BEUDAMED
    3 results · 24ms · 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 ×

    INTRALASE FS3 LASER

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA LLC·Product code HNO·December 10, 2010

    ELECTRO SURGICAL INSTRUMENT COMPANY

    FDA Adverse Event
    Other ·ELECTRO SURGICAL INSTRUMENT COMPANY·Product code FDG·January 22, 2013

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 14, 2014