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

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    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·August 30, 2023

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·December 23, 2022

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 19, 2025

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111451539·BUCK HAMMER NEEDLE ONLY

    IMMULITE HIGH SENSITIVITY CRP, IMMULITE 2000 HIGH SENSITIVITY CRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    CLEARBLUE EASY EARLY RESULT PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·November 21, 2013

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·March 17, 2020

    VISX EXCIMER LASER

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA LLC·Product code LZS·November 5, 2010

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·August 20, 2013

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·October 30, 2013

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·April 11, 2013

    TORNIER

    FDA Adverse Event
    Malfunction ·TORNIER INC·Product code KWS·February 18, 2011

    CARPENTIER-MCCARTHY-ADAMS IMR ETLOGIX ANNUPLASTY RING

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code KRH·June 19, 2008

    IKAZUCHI ZERO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·June 13, 2019

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 19, 2019

    IKAZUCHI ZERO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 20, 2019

    KANEKA PTCA CATHETER CO-R7(IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 21, 2019

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·April 14, 2022