BEUDAMED
    5 results · 47ms · 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 ×

    SPINAL NEEDLE 27GA 3.50 IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·July 8, 2021

    SPINAL NEEDLE 27GA 3.50 IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code BSP·October 1, 2020

    AMS SPARC SLING SYSTEM

    FDA Adverse Event
    Death ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTN·June 11, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 10, 2010

    BIOPATCH 4150

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code FRO·December 18, 2012