BEUDAMED
    8 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.

    SILKON TITANIUM CABLE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377072696·RELINE C Ti Rod, 4.0x300mm Straight

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111031·INSTRUMENT CADDY LARGE

    AMT INTRODUCER: MINI BUTTON DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Arrow GPSCath Balloon Dialation Catheter (150 cm)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CORE SUMEX DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·December 22, 2010

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 4, 2013

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 17, 2014