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

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    Filters Regulation: Us FDA ×

    Instrument kits

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MONACO RTP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    LOUTREX TOPICAL CREAM

    FDA 510(k)
    FDA Unclassified ·Unknown

    CONTOUR® PLUS

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code NBW·February 20, 2025

    BD RAPID DETECTION OF SARS-COV-2 VERITOR¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·November 17, 2021

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 1, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 10, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 5, 2008

    3007566237-2016-01605

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MFR·April 6, 2016