BEUDAMED
    10 results · 32ms · 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

    PRONTO SPOT CHECK PULSE CO-OXIMETER

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code DQA·July 9, 2018

    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

    V SERIES MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    OT VERIO SYNC METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 16, 2014

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·May 12, 2011

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·September 11, 1997

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

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