BEUDAMED
    7 results · 17ms · 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.

    IDENTI-CLAMPS

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

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517499530·Archon Screw, Ø4.0x21mm SD Fixed

    MEDICAL OSCILLOSCOPE MEMORY SCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MONITORS, REMOTE, RMS III

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·April 22, 2014

    FINELINE II

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·October 10, 2012

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·May 19, 2015