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

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    DUPEL IONTOPHORESIS DEVICE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BROWNE MEDICAL SYSTEMS IMAGEPRO

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RUBELLA VIRUS IMMUNOLOGICAL TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    840 VENTILATOR

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

    CVC SET: 3-LUMEN 4FR X 13CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code DQY·February 25, 2014

    HEARTSTRING III PROXIMAL SEAL SYSTEM, 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC.·Product code DXC·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