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

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    SKIN STAPLE REMOVER WITH SPONGE STERILE DISPOSABLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    JOBST Maternity

    FDA UDI
    BSN MEDICAL, INC.·04042809641738·OPAQUE MATERNITY 15-20 MM HG THIGH HIGH ZIG ZAG...

    Shoreline™ ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981177126·Modular Trial, 14 x 13 x 11mm, 7 Deg Lordosis

    BK-6010 CATHETER TUBE HOLDER

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

    OASIS WOUND MATRIX

    FDA 510(k)
    FDA Unclassified ·Unknown

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2014

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·October 8, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 7, 2012

    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