BEUDAMED
    4 results · 21ms · 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 ×

    C-SECTION PACK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code KDD·September 26, 2019

    AMS MONARC SLING SYSTEM

    FDA Adverse Event
    Death ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTN·June 11, 2014

    ZOOM

    FDA Adverse Event
    Malfunction ·EXTERNAL MANUFACTURER·Product code KRG·January 11, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·November 10, 2010