BEUDAMED
    8 results · 41ms · 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.

    WINDSOR MEDICAL MODEL 52

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TiBase

    FDA UDI
    SIRONA Dental Systems GmbH·E27668326410·TiBase AT EV 4.2 GH3 L

    MODIFIED TREVO PROVUE RETRIEVER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO: THE MARGRON HIP REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MARGRON STEM (K032641)

    FDA Adverse Event
    Injury ·PORTLAND ORTHOPAEDICS PTY LTD·Product code KWY·May 31, 2005

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·November 14, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 27, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PR·Product code LWS·June 10, 2015