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 ×

    LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Legacy™4 Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307103301·4.2mmD x 8mmL, 3.5mmD Platform

    COLLOID OSMOMETER 4400

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    THE BODYLOG 500 RET THERAPEUTIC ELECTROMYOGRAPHICS

    FDA 510(k)
    FDA Class 2 ·Neurology

    WALRUS EXTENSION SET COMPONENT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code FPA·June 11, 2010

    ARCHITECT CA 19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code NIG·December 21, 2012

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 19, 2014