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

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    Filters Regulation: Us FDA ×

    T-Line Hernia Mesh

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

    LOUSEBUSTER

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DIGITAL COLOR DOPPLER ULTRASOUND IMAGAING SYSTEM; CONVEX / LINEAR PHASED ARRAY TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Radiology

    VSP SYSTEM

    FDA Adverse Event
    Injury ·3D SYSTEMS·Product code DZJ·December 18, 2020

    PAGEWRITER TC 20 CARDIOGRAPH

    FDA Adverse Event
    Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC·Product code DPS·May 17, 2021

    BREAS VIVO 60

    FDA Adverse Event
    Malfunction ·BREAS MEDICAL AB·Product code NOU·July 31, 2017

    SUNBEAM

    FDA Adverse Event
    Malfunction ·JARDEN CONSUMER SOLUTIONS, DBA SUNBEAM PRODUCTS·Product code IRT·October 7, 2008

    PROMUS ELEMENT ?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 27, 2013

    LEAD MODEL UNK

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·July 22, 2011

    BREAS VIVO 60

    FDA Adverse Event
    Malfunction ·BREAS MEDICAL AB·Product code NOU·September 15, 2015

    BREAS VIVO 60

    FDA Adverse Event
    Malfunction ·BREAS MEDICAL AB·Product code NOU·May 12, 2017

    BREAS VIVO 60

    FDA Adverse Event
    Malfunction ·BREAS MEDICAL AB·Product code NOU·May 12, 2017