BEUDAMED
    8 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    Anjon Bremer Halo System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SELECTCORE VARIABLE THROW BIOPSY DEVICE MODEL 991014, 991514, 991018, 991518, 992018

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

    SMITH & NEPHEW SMF HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BE PLUS LTM PLUG-IN HEADBOX, 64CH (193-256)

    FDA UDI
    EB NEURO SPA·08056446900130·64 channels (193-256) patient-interface for EE...

    I-STAT E3+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·March 31, 2020

    ZERO TIP RETRIEVAL BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FFL·October 7, 2008

    QUICKSITE LV

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code OJX·August 5, 2011

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 27, 2013