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

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    Filters Regulation: Us FDA ×

    Intelli-C

    FDA 510(k)
    FDA Class 2 ·Radiology

    LUMINOS LOTUS MAX

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·March 5, 2025

    ORQIS EXTRACORPOREAL BLOOD PUMPING SYSTEM, MODEL BPS-100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SLEEPMINDER BREATHING FREQUENCY INDICATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LINEAR? ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·June 4, 2025

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Death ·MEDTRONIC MINIMED·Product code OYC·October 15, 2014

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·June 17, 2013

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 23, 2011