BEUDAMED
    21 results · 26ms · Sources: EU EUDAMED, US FDA

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    READS RF TEST KIT FOR IGM RHEUMATOID FACTOR

    FDA 510(k)
    FDA Class 2 ·Immunology

    Eclipse Kiss Zirconia

    FDA 510(k)
    FDA Class 2 ·Dental

    ULTRACLIP II WING AND ULTRACLIP II COIL

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

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 10, 2014

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 9, 2010

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·November 1, 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

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·September 1, 2022

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 7, 2025

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 16, 2022