BEUDAMED
    13 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    8.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    5.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV.·Product code BTR·September 17, 1999

    5.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    8.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV.·Product code BTR·September 17, 1999

    9.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    6.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    7.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    5.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    9.0MM HI LO

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV·Product code BTR·September 17, 1999

    ENDO CLIP 5MM CLIP APPLIER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US·Product code FZP·March 25, 2013

    TOTALCARE SPO2RT

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 22, 2011

    CLEARSTAR PUMP

    FDA Adverse Event
    Malfunction ·ROSS PRODUCTS DIVISION·Product code LZH·April 15, 2008

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·February 23, 2016