BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    CATHETER THORACIC, AXIOM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NIOX VERO

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    OLYMPUS XBF-UC180F-DT8 ULTRASONIC BRONCHOFIBERVIDEOSCOPE USED WITH ALOKA SSD-ALPHA 5/10 ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TAXUS¿ LIBERTÉ¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·October 3, 2012

    LENSX LASER SYSTEM

    FDA Adverse Event
    Injury ·ALCON - LENSX LASERS, INC.·Product code OOE·December 18, 2013

    GYNECARE MESH UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·May 14, 2015

    FREESTYLE AORTIC ROOT BIOPROSTHESIS

    FDA Adverse Event
    Death ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·August 29, 2023

    CONTEGRA

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·August 29, 2023