BEUDAMED
    6 results · 35ms · 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.

    THE SIGNATURE SERIES, M IV

    FDA 510(k)
    FDA Class 2 ·Neurology

    INOGEN SATELLITE CONSERVER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FDI LEVEL I AND LEVEL II GLUCOSE CONTROLS FOR THE EMBRACE NO CODE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·July 22, 2015

    SENSOR¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code EZB·January 29, 2013

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 15, 2010