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

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    DINAMAP VITAL SIGNS MONITOR #1846

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GN Otometrics A/S

    FDA UDI
    NATUS MANUFACTURING LIMITED·05713315003608·Silicone Eartip, 18 mm semi gray, mushroom

    SPIROPRO SPO2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACE -GT REAGENT; ACE LIPASE RAGENT; ACE T4 REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 25, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 5, 2012

    COLLEAGUE CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 10, 2010

    ELLIPSE DR, REF: CD2377-36QC Implantable cardioverter defibrillators (ICDs)

    FDA Enforcement
    Class I ·Terminated·St Jude Medical Inc.·August 14, 2019