BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    KEYMED FIBERSCOPE AUTO DISINFECTOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    JOBST Maternity

    FDA UDI
    BSN MEDICAL, INC.·04042809642612·OPAQUE MATERNITY 20-30 MM HG THIGH HIGH ZIG ZAG...

    Stryker Universal Mesh

    FDA 510(k)
    FDA Class 2 ·Neurology

    FLOW MED 150

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 8, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HLTHCARE CORP·Product code FRN·January 13, 2014

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·November 8, 2012

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020

    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