BEUDAMED
    6 results · 38ms · 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 ×

    MLX 300W XENON LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC.·Product code FCW·May 23, 2019

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Death ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·September 20, 2019

    SUNBEAM SERIES 001388-800 WARM MIST VAPORIZER

    FDA Adverse Event
    Injury ·JARDEN CONSUMER SOLUTIONS / SUNBEAM PRODUCTS, INC.·Product code KFZ·May 2, 2019

    2520274-2013-01435

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·March 13, 2013

    LIGACLIP*MCA MED APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDO·February 25, 2011

    NONE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·February 23, 2008