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

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    ARTHREX CANNULATED INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KTP DISC KIT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TEETHMATE-F

    FDA 510(k)
    FDA Class 2 ·Dental

    AQURE

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code OUG·December 13, 2022

    TRILOGY 100

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

    HUDSON NEONATAL HEATED-WIRE CIRCUIT

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BZO·November 5, 2010

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·January 9, 2013

    RADIFOCUS GLIDECATH

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

    AQURE

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code OUG·August 29, 2022

    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