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.

    BIO MEDICUS BIO CONSOLE 540

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209128587·

    CLEANSE N BOND I

    FDA 510(k)
    FDA Class 2 ·Dental

    ENTity USB Videoscope System

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 6, 2014

    2.8 MM PITON KNOTLESS ANCHOR

    FDA Adverse Event
    Injury ·TORNIER INC·Product code MBI·November 28, 2012

    CONSTELLATION WITH LASER

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 2, 2010