BEUDAMED
    13 results · 40ms · Sources: EU EUDAMED, US FDA

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    MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE

    FDA 510(k)
    FDA Class 2 ·Hematology

    FLOSCOPE MICRODOP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MRT 35-A (TM)

    FDA 510(k)
    FDA Class 2 ·Radiology

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·January 9, 2013

    PI CVC KIT: 4-L 8.5 FRN X 20 CM AGB

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code FOZ·February 25, 2014

    ENDOPATH** ETS FLEX45

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 6, 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