BEUDAMED
    7 results · 18ms · 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 ×

    STEINHAUSER TITANIUM MINI BONE PLATES & SCREWS

    FDA 510(k)
    FDA Class 2 ·Dental

    A.B. DENTAL DEVICES Dental Implants System

    FDA 510(k)
    FDA Class 2 ·Dental

    VENTED VIAL ADAPTER TRANSFER DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 10, 2014

    SIGMA 300 SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·October 8, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·December 10, 2012

    Fujifilm Medical Systems Duodenoscope, Model Numbers ED-200XU, ED-200XT, ED-250XT, ED-310XU, ED-420XL, ED-410XT, ED-410XU, ED-450XL, and ED-450XT. Medical endoscope for the duodenum and upper G.I. tract. Open elevator wire channel duodenoscopes.

    FDA Recall
    Terminated ·Fujifilm Medical Systems U.S.A., Inc.·Product code FDT·August 31, 2015