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

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    Filters FDA Adverse Event ×

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code CGA·July 27, 2016

    IT VITE XLPE LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OQG·March 9, 2018

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 30, 2014

    VIRTUOSAPH PLUS, EVH

    FDA Adverse Event
    Injury ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·January 3, 2013

    GORE TRI-LOBE BALLOON CATHETER

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·November 16, 2010

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·October 19, 2016

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·July 26, 2016