BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    CERVITRAC TRACTION FRAME & CORD

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    Suction Cannula

    FDA UDI
    KOROS U.S.A., INC.·10840199535184·Cooley-Madoff Adult Suction Cannula Small Tip 6...

    POLYFIT ABSORBING ANTIMICROBIAL DRESSINGS (OTC)

    FDA 510(k)
    FDA Unclassified ·Unknown

    LORENZ 1.5 X 4 MM LACTOSORB TAP FREE SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 30, 2014

    UNKNOWN RIGHT REJUVENATE/ABGII HIP

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·October 24, 2012

    EON - IPG

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·August 27, 2010

    MR 5300- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): (1) 782152 (2) 782110

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·May 3, 2024

    MR 5300- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): (1) 782152 (2) 782110

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·May 29, 2024