BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE GMBH·Product code NBW·January 25, 2019

    GLUCOMETER ELITE 4 BASIC

    FDA Adverse Event
    Other ·ARKRAY, INC·Product code NBW·June 6, 2002

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 7, 2014

    ROCKERSWITCH PENCIL

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·August 3, 2011

    COULTER® LH 750 HEMATOLOGY ANALYXZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 29, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 14, 2014