BEUDAMED
    4 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    ENDO STITCH POLYSORB 3/0 7 VIO DLU SU

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL·Product code GCJ·May 29, 2014

    HELICAL BLADE COUPLING SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES (USA) MONUMENT·Product code LXH·February 11, 2013

    XIMATRON C RADIOTHERAPY TREATMENT SIMULATOR

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS UK LTD·Product code KPQ·January 6, 2011

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·March 26, 2018