BEUDAMED
    6 results · 18ms · 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.

    URESIL 150CC BELLOWS RESERVOIR

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

    SYRINGE DRIVER 209

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GYNECARE PROSIMA PELVIC FLOOR REPAIR SYSTEMS

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·June 10, 2014

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 11, 2010

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·December 10, 2012