BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    DTX Studio Clinic 3.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    Sechrist Industries, Inc.

    FDA UDI
    SECHRIST INDUSTRIES, INC.·00899660002918·CABLE ASSY. RDMTR EXTERIOR

    SHINEMOUND ENTERPRISE, INC.

    FDA registration
    SHINEMOUND ENTERPRISE, INC.·2 products·🇺🇸 United States

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 3, 2024

    INTUITIVE SURGICAL ONSITE FOR DA VINCI SURGICAL SYSTEMS

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

    Spacelabs Lifescreen PRO Analyzer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VALIANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·February 9, 2015

    EEA 25MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·November 4, 2008

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FRN·August 17, 2011

    6000CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·July 5, 2013

    BD ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·February 7, 2018

    CAPTURE-R READY-SCREEN (3)

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·February 14, 2013