BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 10, 2009

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 10, 2009

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 10, 2009

    KARL STORZ

    FDA Adverse Event
    Injury ·KARL STORZ ENDOSCOPY·Product code KQT·January 21, 2004

    INTELEPACS

    FDA Adverse Event
    Malfunction ·INTELERAD MEDICAL SYSTEMS INCORPORATED·Product code LLZ·March 7, 2014

    N/A

    FDA Adverse Event
    Malfunction ·STRYKER SUSTAINABILITY SOLUTIONS·Product code NLQ·November 14, 2012

    V-LOC 180 ABS CLOS DEVICE 3-0 CL 18 P-12

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GAM·September 8, 2010