BEUDAMED
    8 results · 33ms · 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 ×

    MD 420/440/460/470/480/490

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

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993200·anteriors; shade B2; mould CS

    LIFE SPINE LUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    uMR Omega

    FDA 510(k)
    FDA Class 2 ·Radiology

    CONSULT HCG TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·March 4, 2025

    MULTI-LINK RX VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·March 7, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014