BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MULTI SPECT 2 [510(K) K913630]

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code IYX·April 13, 2001

    ABLATOR - S

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW ENDOSCOPY ANDOVER MANUFACTURE·Product code GEI·December 3, 2010

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 14, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 3, 2014

    FEMORAL STEM CMK OC MODULAR CEMENTED

    FDA Adverse Event
    Death ·BIOMET FRANCE S.A.R.L.·Product code JDI·October 30, 2017

    STAINLESS STEEL MODULAR HEAD

    FDA Adverse Event
    Death ·BIOMET FRANCE S.A.R.L.·Product code JDI·October 30, 2017

    RINGLOC HIP SYSTEM ACETABULAR BI-POLAR CUP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·October 17, 2017

    COBALT HV BONE CEMENT 40GRAMS-JAPAN

    FDA Adverse Event
    Death ·BIOMET ORTHOPEDICS·Product code LOD·September 23, 2016