BEUDAMED
    7 results · 18ms · 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.

    UNIVERSAL EXAMINATION TABLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    AZIDE AGAR W/5% SHEEP BLOOD

    FDA 510(k)
    FDA Class 1 ·Microbiology

    VENTILATOR PRESSURE ALARM MODEL VPA-100

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 2, 2014

    FLEXTEND

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·October 19, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012

    POLYETHYLENE INLAY W/TANTALUM MARKER/LARGE-10MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·July 25, 2016