BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    CHOLEDOCHOSCOPE/ENDOSCOPE MODIFICATION

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

    Ventura NanoMetalene System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981150631·Ventura NM Trial, 9mm x 20mm x 12mm

    PORTASCAN BLADDER SCANNER, MODEL PA00146

    FDA 510(k)
    FDA Class 2 ·Radiology

    C-JAWS CERVICAL COMPRESSIVE STAPLE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PORTASCAN

    FDA Adverse Event
    Malfunction ·MEDIWATCH UK LTD·Product code ITX·November 17, 2011

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 23, 2014

    ACCU-CHEK ® ACTIVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 21, 2010

    OMNILINK .018 STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIO·January 29, 2013