BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·May 2, 2002

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 10, 2025

    FINELINE II

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code DTB·November 11, 2008

    UNICEL DXC 800

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 19, 2011

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 30, 2013

    PERSONA REVISION TAPERED CEMENTED STEM EXTENSION 13MM DIA +75MM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 9, 2023

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·June 19, 2012

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·June 19, 2012