BEUDAMED
    3 results · 28ms · 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 ×

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 14, 2014

    INTEGRIS ALLURA 15 12 (MONO)

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZI·November 22, 2010

    CERVSPINE-EXP-HEADSCR Ø4 SELF-TAP L14 TI

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KWQ·January 12, 2013