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 ×

    Solitaire Platinum Revascularization Device, Solitaire X Revascularization Device (Solitaire Revascularization Device)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Reveal

    FDA UDI
    Oticon A/S·05707131342904·G20, MINIRITE T 312 2.4G C063 REVEAL

    RUBBER-LIKE POWDER FREE VINYL PATIENT EXAMINATION GLOVES, WHITE COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MIM 5.2 (BRACHY)

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2024

    S-ICD SYSTEM

    FDA Adverse Event
    Injury ·CAMERON HEALTH·Product code LWS·October 16, 2014

    MULTI-LINK RX VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·August 5, 2011

    APEX HIP SYSTEM

    FDA Adverse Event
    Injury ·OMNILIFE SCIENCE, INC.·Product code LPH·June 25, 2013