BEUDAMED
    6 results · 16ms · 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.

    SPECIFIC ALLERGEN MODULES FOR ALASTAT(TM) IGE SYS.

    FDA 510(k)
    FDA Class 2 ·Immunology

    ANYRAY PORTABLE X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ROCCIA® PLIF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·June 18, 2014

    PROFEMUR Z

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGIES·Product code LPH·October 20, 2010

    SILVERHAWK PLAQUE EXCISION SYSTEM

    FDA Adverse Event
    Injury ·EV3 INC.·Product code MCW·December 20, 2012