BEUDAMED
    7 results · 17ms · 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.

    EAR SPECULI

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Tranquil-L™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788221640·TLIF Trial 16x10x32

    MR VESSELLQ XPRESS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ZETA DIAGNOSTIC RETINAL IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·May 20, 2014

    PULSAR GENERATOR

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

    WALLFLEX ENTERAL DUODENAL STENT WITH ANCHOR LOCK DELIVERY SYSTEM, MOD M00565010

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code MUM·September 1, 2010