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.

    CAP-AID (IMPROVED)

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    MODEL EL-1 W/ST MONITOR OPTION (ACRONYM = ELI/STM)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPORICIDIN BRAND DISINFECTANT SPRAY

    FDA 510(k)
    FDA Class 1 ·General Hospital

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    XLD 110V L.A. REF

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 30, 2014

    CORE UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011