BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

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    AGC UNICOMPARTMENTAL KNEE PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    E.W.L. P-TENS MODEL(TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Merit Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code KNT·April 17, 2020

    FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM

    FDA Adverse Event
    Malfunction ·FLEXIBLE STENTING SOLUTIONS·Product code FGE·June 15, 2014

    EXETER FEMORAL STEM +2 HDP CENTRALISERS SMALL CD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code JDI·October 12, 2010

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code LZH·November 14, 2012

    SmartPath to dStream for 1.5T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models: 781260

    FDA Enforcement
    Class II ·Completed·Philips North America Llc·September 15, 2021