BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    MITEK MICRO ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RHYTHMIA HDx Mapping System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SERVO-I VENTILATOR SYSTEM, MODEL 64 87 800 E407E; NAVA OPTION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RHYTHMIA HDX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 14, 2013

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 13, 2011