BEUDAMED
    10 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.

    PHASIX-HIGH FREQUENCY GENERATOR

    FDA 510(k)
    FDA Class 1 ·Radiology

    Optego

    FDA UDI
    Optego Vision USA Inc.·00360843010964·Roller-Shadz®, Charcoal, 100/bag, 6 bags with d...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704262124·

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776417598·Tessier Retromaxillary Chisel 16.5cm OL, 6mm Wi...

    CROWN REMOVER UNIVERSAL

    FDA UDI
    W.H. Holden, Inc.·D9288343060·

    HEMACAL

    FDA 510(k)
    FDA Class 2 ·Hematology

    HEARTRATE PLUS ECG CARDULE #1918

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VALIANT STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·November 15, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 28, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2015