BEUDAMED
    8 results · 20ms · 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.

    COOPER LASER SONICS CUSA MODEL 200

    FDA 510(k)
    FDA Unclassified ·Unknown

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209116041·

    DESILET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Capiox Advance Hardshell Reservoir

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MALLINCKRODT

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code BTS·April 2, 2014

    ENDOPATH** XCEL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·October 5, 2010

    ANEURX STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·November 30, 2012

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015