BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    MYOTEST - NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    P.F.C.

    FDA UDI
    DEPUY (IRELAND)·10603295215622·P.F.C. MODULAR PLUS TIBIAL HEMI WEDGE CEMENTED ...

    POLYPLEX STIMULATING CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    EnSite Velocity Surface Electrode Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·June 10, 2014

    XIA 3 TITANIUM R T R PARALLEL CONNECTOR TOP - SIDE

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code NKB·November 21, 2012

    QUANTUM? MAVERICK?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·June 22, 2015

    Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor 728332 - IQon Spectral CT : IQon Spectral CT

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·July 7, 2021

    OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

    FDA Enforcement
    Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012