BEUDAMED
    12 results · 27ms · Sources: EU EUDAMED, US FDA

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    GRAPHIC CONTROLS BIOTAC ECO ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Humelock II Reversible Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TURBT-RF ELECTRODES AND ELECTROSURGICAL DEVICES

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

    SIMON NITINOL FILTER

    FDA Adverse Event
    Injury ·NITINOL MEDICAL TECHNOLOGIES, INC.·Product code DTK·September 23, 1996

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    SROM*STM LG 36+8L 22X17X230N

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code JDI·February 8, 2013

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 6, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 22, 2014

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    HLS SET ADVANCED

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·March 31, 2021

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022