BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    ADI SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SeaSpine Spacer System - Ventura™ NanoMetalene®

    FDA UDI
    Seaspine Orthopedics Corporation·10889981050269·Ventura NM Trial, 9mm x 28mm x 12mm

    ORTHOPACS

    FDA 510(k)
    FDA Class 2 ·Radiology

    Reprocessed Webster Duo-Decapolar Diagnostic EP Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HU-FRIEDY PERMA SHARP SUTURES

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code GAR·May 26, 2010

    FRESENIUS 2008K

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

    ACCU-CHEK MOBILE TEST STRIPS

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

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·January 29, 2013