BEUDAMED
    115 results · 22ms · Sources: EU EUDAMED, US FDA

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    MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111086·INSTRUMENT CASE LARGE ALUMINUM

    ATAC PAK CREATININE REAGENT AND ATAC CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CELLULAZE LASER

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

    RADIFOCUS GLIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·January 22, 2013

    MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·December 13, 2010

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code KGE·April 4, 2017

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·December 29, 2025

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·May 16, 2024

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 21, 2021

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 6, 2025

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·September 15, 2023

    GUIDE WIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 25, 2025

    RADIFOCUS GUIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·December 5, 2023

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 3, 2018

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 23, 2026

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 11, 2026

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 12, 2021