BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    BIOTIS COLUMBIA SHEEP BLOOD AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981142995·Trial 20x15x9mm, 7 Deg Lordosis, w/Depth Stop

    Stainless Steel Wire

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746049743·WIRE SS POSTED 018 40MM FORM I 10/PK

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971833·

    HEMOHALT HEMOSTASIS PAD

    FDA 510(k)
    FDA Unclassified ·Unknown

    AOS Anterolateral Proximal Humeral Plate

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROTECTA XT CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·June 10, 2014

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·November 5, 2012

    HUDSON NEONATAL VENTILATOR CIRCUIT, HEATED-WIRE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BZO·September 27, 2010

    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