BEUDAMED
    6 results · 27ms · 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 Regulation: Us FDA ×

    GED (GRADUATED ELECTRONIC DECELERATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    DENTORIUM CONVERTIBLE ACRYLIC

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNSTER CERVICAL CAGE, ALIF CAGE, PLIF CAGE, PTLIF CAGE, TLIF CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REPIPHYSIS LIMB SALVAGE SYSTEM

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY INC·Product code KRO·May 21, 2010

    TRANSVENOUS

    FDA Adverse Event
    Injury ·HISTORICAL PUERTO RICO·Product code NVN·January 11, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 3, 2014