BEUDAMED
    4 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    6770372

    FDA Adverse Event
    Malfunction ·August 7, 2017

    VASOVIEW HEM25088284OPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·January 21, 2014

    BIOARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·October 1, 2012

    RESTOR IOL

    FDA Adverse Event
    Other ·ALCON RESEARCH LTD·Product code MFK·July 20, 2010