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

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    Filters FDA Adverse Event ×

    UNKNOWN ORTHOSIS

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code MNI·January 6, 2017

    MONARCH IOL DELIVERY SYSTEM CARTRIDGE

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC/HUNTINGTON·Product code HQL·June 2, 2006

    33M HEMORRHOID STAPLER 4.8MM STAPLES

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL·Product code GDW·March 6, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 25, 2011

    SCD EXPRESS SLEEVE K/L MEDIUM

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/ KENDALL·Product code JOW·February 19, 2008

    MONARCH IOL DELIVERY SYSTEM CARTRIDGE

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC. / HUNTINGTON·Product code KYB·June 30, 2006

    MONARCH IOL DELIVERY SYSTEM CARTRIDGE

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC. / HUNTINGTON·Product code KYB·June 30, 2006