BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNSPECIFIED BY THE COMPLAINANT

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTL·April 3, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 22, 2012

    ANALYTICAL D MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 16, 2010

    VG2 CERVICAL

    FDA Adverse Event
    Injury ·LIFENET HEALTH·Product code MQV·June 28, 2023

    MTF ODL, PARALLEL 8MM

    FDA Adverse Event
    Injury ·MUSCULOSKELETAL TRANSPLANT FOUNDATION D/B/A/ MTF BIOLOGICS·Product code MQV·June 28, 2023

    VG2 CERVICAL

    FDA Adverse Event
    Injury ·LIFENET HEALTH·Product code MBP·June 28, 2023