BEUDAMED
    5 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·October 12, 2012

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 13, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·August 10, 2010

    FOLYSIL SILICONE CATHETER

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code EZL·April 18, 2025

    FOLYSIL SILICONE CATHETER

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code EZL·February 21, 2025