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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    EMIT DESIPRAMINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Screw, Cannulated,7.0x155mm, Full Thread

    FDA UDI
    Pioneer Surgical Technology, Inc.·00846468041397·7.0x155mm, Full Thread

    VISTA P VERTEBRAL BODY REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Origin Coxa Vara Hip Stem

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPRINT QUATTRO SECURE S

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

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·October 4, 2010

    PALINDROME EMERALD 23/40KIT VT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS KENDALL·Product code NYU·November 2, 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