BEUDAMED
    10 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·June 4, 2014

    HCG COMBO DEVICE SP BRAND RAPID TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·January 9, 2013

    REPLY

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA C.R.M., S.R.L.·Product code NVZ·November 4, 2010

    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