BEUDAMED
    4 results · 22ms · 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 ×

    ELEVATE PROLAPSE REPAIR SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·January 10, 2013

    VIRTUOSO VR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code LWS·December 13, 2010

    R3 32MM ID US CRMC LINER 50

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LZO·July 9, 2014

    FEM. MODULAR HEAD - S 36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·March 10, 2021