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

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    Filters FDA Adverse Event ×

    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