BEUDAMED
    9 results · 22ms · 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.

    ABCO SUCTION CANISTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SONTEC OPERATING LARYNGOSCOPE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896080331·SONTEC OPERATING LARYNGOSCOPE MEDIUM SIZE

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111019098·DITTEL SOUND STR 11.5" 16FR

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209105052·

    X-FORCE NEPHROSTOMY BALLOON DILATION CATHETER

    FDA 510(k)
    FDA Unclassified ·Unknown

    U2 Hip Stem, Ti Porous Coated, Matrix

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 5, 2014

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 4, 2010

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·November 29, 2012