BEUDAMED
    6 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.

    CANON AUTOREF R-10

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NEXUS INTRAVENOUS TUBING SETS (NIVTS)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HILTHERA 4.0

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 30, 2014

    FLEXCATH STEERABLE SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·November 21, 2012

    ACTIVA PC

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·September 21, 2010