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

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    MODIFICATION TO CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983023·posteriors; shade A3; size S; lower jaw

    xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND

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

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 28, 2013

    SYNERGY

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 4, 2011

    TI LCP(TM) DISTAL FEMUR PLATE 9 HOLES/236MM-RIGHT

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code HRS·August 6, 2014