BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    KUBTEC X250

    FDA 510(k)
    FDA Class 2 ·Radiology

    VITAL SIGNS MONITOR MODEL M3B

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COMPEL SURGICAL GOWNS

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

    MUSTANG?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·September 24, 2025

    BD ULTRA FINE PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·January 27, 2020

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 27, 2011

    MUSTANG

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·May 2, 2025

    Retractor f/Sciatic Nerve; Part number: 03.100.013; UDI: 10886982070623

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·May 16, 2018