BEUDAMED
    16 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    9616240-2006-00341

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    9616240-2006-00332

    FDA Adverse Event
    Other ·Product code FII·June 1, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    9616240-2006-00339

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    9616240-2006-00340

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 2/14MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 16, 2021

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 2/14MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 26, 2023

    9616240-2006-00350

    FDA Adverse Event
    Malfunction ·Product code FII·June 23, 2006

    9616240-2006-00345

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 6, 2025

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013

    HIRES 90K

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS, LLC·Product code MCM·February 14, 2011

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 12, 2014

    PROLENE HERNIA SYSTEM UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·April 10, 2019