BEUDAMED
    7 results · 26ms · 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.

    IMX ESTRADIOL

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122376·K-WIRE - SINGLE TROCAR THREADED 1.6mm DIA x 230mm

    Guardian 1000

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BLEAS ESIRIUC ANAESTHSIA SYSTEM, MODELS 3000, 2000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PULSE-GENERATOR, PACEMAKER, EXTERNAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code DTE·February 9, 2013

    ONE TOUCH LANCING DEVICE

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·January 6, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014