BEUDAMED
    10 results · 25ms · 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.

    Q750 ELECTROCARDIOGRAPH

    FDA 510(k)

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517134844·Archon ACP Base, Tray

    TRUELOK EVO

    FDA UDI
    ORTHOFIX SRL·18052469471777·TRUELOK EVO NUT WITH WASHER STERILE

    Trial Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964094521·Trial Procedure Kit

    THROMBINEX BOVINE THROMBIN

    FDA 510(k)
    FDA Class 2 ·Hematology

    RATEMINDER III INFUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NA

    FDA UDI
    Zimmer, Inc.·00889024065116·

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 19, 2014

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·October 20, 2010

    HEARTMATE II LVAD

    FDA Adverse Event
    Death ·THORATEC CORP.·Product code DSQ·December 19, 2012