BEUDAMED
    6 results · 19ms · 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 ×

    ENSITE 3000 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Aloka Arietta 850

    FDA 510(k)
    FDA Class 2 ·Radiology

    NIHON KOHDEN CO2 SENSOR KIT, MODEL TG-970P

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·February 28, 2013

    MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·February 10, 2011

    OLYMPUS WM-NP2 WORKSTATION

    FDA Adverse Event
    Malfunction ·KEYMED (MEDICAL & INDUSTRIAL EQUIPMENT), LTD.·Product code FEM·July 7, 2014