BEUDAMED
    8 results · 22ms · 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 Regulation: Us FDA ×

    AIRCAST VENAFLOW ELITE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DUOFERTILITY

    FDA 510(k)
    FDA Unclassified ·Unknown

    BIOMERIX COMPOSITE SURGICAL MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VITEK MASS SPECTROMETER

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code PEX·October 12, 2017

    RENAISSANCE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC·Product code HAW·August 18, 2019

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·May 21, 2013

    ARCHITECT TOTAL T3

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code CDP·September 26, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 13, 2011