BEUDAMED
    25 results · 32ms · Sources: EU EUDAMED, US FDA

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    MASH DERMATOME

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Supplies

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746162954·SUPPLIES-IMPRESSA/SURE DISPENSER GUN

    Supplies

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746034879·SUPPLIES-IMPRESSA/SURE DISPENSER GUN

    Impressa/Sure

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746035050·SUPPLIES-IMPRESSA/SURE DISPENSER GUN

    ABX PENTRA 400 : CRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    St. Louis Band

    FDA 510(k)
    FDA Class 2 ·Neurology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 10, 2014

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 8, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 4, 2012

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 12, 2025

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 14, 2021

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 14, 2022

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 20, 2022

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 31, 2024

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 8, 2025

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 11, 2022

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·September 28, 2023

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·May 25, 2023

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·December 21, 2022

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 4, 2022