BEUDAMED
    6 results · 20ms · 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 ×

    PORTABLE OXYGEN GENERATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BIOCHEM TEMPERATURE/ FIO2 MODULE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MANHANDLER

    FDA 510(k)
    FDA Class 1 ·General Hospital

    THERAKOS XTS SYSTEM

    FDA Adverse Event
    Malfunction ·THERAKOS, INC.·Product code LNR·May 28, 2014

    EMAX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·January 9, 2013

    MEDTRONIC IMPLANT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·November 3, 2010