BEUDAMED
    7 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 ×

    NovoGen Wound Matrix

    FDA 510(k)
    FDA Unclassified ·Unknown

    Brio Device, LLC

    FDA UDI
    SUMMIT MEDICAL PRODUCTS, INC.·00857595005787·Thumb-controlled Articulating Intubation Stylet...

    4CIS SARA Spine System, 4CIS VERTU Spine System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SCENARIA View

    FDA 510(k)
    FDA Class 2 ·Radiology

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 3, 2014

    RESIDENT BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·July 18, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013