BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    REVISION MODULAR NECK H.50MM

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code LZO·April 22, 2020

    FEM. MODULAR HEAD - L 32MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LPH·February 7, 2020

    LIMFFLOW STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·LIMFLOW INC·Product code QWN·March 26, 2025

    AXXESS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL ¿ NEUROMODULATION·Product code GZB·May 28, 2014

    PRODISC-C IMPLANT MEDIUM 5MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·January 7, 2013

    RADIAL JAW 4 BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·November 16, 2010