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.
    Filters Regulation: Us FDA ×

    MODELS 4002/4102/4202 OXY. DELIVERY/CO2 CANNULA

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ULTRAZYME PLUS GAMMA-GT, #64959/65032

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DIGITAL AUDIOMETER/HEARING AID 3100

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

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 10, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 10, 2012

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 23, 2015

    Plastic Cannula Holdex Tube Holder, Item number: 450216. It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code FMI·August 5, 2008