BEUDAMED
    7 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.

    V LANCE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    ENCORE TONGUE SUSPENSION SYSTEM ENCORE REMOVAL-TITRATION KIT

    FDA 510(k)
    FDA Class 2 ·Dental

    BONESOURCE HAC

    FDA 510(k)
    FDA Class 2 ·Neurology

    ADVIA CENTAUR XP HAV TOTAL (AHAVT)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code LOL·May 20, 2014

    PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·August 27, 2010

    MONOBLOCK INSERTER HANDLE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWA·April 11, 2021