BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    27-120601

    FDA Adverse Event
    Injury ·SANTA BARBARA·Product code FTR·June 29, 2005

    POWERPICK, 30 DEG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GFA·May 14, 2024

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    PERMACOL 10X15 1.5MM

    FDA Adverse Event
    Death ·COVIDIEN, FORMERLY TISSUE SCIENCE LABORATORIES, PLC·Product code FTL·September 3, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 20, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 26, 2014

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code LXH·June 10, 2011

    POWERPICK, 45 DEG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GFA·July 18, 2022