BEUDAMED
    6 results · 26ms · 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.

    VTI OXYGEN ANALYZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AGILTRAC .035 PERIPHERAL DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GAITWAY IMPLANT SYSTEM, SURGICAL INSTRUMENT SET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INSYNC III MARQUIS

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NIK·December 13, 2010

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 9, 2014

    DURASTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·December 28, 2012