BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    XRT 400

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERTEX® Reconstruction System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074239217·BONE SCREW 6955414 4.0 X 14MM CORTICAL

    Zuma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981096755·Rasp, 32mm x 25mm x 14mm, 8 Deg

    TERUMO ANGIOGTAPHIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MANGAR BOOSTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 11, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 10, 2011

    FOOT CONTROL

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 13, 2013

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 14, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 3, 2024

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·January 24, 2023

    RADIFOCUS ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·September 26, 2018