED
    10 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 3, 2013

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 10, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 3, 2011

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

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·April 15, 2015

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

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

    BD MICROTAINER® MAP MICROTUBE FOR AUTOMATED PROCESS K2 EDTA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·July 3, 2019