BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    AUSTIN ENDOLYMPH DISPERSMENT SHUNT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CONTOX DRUG SCREEN CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    USCI TEMP. ATRIO-VENTRICULAR ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COBAS 6000 C (501) MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 6, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 27, 2014

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Death ·ZOLL CIRCULATION, INC.·Product code DRM·November 6, 2012

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·September 13, 2010

    NIM 4.0 CONSOLE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code GWF·April 2, 2024